INVENTORS: Krzysztof Matyjaszewski, Nicola Bortolamei, and Andrew Magcnau

CROSS REFERENCE TO RELATED APPLICATIONS

This application claims priority to U.S. provisional applications 61/459,724 filed on 12/17/2010 and provisional application 61/574,890 filed on 8/1 1/11 each entitled Elcctrochemically Mediated ATRP each of which is entirely incorporated herein by reference as if fully set forth herein.

TECHNICAL FIELD OF THE INVENTION

An atom or group transfer polymerization process where the ratio of the activator and deactivator oxidation states of the catalyst complex in the reaction medium is dictated and continuously balanced by electrochemistry. The rate of polymerization can be controlled tlirough the magnitude of the applied potential, current, or total charge passed to the system. The polymerization can be switched "on" and "off at will to control the temperature of the reaction medium.

BACKGROUND OF THE INVENTION

Since their discovery, controlled radical polymerization (CRP) processes have gained increasing attention because CRP couples the advantages afforded by conventional free radical polymerization (RP), to (co)polymerize a wide range of monomers using various commercially viable processes, with the ability to synthesize polymeric materials with predetermined molecular weight (MW), low polydispersity (M _w /M^), controlled composition, site specific incorporated predetermined functionality, selected chain topology and the ability to incorporate bioresponsive or inorganic species into the final product.

Atom transfer radical polymerization (ATRP) is considered to be one of the most successful

CRP processes with significant commercial potential for production of many specialty materials including coatings, sealants, adhesives, dispersants in addition to materials for health and beauty products, electronics and biomedical applications. The process, catalysts, including transition metals and ligands, range of polymerizable monomers and materials prepared by the process have been thoroughly described in a series of co-assigned U.S Patents and Applications including U.S. Patent Nos. 5,763,548; 5,807,937; 5,789,487; 5,945,491 ; 6,1 1 1 ,022; 6,121,371 ; 6,124,41 1 ; 6,162,882; 6,407,187; 6,512,060; 6,538,0 1 ; 6,541 ,580; 6,624,262; 6,624,263; 6,627,314; 6,759,491; 6,790,919; 6,887,962; 7,019,082; 7,049,373; 7,064,166; 7,125,938; 7,157,530; 7,332,550; 7,572,874; 7,678,869; 7,795,355; 7,825,199; 7,893, 173; 7,893,174 and U.S. Patent Applications 10/548,354;

1 1/990,836;12/31 1 ,673; 12/451 ,581 ; 12/921 ,296; 12/877,589; 12/949,466 and 13/026,919 the disclosures of all of which are herein incorporated by reference. These prior art patents and applications describe the range of (co)polymerizable monomers in addition to the topology, architecture and site specific functionality attainable in copolymers prepared by ATRP in addition to detailing a range of composite structures that can be prepared by "grafting from" or "grafting to" a broad range of organic or inorganic materials.

ATRP has also been discussed in numerous publications with Matyjaszewski as co-author and reviewed in several book chapters. [Matyjaszewski, K. et al. ACS Symp. Ser. 1998, 685, 258-283; ACS Symp. Ser. 1998, 713, 96-1 12; ACS Symp. Ser. 2000, 729, 270-283; ACS Symp. Ser. 2000, 765, 52-71; ACS Symp. Ser. 2000, 768, 2-26; ACS Symposium Series 2003, 854, 2-9; ACS Symp. Ser. 2009, 1023, 3-13 and Chem. Rev. 2001, 101, 2921-2990.] These publications are incorporated by reference to provide information on the range of suitable transition metals that can participate in the redox reaction and suitable ligands for the different transition metals to form transition metal complexes suitable for polymerizing broad range of exemplified polymcrizable (co)monomers. The generally accepted mechanism of an ATRP reaction is shown in Scheme 1.

P— X + _t ⁿ /Ligand -— '— P* - ⁺ X- , ⁿ⁺¹ /Ligand kp p -p _m

Scheme 1. General mechanism for the ATRP process

Any transition metal complex ( "/L) capable of maintaining the dynamic equilibrium through participation in a redox reaction comprising the transferable atom or group present on each initiator or dormant polymer chain (P _n -X) to form an active radical (P„") and higher oxidation state transition metal complex (X-M "* ¹ /L) that acts as the deactivator, may be used as the catalyst in ATRP. The creation and maintenance of a low concentration of active species, (P _n ^* ) _» reduces the probability of bimolecular termination reactions, (lc,), which leads to a radical polymerization process that behaves as a "living" system through retention of the stable transferable atom or group (-X) on the vast majority of growing dormant chain ends. The most frequently used ATRP procedure is based on a simple reversible halogen atom transfer catalyzed by redox active transition metal compounds, most frequently copper or iron, that form a catalyst complex with a ligand that modifies solubility and activity of the catalyst, most frequently nitrogen based ligands. The simple procedure may be carried out in bulk, in the presence of organic solvents or in water, under homogeneous or heterogeneous conditions, in ionic liquids, and in supercritical CO _: .

Early ATRP procedures required addition of a sufficiently high concentration of the transition metal complex to overcome the effect of unavoidable increased concentration of the deactivator in the reaction medium while still driving the reaction to the desired degree of polymerization in a reasonable time frame while retaining chain end functionality. Recently a novel approach that allowed a significant reduction in the concentration of added catalyst was developed. [PCTInt. Appl. WO 2005/087819; Camegie Mellon University, 2005; 96 pp.] The driving force was the economic penalty associated with purification procedures coupled with a deeper understanding of the ATRP rate law (Equation 1 , using Cu ¹ as the catalyst metal) which shows that Rp, the polymerization rate, depends only on the ratio of the concentration of [Cu ¹ ] to [X-Cu ¹¹ ], and does NOT depend on the absolute concentration of the copper complexes (Equation 1). Therefore in principle, one could reduce the absolute amount of copper complex to ppm levels without affecting the polymerization rate.

[Cu ¹ ]

R _p = yM][p-] = ,[ K _f .[i] ₀

[X-Cu ¹¹ ]

However, a balance had to be reached between the formed activator species (i.e. Cu'/L, where

L=ligand) and a residual amount of deactivating species (i.e. X-Cu L) which is required for a well- controlled polymerization since both, molecular weight distribution and initial molecular weight, depend on the ratio of the propagation and deactivation rate constants and the concentration of deactivator, formula (2).

This means, for example, that in order to obtain polystyrene with M M _a = -1.2, when targeting a DP-200 and 90% conversion at -100 °C, the actual amount of X-Cu" species required to conduct a controlled reaction is -2 ppm (k _p -10 ³ NT's ^'1 and k^-lO ⁷ M 's ^'1 ), meaning that the concentration of the X-Cu" species could be reduced over 1,000 times from the level typically used in the earlier ATRP polymerization protocols. Unfortunately, if the amount of Cu ¹ is reduced 1 ,000 fold, unavoidable radical-radical termination reactions irreversibly consume the activators present in the reaction media as the polymerization progresses and the reaction slows down or stops; i.e. if -10% of chains terminate and the amount of Cu ¹ initially added to the system was below 10 mole% of the initiator, all Cu ¹ would be consumed by termination. It was recognized that this situation could be overcome if there was constant regeneration of the Cu ¹ activator species by environmentally acceptable organic or inorganic reducing agents to compensate for any loss of Cu ¹ by termination, Scheme 2. Ligand

Scheme 2: Use of reducing agents to continuously reactivate the fraction of deactivator formed by termination reactions. This procedure was named Activator ReGenerated by Electron Transfer (ARGET) ATRP [Macromnlecules 2006, 39, 39-45.] and it was possible to use a range of reducing agents; e.g. tin"-2- ethylhexanoate, ascorbic acid, glucose, amines, excess ligand, and Cu° etc. for ARGET or a source of free radicals, such as AIBN, for Initiators for Continuous Activator Regeneration (ICAR) to constantly regenerate the ATRP activator, exemplified by a Cu ¹ species, from the deactivator, the Cu" species in Scheme 2, formed during termination processes.

The electrochemical mediated ATRP procedure disclosed herein overcomes the limitations of ARGET and ICAR ATRP in that no undesirable byproducts are formed and a ratio of Cu'L:Cu"L can be selected and retained or adjusted throughout the polymerization.

Cyclic voltammetry (CV) has been used for over a decade as an analytical tool to study the redox behavior of numerous transition metal complexes used in an ATRP. One of the earliest studies, [Qiu, }., et al., Macromol. Chem. Phys. 2000, 201, 1625-1631.] determined that the half-sum of the oxidation and reduction peak, the Em value, strongly depends on the nature of the ligand and the halogen and the measured value provided an estimate for the activity of the catalyst complex (CU'L CU ^U L redox couple) in an ATRP, and that this value strongly depends on the nature of the ligand (L) and the halogen. The general trend agreed with the kinetic features of ATRP catalyzed by the corresponding transition metal complex, and a correlation between the measured redox potential and the apparent equilibrium constant of ATRP was observed. The more negative the redox potential of the complex, as measured by CV, the faster the polymerization indicating that, in most cases, the catalytic activity of the transition metal complexes in an ATRP can be predicted from the redox potential of the transition metal complex. Two more recent studies by the primary author, K.

Matyjaszewski, on a broader spectrum of transition metal/1 igand complexes in a number of different solvents confirmed the conclusion that excellent correlation existed between the equilibrium constants with the Cu'VCu' redox potential and the carbon-halogen bond dissociation energies. [Matyjaszewski; et al. Macromole des 2007, 40, 8576-8585 and J. Am. Chem. Soc. 2008, 130, 10702-10713.]

This analytic tool, CV analysis, was used extensively to provide information on the expected properties of the transition metal complex in an ATRP. [Bortolamei, N., et al., Macromolecules, 2010: 43, 9257-67 and Electrochim. Acta, 2010, 55(27): 8312-8318.] CV analysis had always been carried out in the absence of monomer and in the absence of initiator. However, there is a recent paper, by one of the authors of the initial CV paper, (C. Amatore) where the notion of utilizing an electrochemical technique to produce an electrogenerated Fe"Salen complex providing activation of alkyl- and benzyl halide initiators as the initial step of an atom transfer radical addition (ATRA) reaction. [J.

Electroanal. Chem. 2009, 633, 99-105] CV's conducted in the absence and presence of an ATRP initiator showed that reductive cleavage of the R-X bond occurred on the timescale of the CV measurement but suggested that it does not lead to a classical redox-catalysis framework.

Additionally, it was noted that addition of a monomer adversely affected the voltammogram of the studied iron complex. Attempts to polymerize styrene at 110 °C, a temperature at which self initiated polymerization occurs, in the presence of a Fe Salen complex formed by electrolysis resulted in the formation of low molecular weight oligomers with broad polydispersity over a three hour period (MW 1868, M JM„ 1.768). Furthermore, the paper indicates that multiple transition metal/ligand/initiator species were involved in the reaction and determined that activation of alkyl halides by an electrogenerated Fe"Salen complex did not proceed along the redox mediated process usually invoiced in an ATRP and the results presented showed no evidence of the development of a CRP process. These results would teach against using electrochemistry to improve the degree of control an ATRP.

In US201 1/034625A1 the concept of using electrochemically produced free radicals for the initiation of a standard free radical polymerization is considered. The procedure focuses on direct formation of free radicals, substantially hydroxyl radicals, on the basis of electrolysis at anodic electrode surfaces [see paragraphs 0015 and 0019]. While indicating that the procedure could be employed to initiate a CRP this reference provides no evidence of a methodology which would allow manipulation of a redox-active species via electrochemical methods to subsequently control a CRP procedure.

There are no reports in the decade since the first report using cyclic voltammetry as an analytical tool to measure the redox potential of a transition metal complex to determine if electrochemistry could be used to mediate an ATRP. The notion of utilizing an electrochemical technique (i.e. electrolysis) to modulate polymerization kinetics has never been reported. BRIEF DESCRIPTION OF THE INVENTION

Disclosed herein in one embodiment of the invention is an atom or group transfer polymerization process where the ratio of the activator and deactivator oxidation states of the catalyst complex in the reaction medium is continuously balanced, adjusted, controlled, or dictated and maintained by electrochemistry.

According to one embodiment, the present disclosure provides for a polymerization process, comprising: polymerizing free radically (co)polymerizable monomers in the presence of a polymerization medium. The polymerization medium initially comprises at least one transition metal catalyst that can participate in a redox reaction, and an initiator comprising one or more redox transferable atoms or groups, wherein the molar ratio of the oxidation states of the transition metal catalyst are adjusted, controlled, and/or maintained by electrochemistry. The electrochemistry may include adjusting, controlling and/or maintaining one or more of an applied voltage, a current, and a charge passed through the polymerization medium.

In another embodiment of the invention his novel procedure was also applied to aqueous based ATRP, both homogenous and heterogeneous systems. DESCRIPTION OF EMBODIMENTS OF THE INVENTION The following figures illustrate that procedures were developed for controlled

electrochemically mediated ATRP, ("eATRP").

Figure 1 : Schematic of an electrochemical cell listing some of the electrical variables and electrolyte variables targeting an ATRP reaction with a copper catalyst.

Figure 2: Schematic of electrolysis cell configured with a platinum mesh working and counter electrode used in certain eATRP experiments.

Figure 3: Results of conducting cyclic voltammetry (CV) on (A) a solution of MeCN/MA solvent/monomer and (B) a solution of Cu ^u Br2 in MeCN/MA.

Figure 4: Cyclic voltametry of a solution of MeCN/MA Me ₆ TREN/Cu"Br2, in the absence

(black curve), and in the presence of EBP (grey curve), an ATRP initiator.

Figure 5: GPC traces of polymers formed at different conversions during electrochemical mediated ATRP of MA with different applied voltages; (A) E = -0.637 and (B) E = -0.665 V

Figure 6: Illustration of how the polymerization of methyl acrylate can be "switched on" and "switched off" by changing the E(V) between two electrodes.

Figure 7: Increase in molecular weight and change in M,JM _n with conversion during the intermittent polymerization illustrated in Figure 6.

Figure 8: Total charged (Q) and current (I) as a function of time, Exp.2 - E = -0.637

Figure 9: Cyclic voltammetry of Cu"Br ₂ /TPMA and various initiators. In each system the [M] = 4.67 M and [TBAPF ₆ ] = 0.2 M. Molar ratios = [M]:[I]:[Cu"BR ₂ /L] = 300: 1 :0.2.

Figure 10: Cyclic voltammetry of 1 mM Cu"Me ₆ TREN in the absence and presence of different MBrP], recorded at v = 0.05 V/s on Pt, in AN MA 1 :1 + 0.1 M Et NBF ₄ .

Figure 11: Cyclic voltammetry of 1 m M Cu"Me ₆ TREN in the absence (a) and presence (b) of lmM Et _t NBr, recorded at v = 0.05 V/s on Pt, in 0.1 M Et NBF + 0.1 M Et NBF ₄ .

Figure 12: cyclic voltammetry of Cu"Br TPMA and ferrocene.

Figure 13: Current versus time and cyclic voltammetry conducted periodically during polymerization. Polymerization conditions: [MMA] = 4.5 M, [MMA]:[EBPA]:rTPMA]:[Cu"] = 300:1 :0.1 :0.1 , T = 50 °C.

Figure 14: Position of E _¼ , E. _½ and E _¾ applied potentials in optimization series of experiments for MMA showing the exemplary CV of the Cu'/Cu" couple.

Figure 15: (A) Current profile for polymerization of MMA using EBPA showing occurrence of _p after a certain amount of time, exemplary for reaction 16.4. (B) Comparative current profile for polymerization of BA with EBiB initiator under similar conditions.

Figure 16: (A) Cyclic voltammetry of Cu'Trf L (black), Cu"Br/L (gray), and Cu"Br/L with EBiB (dashed) and (B) Current and Coulombs versus time plot.

ΓΒΑ]/[ΕΒϊΒ]/ΓΤΡΜΑ]/[Ου"ΤΓ¾]/[ΤΡΜΑ]/ΓΓ ΒΑΒΓ] = 300/1/0.03/0.03/0.03, [BA] = 3.87 M (43 (v/v) % in DMSO:Anisole), [TBAC10 ₄ ] 0.2 M, T = 40-45 °C. Figure 17: (A) Cyclic voltammetry of Cu"Br L (black), Cu ^M Br/L + EBiB (dash), and Cu"Rr/L + EBiB + convection (gray). (B) First order kinetics versus time plot as a function of E _3pp .

Figure 18: (A) Cyclic voltammetry of PnBA-Br macroinitiator. (B) Plot of mmol electrolyzed (JV) and current (I) versus time. Starting conditions: [PnBA] = 0.02 M, [PnBA]:[DVB]:[TPMA]:[Cu"] = 1 : 12:0.2:0.1, T = 90 °C.

Figure 1 . CV of 1 mM Cu"L ^2f in H,0/OEOMA475 (9/1, v/v) + 0.1 M Et ₄ NBF ₄ recorded at v = 0.1 V/s in the absence (— ) and presence (black solid) of 1 mM HEBriB; the three dots on the CV indicate the E _m values used in the polymerization experiments.

Figure 20: Cyclic voltammetry of 1 mM Cu"L ²⁺ in the absence (a) and presence of 1 mM HEBriB (b) or 2 mM HEBriB (c), recorded at 0.1 V/s in H ₂ 0 + 0.1 M Et ₄ NBF ₄ .

Figure 21. First-order kinetic plots for electrochemical ATRP of OEOMA475 in H ₂ 0 + 0.1 M Et ₄ BF ₄ at E _3?J> = -0.21 V vs SCE. Conditions: [Cu"L ²⁺ ] = 0.1 mM; [OEOMA]/[RX] = 1000 (·), 500 (Y), 200 (A).

Figure 22. CV of miniemulsions at a range of scan rates of Cu" BPMODA and after the addition of Cu"/TPMA at 0.5 V/s.

Figure 23: CV of miniemulsions (A) formulated without Cu"/BPMODA or EBiB, and (B) with and without copper for TPMA. CVs conducted at a scan rate of 0.05 V/s using a glassy carbon electrode.

Figure 24: (A) Current versus time profile for electrolysis (E _app = E _p - 80 mV) and (B) Potential versus time at two / _apps .

Figure 25: (A) First order kinetics versus time plot as a function of an applied C or / and (B) Molecular weight and MJM _a versus time plot for eATRP of B A in DMF.

Figure 26: Cyclic voltammetry of Cu"Br TPMA.

Figure 27: (A) Conversion versus time plot as a function of applied potential. (B) Molecular weight and MJM _a versus time plot for eATRP of BA in DMF.

DETAILED DESCRIPTION

The present disclosure provides for a new radical polymerization process, such as a controlled radical polymerization process. The polymerization process described herein may includes polymerizing free radically (co)polymerizable monomers in the presence of a polymerization medium initially comprising at least one transition metal catalyst that can participate in a redox reaction, and an initiator comprising one or more redox transferable atoms or groups, wherein the molar ratio of the oxidation states of the transition metal catalyst are adjusted, controlled, and/or maintained by electrochemistry. Examples of polymerization processes that are suited to the present process include, for example, atom transfer radical polymerization processes.

Here, and elsewhere in the text the word "control" and/or "controlled", when used in reference to a "controlled" polymerization process means that in the polymerization process conditions are defined whereby the contributions of the chain breaking processes are insignificant compared to chain propagation, so that polymers with predetermined molecular weights, low polydispersity and high site specific functionalities are achievable. Examples of a controlled polymerization processes described herein include controlled radical polymerization (CRP) processes, such as atom or group transfer radical polymerization (ATRP) processes.

As used herein, "polymer" refers to a macromolecule formed by the chemical union of monomers, typically five or more monomers units. The term polymer includes homopolymers and copolymers; including random copolymers, statistical copolymers, alternating copolymers, gradient copolymers, periodic copolymers, telechelic polymers and polymers of any topology including linear polymers, block copolymers, graft polymers, star polymers, bottle-brush copolymers, comb polymers, branched or hyperbranched polymers, and such polymers tethered to particle surfaces or flat surfaces as well as other natural or synthetic polymer structures.

It must be noted that, as used in this specification and the appended claims, the singular forms "a," "and", and "the" include plural referents unless the context clearly dictates otherwise. Thus, for example, reference to "a polymer" includes more than one polymer.

Unless otherwise indicated, all numbers expressing quantities of ingredients, time, temperatures, and so forth used in the present specification and claims are to be understood as being modified in all instances by the term "about." Accordingly, unless indicated to the contrary, the numerical parameters set forth in the following specification and claims are approximations that may vary depending upon the desired properties sought to be obtained by the present invention. At the very least, and not as an attempt to limit the application of the doctrine of equivalents to the scope of the claims, each numerical parameter should at least be construed in light of the number of reported significant digits and by applying ordinary rounding techniques. Notwithstanding that the numerical ranges and parameters setting forth the broad scope of the invention are approximations, the numerical values set forth in the specific examples are reported as precisely as possible. Any numerical value, however, may inherently contain certain errors necessarily resulting from the standard deviation found in their respective testing measurements.

It is to be understood that this invention is not limited to specific compositions, components or process steps disclosed herein, as such may vary. It is also to be understood that the terminology used herein is for the purpose of describing particular embodiments only, and is not intended to be limiting. Any patent, publication, or other disclosure material identified herein is incorporated by reference into this specification in its entirety unless otherwise indicated, but only to the extent that the incorporated material does not conflict with existing definitions, statements, or other disclosure material expressly set forth in this specification. As such, and to the extent necessary, the express disclosure as set forth in this specification supersedes any conflicting material incorporated by reference herein. Any material, or portion thereof, that is said to be incorporated by reference into this specification, but which conflicts with existing definitions, statements, or other disclosure material set forth herein, is only incorporated to the extent that no conflict arises between that incorporated material and the existing disclosure material. Applicant reserves the right to amend this specification to expressly recite any subject matter, or portion thereof, incorporated by reference herein.

According to one embodiment, the present disclosure provides a polymerization process comprising polymerizing free radically (co)polymerizablc monomers in the presence of a polymerization medium initially comprising at least one transition metal catalyst that can participate in a redox reaction and an initiator comprising one or more redox transferable atoms or groups, wherein the molar ratio of the oxidation states of the transition metal catalyst are adjusted, controlled and/or maintained by electrochemistry, such as by applying or changing one or more of an applied voltage, a current, and a charge passed through the polymerization system. Examples of polymerization processes include controlled radical polymerization processes, such as atom transfer radical polymerization (ATRP) processes. General conditions and components for ATRP processes and other controlled radical polymerization processes are known in the art, as shown by the references cited and incorporated by reference herein. For example, examples of transition metal catalysts, radically (co)polymerizable monomers, and initiators comprising one or more redox transferable atoms or groups are described in detail in the references cited and incorporated herein. Suitable transition metal catalysts include transition metals and complexes of transition metals with various ligands, including those transition metal catalyst complexes and ligands shown to be effective in the art for ATRP processes. In certain embodiments, the transition metal catalyst may comprise two different transition metals.

Embodiments of the controlled polymerization processes described herein may be designed so that the polymerization may take place in an electrolysis apparatus comprising at least a cathode and an anode. Non-limiting examples of electrolysis apparatuses are shown in Figures 1 and 2. According to these embodiments, the polymerization process may be controlled by the electrolysis apparatus, for example, by applying or changing one or more of an applied voltage, a current, and a charge passed through the polymerization medium. The electrolysis or electrochemical process may be selected so to control or maintain the ratio of the oxidation states of the transition metal catalyst, such as by providing a concentration for each oxidation state of the transition metal catalyst that is greater than or equal to 0.1% based on the total transition metal added in the polymerization medium.

In specific embodiments, the molar ratio of two oxidation states of the transition metal catalyst at a specific time during the polymerization process may be determined by one or more of the applied voltage, the current, and the total charge passed through the polymerization medium and the current values. For example, in a copper transition metal catalyst based system, the electrolysis may be selected to maintain the concentration of the Cu' and/or Cu" oxidation states of the transition metal catalyst at greater than or equal to 0.1 % by weight based on the total concentration of Cu added to the polymerization medium. According to these embodiments, the rate of the polymerization may be controlled through the magnitude of one or more of the applied voltage, current and charged passed that is applied to the system.

Initial examples of the disclosed electrochemically mediated ATRP (eATRP) process employ a single catalyst complex, Cu/Me ₆ TREN, which is used as an exemplary active transition metal catalyst system in Ihe following discussion but this in no manner limits the utility of the disclosed procedure to the exemplary catalyst. Any transition metal catalyst or transition metal catalyst complex that has been shown, or will be shown, to control an ATRP can be used in the disclosed procedure.

The specific materials selected for the preparation of electrodes used in this disclosure are exemplary materials and should not limit the choice of electrode materials in any manner nor the materials or design of the cell for either batch or continuous electrochemical mediation of the polymerization. One requirement of the disclosed eATRP procedure is that the selected

current potential is applied to a reaction medium that contains all, or precursors of all, reagents required for the polymerization and maintained for a time frame which exceeds a standard CV analysis ^■ of a potential ATRP catalyst complex. Appropriate current/potential values can be selected based upon the standard redox couple (E _x/2 ) determined for the reaction medium including catalyst, monomer and optional solvent in the presence or absence of an initiator. Procedures for selection of an appropriate reduction potential for each desired (co)polymerization reaction with a specific catalyst complex in a specific reaction medium are discussed below. The Ej/2 redox couple for the polymerization medium may be determined by any suitable means, for example, by cyclic voltammetry (CV). If an appropriate charge is selected for a catalyst complex and (co)monomer(s) as disclosed herein, rather surprisingly, electrochemical procedures can provide a method for forming a targeted fraction of the activator species from an added deactivator resulting in initiation of the ATRP by transfer of the transferable atom or group from the added initiator to the formed lower oxidation state transition metal complex thereby initiating controlled copolymerization of a wide range of monomers generating copolymers with low Μ _« Μ _η and high degrees of polymerization.

In certain embodiments, the voltage applied to the polymerization medium may be based on the E| 2 value, as determined for example by CV. The voltage applied to the polymerization medium may be determined by the components in the polymerization. For example, in one embodiment, the voltage applied to the polymerization medium may be based on the as determined by CV, of the at least one transition metal catalyst and the one or more ligands present in the polymerization medium. In another embodiment, the voltage applied to the polymerization medium may be based on the Eia value, as determined by CV, of the at least one transition metal catalyst, the one or more ligands, and the radically (co)polymerizable monomers present in the polymerization medium and optionally any solvent and or any electrolyte present in the polymerization medium. In other embodiments, the voltage applied to the polymerization medium may be based on the E value, as determined by CV, of the at least one transition metal catalyst, one or more ligands, the radically (co)polymerizable monomers, and the initiator comprising one or more redox transferable atoms or groups, present in the polymerization medium and optionally any solvent and/or any electrolyte present in the polymerization medium.

The overall mechanism of an electrochemically mediated ATRP is shown in Scheme 3.

cathodic current

Scheme 3: Procedure for controlling an ATRP by applied electrical potential

The influence of the applied potential, the electrodic area, the concentration profile of Cu' and Cu" during the electro-mediated polymerization, and the solvent-monomer ratio on the crucial features of an ATRP including conversion, polymerization time, molecular weight and polydispcrsity were studied and are reported below. Analysis of these parameters together with the charge-current patterns can provide a deep comprehension of the dynamics of the system, and in particular an understanding of how the heterogeneous electrochemical process affects the homogeneous or biphasic

polymerization procedure.

In various embodiments, the concentration of the transition metal catalyst in the

polymerization medium may be less than 1000 ppm, or in other embodiments less than 500 ppm. For example, starting from a low amount (<1000 ppm, preferably less than 500 ppm) of deactivator (X- Cu"/L), the activator (Cu'/L) may be generated in-situ by electrolysis at a carefully selected reduction potential. When generated, the activator molecules can then react with the redox transferable atom or group, for example, the carbon halogen bond, of the initiator molecules or dormant chain end, P.-Br in scheme 3, forming active radicals through the traditional ATRP mechanism. These radicals can propagate with monomer prior to being returned to the dormant alkyl halide form by reacting with a deactivator molecule (X-CU'VL), or terminate with other radicals with a rate constant of k^. In this system, activator molecules are continuously regenerated at the working electrode {i.e. cathode) to maintain a selected ratio of activator to deactivator and hence control the rate of polymerization. In this manner a constant ratio of activator to deactivator can be maintained in the polymerization medium thereby continuously maintaining the targeted rate of polymerization.

According to certain embodiments, the polymerization process can be started and stopped by changing the applied voltage or current, or switching the applied voltage or current "on" or "ofP'. For example, changing the applied voltage or current or switching the applied voltage or current on or off, the system may provide a simple means to control any reaction exotherm. Indeed, in certain embodiments the reaction temperature may be used as a control to modify and adjust the timeframe, magnitude and voltage of the applied current to maintain the desired reaction rate at a controlled temperature as the reaction progresses. This allows unprecedented control over the polymerization procedure. Mechanical mixing of the reagents in the reaction flask assists in forming a homogeneous reaction medium by providing efficient mass transport of the generated catalyst complex away from the working electrode.

As disclosed herein electrochemical methods provide significant improvements to, and control over, an ATRP by offering readily adjustable "dials", e.g. applied voltage, current, potential, and total charge passed, to manipulate polymerization activation/deactivation, polymerization rates, and selective targeting of one or more redox-active species. In addition, electrochemistry offers an environmentally friendly alternative to current ATRP techniques that use comparable low

concentrations of catalyst complex by elimination of chemical agents to form the activator and a new approach to catalyst removal through electrodeposition.

In one embodiment of the invention the ratio of the two oxidation states of the catalyst complex in an atom or group transfer polymerization process is monitored and balanced by electrochemistry, for example, continuously monitored and/or continuously balanced, thereby dictating the rate of polymerization without formation of any by-products. For example, according to various embodiments, the electrochemistry selected from applied potential, current, and charged passed may be adjusted one or more times during the polymerization process. In specific embodiments, the electrochemistry may be continuously monitored and adjusted over the course of the polymerization reaction.

In specific embodiments, the polymerization medium may further comprise one or more electrolytes. Suitable electrolytes include any ionic compounds that is at least partially soluble in an aqueous phase of the polymerization medium. Non-limiting examples of electrolytes include those listed in US 2001.034625A1 at paragraph 0024. In certain embodiments, the electrolyte may comprise the same counterion that is present on the first added transition metal salt that forms the at least one transition metal catalyst. For example, in embodiments where Cu"Br ₂ is added as the transition metal salt which will form the transition metal catalyst, the electrolyte may also comprise a Br ^' counterion. In other embodiments, the electrolyte may comprise a different counterion than the anion present on the first added transition metal salt that forms the at least one transition metal catalyst. For example, in embodiments where Cu"Br ₂ is added as the transition metal salt which will form the transition metal catalyst, the electrolyte may comprise a OTf ^' (triflate or trifluoromethanesulfonate) counterion. In certain embodiments, the electrolyte may comprise a quaternary ammonium complex or a triflate anion. In specific embodiments where the polymerization medium further comprises an electrolyte, the electrochemistry may be selected from an applied voltage and a current, and may be selected to retain at least 0.1 % by weight concentration (based on total transition metal present) of an activator state of the transition metal catalyst and a deactivator state of the transition metal catalyst in the polymerization medium throughout the time period(s) when an active polymerization is desired.

Additional embodiments of the procedures are disclosed that allow a well controlled ATRP to be conducted with low concentrations of catalyst, very low concentrations of activator in a full range of solvents, including organic solvents, water, and biphasic systems.

The disclosed procedure allows one to dictate the concentration of both the activator and the deactivator in the reaction medium by adjusting the electronic potential of the current, or rate of flow of the charge. Indeed the electronic potential can, indeed should, be adjusted to match the catalyst system selected for the polymerization while providing optimal control over the radical polymerization of selected (co)monomers. The system provides additional control over the polymerization process by monitoring; total charged passed (Q) and current (I) values. Another method consists of placing a constant current (galvanostatic method) upon the electrochemical system and if desired measuring the variation of the voltage supplied at the working electrode.

According to certain embodiments, the transition metal catalyst may be a transition metal catalyst complex and comprise one or more ligands, and in specific embodiments may comprise two different ligands. Ligands may be used for a variety of reasons, for example, but not limited to, adjusting the solubility of the transition metal catalyst in the polymerization medium, or to control the reactivity of the transition metal catalyst. Suitable ligands for ATRP polymerization processes are known in the art and described in detail in the references incorporated herein. In specific embodiments, the ligands may include nitrogen containing ligands such as, but not limited to bipyridyl (bipy) based ligands, substituted pyridines (such as TPMA), and polyamines (such as Me ₆ TREN), and the like.

In certain embodiments, the relative concentration of a higher oxidation state transition metal catalyst and a lower oxidation state transition metal catalyst may be adjusted through the magnitude of the voltage or current applied to the system, thus controlling the polymerization of the radically (co)polymerizable monomers with the at least one transition metal catalyst and the one or more ligands. For example, the relative activity of a catalyst complex formed with selected ligand(s) can be adjusted, i.e. the ratio of Mt7L to Mt* ^+I /L, to provide control over the polymerization of a range of monomers just by changing the applied voltage. The rate of the polymerization is controlled by the selected ratio of Ml" to X-Mt"* ¹ with the rate increasing as the value of Mt7X-Mt ⁿ⁺¹ increases. More active catalysts require less activator in the system when polymerizing active monomers. Indeed as exemplified in the experimental section this is a novel tool that expands the range of monomers that can be polymerized in an expanded range of solvents including water.

If desired, the transition metal catalyst can be removed from the contacting polymer solution by clectrodeposition, leaving the added ligand(s) in solution. For example, the concentration of the transition metal catalyst in the polymerization medium may be reduced by electrodeposition of the transition metal onto the surface of one of the electrodes. The solvent/ligand unreacted monomer mixture can be removed from the polymer and recycled whereupon the ligand can react with the first deposited transition metal, optionally in the presence of a halogen containing electrolyte and in (he absence of an initiator to reform a soluble transition metal complex suitable for a further electrochemically mediated ATRP of additional monomeris) after addition of an initiator. In other embodiments, the transition metal catalyst or transition metal catalyst complex may be formed in-situ directly from electrolysis of the solid transition metal deposited on an electrode. In one embodiment, a transition metal catalyst complex may be formed in-situ directly from a reaction of a solid transition metal deposited on an electrode with one or more ligands in the polymerization medium.

Therefore another embodiment of the invention comprises electrodeposit ion of a transition metal and reformation of a soluble transition metal complex by subsequent reverse reaction with a contacting ligand in the presence of a (pseudo)halogen electrolyte. This embodiment can also be employed in "normal" ATRP reactions for catalyst removal and recycling expensive ligands.

As shown in Scheme 3 a controlled predetermined fraction of an air stable Cu"Br ₂ /Me ₆ TREN catalyst complex initially formulated in, or added to, the polymerization media can be "at will" electrochemically reduced to Cu'Br e ₆ TREN by application of a selected cathodic potential to invoke a controlled polymerization, whereby the formed activators (i.e. Cu'Br/Me ₆ TREN) then react with an ATRP initiator molecule exemplified herein by an alkyl halide, further exemplified herein by a molecule with a transferable bromine, forming the corresponding deactivator (i.e. Cu"Br2/Me ₆ TRE ) and radicals capable of monomer addition in a reversible fashion. This dynamic equilibrium mediates the polymerization allowing concurrent growth of polymeric species resulted in a control polymerization and polymers with predetermined molecular weights and low M _w M„. Therefore, electrochemical activation of ATRP provides significant improvements to this polymerization procedure by offering additional tools for polymerization control and an environmentally friendly alternative to the chemical reduction of Cu" to Cu ¹ .

The objectives initially targeted, and subsequently met, to exemplify this novel procedure include, but are not are not limited to, the following bullet points:

• Provide an understanding of the influence of each of the components of the electrolyte un an ATRP.

· Demonstrate polymerization control with specifically selected applied potential, or current, with alkyl (meth)acrylate(s) as exemplary monomers;

• Demonstrate that the ratio of Cu' to Cu" copper salts forming partially soluble catalyst complexes with active ligands, e.g. Me ₆ TREN or TPMA, can be adjusted to control polymerization of a broad range of radically poiymerizable monomers. This concept is based on the idea that the applied constant electric current can control the relative concentrations of Cu ¹ and Cu" in the reaction medium and hence the kinetics, or instantaneous rate of the polymerization reaction for a range of monomers.

• Demonstrate preparation of macromolecules with complex topology.

• Develop an aqueous electrochemical system this is desired since:

" The vast majority of electrochemistry is conducted in aqueous media.

^■ Bio-rcsponsive molecules are water soluble but can undergo

undesired conformational changes in the presence of organic media.

• Identify a mixed catalyst complex for bi-phasic ATRP.

• Demonstrate catalyst removal by electrodepositing copper

Various embodiments of the polymerizations described herein may include a polymerization medium where the medium is selected from the group consisting of an organic medium, an aqueous medium, and a biphasic medium. Controlled/living/ radical polymerizations (C LRPs) described herein performed in aqueous media are very attractive both from economic and environmental points of view. In addition to the synthesis of water soluble polymers from polar monomers using the processes described herein, aqueous media can be used for the polymerization of nonpolar monomers in biphasic systems, for example, through emulsion, microemulsion, or miniemulsion techniques.

In one embodiment a mixture of reagents/ligands is employed in order to adapt emulsion systems to the eATRP process. Significant reaction modifications and mechanistic considerations must be taken into account in order to conduct a successful "triphasic" controlled polymerization. In a non-limiting exemplary formulation of an eATRP miniemulsion comprising an oil soluble BPMODA based catalyst system requires the addition of a second more hydrophilic catalytic complex

(CU'VTPMA), reduced reaction temperatures (65 °C), and addition of a supporting electrolyte

(TEABF ₄ ) to efficiently activate the relatively isolated oil soluble dispersed BPMODA catalyst complex. Mechanistically, addition of a second copper ligand complex creates various pathways through which electrochemical activation of the dispersed catalyst could occur and overcomes the dual heterogeneous nature of the system comprising an oil/water and an electrode/water interface. The hydrophilic catalyst complex and/or bromine anions serve as electron messengers transporting electrons from the electrode to the organic phase by reacting with the more water soluble Cu" ligand complex(es) and initiator/dormant chain end(s) at, or close to, the phase boundary. The dual ligand communication pathway between an electrode and the dispersed organic phase operates in all stable biphasic polymerization media including microemulsion, miniemulsion and the ab initio emulsion system. Inverse emulsion systems could be controlled in a similar manner with an oil-soluble catalyst complex acting to shuttle the charge from the electrode to the dispersed aqueous phase.

In contrast to the remarkable success of ATRP in organic solvents, aqueous ATRP has been found to suffer from some limitations, especially in control and targeted degree of polymerization

(DP). [J. Polym. Sc , Part A: Polym. Chem. 1998, 36, 1417-1427] Aqueous ATRP is usually fast with relatively high K _A7RP . [Client. Rev. 2007, 107, 2270-2299] In addition, the halidophilicity (K _x ) of CU"L ²⁺ , i.e. association of X ^" to Cu ⁿ L ² * is low and the deactivator XCu"L ⁺ is not always stable toward dissociation. [Macromolecules 2004, 37, 9768-9778] Furthermore, certain CU'L ⁺ complexes are unstable in water and may undergo disproportionation. In fact, control over an aqueous polymerization was improved by using high [X ^" ], which helps to suppress deactivator dissociation. Developing successful aqueous ATRP requires taking all these issues into consideration. These limitations are overcome in an eATRP.

In a copper mediated aqueous eATRP the reaction mixture initially contains monomer, initiator, and Cu"L ²⁺ (or Cu"L ^2t + X-Cu"L*). No polymerization occurs under these conditions, as there is no Cu'L ⁺ activator in solution. The reaction starts only when a potential (E _m ) is applied to the cathode so that reduction of Cu ^u L ²⁺ to Cu'L ⁺ occurs at the electrode. The value of E _m can be appropriately chosen to achieve a continuous production of a small quantity of Cu'L ⁺ and consequently control the concentration of R ^* throughout the reaction. The livingness of the polymerization process is ensured by the combination of low [R ^* ] and very high [Cu"L ^J+ ]/[Cu'L ^* ]. The overall rate of the process and the degree of control over polymerization can be tuned by adjusting £ _app .

One embodiment of the invention describes an electrochemical ATRP water based polymerization process by setting the E _m to provide a combination of low [R ^* ] and high

[Cu"L ²⁺ ]/[Cu'L ⁺ ] ratio, as high as 99.9/0.1. Indeed the overall rate of the process and the degree of control over the polymerization can be tuned by adjusting the E _app .

Although development of AGET (Activators Generated by Electron Transfer) ATRP gives good results in terms of both control and DP, the appropriate ratio [Cu"]/[reducing agent] and the nature of the reducing agent is critical. [J. Polym. Sci. Part. A. Polym. Chem. 2009, 47, 1771 -1781] The ideal process should have a constant, high Cu'VCu ¹ ratio, which can hardly be achieved by a single addition of reducing agents. This limitation can be overcome in an eATRP as no added agents are required. In another embodiment targeting environmentally benign systems the concentration of transition metal in the polymerization medium is less than 1000 ppm, preferably less than 500 ppm and more preferably less than 100 ppm.

In another embodiment of the invention directed at preparing block copolymers with a single catalyst complex the degree of polymerization and dispersity of each block can be tuned by adjusting fapp to attain optimal control over each block. After the first monomer is converted to a first segment the second monomer can be added and the E _w adjusted to provide the desired level of control for the polymerization of the second segment(s) without changing the catalyst. Optionally if a "clean" second block, i.e. without incorporation of any residual "first" comonomers, is desired the current can be switched "off' and first comonomers removed leaving the catalyst complex present in the pure first block macroinitiator prior to adding the second comonomers then switching the second polymerization "on" by selecting the desired £" _app . Various features of the present invention will become more apparent upon consideration of the following examples. The various embodiments of this disclosure described in the following examples are not to be considered as limiting the invention to their details. All parts and percentages in the examples, as well as throughout this specification, are by weight unless otherwise indicated.

EXAMPLES AND DISCUSSION OF EXAMPLES

The IUPAC definition of terms used in electrochemical reactions are summarized in Chapter 1 of the Handbook of Electrochemistry, Edited by C.G. Zoski; Elsevier, 2007, and will be employed in the following discussion. This Handbook of Electrochemistry also provides information on selection of electrodes for the disclosed process. The electrodes used in the initial examples are chosen as exemplary materials and do not limit the choice of electrode materials in any manner. Definitions of terms, equations and important relationships are also provided in Electrochemical Methods, Fundamentals and Applications, A. J. Bard, L. R. Faulkner, second edition John Wiley & Sons, 2001. Chapter 1 1 of the book also provides a discussion on bulk electrolysis methods.

Abbreviations

Tris((2-dimethylamino)ethyl)amine) ME ₆ TREN

Tris 2-pyridylmethylamine TPMA

Bis(2-pyridylmethyl)octadecylamine BPMODA

Ethyl a-bromophenylacetate EBPA

Ethyl a-bromoisobutyrate EBiB

Ethyl 2-bromopropionate EBP

Hexadecane HD

Methyl bromopropionate MBrP

Tetrabutylammonium hexafluorophosphate TBAPF ₆

Tetrabutylammonium bromide TBABr

Tetrabutylammonium perchlorate TBACIO ₄

Tetraethylammonium tetrafluoroborate E NBF4

Tetraethylammonium bromide Et ₄ NBr

2-hydroxyethyl 2-bromoisobutyrate HEBriB

Acetonitrile MeCN

Dimethylsulfoxide DMSO

Poly(ethylene glycol) methyl ether methacrylate OEOMA47J

Ethylene glycol diacrylate EGDA

2-hydroxyethyl acrylate HEA

In order to determine if the concept of utilizing electrochemistry to control an ATRP, summarized in Scheme 3, was indeed possible an electrochemical cell was constructed. The desired functions of the cell are represented in Figure 1. It was envisioned, and then confirmed that, as shown in Scheme 3, the ATRP equilibrium could be controlled by subjecting the reaction medium to a specifically selected applied voltage, (E _app ). The exemplary electrochemical cell was designed to be suitable for both electrolysis of Cu" and to provide control over a standard ATRP. A pear shaped five neck jacketed flask was selected as the foundation for a laboratory electrochemical cell and was equipped with a "rare earth" stirring element, a N ₂ purge, and a peristaltic pump for cooling. Each of the necks was fitted with either: a silver/silver (Ag Ag+) ion reference electrode, a platinum mcsh/disk working electrode, a platinum mesh counter electrode, and an inlet/outlet port for samples and reagents. A silver/silver reference electrode, a Pleskov electrode, was selected as reference electrode because it is well suited for electrochemistry in organic media; specifically the initial examples conducted with MeCN as solvent. The counter electrode was designed to be enclosed in a separate fritted compartment to reduce diffusion of oxidized species at the counter electrode into the polymerization occurring in the main compartment of the reactor. Therefore, the counter electrode was jacketed within a fritted compartment. The working electrode was made of a platinum mesh. A mesh was selected over a disk/button working electrode because of its larger relative surface area, although a platinum button working electrode was used for all analytical cyclic voltammetry (CV) measurements conducted prior to the addition of an initiator. Fabrication of all electrodes was undertaken within the laboratory, since they are not commercially available, and comprise a standard conductive wire encased in a glass compartment. The wire was soldered to platinum wire and coated with a chemically stable epoxy coating. A schematic of the reaction flask is shown in Figure 2.

As exemplified in the following examples application of electrochemical techniques to ATRP introduces a unique and novel strategy to dynamically control this redox driven polymerization process. The initial experiments demonstrated that any desired fraction of the catalyst complex in an ATRP reaction medium formulated with air stable Cu"Br2/Me<iTREN catalyst complex can be "on demand" reduced to provide targeted levels of Cu'Br/MeeTREN activators to invoke or trigger polymerization. The extent and rate of reduction is dictated by the initially applied potential (E _aff ) allowing one to control the efficiency and rate of initiation from the added (pseudo)alkyl halide initiator. The ratio of Cu Me ₆ TREN:Cu"Br ₂ /Me ₆ TREN can be adjusted throughout the polymerization reaction to provide optimum control when taking into account the gradual increase in viscosity as the polymer chain increases in molecular weight and, with certain monomers, the change in polarity of the reaction medium as the reaction progresses. Further to this point, electrochemical methods allow lower oxidation state catalyst (Cu'Br/MesTREN) to be reverted back to their original higher oxidation state under an anodic potential providing a means to continuously balance the ratio of lower to higher states of the transition metal complex and if desired deactivate an ongoing polymerization.

• Therefore in one embodiment of the invention alterations of polymerization rates through switching, or continuous adjusting of the catalyst oxidation states, allows enhanced levels of polymerization control and in essence enables precise modification of macromolccular species at any specified time during the polymerization.

Example 1: Influence of an Added Electrolyte on Polymerization of Methyl Acrylate A series of control experiments were conducted focusing on understanding the influence of addition of an electrolyte to an ATRP. It is envisioaed that any salt will suffice as long as it is soluble in the reaction medium. A variety of different acids and bases can be employed, indeed any molecule which is composed of ions or compounds which can be made into ions, including ionic liquids, are potential electrolytes. TBAPF ₆ was selected as an exemplary electrolyte due to its stability at a wide range of electrolytic potentials in MeCN. Two polymerizations were conducted utilizing copper wire as a reducing agent, one without and one with an electrolyte. The results are reported in Table 1. The system without an added electrolyte, entry 1 , proceeded rapidly achieving a final conversion of 88 % in 3 hours while maintaining linear first order kinetics and a strong correlation between experimental and theoretical molecular weights. Addition of TBAPF ₆ to the polymerization system resulted in slightly improved control, entry 2. First order kinetic behavior was observed, indicating the maintenance of a constant concentration of radicals throughout the polymerization, and molecular weights values clearly matched those of the theoretical values while attaining a narrow molecular weight distribution. These results confirmed that the addition of an electrolyte, with bulky non- coordinating counter ions has little, or no, adverse effects on an ATRP. This procedure of adding an electrolyte also provides a means to control the concentration of a desired counterion in the reaction medium.

Interestingly, switching the electrolyte anion from PF ₆ ^" to bromide (Table 1, entries 2 and 3) changed the behavior of the system and a lower than targeted MW was obtained, entry 3, indicating lower initiation efficiency due to early termination reactions but a subsequent controlled

polymerization. Upon increasing the concentration of the TBABr electrolyte, entry 4, lower final conversions and slower polymerization rates occurred. This behavior may be explained due to the fact that in a standard ATRP excess bromide ions are capable of displacing the Me ₆ TREN ligand in the active transition metal complex, in agreement with the conclusions in a speciation paper by

Bortolamei et al. [Macromolecules, 2010 9257].

Example 2: Electrochemically Mediated Polymerization of Butyl Acrylate (ΒΛ).

An initial scouting experiment was performed with butyl acrylate as monomer at the selected Ei _fl . The potentiometric charge was selected to provide a target conversion of 90% in 4 hours (14,400 seconds). The initial reaction conditions were: [M] ₀ = 5.56 M, [R-X] ₀ = 0.0278 M, [Cu"Br ₂ ] = 0.00139 M based on the knowledge that Ap for methyl acrylate at 30 °C = 16,600 M ^" ' s ^' ' and /-ATRP for Cu/Me ₆ TREN at 22 °C with MeBrP as initiator = 2.9 IT*. It was calculated that the concentration of radicals in the system should be 9.622 x E ^"9 which would require E° = E1 2 = 0.30 V to generate the required catalyst ratio of Cu'Br/Cu"Br2 = ~0.12. Results of this experiment are reported in Table 2. Table 1: Control polymerizations to determine influence of electrolyte on ATRP

Exp. ATRP System Electrolyte [Electro] [Cu°] time conv. ^b Mn.theo M _n ,GPC loff

W . [MA]:[EBP]:[Me ₆ TRE ]:(Cu"Br ₂ ] (M) (mm ^J /mL) (mm) (h) (%) (g/mole) (g/mole)

1 500:1:0.05:0.05 None 0 40/53 3.0 88.4 38,174 32241 1.11 1.18

2 500:1 :0.05:0.05 TBAPFe 0.11 40/53 2.6 89.3 38,571 39,764 1.07 0.97

3 500:1 :0.05:0.05 TBABr 0.11 40/53 3.4 75.0 32,428 26774 1.15 1.21

4 500:1 :0.05:0.05 TBABr 0.33 40/53 3.5 53.6 23,204 20,193 1.50 1.15 a - All polymerizations: [M] = 5.56 M in eCN.Temp = 30 °C, b - Determined by ¹ H N R.

Table 2: Polymerization of BA with potentiostatic conditions

ATRP [M]/[q/[L]/[Cu"] E time Conv. M„,u,. ₀ M„,GPC M _w /M _n

System (V) (h) (%) (g/mole) (g/mole)

BA/EBP/Me ₆ TREN/Cu"Br ₂ 300/1/0.2/0.2 -0.668 3.0 71.1 27,638 19,089 1.09

All polymerizations were conducted with [M] = 3.3 M (50 (v/v) MeCN, {TBAPF ₆ ] = 0.1M, T = Room Temperature and reaction volume of 16 mL.

Table 3: Electrochemically mediated ATRP of MA as a function of applied potential.

Exp. ATRP [M]/[l]/[L^Cu»] £ [CulMCull] time P M _n ,lh«o Mn,GPC M _w /M„

[#) System (V) (target) (h) (%) (g/mole) (g/mole)

1 MA/EBP/Me _e TREN/Cu"Br ₂ 500/1/0.2/0.2 -0.62 0.14 7.0 52 22,371 23,755 1.08

2 MA EBP Me _e TREN/Cu°Br ₂ 500/1/0.2 0.2 -0.69 1.0 5.0 83 35,271 26,795 1.08

3 MA EBP e ₆ TREN/Cu ^ll Br ₂ 500/1/0.2/0.2 -0.72 3.0 3.8 68 29,144 26,795 1.09 a -All polymerizations were conducted with [M]= 5.56 (50 (v/v) MeCN. rjTBAPFg] = 0.1 , T = room temperature and reaction volume of 16 mL.

The final value for MJM„ = 1.09 indicates an acceptable level of control throughout the reaction and the preparation of a well defined polymer. However minor tailing in the GPC curves indicates that further control could be exerted on the reaction if the applied charge was changed as the

polymerization progressed.

Example 3: Electrochcmically Mediated Polymerization of Methyl Acrylate.

3A. Selection of appropriate E _app

As a consequence of these results a series of control CVs were performed to check for any additional reduction/oxidation reactions involving any of the other reagents, besides generation of the desired Cu ^M Br ₂ /L complex, before conducting a second experiment, namely polymerization of methyl acrylate with Οι"ΒΓ ₂ /Μο ₆ ΤΡνΕΝ. All CVs were conducted under conditions identical to that envisioned as suitable for the polymerization, i.e. those given in Table 3.

The initial evaluation was a potential sweep (i.e. CV) of the 50% (v/v) monomer/solvent reaction media, no significant oxidation or reduction was observed over a range of two volts, Figure 3A. At this point, Cu"Br ₂ was injected into the reaction system and another CV was conducted, Figure 3B. As expected, the Cu ⁿ Br ₂ solution in the mixture of monomer and solvent had a clear oxidation and reduction peak at positive potentials between 0.65 and 0.90 V (Ε _1/2 = 0.780 V). Similar results are reported in literature for Cu" salts, but it should be noted that these potentials are at different locations than may have been expected from prior analytical CV work on ATRP catalysts due to the selection of a different reference electrode; Ag Ag+ instead of a saturated calomel electrode (SCE), which is based on the reaction between elemental mercury and mercury(I) chloride. These values can be converted to be SCE if required and indeed would be if the reference electrode is changed to ferrocene. In order to generate the additional information for an eATRP two additional CVs were performed by sequentially first adding the ligand, Me ₆ TREN, Figure 4 black curve, and then a low molecular weight initiator, ethyl 2-bromopropionate (EBP) was added and a significant shift in the Ei _/2 was observed, Figure 4 - grey curve.

This was the first time that a systematic CV analysis of precursors for an ATRP had been conducted and indicates that such a systematic analysis should be conducted prior to applying eATRP to a new monomer or with a new catalyst. The Em was now ca. -0.67 V instead of 0.78 V vs Ag Ag ⁺ . This curve was used as the base for all the polymerizations reported in Table 3 and for the Nernstian calculations. It should be noted that before each polymerization, a CV was run to check for any unexpected behavior and to confirm that the E _1/2 was consistent with the results given in Figure 4. Upon adding the initiator the shape of the CV changed, Figure 4 gray line, which could now be expected due to the presence of additional Cu"Br ₂ generated in the presence of the initiator due to the reaction of the electrochemically generated Cu'Br (Formula 3) re-oxidation reaction with the alkyl halide (Formula 4) to form a radical. Therefore additional cathodic current is required, which accounts for the CV curve remaining at a -2.0 μΑ instead of returning to -1.25 μΑ. Cu ⁿ Br ₂ /L + e- ^» Cu'Br/L + Br ( ₃ )

Cu'Br/L + RX - Cu"Br ₂ /L + R - (4)

Tlie Nemst equation, shown below (Formula 5), was used to calculate the potential required to generate and maintain a variety of different [Cu']/[Cu ⁿ ] ratios from the CV shown as vertical lines in Figure 4, grey curve w/o EBP, also shown in Table 3. At room temperature (RT/nF) is a constant, with a value of 0.02569 V, as our system is a one electron process (n = I).

E = E° + RT/nF Ln [0]/[R] (5)

Indeed the ernst equation can be employed to determine the absolute values for the concentration of each the activator and deactivator transition metal complex and the applied voltage can be selected to retain at least 0.1% of both the activator and deactivator in the contacting electrolyte when a controlled ATRP with an active catalyst complex is targeted for use in a polar medium such as water.

The changes in the shape and position of the CV measured in the presence of different components required for a controlled ATRP indicate that each polymerization reaction may require a similar set of measurements prior to selecting electrochemical conditions for formation of the desired ratio of oxidation states in the selected transition metal complex.

3B. Examination of reaction parameters

The first series of polymerizations of methyl acrylate were designed to probe the effect of changing the magnitude of the applied potential, E _a/P . The results arc summarized in Table 3.

Theoretically, assuming Nemstian behavior and a reversible system exists, the relative concentrations of [Cu ⁿ Br ₂ L] and [Cu"Br L] should be tunable through the applied potential and concomitantly the polymerization rate. The first polymerization conducted with electrochemical control was conducted at the previously determined value (Table 3, entry 2). Linear first order kinetics were observed and a good correlation between theoretical and experimental molecular weight values. A narrow Ai M _n was observed throughout the polymerization and progressively increasing molecular weight of the polymers with conversion, as shown in the GPC traces of samples of polymer taken from the reaction after different times, and therefore at different degrees of monomer conversion (p), in Figure 5. The curves moved cleanly to higher molecular weight.

Assuming a reversible or quasi-reversible system exists, as previously established with ATRP catalytic systems, the relative concentrations of Cu ^l: Br ₂ Me ₆ TREN and Cu'Br/Me ₆ TREN and concomitantly the polymerization rate should be tunable through the applied potential. Two additional polymerizations were conducted; one with an increase and the other a decrease of the applied potential; to -0.72 and -0.62 V, respectively, Table 3 entries 1 and 3. An enhanced polymerization rate was observed at the higher potential, a higher ratio of [Cu'yfCu ¹¹ ] = 3.0, whereas a lower potential provided a lower ratio of [Cu']/[Cu"j = 0.14, and accordingly a reduced rate of polymerization. Initial slopes in the first order kinetic plots revealed an approximate rate enhancement of 2.4 fold by adjusting the from -0.66 V to -0.72 V. The rate dependence should result from the adjustment of the relative concentrations of Cu'Br/Me ₆ TREN and Cu Br ₂ Me ₆ TREN, which dictate the overall rate of polymerization in ATRP. More negative potentials induce a faster reduction rate of Cu"Br/Me ₆ TREN, and an increase in the [CutyfCu ¹¹ ] ratio, hence, results in higher rates of polymerization. In all cases, similar correlations between theoretical and experimental molecular weights were observed and narrow molecular weight distributions were maintained even with enhanced polymerization rates. GPC results illustrate clear shifts in molecular weight to higher values and monomodal distributions for all polymerizations.

3C. Switching a polymerization reaction "on" and "off'

The final experiment in Table 4 was designed to demonstrate that designed changes in the applied potential could effectively "turn on" and "shut down" a polymerization. In the first hour of the experiment no potential was applied and no reaction occurred; no conversion of monomer was observed which shows that an applied potential is required to reduce a fraction of the Cu" species to the Cu ¹ species and activate the polymerization. Then a potential of -0.693 V was applied for 45 minutes. During this time approximately 30 % of monomer was consumed, Figure 6 - left. After 45 minutes the potential was changed to -0.45 V for 1 hour. The polymerization soon halted, although there was a 10-15 minute lag time as the low concentration of Cu ¹ species was slowly converted into the Cu" species, once the change in the potential occurred. The time lag could be adjusted by varying the concentration of transition metal and/or the ratio of higher to lower oxidation states in the steady state. The reversible nature of this redox process and an ability to reinitiate polymerization was demonstrated by applying a potential of -0.693 V for 1 hour. As soon as this increased potential was applied, polymerization began again, increasing the overall consumption of monomer in the next hour to over 60 %. Finally, the polymerization was switched off a second time by reverting to a less negative potential. The molecular weight values of the polymer chains correlated strongly with the theoretically predetermined values, Figure 7 - left scale, and a low M _w /M _n was maintained during the whole duration of the polymerization, Figure 7 - right hand scale. Lastly, GPC curves, Figure 5B, showed that the molecular weight increased with conversion without any detectible coupling or substantial number of termination events.

3D. Examining potentiostatic outputs

In addition to the kinetic analysis of the polymerization, the potentiostatic outputs; total charged passed (Q) and current (1) values were recorded as the polymerization proceeded. Essentially dQ/dt (coulombs/s) is equal to the current (amperes (C s)). From Figure 8, it is clearly visible that more charged passed through the reaction during the polymerization than was required to completely reduce the total amount of Cu ⁿ Br ₂ initially present in the reaction medium. Theoretically, if all Cu"Br ₂ Table 4: Polymerization of MA under potentiostatic conditions

Exp. ATRP [M]/[I]/[L)/[Cu"] E Eli [CuI]/[CuII] time Conv." M„,GPC M„/M„

(#) System (V) (V)/(h) (target) (h) (%) (g mole) (g/mole)

2 MA EBP Me¾TREN/Cu"Br ₂ 500/1/0.2/0.2 -0.693 -0.693/5.0 1.0 5.0 83 35,271 26,795 1.08

3 MA/EBP Mc6TREN/Cu"Br ₂ 500/1/0.2/0.2 -0.688 -0.716/3.8 3.0 3.8 68 29,144 26,795 1.09

4 MA/EBP/Me REN/Cu^ 500/1/0.2/0.2 -0.697 -0.668/7.0 0.33 6.8 75 32160 31645 1.10

5 MA/EBP/Me¾TREN/Cu"Br ₂ 500/1/0.2/0.2 -0.696 on/off 1.0 4.8 67 28,856 24969 1.08

[a] - All polymerizations were conducted with [ ] = 5.55 M (50 (v/v) eCN, [TBAPF ₆ ] = 0.1M, T = room temperature and reaction volume of 12 mL.

[b] - Determined by Ή NMR.

Table 5: Influence of fCu"Br ₂ /Ll on AMP ATRP

Exp. ATRP [M]/[l]/[L]/[Cu"] £ time Mn.theo M _n ,GPC M _w /M„

(#) System (V)/h (h) (%) · (g/mole) (g/mole)

1 A/EBP Me ₆ TREN/Cu"Br ₂ 500/1 /OJ2/0.2 -0.668 7 75 32,160 31 ,645 1.10

2 MA/E B P/Me ₆ TRE N/C u"B r ₂ 500/1/0.05/0.05 •0.666 5.33 81 35,025 35,996 1.09

3 MA EBP/Wle _e TREN/Cu"Br ₂ 500/1/0.025/0.025 -0.666 5.33 91 38,918 31 ,337 1.06

was converted to Cu'Br, then Q would equal 3.387 coulombs. This point is identified in Figure 8 as point (b). This value is calculated by the product of the moles of Cu"Br ₂ put into the reactor (i.e. 3.51 x 10 ^'5 mol) and Faraday's constant (9.64853 x 10 ⁴ C/mol), Equation 6 below.

The additional charged passed can be accounted for because in an ATRP as Cu'Br is formed it reacts with alky halides thereby regenerating the corresponding Cu ⁿ Br ₂ species. A second point was identified as (a), were the charge passed and current change slope. These points arc of interest because this is the time when the level of control over polymerization begins to be reduced. Excessive reduction of Cu"Br ₂ could be responsible for this loss of control. This leads to the conclusion that a two step, or multi-step, potential is required to gain and retain optimum control throughout the polymerization. An initial higher potential to generate Cu'Br quickly and then a lower applied potential to maintain the desired/targeted [Cu'Br] while accounting for terminated chains. This value for applied potential should diminish as the reaction progresses. This is exemplified later in the optimal polymerization of methyl methacrylate (MMA), where in contrast to BA, a switching between two potentials provided the best possible control.

These results indicate that additional control of polymerization rate can be accomplished by applying different potentials at different periods of the polymerization and that it is necessary to maintain appropriate concentrations of Cu' and Cu" to preserve maximum control. The symmetrical GPC traces from entry 4 in Table 4 display a gradual increase in molecular weight, Figure 5B, indicating a high level of control over the kinetics of the polymerization reaction.

Example 4: Control Experiments

While the above examples provide proof that electrochemical mediation of an ATRP is indeed possible a series of experiments was conducted in order to gain detailed information on how each component of the ATRP reaction medium influenced the overall level of control in order to provide parameters to expand the utility of the process to new catalysts, new polymerization media and new polymer architectures.

4A. Influence of the concentration of transition metal complex on level of control in an electro-chemical ATRP process

The concentration of transition metal complex, exemplified in the initial examples by cupric bromide in the presence of MeeTREN as the ligand, was progressively decreased from 400 ppm to 50 ppm. The reaction conditions/results are summarized in Table 5. As the concentration of catalyst was dropped from 400 ppm to 50 ppm three general trends were observed.

• Lower catalyst concentrations resulted in lower M _w M„ values a polymer with a

M _w M„ distribution of 1.06, the lowest yet achieved while also achieving a high conversion. • The 50 ppm system appeared to have the most linear first order kinetic behavior.

• As expected, lower amounts of catalyst resulted in a lower amount of charged passed, or species electrolyzcd.

Nevertheless at each concentration of catalyst, more charge was passed than required to reduce the initial Cu"Br ₂ present, indicating some termination reactions still occurred. The symmetrical GPC curves moved cleanly to higher molecular weight as conversion increased.

In one embodiment of the invention the reaction can be conducted with concentration of catalyst below 500 ppm, optionally below 100 ppm and optimally as low as 50ppm.

4B. Influence of initiators

The relative activity of each initiation system can be observed through the cathodic peak height compared to the Cu'VCu' cathodic peak high without initiator present, Figure 9. In each system the [ ] = 4.67 M and [TBAPF ₆ ] = 0.2 M. Molar ratios = [M]:[l]:[Cu"BR ₂ /L] = 300: 1 :0.2. The left hand scale differs for Figures 9(A), (B), and (C). Figure 9 shows this relationship with three initiators (EBP A, EBiB, and EBP) under conditions suitable for an ATRP polymerization. In this series of measurements the catalyst complex was formed with TPM A as ligand and cupric bromide as the transition metal salt. Moving from the most active to least active initiator, i.e. from the initiator with the lowest k _a- , to that with the highest, the relative difference in cathodic heights becomes smaller. EBPA resulted in the largest difference while completely eliminating the anodic portion of the half wave. On the other hand, EBP resulted in very little difference and almost no change in the CV shape, indicating little catalytic activity of the alkyl halide. In addition to the relative activities of each initiator, slight variations in the catalyst complex half waves were observed. Methyl acrylate (MA) and methyl methacrylate (MMA) were the most similar and appeared to have more positive potentials indicating some stabilization of the electron transfer process, whereas styrene was the least positive and potentially the least stabilizing of the three monomers.

4C. Influence of the concentration of the monomer and the initiator

Cyclic voltammetry measurements were carried out to investigate the influence of the concentration of the monomer and the initiator on the reaction. The system under study used the following components:

Catalyst (precursor) Cu"(OTf)2, L = Me ₆ TREN

Halide ion Bromide

Initiator (I) Methyl 2-bromopropionate (MBrP)

Monomer (M) Methyl acrylate (MA)

Solvent (S) Acetonitrile (AN)

Electrolyte (E) E NBF,

Temperature 25°C The primary reactions involved during the electroregeneration of Cu in ATRP conditions are the following:

(7) Cu»L+ e Cu'L EO-cuI culL. ^ct. cuIlL/cJL

(8) Cu'L + RX ^: ^== X-Cu"L + R* K _A TRP, k∞

χα,ΐ'ινχα,Ί.

(11) X-Cu'L Cu'L + X ^" l/Ac„Ii. ₊ x, &i,xculi.

Considering Cu'L as the species responsible for the activation of RX (reaction shown in equation 8), the rate of polymerization, or degree of catalysis, is directly correlated with its rate of regeneration, which in principle depends on reactions (7), (10) and (1 1). If we consider a rather active initiator like MBrP (* ^■ „, ~ 2000 M ^" 's ^' ' in pure CH ₃ CN), after reaction (7) the concentration of Cu'L near the electrode surface is very low because of the homogeneous activation reaction (8); furthermore, aAer one catalytic cycle all the Cu" is present as XCu"L (logmcuIlL = 6.1 in pure CH ₃ CN), and therefore the electrodic process correlated with the degree of catalysis is underlined by the reaction (10). Figure 10 reports the effect of the concentration of initiators on the voltammetric cycle recorded starting with CU"L, recorded at v = 0.05 V/s on Pt, in AN MA 1 : 1 + 0.1 M Et ₄ NBF . The first cathodic wave is the monoelectronic reduction of Cu"L (reaction 7): in absence of initiator, this is the only process involved since the catalytic cycle can not switch on. Therefore, the voltammetric response is totally reversible. After the addition of an initiator, MBrP, a second wave appears at more negative potential, because of the reduction of XCu"L produced by the homogeneous reaction (8), and the reversibility of the first peak is lost since the concentration of Cu'L is very low. In the presence of higher ratios of [MBrP]/[Cu"L] the cathodic peak current XC _U »L increases, meaning higher degrees of catalysis.

4D. Influence of the concentration of the monomer and solvent

The same approach was used to investigate the effect of the monomer/solvent ratio on the degree of catalyst activity. The CV of ImM Cu ⁿ Mc ₆ TREN in the presence of lOmM MBrP and 0.1 M E tNBF* at different AN MA ratio* 0.1 M Et NBF., recorded at v = 0.05 V/s on Pt. V ₀ = 15 mL, MA step addition = 5mL. In this case, the experiment was influenced by a certain approximation. In fact, the MA step additions entail dilution of the reaction medium; tins problem was overcome considering the direct proportionality between the peak current l _p and the bulk concentration of the electroactive species C*, given by the Randles-Sevcik equation (12):

It was assumed that the changes in the diffusion coefficient D after the MA stepwise additions were negligible. The voltammetric responses are quite similar to those shown in Figure 10; however, increasing the ratio MA AN results in a slight reduction in the activity of the catalyst, since the reduction peak current _pc .of XCu"L decrease with higher ratio M A/ AN which indicates that catalyst activity changes with comonomer/soivent ratio and the correct potential should be selected and applied for maximum control.

4E. Selecting the applied potential

Selecting the correct applied potential, E _m . is of primary importance when conducting potcntiostatic electrolysis. In particular, two main conditions can be used:

• electrolysis under diffusive control: in this case, E _m « E^ and the overall rate of the reaction is controlled by the rate of the diffusion of the reactants to the electrode surface rather than the rate of the reaction itself or;

· electrolysis under kinetic or chemical control: herein, E _m > E^ and the overall rate of the reaction is controlled by the rate of the reaction itself rather than the rate of the mass transport of the reactants to the electrode surface.

In addition to these considerations, the choice of E^, should be appropriate in order to avoid other undesired electron transfers. In ATRP systems, one of these factors is the further reduction of Cu ¹ to Cu°, this is expected to occur at potentials more negative than that of the Cu'VCu' redox couple when disproportionation is not thermodynamically favoured. Figure 1 1 , which shows the CV of l nM Cu"Me ₆ TREN in the absence (a) and presence (b) of lmM EtjNBr, recorded at v = 0.05 V/s on Pt, in 0.1 M Et ₄ BF + 0.1 Et^NBF^, confirms these expectations: the first cathodic peak, curve (b), corresponds to the reduction (VL/CU'L, whereas the second peak, curve (a), at, at more negative potential is indicative of electrodeposition of Cu° on the electrode surface, since the back scan is characterized by the so-called anodic-stripping peak, having the typical symmetric shape with high peak current. During this process, the electrodeposited Cu° is oxidised to Cu ¹ ion that undergoes complexation in solution and subsequent oxidation to Cu ⁿ L. This electrochemical picture is confirmed when the starting species is Br ^' Cu"L, Figure 11 curve (b)j in this case, both the

BrCu"L BrCu'L and BrCu'L/Cu ⁰ +Br+L redox processes are shifted toward more negative potentials because of the stabilization induced by the halide ion, while the anodic stripping is unchanged since it is independent of the presence of the ligands in solution.

These observations point out that there is always a lower limit for E _m in order to avoid the electrodeposition of the transition metal; furthermore, the presence of 1 equivalent of halide ion is necessary to produce the ternary complex BrCu"L to investigate E _m in the diffusive region of the BrCu"L/BrCu'L redox couple.

The results also confirm that copper can be removed from the reaction by electrodeposition and that the catalyst complex can be reformed by reaction of deposited Cu° with ligands present in the reaction medium.

4F. Influence of solvent

The next series of reactions were designed to evaluate the influence of solvent. Numerous reports in incorporated references have shown well controlled ATRP reactions occur in DMSO as solvent. One reaction was conducted with DMSO as solvent, this required a new reference electrode, and exhibited an initially faster reaction in comparison to the reactions conducted in MeCN. The DMSO system experienced a significant exotherm, which would have further increased the k _p of methyl acrylate. Nevertheless two advantages of the DMSO system should be noted:

· no clogging of the vycor frit was noticed and

• DMSO will allow further expansion in the selection monomers that can be

polymerized by eATRP to include more polar monomers, if it is selected as the solvent.

Anisole is a more hydrophobic solvent than acetonitrile. In the initial evaluation of the CV analysis when using such a hydrophobic solvent (i.e. low conductivity) high solvent resistance was observed. In response to this, the molarity of supporting electrolyte was increased from 0.1 M to 0.2 M to achieve better conductivity. Furthermore, since it is the IUPAC standard, it was considered important to begin reporting standard potentials against ferrocene. Figure 12 illustrates two couples; one of the copper ligand complex (Cu ^u Br ₂ TPMA) and the ferrocene ferrocenium standard. A difference of ca. 0.72 V exists between the two couples.

The first polymerization conducted in anisole was methyl acrylate. This monomer was chosen because of the success in the MeCN system. Cyclic voltammetry was conducted of the solvent and monomer background and a limited current was observed in a range of 3.5 V reflecting the relative stability of the system. Further CV analysis was carried out, shown in Figure 9 C, by first recording the copper complex of interest and then after addition of the alkyl halide initiator. Methyl acrylate was successfully polymerized by eATRP in anisole at T = 50 °C. High conversion values over 90 % within 5 hours, linear first order kinetic behavior was observed, and a linear increase in molecular weight with conversion was observed with M M _n values around 1.1 which shows that no significant coupling is occurring during polymerization.

Example 5: Polymerization of Methyl Methacrylate

SA. As previously discussed background CVs of the solvent and monomer were carried out along with characterization of the initiator activity. Similar to the MA system a 3.5 V range was observed and no significant current passed until reaching the cathodic and anodic discharges. EBPA was selected as the initiator for MMA as it showed high activity in the CV analysis, Figure 9A. To further exemplify that eATRP can be applied to a range of catalysts a copper triflate based catalyst, Cu"(Trf) ₂ A. was used in conjunction with one equivalent of TBABr to convert the complex to their more active Cu ⁿ Br L catalyst. A background of MMA anisole with supporting electrolyte (TBAPF ₆ ) was conducted and no significant current passed, either cathodically or anodically, from ca. -1.5 to 2 V showing the stability of the reaction medium. After confirming the stability of the reaction medium, Cu"(Trf) ₂ TPMA was injected into the reaction medium and an additional CV was recorded. A reversible couple was observed at ca. 0.659 V that shifted to 0.315 V after addition of the bromine electrolyte. This corresponds to ca. 0.344 V more negative potential. After addition of the copper catalyst, the initiator was introduced to the system. Since the monomer to be polymerized was MMA, EBPA was selected as the initiator. The CVs were recorded before and after addition of the initiator and as expected, a large increase in the cathodic current and decrease in the anodic current were observed, since with a very active initiator such as EBPA, a large portion of the electro-generated Cu ¹ is converted back into Cu".

Figure 13 shows a typical current versus time profile of the MMA system in anisole where the CV's were conducted periodically during polymerization. Polym6risation conditions: [MMA] = 4.5 M, [MMA]:[EBPA]:[rPMA]:[Cu ⁿ ] = 300: 1 :0.1 :0.1 , T = 50 °C. Two current profiles are shown which represent the two polymerizations conducted. The black curve is that of the E _app = having initial current values between -1 mA and -0.4 mA, whereas E _m = Em had current values at a maximum of - 0.4 mA. The high current values (black line) in combination with EBPA are most probably responsible for the early termination events occurring in the cathodic peak system. Based upon this assumption, a system where Cu ¹ is slowly fed into the polymerization system would generate better results. Nevertheless, the eATRP in anisole was proven to be a successful system for MMA. The eATRP of MMA conducted at T = 60°C resulted in a successful polymerization. Near quantitative consumption of monomer (ca. 98-100 %) was observed and linear first order kinetics. The molecular weight increased linearly with conversion although it was slightly lower than the theoretical values and the molecular weight distribution was narrow (MJM _a <1.3) the current profile resembled that of the MA system except with different time scales, each reaching minimal current values around -200 mA.

5B. Optimization of MMA Polymerization

TBACIO4 (4.69 mmol, 1.6051 g), was added to an electrochemical cell equipped with the electrodes and a condenser and flushed with nitrogen. Deoxygenated DMF (13.1 mL) and MMA (0.0907 mol, 9.7 mL) were transferred into the cell via gastight syringe. A stock solution Cu" / TPMA / Br ^' in DMSO (0.027 mmol, 0.18 mL for 300 ppm reactions, [Cu ¹¹ ] = 0.15 M; 0.009 mmol, 0.18 mL for 100 ppm reactions, [Cu ¹¹ ] = 0.05 M) was added and subsequently bubbled with nitrogen. A CV of the Cu'VCu ¹ couple was conducted to detect the possible range of applied potentials Ea- _P . The initiator EBPA (0.3 mmol, 0.053 mL) was added, followed by further bubbling for lOmin. A CV of the Cu"/Cu' + initiator system was conducted. Several potentials were defined on the basis of cathodic and anodic peak potential value (E^ and Epa, determined by CV).

Within this application the average potential between E^ and Ep, is defined as E _{1 2} . The potential difference Δ = Em - E _p c was defined and subtraction of Δ from E^ was assigned as E.1/2. The average potential between Epc and Em was defined as Ei . Figure 14 illustrates their location within the CV of the Cu'/Cu" couple. The reaction was started by applying the selected E^.

The current profile of the eATRP of MMA using EBPA as initiator, showed a significant drop in current after a certain time, the time that this drop is observed is defined as t _d ^-,, and subsequently continued trending downwards, see Figure 15(A). Application of a more negative potential or conducting the reaction at a higher temperature decreased the time period until t^ occurred.

Comparison of the current profile shape shows that a much higher slope of the current occurs in electrolysis of BA using EBiB, Figure 15(B), as initiator than for MMA with using EBP A.

Table 6 summarizes the reaction conditions for the polymerization of MMA in which variation and switching of applied potential during the reaction and the corresponding time ta _mp ; variation of temperature and initial Cu" catalyst concentration are summarized.

Table 6. A lication of two different a lied otentials to an eATRP

These experiments show that switching of the applied potential from a more negative potential to a more positive potential after t^, and decreasing reaction temperature not only improved the polydispersity but it also reduced the induction period and improved the symmetry of the GPC signals due to less formation of shoulders at higher molecular weight and less tailing at lower molecular weights.

Therefore in one embodiment of the invention two different applied potentials are applied to improve the overall level of control in an electrochemically mediated ATRP, the first a more negative potential to rapidly reduce the higher oxidation state transition metal complex to the lower oxidation state then a more positive potential to maintain the targeted ratio of two oxidation states of the transition metal complex.

Example 6: Exemplifying eATRP for a Broader Range of Monomers

The following examples expands the range of monomers by exemplifying application of an eATRP to a broader variety of monomers by defining conditions appropriate for the polymerization of ethyl acrylate (EA), butyl acrylate (BA) and styrene (sty).

6A. Polymerization of butyl acrylate

Run conditions were [BA]/[EBiB]/|TPMA]/[Cu ^ll Trf2]/[TPMA]/[TBABr] =

300/1/0.03/0.03/0.03, [BA] = 3.87 M (43 (v/v) % in DMSO:Anisole), [TBACIO4] 0.2 M, T = 40- 45 °C. Figure 16A provides the CV traces of the Cu species under a variety of conditions prior to electrolysis. As expected, addition of Br ^" to the system shifted the Cu"/Cu' catalyst couple ca. 200 mV (black to grey trace). Next, after addition of the initiator a large catalytic response was observed due to the regeneration of Cu" (dashed trace). Figure 16B shows the current and charge passed versus time. A rapid decay in current was observed approaching negligible values (10-15 uA). Rapid conversion of Cu" to Cu ¹ is observed in the early stages whereas a minimal amount of charge is required to maintain the Cu"/Cu' ratio. GPC for polymer samples collected during both experiments show narrow monomodal distributions of the polymeric species.

After conducting the initial experiments detailed above in Examples 2 and 6A, it was decided it would be appropriate to use DMF instead of DMSO as it provided several additional advantages including: (1) enhancement of K _A m< - in comparison to anisole, (2) increase the conductivity of the reaction medium, there is a large drop in resistance when incorporating DMF versus anisole, and (3) improve the solubility of Sty, MMA, and BA polymers in the reaction medium.

6B. Optimizing reaction conditions for polymerization of butyl acrylatc

6B 1) [BAJ/tEBiBl/tTPMAJ/tCu^rrf _! j lTPMAl rTBABr] = 300/1/0.09/0.09/0.09, [BA] =

3.87 M, [TBACIOJ 0.2 M, T = 44 °C. 300 ppm catalyst was used in each instance. Three different voltammograms were obtained for the polymerization mixture prior to electrolysis, Figure 17A. As expected, a typical copper couple was observed with quasi-reversible behavior in reference to Ag/Agl. Anodic and cathodic peaks were separated by ca. 80 mV under fully compensated conditions. After addition of an initiator a large catalytic response was observed due to the regeneration of Cu" resulting in an increased cathodic response. Each of these voltammograms was conducted under typical stagnant conditions. The final CV was conducted with stirring. Three clear regions were observed: (1) onset of reduction of Cu" (2) a proportional/linear increase in cathodic current with potential and (3) a limiting current region (at diffusion controlled limits). An equation was developed which describes the limiting current value (; ^' i(t)) as a function of time when using a potential value within the limiting current region. This specific CV indicates where no further rate enhancement is possible by providing a more negative potential.

6B 2) Reaction conditions: [BA]/[EBiB]/[TPMA]/[Cu"Trf ₂ ]/[TPMA]/[TBABr] =

300/1/0.09/0.09/0.09, [BA] = 3.87 M, [TBACIO ₄ ] 0.2 M, T = 44 °C. Four different polymerizations were conducted with identical formulations but increasingly more negative potentials. A clear trend is observed, Figure 17B: increasingly negative potentials provide an increase in apparent rate coefficients. However, a limiting region exists somewhere between 80-120 mV past the whereby a small rate enhancement was observed. Surprisingly the molecular weight and M M _n data in each experiment displayed similar behavior. When applying more positive potential (2T _P and Em) lower MJM _a values were observed indicative of the presence of a larger amount of Cu" in the system.

Rapid conversion of Cu" to Cu ¹ is observed in the early stages, typically less than 30 minutes whereas a minimal amount of charge is required to maintain the Cu ^u /Cu' ratio. Also the initial current values were larger with a larger E _m which generally can be related to the rate of reduction of Cu" to Cu ¹ and therefore indicates the relative concentration of Cu"

6B 3) Reaction conditions: [BA]/[EBiB]/[TPMA]/[Cu"Trf ₂ ]/|TPMA]/[TBABr] =

300/1/X/X/X, [BA] = 3.87 M, [TBACIO ₄ ] 0.2 M, T = 44 °C. The next variable which was investigated was the concentration of Cu" initially added to the system. The E _app in all instances was 80 mV more negative than the cathodic peak potential (E _p c). It was predicted that higher

concentrations of copper should yield increased rates of polymerization and lower M„/M _n values.

Pseudo-first order kinetic plots were generated to examine the function of the concentration of copper. As the concentration of copper increases the rate of polymerization was observed to increase to a root dependence of the relative copper concentrations. The increase in molecular weight was linear with respect to conversion in all cases, however, the Cu" concentration had a profound impact on the MJM _B values as the polymerization proceeded with higher concentrations of copper leading to lower w/ „ values. As we know the MJM _a value corresponds to the following equation:

The current profiles also reflect the relative concentration of Cu" in the system.

6B 4) In an effort to further improve the eATRP process the effect of minimization of the supporting electrolyte was investigated. Reaction conditions:

[BA]/[EBiB]/[TPMA]/[Cu ^1, Trf ₂ ]/|TPMA]/[TBABr] = 300/1/0.9/0.9/0.9, [BA] = 3.9 M, [TBACIO ₄ ] = X M, T = 44 °C. The E _apfl in all instances was 80 mV more negative than the cathodic peak potential {E _p c)- The relative resistance of the reaction medium was clearly observed when decreasing the concentration of TBACIO ₄ and the resistance values were progressively increased from 500 to 14,500 ohms at 0.2 M to 0 M, respectively. When examining the rate of polymerization as a function of supporting electrolyte, a visible reduction in the apparent rate constant can be observed as the concentration of supporting electrolyte is decreased. When no supporting electrolyte was used polymerization still occurred, however a large induction period was observed. Without being limited by the proposed mechanism it is believed that the decrease in the rate of polymerization can be explained as a result of an increase in the resistance of the solution. When all process involved in the reaction are fast, this leaves the electron transfer of the reaction as the limiting factor. Measurements of the electron transfer constant for the electrode .(Tsec)) are determined in the following equation:

were R _s [Ω] is the solution resistance and C _d [F] is the capacitance.

Therefore, as the solution resistance increases the time of electron transfer become longer and ultimately slows the polymerization (this phenomena is also in relation to migration of ions to the WE and CE). This is bolstered by the current profiles where a decrease in current is observed with less supporting electrolyte. However the change in rate had no effect of either M _a or MJM _n .

In one embodiment of the invention the rate of polymerization is modified by the concentration of the added electrolyte.

6C. Polymerization of styrene

TBACIO ₄ (4.69 mmol, 1.6051 g) was added to an electrochemical cell fitted with the electrodes and a condenser then the flask was flushed with nitrogen prior to the addition of deoxygenated DMF (12.4 mL), and styrene (0.0907 mol, 10.4 mL) via a gastight syringe. A stock solution of Cu'VTPMA/Br in DMSO (300 ppm of Cu", 0.027 mmol, 0.18 mL, [Cu ⁿ ] = 0.15 M) was added then the reaction mixture was bubbled with nitrogen for 15 min. A CV of the Cu'VCu ¹ couple was conducted to detect the cathodic peak potential Epc. The initiator EBiB (0.3 mmol, 0.044 mL) was added, followed by further bubbling with nitrogen for 5 min. then the C V of the Cu'VCu ¹ + initiator system was conducted. The reaction was started by applying the cathodic peak potential Epc at a temperature of 90°C. The experimental molecular weights were slightly higher than the theoretical, which suggests termination of radicals in the early phase of the reaction however the GPC signal did not show any shoulder at higher molecular weights, nor significant tailing to lower molecular weight region.

Example 7: Preparation of Polymers with More Complex Topologies.

The anisole system was in part developed in order to be directly applicable to synthesis of more complex architectures through TRP. Anisole, in addition to being suitable solvent for a wide range of monomers, is also commonly used in the synthesis of stars and brushes through ATRP.

7A PrtBA-stars. The first eATRP synthesis of star macroraolecules was attempted with

P«BA-Br macroiiutiators under potentiostatic conditions. Starting conditions for star synthesis: [PnBA] = 0.02 M, [PnBA]:[DVB]:[TPMA]:[Cu ^H ] = 1 : 12:0.2:0.1 , T = 90 °C. An initial CV was recorded for the macroinitiator (MI) to determine a suitable potential for synthesis of P«B A stars, which was selected to be at the cathodic peak, indicated by dashed circle in Figure 18(A). The decay of current was slower than typical eATRP polymerization systems, and reached a near steady state at ca. -0.05 mA, Figure 18(B). Once the current reached its steady state no additional Mi's were incorporated into the star. In addition, the mmol of Cu ⁿ electrolyzed during star synthesis never reached full conversion of the initially added Cu". The E _i?p would correspond to a radio of

[Cu"]/[Cu'] = ~ 0.07, meaning that a maximum of ca. 14 mmol should have been possible. This experiment showed that ca. 1 1 mmol of Cu" was converted to Cu'. The GPC traces of samples collected as the polymerization progressed showed almost quantitative consumption of the inacroinitiators, although a small tail was observed in the final star indicating that some lower molecular weight species existed, which were either a result of terminated chains during macroinitiator synthesis or from termination reactions during the activation stage of the star synthesis from the added macroinitiators. NMR revealed near complete consumption of divinyl benzene (DVB) after ca. 9 h. The final molecular weight and molecular weight distribution of the star polymer was 60,000 g/mol and 1.40 respectively.

Example 8: Controlled Aqueous ATRP of OEOMA

Cu ^lw TPMA, which is one of the most active complexes used in ATRP, was chosen as the catalyst system. In cyclic voltammctry screening the CU"L ²⁺ exhibits a reversible peak couple with £°' = -0.245 V vs SCE, Figure 19. Addition of a large excess of Br ^" to the solution does not significantly affect this CV response, indicating that the Κχ of Cu ^ll L ²⁺ is very small, Figure 20 curve a. The full reversibility of the response at very low scan rates confirms that CU'L ⁺ is quite stable in H ₂ 0 with a lifetime of at least few seconds, the time scale of CV. Using the above reported £°' value together with other available thermodynamic data, the value of K _D was estimated to be 6.8* 10 ^'3 for the disproportionation of Cu'L ⁺ . The CV response of Cu"L ²⁺ drastically changes when an equimolar amount of the initiator, 2-hydroxyethyl 2-bromoisobutyrate (HEBriB) is added, Figure 20 curve b. The cathodic peak approximately doubles in height while the anodic one decreases, clearly indicating that Cu'L ⁺ rapidly reacts with HEBriB. On the basis of thermodynamic data available in the literature, the estimated ^ATRP value for this system isl .5x 10 ^" ', which is 4 orders of magnitude higher than that measured for an analogous system in CH ₃ CN. An estimate of the activation rate constant based on voltammetric analysis of the system Cu"L ²⁺ + HEBriB at different concentration ratios are shown in Figure 20 curves b and c, and different scan rates provide a very large value for k _Kl ≥2.5* 10* M ^" 's ^" '.

The above described voltammetric analyses show that the system under investigation has all the characteristics that make aqueous ATRP reactions very difficult to control; low K _x , high K _MW , and extremely rapid activation. Therefore, it represents an excellent test of the potential of the proposed electrochemical method to resolve problems still facing application of ATRP to certain systems, herein exemplified by aqueous ATRP.

The electrogeneration of the active catalyst was carried out under potentiostatic conditions starting from the catalytic system Cu"L ²⁺ /HEBriB 1 : 1 in ¾0 + 10% OEOMA ₄₇ 5 (MW = 475 gmol ^"1 ). The effect of E _ipp on the degree of control over polymerization was first investigated. Three E _app values around E" were applied, points marked on Figure 1 , and the results are summarized in Table 7 (entries 1-3). The driving force of the electrochemical process is given by AG* = F(E _pp - E") and the [Cu"L ² ]/[Cu'L ⁺ ] ratio at the electrode surface is closely related to that dictated by the Nemst equation. At the beginning of the electrolysis there is only Cu"L ⁺ in solution, so the current has to decay as Cu" is converted to Cu ¹ , approaching a constant value corresponding to the [Cu ⁿ L ²⁺ ]/[Cu'L ⁺ ] ratio required by -¾, _ρ . However, CU'L* is engaged in a reversible reaction with the initiator and the formed dormant species, which represents a continuous perturbation to the equilibrium concentrations imposed by E _ipp . Therefore, whether a constant [Cu ^,, L ²⁺ ]/[Q-'l-. ⁺ ] ratio can be imposed in the bulk solution depends on the mutual rates of electrogeneration and disappearance of Cu'L* and therefore will depend on E _m .

At E _m = -0.55 V, which is « E ³ ', the electrode process is under diffusion control and Cu"L ²⁺ is almost quantitatively converted to Cu'L ^* in a relatively short time; the current rapidly decreases to very small values. The overall rate of the process was rather high, with 79% of monomer conversion in less than 30 min, but control over polymerization was poor. The ln([M]/[M]o) vs time plot deviated significantly from linearity, while the molecular weight distribution of the formed polymer was very broad and the final experimental M„ was 3 times larger than the theoretical one, Table 7, entry 1. These features are typical of an uncontrolled polymerization dominated by termination reactions, such as bimolecular radical-radical coupling reactions.

With £Ό _Ρρ = -0.31 V, the current decays much less rapidly than in the case of the electrolysis at -0.55 V, but tends to a constant value after a long period. Under these conditions, the rate of polymerization decreased without significant improvement in the control, Table 7, entry 2.

With E _m = -0.21 V, the current decays very slowly, approaching a constant value (~ -250 uA) within a short period. Under these conditions £ _w > which implies an equilibrium

[Cu"L ²⁺ /[Cu'L ⁺ ] ratio » 1. In this case, the process is under a good control as judged by the linearity of the first-order kinetic plot, _n increases linearly as a function of monomer conversion and polymers with MJM _a ~ 1.2 are obtained and nearly quantitative monomer conversion. This striking improvement of control is achieved with low charge consumption. This is a clear evidence of a drastic decrease of the termination events due to a good balance between [Cu'l ] and [Cu ⁿ L ²⁺ ].

To promote the formation of XCu"L ⁺ some experiments were run in the presence of a large excess of X ^" (Table 7, entries 4-5). As shown, the presence of X~ produces a noticeable improvement of MW distribution without any loss in the rate of monomer conversion. Furthermore, the overall rate of the process does not decrease due to the formation of inactive Cu'X„ species as was found in organic solvents when excess X ^" is added. [Macro olecules, 2010, 42, 9257-9267; Chem. Commun. 2011, 47, 3580-3582.] Linear first-order kinetic plots were observed for all the polymerizations carried out with [Cu"L ²⁺ ] = 0.1 mM, Figure 21. In particular, experiments with different degrees of polymerization gave a fairly constant slope, d(ln [ ]o [M])/dt, suggesting that the radical concentration is unaltered.

8B. eATRP of OEOMA ₄₇₅ in water in the presence of added salts

PBS buffer was selected as an exemplary salt since it is employed in reactions seeking bio- conjugation of a protein with a water soluble polymer. Since £*' shifts to -0.326 in this medium was adjusted to -0.275 V. Although several interferences perturbing the ATRP equilibrium are possible (e.g., highly insoluble Cu'^PO^ and/or stable Cu'(H ₂ P0 ₄ ) ₂ and Cu'Cl ₂ ^" may form [Chem. Commun. 2011, 47, 3580-3582], excellent results were observed both in terms of conversion and MJM _a , Table 7, entry 5. Indeed, neither displacement of the ligand nor loss of catalysis was observed by CV analysis of the system.

The effect of targeting different DPs was explored (Table 7, entries 6-8) using 0.1 mM Cu"L ² 6.4 mol ppm with respect to solvent, and different concentrations of monomer. All polymerizations displayed linear ln([M]/[M] ₀ ) vs time plots which, together with low MJM _B values of the final polymer, is indicative of ATRP under good control. However, the experimental M _a was significantly higher than the theoretically predicted one. This is due to low initiation efficiency at the beginning of the polymerization. Improvement was obtained with PBS buffer, Table 7, entry 9. In conclusion, aqueous eATRP overcomes the most serious drawbacks associated with conventional aqueous ATRP. The balance between Cu"l.. ²⁺ and CU'L ⁺ , which is crucial for control, can be regulated by appropriate selection of £ _app by following the simple CV analysis herein disclosed for each targeted monomer and initiator. The best results were achieved at E _apg >

providing excellent control over MW and MW distribution, accompanied by a fast reaction and a low charge consumption. Remarkably, phosphates and halide ions can not only be tolerated but can have a beneficial effect on the level of control over the polymerization. This last observation could be attractive for biological systems.

Example 9: eATRP Minicmulsion.

Initial experimentation involved preparation of a miniemulsion and characterization using CV.

CV traces representing the cathodic and anodic discharges of the miniemulsion system were examined in the absence of Cu/TPMA, Figure 22. When viewing CV's conducted in the cathodic direction the reduction of protons begins around -1.6 V to generate ¾ whereas in the anodic direction oxidation of water occurs to generate O ₂ at around 1 V, these discharges may not be water but rather monomer. Upon closer examination of the cathodic CV a small current response can be seen around between 0.2 and -0.1 V, indicative of the presence of Cu BPMODA catalyst in the system. Larger potentials were not probed in these CV experiments due to passivation of the electrode. After identifying the current response of Cu"/BPMODA further scans were recorded at various scan rates. As expected, the BPMODA couple current increased with increasing scan rate. The larger scan rates allowed accurate identification of the catalyst couple. The intensity of the current indicates that the catalyst complex is for the most part inaccessible to the electrode and resides within or at the surface of the miniemulsion particles or organic phase.

The addition of Cu'/TPMA significantly changed the response, Figure 22. The TPMA response resembles that of a transition metal complex participating in catalytic behavior, as indicated by the large cathodic and small anodic current. This behavior indicates that Cu'VTPMA is regenerated by participating in homogenous bulk reactions, presumably those shown in the following equations, direct activation of the initiator (14) and electron transfer with Cu' BPMODA (15):

Cu'/TPMA + RX <→ Cu'VTPMA + R ^* (14) Cu'/TPMA + Cu'VBPMODA→ Cu'VTPMA + Cu'/BPMODA (15)

In addition the large current response indicates that Cu TPMA is assessable to the electrode and remains mostly within the aqueous phase. Table 7: Electrochemical aqueous ATRP of OEOMA ₄₇ 5 at 25°C

[a] [CuV*] = 1 mM. [b] [Cu ⁿ L ²⁺ ] = 0.1 mM. [c] 0.1 M. [d] 0.137 M NaCl + 2.7 mM KCI + 1 1.9 mM (Na ₂ (HP0 ₄ )+KH ₂ P0 ₄ ) in H ₂ 0; pH = 7.4. [e] Determined by Ή NMR.

[fj Determined by GPC-MALLS

Table 8: Summary of miniemulsions by eATRP.

Ent. Exp. ^app Temp. [HD]:[Brij] ^a Solids ⁶ [E] DLS time A»MR lGPC MJM _n

(#) m (V) (°C) wt. (%) vs M (%) M nm/PDI 00 (%)

1 2-79 -0.550 65 5.4:4.6 19.7 0.019 143/0.147 10 n/a n a 22,751 1.96

2-80-1 -0.310 65 5.4:4.6 1 .7 0.019 131/0.162 2.5 n/a n/a 39,1 10 14.1

3 2-82 -0.296 65 3.7:4.6 19.7 0.020 143/0.147 4.0 63.8 32,941 17,238 1.93

All reactions have the following molar ratios: [BA]/rEBiB]/[BPMODA]/[TPMA]/[Cu"] = 400/1/0.4/0.4/0.8

[a] - (m _HO m _BA )*100. [b] - solid content = (m _B A/(m _t o..meiecm _> ))*100. [c] - without Cu BPMODA

A series of control experiments were conducted to investigate the origin o the Cu"/TPMA catalytic response, as shown in Figure 23(A). The black curve represents a miniemulsion system formulated with both TPMA and BPMODA ligands and EBiB as initiator. This CV represents the total catalytic response from both Cu"/BPMODA and EBiB interacting with Cu'/TPMA. A second miniemulsion was then formulated without Cu'VBPMODA which is represented by the dark grey curve. As evident from the CV, there is a substantial decrease in the current response when

Cu"/BPMODA is not present. This result confirms that indeed Cu' TPMA interacts with

Cu'VBPMODA. A third formulation was made, where initiator was not added, which also resulted in a significant decrease in current as compared to the system containing all reagents (light grey curve). These results confirm that both chemical pathways exist simultaneously and may indicate that Cu'/TPMA reacts at a faster rate with EBiB than with CU'VBPMODA.

Figure 23(B) represents a miniemulsion formulated without EBiB while still containing Cu'VBPMODA. TPMA ligand, that had not been precomplexed with Cu, was then added to the reaction medium. Interestingly, the TP A complex couple appeared (black curve) which indicates that ligand exchange occurred. The TPMA effectively stole the Cu from the preformed Cu/BPMODA complex. Afterward, a second charge of Cu" was added for complexation with TPMA which resulted in an increase in current as expected (grey curve).

After conducting these control reactions to illustrate the mechanism through which electron transfer occurs in a biphasic reaction medium, three miniemulsion polymerization reactions were conducted as summarized in Table 8. The first polymerization was conducted utilizing a potential past the cathodic peak to ensure efficient and rapid reduction of Cu"/TPMA to Cu'/TPMA. The polymer obtained after 10 h reaction displayed a high molecular weight and a relatively broad M _w M _n . The uncontrolled behavior of this system was attributed to the large reducing potential applied to the polymerization. Therefore, a second polymerization was conducted with a lower applied potential, entry 3. Similar to the first polymerization the resulting polymer exhibited a higher molecular weight with a broad M,JM _a . Owing to the fact that Cu' TPMA can react with EBiB and to demonstrate that Cu'VBPMODA is required to obtain any level of control a third polymerization was conducted without addition of BPMODA (entry 2). This polymerization resulted in preparation of a polymer with a very high value for M„M_, reaching a value of 14. The results exemplify the profound effect of having a hydrophobic ligand (BPMODA) present in the system.

Most importantly the results indicate that the presence of both a hydrophilic and a hydrophobic ligand provides an e(ATRP) emulsion system and leads to the conclusion that development of a more active hydrophobic ligand, such as an AlkMejTREN ligand, which would allow lower temperature miniemulsions to be conducted and be well suited for eATRP in

miniemulsion systems. Such an active hydrophobic catalyst complex could, indeed should, function with a less active hydrophilic ligand, such as 2, 2-bipyridene, that would not act to reduce the concentration of the catalyst in the dispersed phase. Improved control would result if the less reactive catalyst resides predominately in the aqueous phase otherwise lower concentrations of XCu"/L will be retained in the oil phase and if there in no deactivator, there is no control. So preferentially one should either match the reactivity of both hydrophilic and hydrophobic catalyst complexes and/or put the less reactive complex in the aqueous phase.

In one embodiment of the invention control of an emulsion polymerization is attained by addition of a hydrophilic ligand.and a hydrophobic ligand.

Example 10: Galvanostatic eATRP

Galvanostatic conditions are attractive from an industrial standpoint because they allow the elimination of the reference electrode.

Reaction conditions: [BA]/|EBiB]/[TPMA]/[Cu ^1, Trf ₂ ]/[TPMA]/rTBABr] = 300/1/0.9/0.9/0.9,

[BA] = 3.9 M, [TBACIO4] 0.2 M, T = 44 °C. The current profile shown in Figure 24 A was obtained at an Ea _PP 80 mV more negative than the cathodic peak potential (Epc). This profile was used to determine the appropriate currents for the galvanostatic polymerization. This current profile was divided up into two main regimes: (1) initial reduction of Cu" to Cu ¹ and (2) maintenance of the current to compensate for termination events during polymerization. The area under the current profile was calculated to determine the total charged passed in each regime, afterward this value was divided by the desired time of that regime (i.e. this is an average current). Two current values were determine as shown in Figure 24 A and applied to begin polymerization. The potential at the working electrode was monitored as the polymerization proceeded, as shown in Figure 24 B. As the polymerization took place the E remained in close proximity to the Cu'VCu ¹ couple, however, near the end of each current stage it began to shift to more negative potentials. This indicates that in the vicinity of the electrode, nearly all Cu ⁿ was converted to Cu', and therefore the potentiostate began to apply a stronger reducing potential to maintain these current values. The resulting polymerization results are shown in Figure 25 (A & B). The rate of polymerization was slower in comparison to the potentiostatic experiment simply because of a smaller applied current. In regard to polymerization control, the polymerization displayed a linear increase in molecular weight with conversion and low M _w /M _a values during the course of the polymerization confirming that galvanostatic eATRP are possible.

Example 11: Copper removal and catalyst regeneration in an tATRP

11 A. As discussed above in section 4E, one of the significant advantages of eATRP is the ability to remove then recycle the transition metal from the polymerization medium. Therefore a variety of different potentials were applied to either deposit Cu on the Pt working electrode, or strip the bound copper from the working electrode, and/or promote polymerization of BA. Reaction conditions: rBA]/rEBiB]/[TPMA]/[Cu ^ll Trf ₂ ]/[TP A]/[TBABr] = 300/1/0.03/0.03/0.03, [BA] = 3.9 M, [TBACIO4] 0.2 M, T = 45 °C. 100 ppm catalyst was used in this polymerization. Figure 26 shows that with a sufficiently negative potential that Cu° deposition is possible. Figure 27A shows that the reaction rate slows when this process is occurring, between 1.5 and 2.45h and increases again when the potential is changed to reform Cu" seen after 3 h in Figure 27A. Chain end functionality is not affected by this reduction in concentration of catalyst and continues to increase in a regular manner throughout the reaction, Figure 27 B.

11 B. Initial reaction conditions: [BA]/[EBiB]/[TPMA]/[Cu"Trf ₂ ]/rTBABr] =

300/1/0.09/0.09/0.09, [BA] = 3.9 M, [TBAC10 ₄ ] 0.2 M, T = 60 °C. 300 ppm catalyst was in this polymerization. After 1.5. hr conversion was 72%, see Table 9, the temperature of the reactor was increased to 60 °C, an applied potential was adjusted to be past that of the Cu° deposition peak was applied. The current profile shows a decrease in the current indicating the depletion of Cu in the reaction medium. The process is rather slow and required nearly 9 h for the current to reach nominal values. A UV-Vis calibration curve was generated so that the concentration of copper could be determined before and after the deposition and the resulting concentration of copper can be seen in

Table 9. This process resulted in nearly 85 % of the Cu being removed from the reaction vessel. There was visual confirmation of the copper deposition on the platinum electrode.

Table 9: Summary of polymer characterization and copper concentration before and after electrodeposition .

time Conversion w, M M _W (Cu]

<h) (%) (mM) polymerization 1.5 72.0 28,000 1.09 1.15 deposition #1 1.5 80.1 28,300 1.09 0.78 deposition #2 14 96.9 28,600 1.12 0.18

In one embodiment of the invention the reaction is initially exposed to a larger potential to quickly generate the desired concentration of Cu'Br and then the applied potential is lowered to maintain the [Cu'Br] at a lower constant level thereby providing a lower concentration of propagating radicals to generate a reduced fraction of terminated chains.

Another embodiment allows the synthesis of well-controlled polymers using a low amount of catalyst by using electrochemistry to directly reduce a targeted fraction of the X-Mt ^x+1 deactivator to the Mt ^x activator, exemplified in these initial examples by a X-Cu" deactivator and Cu ¹ activator.

In another embodiment of the invention the polymerization reaction can be started and stopped by changing the potential applied to the reaction medium. This is a convenient procedure for controlling any exotherm in a polymerization reaction by incorporating a feedback loop into the electrochemical control process.

In a further embodiment the rate of polymerization can be controlled through the magnitude of the voltage applied to the system.

The embodiments disclosed herein can be summarized as, but are not limited to, allowing dynamic modulation of polymerization rates through electrochemical means, allowing "on demand" polymerization initiation, cessation, and rejuvenation of a controlled/living radical polymerization process thereby providing an enhanced level of polymerization control through an external potential source, i.e. potentiostat, affording complete kinetic control by the magnitude of E _m . The disclosed procedure can additionally offer adjustable "dials", e.g. current, potential, and total charge passed, to manipulate/control polymerization activation/deactivation, polymerization rates, and selective targeting of electro-active species which thereby affords complete kinetic control by the magnitude of applied potential, without addition of chemical reducing agents, at low catalyst concentrations.