ALKOXYSILALKYLENESILANE COMPOUND

CROSS REFERENCE TO RELATED APPLICATIONS

[0001] This application claims the benefit of U.S. Provisional Patent Application Serial No. 63/392,299 filed on 26 July 2022 under 35 U.S.C. §119 (e). U.S. Provisional Patent Application Serial No. 63/392,299 is hereby incorporated by reference.

TECHNICAL FIELD

[0002] A carbamate-functional alkoxysilalkylenesilane compound and methods for its preparation and use are provided. The compound can be reacted with polyorganosiloxane having a silanol moiety to form a polyalkoxy-functional polyorganosiloxane, which is useful in condensation reaction curable compositions.

INTRODUCTION

[0003] Polyalkoxy-functional polydiorganosiloxanes are useful in moisture curable polyorganosiloxane compositions. Polyalkoxy-functional polyorganosiloxanes can be synthesized by endcapping vinyl-functional polyorganosiloxanes with polyalkoxy-functional hydrogensiloxane oligomers via hydrosilylation reaction as described, for example, in U.S. Patents 10968317, 11098163, 11168181, and 11161939 or PCT Patent Application Publication W02020-0231755. However, this endcapping process suffers from the drawbacks of relatively high cost and relatively small number of vinyl-functional polyorganosiloxanes that are commercially available, resulting in a limited selection of costly polyalkoxy-functional polyorganosiloxane products.

SUMMARY

[0004] A carbamate-functional alkoxysilalkylenesilane compound is provided.

Methods for the preparation and use of the compound are also provided. The compound can be used in a silylation reaction to cap a silanol moiety of a polyorganosiloxane. The resulting polyalkoxy-functional polyorganosiloxane is useful in condensation reaction curable polyorganosiloxane compositions.

DETAILED DESCRIPTION

[0005] The compound introduced above may comprise formula: each R ¹ is independently selected from the group consisting of a hydrogen atom and an alkyl group of 1 to 6 carbon atoms, with the proviso that two instances of R ¹ may be bound together to form a cyclic moiety; each R ² is independently selected from the group consisting of alkyl groups and aryl groups;

D is an alkylene group; and each R ⁴ is an independently selected alkyl group of 1 to 6 carbon atoms.

[0006] In the formula for the compound, each R ¹ may be the same or different. The alkyl group for R ¹ has 1 to 6 carbon atoms and is exemplified by methyl, ethyl, propyl (including n- propyl and isopropyl), butyl (including n-butyl, t-butyl, sec-butyl, and isobutyl), pentyl (including n-pentyl and branched saturated hydrocarbon groups of 5 carbon atoms), and hexyl (including n-hexyl and branched saturated hydrocarbon groups of 6 carbon atoms). Alternatively, two instances of R ¹ may be bonded together to form a cyclic secondary amine moiety with the nitrogen atom shown in the formula for the compound. Alternatively, each R ¹ may be independently selected from the group consisting of hydrogen and alkyl groups of 1 to 4 carbon atoms. Alternatively, each R ¹ may be selected from the group consisting of hydrogen, methyl, and ethyl.

[0007] In the formula for the compound, each R ² may be the same or different. Each R ² is independently selected from the group consisting of alkyl groups and aryl groups. The alkyl group may have 1 to 6 carbon atoms and is as described above for the alkyl group for R ¹ . Suitable aryl groups for R ² may have 6 to 12 carbon atoms and are exemplified by phenyl, tolyl, xylyl, and naphthyl; alternatively phenyl. Alternatively, each R ² may be an alkyl group of 1 to 6 carbon atoms. Alternatively, each R ² may be methyl or ethyl. Alternatively, each R ² may be methyl.

[0008] In the formula for the compound, D is an alkylene group, which may have 2 to 20 carbon atoms, alternatively 2 to 10 carbon atoms, alternatively 2 to 8 carbon atoms, alternatively H ₂

2 to 6 carbon atoms, and alternatively 2 to 4 carbon atoms. Examples include {also drawn: -CH2-CH2-}, ₃ . {also drawn: drawn -CH(CH ₃ )-CH ₂ -}, -CH2-CH2-CH2-CH2-

, -CH2-CH(CH ₃ )-CH2-, and -CH(CH ₃ )-CH2-CH2-. Alternatively, each D may be selected from the group consisting of -CH2-CH2- and -CH(CH ₃ )-.

[0009] In the formula for the compound, each R ⁴ may be the same or different. Each R ⁴ is an independently selected alkyl group. The alkyl group may have 1 to 6 carbon atoms and is as described above for the alkyl group for R ² . Alternatively, each R ⁴ may be an alkyl group of 1 to 4 carbon atoms. Alternatively, each R ⁴ may be methyl or ethyl. Alternatively, each R ⁴ may be methyl.

Methods for Making the Compound

[0010] The compound described above may be prepared by a method comprising:

1) combining, under conditions to effect reaction, starting materials comprising

C) a carbamate salt;

D) a hydridochlorosilane of formula ClSiR ² 2H, where R ² is as described above; and optionally H) the solvent; thereby forming a reaction product comprising

E) a carbamate-functional hydridosilane of formula R ¹ 2NC(=O)O-SiR ² 2H where R ¹ and R ² are as described above; and

J) a side product; and

2) combining, under conditions to effect hydrosilylation reaction, starting materials comprising:

E) the carbamate-functional hydridosilane;

F) an alkenyl-functional alkoxysilane of formula R ³ Si(OR ⁴ ) ₃ , where R ³ is an alkenyl group and R ⁴ is as described above;

G) a hydrosilylation reaction catalyst; optionally H) the solvent; thereby forming a reaction product comprising:

I) the carbamate-functional alkoxysilalkylenesilane compound described above. [0011] Starting material C), the carbamate salt used in step 1) of the method above, may be commercially available. For example, ammonium carbamate of formula H2N-C(=O)OH ■ NH3 is available from Sigma Aldrich Inc. of St. Louis, Missouri, USA.

[0012] Alternatively, the method for preparing the compound may comprise an optional step for forming the carbamate salt. In an optional additional step, starting material A) an amine having a formula selected from the group consisting of R ¹ 2NH, R ¹ NH2, or a combination thereof (where R ¹ is as described above) may be used. Suitable amines are known in the art and commercially available. For example, the amine may be a dialkylamine such as diethylamine (HN(CH ₂ CH ₃ ) ₂ ) or dimethylamine (HN(CH ₃ ) ₂ ). Dialkylamines are commercially available from various sources, such as Sigma Aldrich Inc. of St. Louis, Missouri, USA. Alternatively, the amine may be a monoalkylamine, such as propylamine (H2NCH2CH2CH3) or butylamine (H ₂ NCH ₂ CH ₂ CH ₂ CH ₃ ). Alternatively, the amine may be a cyclic secondary amine. Alternatively, a combination of a dialkylamine and a monoalkylamine may be used.

[0013] Starting material B) is carbon dioxide of formula CO ₂ , which is known in the art and commercially available. For example, gaseous CO2 may be purchased from various sources, such as Air Products and Chemicals of Allentown, Pennsylvania, USA. Solid CO2 (cardice) may also be purchased from various sources such as EZPro Delivery.

[0014] Starting material H) is a solvent that may optionally be used in the method. Solvents that can be used herein are those that help fluidize the starting materials, but essentially do not react with the starting materials. The solvent may be selected based on solubility of the starting materials and volatility of the solvent. The solubility refers to the solvent being sufficient to dissolve and/or disperse a starting material. Volatility refers to vapor pressure of the solvent. The solvent used for preparing the carbamate salt may comprise an aromatic hydrocarbon such as benzene, toluene, ethylbenzene, or xylene; an aliphatic hydrocarbon such as heptane, hexane, or octane; a halogenated hydrocarbon, such as dichloromethane or chloroform; or a combination of two or more thereof. Such solvents are known in the art and are commercially available.

[0015] The optional step recited above for forming the carbamate salt may be performed by any convenient means, such as adding the amine, and when present the solvent, into a reaction vessel and bubbling gaseous CO2 through the vessel, or by adding cardice to a reaction vessel containing the amine, and when present the solvent. The headspace in the reaction vessel may be kept under inert conditions, such as with an inert gas (e.g., nitrogen) during formation of the carbamate salt. The carbamate salt formed may have formula R ¹ ₂ NH ₂ ⁺ R ¹ ₂ NC(=O)O-, where R ¹ is as described above. In this method, forming the carbamate salt according to the optional step may be performed before step 1). The amount of B) the carbon dioxide is not critical, but may be a molar excess with respect to A) the amine. [0016] In step 1) of this method, starting materials comprising C) the carbamate salt described above and D) a hydridochlorosilane of formula ClSiR ² 2H, where R ² is as described above, are combined under conditions to effect reaction of the carbamate salt and the chlorine.

Hydridochlorosilanes are known in the art and may be prepared by known methods, such as the Direct Process. Examples of hydridochlorosilanes include dimethylchlorosilane (Me^HSiCl) and phenylmethylchlorosilane (PhMeHSiCl), which are commercially available from Sigma Aldrich Inc.

[0017] Additional solvent may be added in step 1). The solvent in step 1) may be the same as, or different from, the solvent used for forming the carbamate salt, if used. The hydridochlorosilane and the solvent may optionally be combined, e.g., by mixing, before adding the hydridochlorosilane to the carbamate salt in the reaction vessel described above. Step 1) produces a reaction product comprising a carbamate-functional hydridosilane and a side product. The carbamate-functional hydridosilane may have formula R ¹ 2NC(=O)O-SiR ² 2H, where R ¹ and R ² are as described above.

[0018] Step 1) may be performed by mixing starting materials comprising C) the carbamate salt and D) the hydridochlorosilane (and H) the solvent, when present). Mixing may be performed at RT, alternatively with heating to a temperature that will not decompose the carbamate, e.g., < 150 °C. Alternatively, step 1) may be performed with cooling. Step 1) may be performed under inert, dry conditions. Step 1) produces a reaction product comprising E) a carbamate-functional hydridosilane and a side product. . The method may optionally further comprise purifying the reaction product by any convenient means such as filtration, distillation and/or stripping to recover E) the carbamate-functional hydridosilane and remove all or a portion of H) the solvent, if used and/or any side product that may form, such as an alkylammonium chloride of formula R^N ^4- Cl’, where R ¹ is as described above.

[0019] The carbamate-functional hydridosilane, E), produced as described above may have formula R ¹ 2NC(=O)O-SiR ² 2H, where R ¹ and R ² are as described above. The carbamate- functional hydridosilane is used in step 2) of the method described above, which comprises combining, under conditions to effect hydrosilylation reaction, starting materials comprising: E) the carbamate-functional hydridosilane, F) an alkenyl-functional alkoxysilane, G) a hydrosilylation reaction catalyst, and optionally H) the solvent.

[0020] Starting material F) is an alkenyl-functional alkoxysilane that may have formula R ³ Si(OR ⁴ )3, where R ³ is an alkenyl group and R ⁴ is as described above. Alkenyl-functional alkoxysilanes are known in the art and are commercially available. Examples include vinyltrimethoxysilane, vinyltriethoxysilane, allyltrimethoxysilane, allyltriethoxysilane, hexenyltrimethoxysilane, and hexenyltriethoxysilane, all of which are commercially available, for example, from Gelest, Inc. of Morrisville, Pennsylvania, USA.

[0021] In the method described above, the amounts of starting materials E) and F) are not critical, however, starting materials E) and F) may be used in a weight ratio, E)/F), of 1/1 to 1/5, alternatively 1/1 to 1/3.

[0022] Starting material G) is a hydrosilylation reaction catalyst. This catalyst will promote a reaction between the alkenyl groups in F) the alkenyl-functional alkoxysilanes and the silicon bonded hydrogen atoms in E) the carbamate-functional hydridosilane. Said catalyst comprises a platinum group metal. The platinum group metal may be selected from the group consisting of platinum, rhodium, ruthenium, palladium, osmium, and iridium. Alternatively, the platinum group metal may be platinum. The hydrosilylation reaction catalyst may be the platinum group metal or a compound or complex of the platinum group metal. For example, the hydrosilylation reaction catalyst may be a compound such as chloridotris(triphenylphosphane)rhodium(I) (Wilkinson’s Catalyst), a rhodium diphosphine chelate such as [1,2- bis(diphenylphosphino)ethane] dichlorodirhodium or [1,2- bis(diethylphospino)ethane]dichlorodirhodium, chloroplatinic acid (Speier’s Catalyst), chloroplatinic acid hexahydrate, platinum dichloride, or a complex of such a compound with an organopolysiloxane such as l,3-diethenyl-l,l,3,3-tetramethyldisiloxane complexes with platinum (Karstedt’ s Catalyst) or Pt(O) complex in tetramethyltetravinylcyclotetrasiloxane (Ashby’s Catalyst). Alternatively, the compound or complex may be microencapsulated in a matrix or coreshell type structure. Hydrosilylation reaction catalysts are known in the art, for example, as described in PCT Patent Application Publication WO2021/081822 and the references cited therein. Hydrosilylation reaction catalysts are commercially available, for example, SYL-OFF™ 4000 Catalyst and SYE-OFF™ 2700 are available from Dow Silicones Corporation of Midland, Michigan, USA.

[0023] The amount of G) the hydrosilylation reaction catalyst is sufficient to catalyze hydrosilylation reaction of the silyl hydride moiety of starting material E) and the alkenyl group of starting material F), and the amount depends on various factors including the reaction conditions and species of starting materials E) and F) selected, however the amount may be sufficient to provide the platinum group metal in an amount of at least 5 ppm, alternatively at least 50 ppm, alternatively at least 100 ppm, alternatively at least 200 ppm, and alternatively at least 400 ppm, based on combined weights of starting materials E) and F); while at the same time the amount of G) the hydrosilylation reaction catalyst may be up to 10,000 ppm, alternatively up to 5,000 ppm, alternatively up to 2,000 ppm, alternatively up to 1,000 ppm, alternatively up to 600 ppm, on the same basis. [0024] Starting material H) is a solvent as described above, which may be the same as or different from the solvent used in step 1) and/or in the optional step for forming the carbamate salt. One or more of the starting materials described above for use in step 2) may be dissolved or dispersed in a solvent before combining in step 2). For example, the hydrosilylation reaction catalyst may be dissolved in a hydrocarbon solvent, such as toluene, before use in step 2). The amount of solvent used in step 2) is not critical and may be, for example 0 to 95 weight %, alternatively > 0 weight % to 90 weight %, based on combined weights of starting materials E), F), G), and H).

[0025] Step 2) may be performed by any convenient means, such as mixing and heating. The same reaction vessel for step 1) may be used. Alternatively a different reaction vessel may be used. The vessel may be purged with an inert gas such as nitrogen. The starting materials may be added in any order. Alternatively, E) the carbamate-functional hydridosilane and H) a solvent may be added to the reaction vessel. Thereafter, a portion of F) the alkenyl-functional alkoxysilane may be added, and the contents of the vessel may be mixed. Starting material G), the hydrosilylation reaction catalyst may be dissolved in H) the solvent. A portion of the resulting catalyst/solvent solution may be added to the reaction vessel with mixing. Step 2) may be performed at RT. Alternatively, in step 2), the contents of the reaction vessel may be heated, at a temperature up to 150 °C for a time sufficient to complete reaction, alternatively at 70 °C for up to 18 h. Thereafter, one or more additional portions of F) the alkenyl-functional alkoxysilane may be added and the catalyst/solvent solution may be added with mixing and heating. Between additions, volatiles may be removed by any convenient means such as stripping, at RT or with heating and optionally with reduced pressure.

[0026] Step 2) produces a hydrosilylation reaction product comprising I) the carbamate- functional alkoxysilalkylenesilane compound described above. The method may optionally further comprise one or more additional steps. For example, I) the compound may be recovered from the hydrosilylation reaction product by any convenient means such as filtration, stripping and/or distillation optionally with heating and/or reduced pressure.

[0027] The method described above is illustrated in Scheme 1 and Examples 1 and 2, hereinbelow. Scheme 1 - Exemplary Method for Forming the Compound

Optional Step and Step 1 ):

[0028] The hydrosilylation reaction product produced by the method described above comprises a combination of compounds with linear and branched linkers (P adduct and a adduct, respectively) represented by D in the formula for the compound shown hereinabove.

[0029] Alternatively, the compound shown by the formula hereinabove may be prepared by an alternative method comprising:

1) combining, under conditions to effect hydrosilylation reaction, starting materials comprising

F) an alkenyl-functional alkoxysilane of formula R ³ Si(OR ⁴ )3, where R ³ is an alkenyl group and R ⁴ is as described above;

D) the hydridochlorosilane of formula ClSiR ² 2H, where R ² is as described above;

G) the hydrosilylation reaction catalyst; and optionally H) the solvent; thereby forming a hydrosilylation reaction product comprising

E’) a chlorodialkyl((trialkoxysilyl)alkylene)silane of formula ClSiR ² 2-D- Si(OR ⁴ )3; where R ² , D and R ⁴ are as described above; and

2) combining, under conditions to effect reaction, starting materials comprising

E’) the chlorodialkyl((trialkoxysilyl)alkylene)silane;

C) the carbamate salt; and optionally H) the solvent; thereby forming a reaction product comprising 1) the carbamate-functional alkoxysilalkylenesilane compound described above, and

J’) a side product.

[0030] In this alternative method, C) the carbamate salt may be commercially available, or may be prepared in an optional step in the same manner as described hereinabove. When used in this alternative method, the optional step may be performed before or after step 1). However, step 1) of this alternative method comprises combining, under conditions to effect hydrosilylation reaction, starting materials comprising: F) the alkenyl- functional alkoxysilane, D) the hydridochlorosilane, G) the hydrosilylation reaction catalyst, and optionally H) the solvent, each of which is as described hereinabove. Step 1) may be performed in a different reaction vessel than the optional step of forming the carbamate salt, described above, is used. The starting materials may be added to the vessel in any order. Step 1) may comprise mixing and heating the starting materials. Alternatively, H) the solvent and F) the alkenyl-functional alkoxysilane may be combined in the reaction vessel with mixing. The hydridochlorosilane may be added, followed by a catalyst/solvent solution (prepared as described above). The vessel contents may be mixed, optionally with heating at, e.g., 30 °C, for a time sufficient to effect hydrosilylation reaction, e.g., up to 72 hours. Alternatively, the reaction mixture may be cooled to control the exothermic hydrosilylation reaction. The resulting hydrosilylation reaction product comprises E’) a chlorodialkyl((trialkoxysilyl)alkylene)silane. The chlorodialkyl((trialkoxysilyl)alkylene)silane may comprise ClSiR ² 2-D-Si(OR ⁴ )3; where R ² , D and R ⁴ are as described above. This may be a mixture having both linear and branched linkers, D. The method may optionally further comprise recovering the chlorodialkyl((trialkoxysilyl)alkylene)silane from the hydrosilylation reaction product by any convenient means such as filtration, stripping, and/or distillation with heating and/or reduced pressure.

[0031] Step 2) of this alternative method comprises combining, under conditions to effect reaction, starting materials comprising: E’) the chlorodialkyl((trialkoxysilyl)alkylene)silane prepared as described above; C) the carbamate salt described above; and optionally H) the solvent. The solvent may be the same as or different from the solvent used in step 1) and/or the optional step, when present. Step 2) may be performed in the same reaction vessel used for step 1) or a different reaction vessel. Step 2) may be performed, for example, by mixing the carbamate salt and the solvent (e.g., benzene) in the reaction vessel. The vessel may be purged with an inert gas, such as nitrogen. The chlorodialkyl((trialkoxysilyl)alkyl)silane may be added, e.g., metered into the reaction vessel intermittently or continuously until all has been added, at RT. The reaction vessel may be heated or cooled to control the exothermic hydrosilylation reaction. The resulting mixture may be stirred for a period of time at RT to complete the reaction, e.g., up to 18 hours. The reaction product of step 2) comprises I) the carbamate- functional alkoxysilalkylenesilane compound and K) a side product. The method may further comprise one or more additional steps, such as recovering the compound from the reaction product by any convenient means such as filtration, stripping, and/or distillation at RT or elevated temperature, optionally with reduced pressure.

[0032] This alternative method is illustrated below in Scheme 2 and Examples 1, 4, and 5, herein below.

Scheme 2 - Exemplary Method for Making the Compound

+

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Step 2): ^{N H} 4 ^Cl

[0033] The reaction product produced by the alternative method described above comprises a combination of compounds with linear and branched linkers (P adduct and a adduct, respectively) represented by D in the formula for the compound shown hereinabove.

Preparing a Polyalkoxy-functional Polyorganosiloxane using the Compound [0034] The compound described above is useful in a silylation reaction for capping a silanol moiety. A method for capping a silanol moiety of a polyorganosiloxane comprises: 1 ) combining, under conditions to effect silylation reaction, starting materials comprising: I) the compound of the formula above; and II) a polyorganosiloxane having a silanol moiety. This method may further comprise preparing 1) the compound by practicing a method described above before step 1 ). This method produces a reaction product comprising a polyalkoxyfunctional polyorganosiloxane.

[0035] The polyorganosiloxane having the silanol moiety, II), is not specifically restricted, provided that II) the polyorganosiloxane has, per molecule, at least one silicon bonded (HO1/2) group capable of a capping reaction with the carbamate functionality of I) the compound. The polyorganosiloxane may be linear, branched, cyclic, or resinous. The polyorganosiloxane may comprise unit formula: (R ⁵ 3SiOi/2)a(R ⁵ 2SiO2/2)b(R ⁵ SiO3/2)c(SiO4/2)d(HOi/2)e, where each R ⁵ is independently selected from the group consisting of a monovalent hydrocarbyl group (e.g., alkyl, alkenyl, and aryl) and a monovalent halogenated hydrocarbyl group (e.g., haloalkyl, haloalkenyl, and haloaryl); subscripts a, b, c, d, and e represent average numbers of each unit per molecule and have values such that a > 0, b > 0, c > 0, d > 0, and e > 1 , and 2 < (a + b + c + d) < 10,000. Alternatively, the subscripts may have values such that 2 < (a + b + c + d) < 2,000; alternatively 2 < (a + b + c + d) < 1,000. Suitable alkyl groups for R ⁵ are as described and exemplified above for R ² . Suitable aryl groups for R ⁵ are as described and exemplified above for R ² . Suitable alkenyl groups for R ⁵ are as described and exemplified above for R ³ . The monovalent halogenated hydrocarbyl groups are monovalent hydrocarbyl groups, as described above, except that at least one hydrogen atom has been formally replaced with a halogen atom. For example, haloalkyl groups include chloromethyl and fluoromethyl. Alternatively, each R ⁵ may be an alkyl group such as methyl or ethyl, or an aryl group such as phenyl. Alternatively, each R ⁵ may be selected from methyl and phenyl. Alternatively, each R ⁵ may be methyl.

[0036] Alternatively, II) the polyorganosiloxane having the silanol moiety may be a polydiorganosiloxane, such as bis -hydroxy 1-terminated polydiorganosiloxane (e.g., where in the unit formula above a = c = d = 0, b > 1, and e = 2) of formula described above and subscript x represents degree of polymerization and has an average value of 1 to 2,000, alternatively 1 to 1,000. Alternatively, each R ⁵ may be independently selected from the group consisting of alkyl groups, alkenyl groups, and aryl groups. Alternatively, each R ⁵ may be an alkyl group such as methyl or ethyl, or an aryl group such as phenyl. Alternatively, each R ⁵ may be selected from methyl and phenyl. Alternatively, each R ⁵ may be methyl. The bis -hydroxy 1-terminated polydiorganosiloxane is exemplified by i) bis-hydroxyl-terminated polydimethylsiloxane, ii) bis-hydroxyl-terminated poly (dimethylsiloxane/methylphenylsiloxane) , iii) bis-hydroxyl-terminated poly(dimethylsiloxane/diphenylsiloxane), or iv) a combination of two or more of i) to iii).

[0037] Suitable polyorganosiloxanes having the silanol moiety are known in the art and are commercially available. For example, polyorganosiloxane resins with various silanol contents are available from The Dow Chemical Company of Midland, Michigan, USA, as described, for example, in the Silicone resins and intermediates Selection guide at Silicone Resins and Intermediates Selection Guide (dow.com). Polydiorganosiloxanes with silanol moieties are also available from The Dow Chemical Company of Midland, Michigan, USA, under the tradename XIAMETER™ OHX Polymers. Examples are described, for example, in the XIAMETER Brand Sealant Formulation Materials for North America (dow.com).

[0038] Capping the silanol moiety of the polyorganosiloxane with the compound produces a polyalkoxy- functional polyorganosiloxane. For example, the capped polyorganosiloxane may comprise unit formula: (R ⁵ 3SiOi/2) _a (R ⁵ 2SiO2/2)b(R ⁵ SiO3/2)c(SiO4/2)dR ⁶ e, where R ⁶ is a group of formula subscripts a, b, c, d, and e are as described above.

[0039] When the bis-hydroxyl-terminated polydiorganosiloxane is capped, the resulting polyalkoxy-functional polyorganosiloxane comprises formula: x and R ⁵ , R ² , D, and R ⁴ are as described above. The polyalkoxy-functional polyorganosiloxane described above may be useful, e.g., as a crosslinker, in moisture curable polyorganosiloxane compositions. EXAMPLES

[0040] The following examples are provided to illustrate the invention to one skilled in the art and are not to be interpreted as limiting the scope of the invention set forth in the claims.

Starting materials used in the examples are described in Table 1.

Table 1 - Starting Materials

Example 1 - Synthesis of O-dimethylsilyl-N.N-diethylcarbamate

[0041] To a dry 250 mL round-bottom flask, cooled in an ice bath, was added through a rubber septum, under positive N2 pressure and with stirring, dichloromethane (100 mL) and diethylamine (16.9 mL, 12.0 g, 164 mmol, 2.0 equiv.). To the mixture was cautiously added solid CO2, until the solution was saturated, followed by a solution of dimethylchlorosilane (10.0 mL, 8.52 g, 90.0 mmol, 1.1 equiv.) in dichloromethane (10 mL) via syringe over 10 minutes. CO2 was periodically added over the following 30 minutes, then the mixture was allowed to warm to room temperature. The mixture was quickly filtered through a disposable frit and the dichloromethane was removed at ambient temperature under reduced pressure. The residue was dissolved in hexane and filtered through a disposable frit. The hexane was removed under reduced pressure to give a crystalline white solid (11.94 g, 68.1 mmol, 83%). ¹ H NMR analysis confirmed the presence of O-dimethylsilyl-7V,lV-diethylcarbamate.

Example 2 - Synthesis of dimethyl(2-(trimethoxysilyl lethyl )sil yl diethylcarbamate (ETM- carbamate-NEt2)

[0042] The following procedure was conducted in a dry, nitrogen-purged glove box. To a dry 40 mL vial was added CMimethylsilyl-2V,jV-diethylcarbamate (2.60 g, 14.8 mmol) and dry toluene (25 mL). To the solution was added vinyltrimethoxysilane (1.25 mL, 8.15 mmol, 0.55 equiv.) and the mixture was stirred (magnetic stirrer). A solution of Karstedt’s catalyst in toluene (“Pt solution”, 2.5 wt% Pt, 10.4 pL) was added. The mixture was stirred at 70°C for 3 h, and the progress of the reaction was monitored via gas chromatography. A second portion of vinyltrimethoxysilane (1.25 mL, 8.15 mmol, 55 equiv.) was then added, and the mixture was stirred at 70°C for 18 h. An additional volume of Pt solution (10.4 pL) was added, and the mixture was stirred at 70°C for 6 h. An additional volume of Pt solution (10.4 pL) was added, and the mixture was stirred at 70°C for 18 h. Volatiles were removed under reduced pressure at RT. NMR, ¹³ C NMR, and GC showed a clean reaction to form a ca. 9:1 mixture of B/a hydrosilylation products (dimethyl(2-(trimethoxysilyl)ethyl)silyl diethylcarbamate), with ca. 15- 25% unreacted dimethylhydridosilyl diethylcarbamate.

Preparation Example 3 - Synthesis of Chlorodimethyl((trimethoxysilyl)ethyl)silane

[0043] The following procedure was conducted in a dry, nitrogen-purged glove box. A dry 250 mL round-bottom flask was charged with dry toluene (100 mL) and vinyltrimethoxysilane (8.3 mL, 8.0 g, 54 mmol). To the stirring solution was added dimethylchlorosilane (6.6 mL, 5.6 g, 59 mmol, 1.1 equiv.) followed by a solution of Karstedt’s catalyst in toluene (2.5 wt% Pt, 22.5 pL). The mixture was stirred at 30°C for 72 hours and then filtered through a pad of alumina. The toluene was removed under reduced pressure at ambient temperature. and ¹³ C NMR spectroscopy and GC showed no residual vinyltrimethoxysilane or dimethylchlorosilane and confirmed the product contained ca 14 wt% toluene, and was a mixture of the B addition product (86%) and a addition product (14%). Mass of product was 15.0 g (12.6 g at 84 wt%, 51.9 mmol, 96%).

Example 4 - Synthesis of dimethyl(2-(trimethoxysilyl)ethyl)silyl dimethylcarbamate (ETM- carbamate-NMe2)

© ©x O M NH

(

[0044] The following procedure was conducted in a dry, nitrogen-purged glove box. To a stirring solution of dimethylammonium dimethylcarbamate (1.4 mL, 11.0 mmol, 1.3 equiv.) in dry benzene (20 mL) in dry 40 mL vial at ambient temperature was added, dropwise over ca. 2 minutes, neat chlorodimethyl(2-(trimethoxysilyl)ethyl)silane with a purity of 84% prepared as described in Example 3 (2.5 mL, 8.44 mmol). The mixture was stirred for 18 h. The mixture was filtered, and the filtrate was placed under vacuum to give a pale brown liquid. The liquid was diluted with hexanes (8 mL) and filtered through a 0.45 pm PTFE filter. The filtrate was placed under vacuum to give a colorless liquid, and NMR confirmed the presence of dimethyl(2- (trimethoxysilyl)ethyl)silyl dimethylcarbamate as a mixture of B and a addition products. Example 5 - Synthesis of Dimethyl(2-(trimethoxysilyl)ethyl)silyl carbamate (ETM-carbamate- NH ₂ )

[0045] The following procedure was conducted in a dry, nitrogen-purged glove box. To a vigorous stirring suspension of ammonium carbamate (1.002 g, 12.8 mmol, 1.5 equiv.) in dry benzene (20 mL) in a 80 mL glass jar at ambient temperature was added via a syringe, dropwise over 2 minutes, chlorodimethyl(2-(trimethoxysilyl)ethyl)silane with a purity of 84% (ca. 2.5 mL, 2.44 g, 2.05 g at 84 wt% purity, 8.44 mmol) prepared in Example 3. After stirring at ambient temperature for 1 h, the mixture was filtered through a glass frit. The filtrate was placed under vacuum to give a pale brown oil, and NMR confirmed the presence of dimethyl(2- (trimethoxysilyl)ethyl)silyl carbamate (1.70 g, 6.34 mmol, 75%).

Example 6 - Capping Hydroxyl-Terminated Polydimethylsiloxane

HOJlo J 10 J OH J? J:^^ ^Si (OMe) ₃

[0046] A dental cup was charged with PDMS-OH and a capping agent prepared as described above in one of Examples 2, 4, and 5. After mixing on a speedmixer for 5 min, the reaction mixture was kept at room temperature in a closed container or under vacuum. The reaction progress was monitored by proton ^! H NMR through the disappearance of SiOH moiety. When the reaction was complete, formation of the bis-trialkoxy -terminated PDMS was confirmed by ²⁹ Si NMR. Viscosity of the capped polydimethylsiloxane was measured by ARES rheometer (25 mm parallel cone and plate, Cone angle 0.0999 radians, Gap 0.0508 mm, The test is a steady rate sweep from 0. 1 to 10 1/s with 10 points per decade). INDUSTRIAL APPLICABILITY

[0047] The examples above show that a carbamate-functional alkoxysilalkylenesilane compound can be successfully prepared by the method described herein. The examples further show that the compound can successfully be used to cap silanol moieties of a polyorganosiloxane. These examples indicate that a wide range of polyalkoxy-functional polyorganosiloxanes can be prepared using the carbamate- functional polyalkoxysilylalkylenesilane compound of this invention to cap different commercially available silanol-functional polyorganosiloxanes due to the ready availability of various polyorganosiloxanes with silanol moieties, which may be, e.g., linear, branched, or resinous. The carbamate-functional alkoxysilylalkylenesilane compound undergoes silylation reaction to cap silanol moieties with one or more of the following benefits: the reaction proceeds without the addition of a catalyst, at RT, with no or relatively low viscosity increase; and the product may be clear (not hazy).

DEFINITIONS AND USAGE OF TERMS

[0048] Unless otherwise indicated by the context of the specification: all amounts, ratios, and percentages herein are by weight; the articles ‘a’, ‘an’, and ‘the’ each refer to one or more; and the singular includes the plural. The SUMMARY and ABSTRACT are hereby incorporated by reference. The terms “comprising” or “comprise” are used herein in their broadest sense to mean and encompass the notions of “including,” “include,” “consist(ing) essentially of,” and “consist(ing) of. The use of “for example,” “e.g. ” “such as,” and “including” to list illustrative examples does not limit to only the listed examples. Thus, “for example” or “such as” means “for example, but not limited to” or “such as, but not limited to” and encompasses other similar or equivalent examples.

[0049] “Yield” means molar amount carbamate-functional alkoxysilylalkylenesilane compound produced / molar amount carbamate -functional alkoxysilylalkylenesilane compound possible based on the amount of limiting reagent. “Selectivity” means the ratio of linear isomer/branched isomer of the carbamate-functional alkoxysilylalkylenesilane compound (where isomers have the same molecular weight).

[0050] The abbreviations used herein have the definitions in Table 4. Table 4 - Abbreviations

Test Methods

[0051] The GC test methods used in this application were performed as follows: Chromatograms were recorded using two methods. (1) (The chromatographic equipment consisted of a Hewlett Packard 5890 Series II GC equipped with a flame ionization detector and Hewlett Packard 6890 Series Autoinjector. The separation was made with a 30m HP-5 column, with 78 mL/min helium flow and 1.05 mL/min column flow. The samples were prepared as 100 pL in 1 mL dichloromethane. An injection volume of 2 p L was used, with an injector temperature of 180 °C and a detector temperature of 300 °C, and data was collected for 36.33 minutes. The oven method consisted of holding an initial temperature of 40 °C for 1 minute, followed by a ramp of 5 °C/min to 150 °C, a ramp of 15 °C/min to 275 °C, ending with holding the final temperature of 275 °C for 5 minutes.) (2). Agilent Technologies 7896A GC system fitted with a 7693 autosampler and connected to a 5975C mass spectrometer. Column: Agilent DB-5MS (phenyl-arylene, 30 m x 250 pm x 0.25 pm). Inlet temp: 250°C. Oven program: 50°C for 1 min; 10°C/min to 275°C; 275°C for 5 min. Total run time: 28.5 min. Mass spectrometer operated in chemical ionization mode I positive ion mode with methane as the reagent gas. Mass range: 50-1000. Solvent delay: 3.5 min.

[0052] The NMR test methods used in this application were performed as follows: (Proton ( ¹ H) and ¹³ C nuclear magnetic resonance (NMR) spectra were recorded on Agilent 500-MR or Varian NMR spectrometer operating at 500 MHz. Carbon ( ¹³ C) and silicon ( ²⁹ Si) NMR spectra were recorded on an Agilent 500 MHz DD2 system with a 16mm silicon free AutoZ probe. Peak frequencies are recorded in ppm. ¹ H samples were run with 100 pL sample in 1 mL deuterated chloroform (CDCh) or benzene (CeDe), while ²⁹ Si and ¹³ C samples were run with 2 mL sample in 3 mL deuterated chloroform with Cr(acac)3.) The ¹ H NMR spectra were referenced internally to residual protons in the deuterated solvents. The ¹³ C NMR spectra were referenced internally to the deuterated solvent.