TECHNICAL BACKGROUND Polymers of ethylene and other olefins are important items of commerce, and these polymers are used in a myriad of ways, from low molecular weight polyolefins being used as a lubricant and in waxes, to higher molecular weight grades being used for fiber, films, molding resins, elastomers, etc. In most cases, olefins are polymerized using a cata- lyst, often a transition metal compound or complex. These catalysts vary in cost per unit weight of polymer produced, the structure of the polymer produced, the possible need to remove the catalyst from the polyolefin, the toxicity of the catalyst, etc. Due to the commercial importance of polymer- izing olefins, new polymerization catalysts are constantly being sought.

Arylaminotropones are useful as chemical intermediates, for instance in the synthesis of pharmaceuticals and pesti- cides.

Nickel complexes of various neutral ligands and mono- anionic ligands are known as catalysts for the polymeriza- tion of ethylene and other olefins, see for instance (for monoanionic ligands) US6060569, W09830609 and W09842664, which are incorporated by reference herein for all purposes as if fully set forth. None of these references describe the use of aminotropones as ligands for nickel containing olefin polymerization catalysts.

kuchi, Bull. Chem. Soc. Jpn., vol. 51, p. 2338 (1978); T.

Nozoe, Bull. Chem. Soc. Jpn., vol. 51, p. 2185 (1978); and W. R. Brasen, J. Am. Chem. Soc., vol. 83, p. 3125 (1961).

The methods described in these references are different from the methods described herein. In addition, yields of the desired 2-anilinotropones are generally lower than reported herein, and/or sterically hindered less basic arylamines are not used in the synthesis thereof.

SUMMARY OF THE INVENTION One aspect of the present invention concerns a first process for the polymerization of olefins, comprising the step of contacting, at a temperature of about-100°C to about +200°C, one or more olefins with an active catalyst comprising a nickel complex of an anion of the formula wherein: R2 is hydrocarbyl or substituted hydrocarbyl, provided that R2 is attached to said nitrogen atom in (I) by an atom that has at least 2 other atoms that are not hydrogen at- tached to it; and R3, R4, R5, R6 and R are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl or a functional group, provided that any two of R3, R4, R5, R6 and R7 vicinal to one another may form a ring.

Another aspect of the present invention concerns a sec- ond process for the polymerization of olefins, comprising the step of contacting, at a temperature of about-100°C to about +200°C, one or more olefins with a compound of the formula

wherein: R2 is hydrocarbyl or substituted hydrocarbyl, provided that R2 is attached to said nitrogen atom in (I) by an atom that has at least 2 other atoms that are not hydrogen at- tached to it; R3, R4, R5, R6 and R are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl or a functional group, provided that any two of R3, R4, R5, R6 and R7 vicinal to one another may form a ring; Ll is a monodentate monoanionic ligand into which an olefin molecule may insert between L1 and the nickel atom, and L2 is an empty coordination site or a monodentate neutral ligand which may be displaced by an olefin, or L1 and L2 taken together are a monoanionic bidentate ligand into which an olefin may insert between said monoanionic bidentate li- gand and the nickel atom; and provided that when L1 and L2 taken together are then a cocatalyst is also present.

In the above-mentioned processes, (II) and/or the nickel complex of (I) may in and of themselves be active catalysts, or may be"activated"by contact with a cocata- lyst/activator, as exemplified by the case when L1 and L2 taken together are (I).

The present invention also concerns a compound of the formula

wherein: R2 is hydrocarbyl or substituted hydrocarbyl, provided that R2 is attached to said nitrogen atom in (I) by an atom that has at least 2 other atoms that are not hydrogen at- tached to it; and R3, R4, R, R and R are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl or a functional group, provided that any two of R3, R4, R5, R6 and R7 vicinal to one another may form a ring; L1 is a monodentate monoanionic ligand, and L2 is a monodentate neutral ligand or an empty coordination site, or Li and L2 taken together are a monoanionic bidentate ligand.

Another aspect of the present invention is a process for making 2-arylamino substituted tropones, comprising the step of contacting, in solution at a temperature of about 20°C to about 150°C, a first compound of the formula a second compound of the formula HNR9Rl9 (IV), a palladium compound, a base capable of deprotonating said second com- pound, and a third compound which is a mono-or diphosphine in which all of the bonds to phosphorous are to carbon at- oms, wherein:

R3, R4, R5, R6 and R7 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl or a functional group, provided that any two of R3, R4, R5, R6and R 7vicinal to one another may form a ring; R8 is a group such that the conjugate acid of-OR8 has a pKa of <0 in water at 20°C ; R19 is hydrocarbyl, substituted hydrocarbyl or hydrogen; and R9 is aryl or substituted aryl.

Still another aspect of the present invention is a com- pound of the formula wherein: R3, R, R, R6 and R7 are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl or a functional group, provided that any two of R3, R4, R5, R6 and R7 vicinal to one another may form a ring; and Rll, R12 R13, R14 and Rl-5 are each independently hydrogen, hydrocarbyl substituted hydrocarbyl or a functional group, provided that any two of R, R12, R13, R14 and Rl5 vicinal to one another taken together may form a ring; provided that: both of R11 and R15 are not hydrogen; and/or the total of the Hammett 6 constants for R11, R12 R13, R14 and R'5 is about 0.50 or more; and/or an Es for one or both of R11 and R15 is-0.10 or less.

A further aspect of the present invention is an anion of the formula

wherein: R2 is hydrocarbyl or substituted hydrocarbyl, provided that R2 is attached to said nitrogen atom in (I) by an atom that has at least 2 other atoms that are not hydrogen at- tached to it; and R3, R4, R, R6 and R are each independently hydrogen, hydrocarbyl, substituted hydrocarbyl or a functional group, provided that any two of R3, R4, R5, R6 and R7 vicinal to one another may form a ring.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS Herein, certain terms are used. Some of them are: A"hydrocarbyl group"is a univalent group containing only carbon and hydrogen. As examples of hydrocarbyls may be mentioned unsubstituted alkyls, cycloalkyls and aryls.

If not otherwise stated, it is preferred that hydrocarbyl groups herein contain 1 to about 30 carbon atoms.

By"substituted hydrocarbyl"herein is meant a hydro- carbyl group that contains one or more substituent groups which are inert under the process conditions to which the compound containing these groups is subjected. The sub- stituent groups also do not substantially interfere with the process. If not otherwise stated, it is preferred that sub- stituted hydrocarbyl groups herein contain 1 to about 30 carbon atoms. Included in the meaning of"substituted"are heteroaromatic rings. When a heteroaromatic ring is pres- ent, it may be attached to another group through the het- eroatom. In substituted hydrocarbyl all of the hydrogens may be substituted, as in trifluoromethyl.

By" (inert) functional group"herein is meant a group other than hydrocarbyl or substituted hydrocarbyl which is inert under the process conditions to which the compound

containing the group is subjected. The functional groups also do not substantially interfere with any process de- scribed herein that the compound in which they are present may take part in. Examples of functional groups include halo (fluoro, chloro, bromo and iodo), ether such as-OR22 wherein R22 is hydrocarbyl or substituted hydrocarbyl. In cases in which the functional group may be near a nickel atom the functional group should not coordinate to the metal atom more strongly than the groups in those compounds are shown as coordinating to the metal atom, that is they should not displace the desired coordinating group.

By"olefin"is meant a compound containing one or more olefinic double bonds. In the event that the compound con- tains more than one olefinic double bond, they should be non-conjugated. As examples of olefins may be mentioned cy- clopentene, a styrene, a norbornene, and compounds of the formulas R17CH=CH2 wherein R17 is hydrogen or alkyl.

By an oligomerization or polymerization"co-catalyst" or"catalyst activator"is meant a compound that reacts with a transition metal compound to form an activated catalyst species. A preferred catalyst activator is an"alkyl alumi- num compound", that is, a compound which has at least one alkyl group bound to an aluminum atom. Other groups such as alkoxide, hydride, and halogen may also be bound to aluminum atoms in the compound.

By"neutral Lewis base"is meant a compound, which is not an ion, that can act as a Lewis base. Examples of such compounds include ethers, amines, sulfides, and organic ni- triles.

By"neutral Lewis acid"is meant a compound, which is not an ion, that can act as a Lewis acid. Examples of such compounds include boranes, alkylaluminum compounds, aluminum halides, and antimony [V] halides.

By"cationic Lewis acid"is meant a cation that can act as a Lewis acid. Examples of such cations are sodium and silver cations.

By an"empty coordination site"is meant a potential coordination site on a metal atom that does not have a li- gand bound to it. Thus if an olefin molecule (such as an ethylene molecule) is in the proximity of the empty coordi- nation site, the olefin molecule may coordinate to the metal atom.

By a"ligand into which an olefin molecule may insert" between the ligand and a nickel atom is meant a ligand coordinated to the nickel atom into which an olefin molecule or a coordinated olefin molecule (such as an ethylene molecule or a coordinated ethylene molecule) may insert to start or continue a polymerization. For instance, this may take the form of the reaction (wherein L is a ligand): By a"ligand which may be displaced by an olefin"is meant a ligand coordinated to a transition metal, which when exposed to an olefin (such as ethylene) is displaced as the ligand by the olefin.

By a"monoanionic ligands meant a ligand with one negative charge.

By a"neutral ligands meant a ligand that is not charged.

"Alkyl group"and"substituted alkyl group"have their usual meaning (see above for substituted under substituted hydrocarbyl). Unless otherwise stated, alkyl groups and substituted alkyl groups preferably have 1 to about 30 car- bon atoms.

By a"styrene"herein is meant a compound of the for- mula

(XXXIV) wherein R43, R44, R45, R46 and R47 are each independently hydro- gen, hydrocarbyl, substituted hydrocarbyl or a functional group, all of which are inert in the polymerization process.

It is preferred that all of R43, R44, R45, R46 and R47 are hy- drogen. Styrene (itself) is a preferred styrene.

By a"norbornene"is meant ethylidene norbornene, dicy- clopentadiene, or a compound of the formula wherein R40 is hydrogen or hydrocarbyl containing 1 to 20 carbon atoms. It is preferred that R40 is hydrogen or alkyl, more preferably hydrogen or n-alkyl, and especially prefera- bly hydrogen. The norbornene may be substituted by one or more hydrocarbyl, substituted hydrocarbyl or functional groups in the R40 or other positions, with the exception of the vinylic hydrogens, which remain. Norbornene (itself), dimethyl endo-norbornene-2,3-dicarboxylate, t-butyl 5- norbornene-2-carobxylate are preferred norbornenes and nor- bornene (itself) is especially preferred.

By a"z-allyl group"is meant a monoanionic ligand with 3 adjacent sp2 carbon atoms bound to a metal center in an 3 fashion. The three sp2 carbon atoms may be substituted with other hydrocarbyl groups or functional groups.

By"aryl"is meant a monovalent aromatic group in which the free valence is to the carbon atom of an aromatic ring.

An aryl may have one or more aromatic rings which may be fused, connected by single bonds or other groups.

By"substituted aryl"is meant a monovalent aromatic group substituted as set forth in the above definition of "substituted hydrocarbyl". Similar to an aryl, a substi- tuted aryl may have one or more aromatic rings which may be fused, connected by single bonds or other groups; however, when the substituted aryl has a heteroaromatic ring, the free valence in the substituted aryl group can be to a het-

eroatom (such as nitrogen) of the heteroaromatic ring in- stead of a carbon.

The polymerizations herein are carried out by a nickel complex of anion (I). In (I), and in all complexes and com- pounds containing (I) or its parent conjugate acid, it is preferred that: R3, R4, R5, R6 and R are all hydrogen; and/or R2 is aryl or substituted aryl, especially phenyl or substituted phenyl.

Useful groups for R2 include, for example which may be substituted in any or all of their ring posi- tions. It is preferred that at least one position next to (ortho) the free valence of the aryl ring be substituted, and more preferred that both of these positions be substi- tuted. In particular it is more preferred that R2 is wherein each of Roll, R12, Rl3, R14 and R15 are independently hydrogen, hydrocarbyl substituted hydrocarbyl or a functional group, provided that any two of Roll, R12, R13, R14 and R15 vicinal to one another taken together may form a ring. In one particularly preferred form both R11 and R15 are not hydrogen, and/or R12, R13 and R14 are hydrogen. In another preferred form R11 and R15 are each independently chosen from the group consisiting of alkyl containing 1 to 6 carbon atoms, perfluoroalkyl, alkoxy, phenyl and halo, more preferably alkyl containing 1 to 4 carbon atoms, phenyl and halo. Particularly preferred are when R11 and R13 are both i- propyl or phenyl, or when R"is methyl and R15 is trifluoromethyl. Preferred specific groups (VI) are shown in Table 1.

Table 1

R R R R R Me H H H Me IPr H H H iPr TBu H H H H TBu H H H Me -Cl H. H H Cl- Br H H H Br F F F F F H CF3 H CF3 H Ph H H H Ph FHHHF All of the complexes of (I) can be made from the corre- sponding tropone In turn (VII) can be made by the process described below, using a palladium catalyst in the presence of a phosphine compound.

In a process to make (VII) the appropriately substi- tuted arylamine, (IV) (and preferred substitution is the same as in (I)), is reacted with an appropriately substi- tuted tropone ester (and preferred substitution is as in (I)), in the presence of a base, a palladium compound and a mono-or diphosphine. This reaction is carried out in solu- tion, although not all of the ingredients must be totally soluble at all times, all of the starting materials, except the base, should be at least somewhat soluble. Preferred solvents are relatively inert to all of the ingredients and products, and include hydrocarbon solvents such as toluene, and ethers such as 1,4-dioxane, ethyl ether and tetrahydro- furan.

The palladium compound may be a Pd [II] compound or a Pd [0] compound, such as palladium acetate, PdX2 wherein each X is independently halogen, and palladium bis (dibenzylideneacetone), which is preferred. The phos- phine may be a mono-or diphosphine in which all three of the bonds to phosphorous are to separate carbon atoms. It is preferred that the phosphine be somewhat sterically hin- dered. Useful phosphines include (o-tolyl) 3P, (t-Bu) 3P, 1, 1'-bis (diphenylphosphino) ferrocene, bis (2- diphenylphosphinophenyl) ether, 2- (di-t- butylphosphino) biphenyl, 2- (dicylohexylphosphino) biphenyl, and wherein each R10 is independently aryl or substituted aryl and preferably all of Rl° are phenyl (this compound is sometimes abbreviated"BINAP"). A preferred phosphine is (XI).

The base may be any metal salt, preferably an alkali metal salt, which can serve as an acceptor for the proton liberated from the arylamine during the process. The base should have at least sparing solubility in the process solvent. Useful bases include alkali metal carbonates such as cesium carbonate, alkali metal phosphates such as potassium phosphate (K3PO4), alkali metal alkoxides such as potassium t-butoxide, and alkali metal amides such as sodium hexamethyldisilamide.

In the process to make (VII) ratios of the various in- gredients are not critical, but to make efficient and eco- nomical use of the various ingredients, it is preferred that:

the molar ratio of (III): (IV) is about 0.1 to about 1.0, more preferably about 0.8 to about 0.9; the amount of gram-atoms of palladium (in whatever form the Pd is added) is about 0.01 to about 10 percent of the number of moles of tropone, more preferably about 0.5 to 1.5 percent; and/or the number of equivalents of base to moles of tropone is preferably about 1.0 to about 4.0, more preferably about 1.2 to about 1.6.

The process to make (VII) is preferably carried out at a temperature of about 20°C to about 150°C, more preferably about 50°C to about 120°C, and especially preferably about 70°C to about 90°C. It is preferred to carry out the proc- ess in the absence of water (and other active hydrogen com- pounds) and oxygen, especially in the absence of oxygen.

This is conveniently carried done by carrying out the proc- ess under an inert gas such as nitrogen or argon. The time required for this process is also not critical, 3 to 48 hours, more typically 12-15 hours, being useful ranges.

In the process to make (VII), (III) is one of the starting materials. In (III), R8 is a group such that the conjugated acid of R80-has a pKa of <0. Useful groups for R8 include R16S02-, wherein R16 is perfluorohydrocarbyl, espe- cially perfluoroalkyl, and p-tolyl. A preferred group for R8 is R16S02-, wherein R16 is perfluoroalkyl, especially trifluo- romethyl (sometimes called the"triflate"group). (III) may be made by methods known in the art, for instance the prepa- ration of 2-triflatotropone is found in A. M. Echavarren, et al., J. Am. Chem. Soc., vol. 110, p. 1557 (1988), which is included by reference herein.

The process to make (VII) (and hence (X)) herein pro- duces these types of compounds in improved yields and/or al- lows the production of compounds which cannot be produced by simple nucleophilic displacements, for instance using aro- matic amines (IV) in which the amine group is sterically hindered by substitution at one or both of the ortho posi-

tions, and/or the amine has reduced bascisity because the aromatic group bears electron withdrawing substituents.

In (IV) (and in any of the arylaminotropones subse- quently produced) it is preferred that Rl9 is alkyl, substi- tuted alkyl or hydrogen, more preferred that it is alkyl or hydrogen, and especially preferred that it is hydrogen.

The steric effect of various groupings has been quanti- fied by a parameter called Es, see R. W. Taft, Jr., J. Am.

Chem. Soc., vol. 74, p. 3120-3128 (1952), and M. S. Newman, Steric Effects in Organic Chemistry, John Wiley & Sons, New York, 1956, p. 598-603, both of which are hereby incorpo- rated by reference herein for all purposes as if fully set forth. For the purposes herein, the Es values are those for o-substituted benzoates described in these publications. If the value for Es for any particular group is not known, it can be determined by methods described in these publica- tions. For the purposes herein, the value of hydrogen is defined to be the same as for methyl (0.00). Representative values for Es are (taken from Table V in Taft and Series 2-2 through 2-10 in Newman)-OCH3 +0.97,-Br +0.01,-I-0.20, CH3CH2-0. 07, CH3CH2CH2--0. 36, i-C3H7--0. 47, t-C4H9--1. 54, C6H5--0. 90. In one preferred form of (X) the Es for either of the ortho substituents is-0.10 or less, preferably about -0.25 or less, and especially preferably about-0.50 or less.

Another preferred form of (X) is when the phenyl ring has electron withdrawing groups attached to it. The elec- tron withdrawing ability of various substituents may be measured by the Hammett constant, see for instance H. H.

Jaffe, Chem. Rev., vol. 53, p. 191-261 (1953), especially Table 7, which is hereby included by reference. Since Ham- mett substituents constants are often not calculated for or- tho substituents, for any ortho substituent the Hammett con- stant will be taken as the Hammett para constant (Cpara). The total of all the a constants for all of the substituents on the phenyl ring is about 0.50 or more, more preferably about 0.75 or more.

It is also preferred in (I) (and in compounds in which it occurs) that provided that one or more of the following obtains: both of R1l and R15 are not hydrogen; the total of the Hammett a constants for R", R12 12, R and R'5 is about 0.50 or more; and an Es for one or both of Rll and Rls is- 0.10 or less. The more preferred forms for (X) are also preferred in (I).

Herein (VII) may be converted to a nickel complex such as (II), and in turn (II) may be active in and of itself and thus useful directly as an olefin polymerization catalyst, or may be converted to an active polymerization catalyst by contact with one or more other compounds (so-called cocata- lysts). Thus (VII) may be converted to its anion by reac- tion with a strong base such as sodium hydride, and this an- ion (which is actually (I)) may be reacted with an appropri- ate nickel compound to form (II). Useful nickel compounds include: (Ph3P) 2Ni (Ph) (Cl) (see Example 13) which gives (II) in which L1 is Ph, and L2 is Ph3P ; (TMEDA) 2Ni (Ph) (Cl) in the presence of a"trapping li- gand"L2 such as pyridine, which specifically gives (IX) for instance in which L1 is Ph, and L2 is pyridine; (Ph3P) 2NiCl2 which gives (II) in which Ll is Cl, and L2 is Ph3P ; and ( (allyl) Ni (X)) 2 which gives (II) in which L1 and L2 taken together are n-allyl.

Methods of synthesis of these types of nickel complexes may also be found in previously incorporated US6060569, W098/30609 and W098/42664, and R. H. Grubbs., et al., Or- ganometallics, vol. 17, p. 3149 (1988), which is also incor- porated by reference herein for all purposes as if fully set forth.

In (II) useful groups L1 include halide (especially chloride), hydrocarbyl and substituted hydrocarbyl espe- cially phenyl and alkyl and particularly phenyl, methyl, hy- dride and acyl. Useful groups for L2 include phosphine such as triphenylphosphine, nitrile such as acetonitrile, ethers

such as ethyl ether, pyridine, and tertiary alkylamines such as TMEDA (N, N, N', N'-tetramethyl-1, 2-ethylenediamine). A1- ternatively L1 and L2 taken together may be a s-allyl n- benzyl group such as wherein R is hydrocarbyl.

In (II) when an olefion (such as ethylene) may insert between L1 and the nickel atom, and L2 is an empty coordina- tion site or is a ligand which may be displaced by an olefin (such as ethylene), or L1 and L taken together are a biden- tate monoanionic ligand into which an olefin (such as ethyl- ene) may be inserted between that ligand and the nickel atom, (II) may by itself catalyze the polymerization of an olefin. Examples of L1 into which an olefin (and particu- larly ethylene) may insert between it an the nickel atom are hydrocarbyl and substituted hydrocarbyl especially phenyl and alkyl and particularly methyl, hydride and acyl, and ligands L2 which an olefin (and particularly ethylene) may

displace include phosphine such as triphenylphosphine, ni- trile such as acetonitrile, ether such as ethyl ether, pyri- dine, and tertiary alkylamines such as TMEDA. Ligands in which L1 and L2 taken together are a bidentate monoanionic ligand into which an olefin (and particularly ethylene) may insert between that ligand and the nickel atom 71- allyl-or s-benzyl-type ligands (in this instance, sometimes it may be necessary to add a neutral Lewis acid cocatalyst such as triphenylborane to initiate the polymerization, see for instance previously incorporated W098/30609). For a summary of which ligands an olefin (and particularly ethyl- ene) may insert into (between) the ligand and nickel atom) see for instance J. P. Collman, et al., Principles and Ap- plications of Organotransition Metal Chemistry, University Science Book, Mill Valley, CA, 1987, included herein by ref- erence. If for instance L1 is not a ligand into which an olefin (such as ethylene) may insert between it and the nickel atom, it may be possible to add a cocatalyst which may convert L1 into a ligand which will undergo such an in- sertion. Thus if Ll is halo such as chloride or bromide, or carboxylate, it may be converted to hydrocarbyl such as al- kyl by use of a suitable alkylating agent such as an alkyla- luminum compound, a Grignard reagent or an alkyllithium com- pound. It may be converted to hydride by used of a compound such as sodium borohydride.

In (II) when Ll and L2 taken together are (I), in the polymerizations a cocatalyst (sometimes also called an activator) which is an alkylating or hydriding agent is also present in the olefin polymerization. It is preferred however that L1 and L2 taken together are not (I). A preferred cocatalyst is an alkylaluminum compound, and particularly preferred are trialkylaluminum compound such as trimethylaluminum, triethylaluminum and tri-i-butylaluminum, and trimethylaluminum is especially preferred. More than one such cocatalyst may be used in combination.

In the polymerizations herein homo-or copolymers of the various olefins may be produced. A preferred olefin (or

combination of olefins) is R17CH=CH2 wherein R17 is hydrogen or n-alkyl containing 1 to 15 carbon atoms, and especially preferred is when R17 is hydrogen or methyl (ethylene or pro- pylene, respectively), and more preferred is when R17 is hy- drogen (ethylene).

In the polymerization processes herein, the temperature at which the polymerization is carried out is about-100°C to about +200°C, preferably about-60°C to about 150°C, more preferably about-20°C to about 100°C. The pressure of the olefin (if it is a gas) at which the polymerization is car- ried out is not critical, atmospheric pressure to about 275 MPa being a suitable range. Generally speaking the response of the catalyst, and hence the polymer produced, to the ef- fects of temperature and pressure are similar to other nickel catalysts, see for instance US5880241 (incorporated by reference herein for all purposes as if fully set forth).

As shown in Table 3 as the temperature increases catalyst productivity increases until about 80°C (at least under these particular polymerization conditions and this cata- lyst) and then starts decreasing, and the branching level increases as the temperature increases. Up to a point at least, increasing the ethylene pressure (Table 4) increases catalyst productivity, decreases branching, and increases polymer molecular weight. It is also believed that as the ethylene pressure increases, it becomes more important that the ethylene used be of high purity. The effect of catalyst loading (Table 5) is somewhat uncertain since in Example 54 there was a large exotherm.

The polymerization processes herein may be run in the presence of various liquids, particularly aprotic organic liquids. The catalyst system, monomer (s), and polymer may be soluble or insoluble in these liquids, but obviously these liquids should not prevent the polymerization from oc- curring. Suitable liquids include alkanes, cycloalkanes, selected halogenated hydrocarbons and aromatic hydrocarbons.

Specific useful solvents include hexane, toluene, benzene, chlorobenzene, tetrahydrofuran, methylene chloride and

1,2,4-trichlorobenzene. The effects of various solvents on the polymerizations are shown in Table 7.

Various polar compounds such as ethyl acetate, trieth- ylamine, water and ethanol may be present in the polymeriza- tion, although in some instances the yields may be reduced (see Table 6). The polymerization may also be carried out in the presence of air. It is noted that the polymerization proceeds with some of these additives even though they may contain active hydrogen atoms (water, ethanol).

The olefin polymerizations herein may also initially be carried out in the"solid state"by, for instance, support- ing the nickel compound on a substrate such as silica or alumina, activating if necessary it with one or more cocata- lysts and contacting it with the olefin (s). Alternatively, the support may first be contacted (reacted) with a cocata- lyst (if needed) such as an alkylaluminum compound, and then contacted with an appropriate Ni compound. The support may also be able to take the place of a Lewis or Bronsted acid, for instance, an acidic clay such as montmorillonite, if needed. Another method of making a supported catalyst is to start a polymerization or at least make a nickel complex of another olefin or oligomer of an olefin such as cyclopentene on a support such as silica or alumina. These"heterogene- ous"catalysts may be used to catalyze polymerization in the gas phase or the liquid phase. By gas phase is meant that a gaseous olefin is transported to contact with the catalyst particle.

In all of the polymerization processes described herein oligomers and polymers of the various olefins are made.

They may range in molecular weight from oligomeric olefins, to lower molecular weight oils and waxes, to higher molecu- lar weight polyolefins. One preferred product is a polymer with a degree of polymerization (DP) of about 10 or more, preferably about 40 or more. By"DP"is meant the average number of repeat (monomer) units in a polymer molecule.

Depending on their properties, the polymers made by the processes described herein are useful in many ways. For in-

stance if they are thermoplastics, they may be used as mold- ing resins, for extrusion, films, etc. If they are elasto- meric, they may be used as elastomers. If they contain functionalized monomers such as acrylate esters, they are useful for other purposes, see for instance previously in- corporated US5880241.

Depending on the process conditions used and the polym- erization catalyst system chosen, polymers, even those made from the same monomer (s) may have varying properties. Some of the properties which may change are molecular weight and molecular weight distribution, crystallinity, melting point, and glass transition temperature. Except for molecular weight and molecular weight distribution, branching can af- fect all the other properties mentioned, and branching may be varied (using the same nickel compound) using methods de- scribed in previously incorporated US5880241.

It is known that blends of distinct polymers, that vary for instance in the properties listed above, may have advan- tageous properties compared to"single"polymers. For in- stance it is known that polymers with broad or bimodal mo- lecular weight distributions may be melt processed (be shaped) more easily than narrower molecular weight distribu- tion polymers. Thermoplastics such as crystalline polymers may often be toughened by blending with elastomeric poly- mers.

Therefore, methods of producing polymers which inher- ently produce polymer blends are useful especially if a later separate (and expensive) polymer mixing step can be avoided. However in such polymerizations one should be aware that two different catalysts may interfere with one another, or interact in such a way as to give a single poly- mer.

In such a process the Ni containing polymerization catalyst disclosed herein can be termed the first active po- lymerization catalyst. Monomers useful with these catalysts are those described (and also preferred) above. A second active polymerization catalyst (and optionally one or more

others) is used in conjunction with the first active polym- erization catalyst. The second active polymerization cata- lyst may be another late transition metal catalyst, for ex- ample as described in previously incorporated W098/30609, US5880241 and US6060569, as well as in US5714556 and US5955555, which are also incorporated by reference herein for all purposes as if fully set forth.

Other useful types of catalysts may also be used for the second active polymerization catalyst. For instance so- called Ziegler-Natta and/or metallocene-type catalysts may also be used. These types of catalysts are well known in the polyolefin field, see for instance Angew. Chem., Int.

Ed.. Engl., vol. 34, p. 1143-1170 (1995), EP-A-0416815 and US5198401 for information about metallocene-type catalysts, and J. Boor Jr., Ziegler-Natta Catalysts and Polymeriza- tions, Academic Press, New York, 1979 for information about Ziegler-Natta-type catalysts, all of which are incorporated by reference herein for all purposes as if fully set forth.

Many of the useful polymerization conditions for all of these types of catalysts and the first active polymerization catalysts coincide, so conditions for the polymerizations with first and second active polymerization catalysts are easily accessible. Oftentimes the"co-catalyst"or"activa- tor"is needed for metallocene or Ziegler-Natta-type polym- erizations. In many instances the same compound, such as an alkylaluminum compound, may be used as an"activator"for some or all of these various polymerization catalysts.

In one preferred process described herein the first olefin (s) (the monomer (s) polymerized by the first active polymerization catalyst) and second olefin (s) (the mono- mer (s) polymerized by the second active polymerization cata- lyst) are identical, and preferred olefins in such a process are the same as described immediately above. The first and/or second olefins may also be a single olefin or a mix- ture of olefins to make a copolymer. Again it is preferred that they be identical particularly in a process in which

polymerization by the first and second active polymerization catalysts make polymer simultaneously.

In some processes herein the first active polymerization catalyst may polymerize a monomer that may not be polymerized by said second active polymerization catalyst, and/or vice versa. In that instance two chemically distinct polymers may be produced. In another scenario two monomers would be present, with one polymerization catalyst producing a copolymer, and the other polymerization catalyst producing a homopolymer, or two copolymers may be produced which vary in the molar proportion or repeat units from the various monomers. Other analogous combinations will be evident to the artisan.

In another variation of this process one of the polym- erization catalysts makes an oligomer of an olefin, prefera- bly ethylene, which oligomer has the formula R7°CH=CH2, wherein R7° is n-alkyl, preferably with an even number of carbon atoms. The other polymerization catalyst in the pro- cess them (co) polymerizes this olefin, either by itself or preferably with at least one other olefin, preferably ethyl- ene, to form a branched polyolefin. Preparation of the oli- gomer (which is sometimes called an a-olefin) by a second active polymerization-type of catalyst can be found in pre- viously incorporated US5880241 as well as US6103946 (also incorporated by reference for all purposes as if fully set forth).

Likewise, conditions for such polymerizations, using catalysts of the second active polymerization type, will also be found in the appropriate above mentioned references.

Two chemically different active polymerization catalysts are used in this polymerization process. The first active polymerization catalyst is described in detail above. The second active polymerization catalyst may also meet the limitations of the first active polymerization catalyst, but must be chemically distinct. For instance, it may have a different transition metal present, and/or utilize a different type of ligand and/or the same type of

ligand which differs in structure between the first and second active polymerization catalysts. In one preferred process, the ligand type and the metal are the same, but the ligands differ in their substituents.

Included within the definition of two active polymeri- zation catalysts are systems in which a single polymeriza- tion catalyst is added together with another ligand, pref- erably the same type of ligand, which can displace the original ligand coordinated to the metal of the original ac- tive polymerization catalyst, to produce in situ two differ- ent polymerization catalysts.

The molar ratio of the first active polymerization catalyst to the second active polymerization catalyst used will depend on the ratio of polymer from each catalyst de- sired, and the relative rate of polymerization of each cata- lyst under the process conditions. For instance, if one wanted to prepare a"toughened"thermoplastic polyethylene that contained 80% crystalline polyethylene and 20% rubbery polyethylene, and the rates of polymerization of the two catalysts were equal, then one would use a 4: 1 molar ratio of the catalyst that gave crystalline polyethylene to the catalyst that gave rubbery polyethylene. More than two ac- tive polymerization catalysts may also be used if the de- sired product is to contain more than two different types of polymer.

The polymers made by the first active polymerization catalyst and the second active polymerization catalyst may be made in sequence, i. e., a polymerization with one (either first or second) of the catalysts followed by a polymeriza- tion with the other catalyst, as by using two polymerization vessels in series. However it is preferred to carry out the polymerization using the first and second active polymeriza- tion catalysts in the same vessel (s), i. e., simultaneously.

This is possible because in most instances the first and second active polymerization catalysts are compatible with each other, and they produce their distinctive polymers in the other catalyst's presence. Any of the processes appli-

cable to the individual catalysts may be used in this polym- erization process with 2 or more catalysts, i. e., gas phase, liquid phase, continuous, etc.

Catalyst components which include Ni complexes of (I), with or without other materials such as one or more cocata- lysts and/or other polymerization catalysts are also dis- closed herein. For example, such a catalyst component could include the Ni complex supported on a support such as alu- mina, silica, a polymer, magnesium chloride, sodium chlo- ride, etc., with or without other components being present.

It may simply be a solution of the Ni complex, or a slurry of the Ni complex in a liquid, with or without a support be- ing present.

The polymers produced by this process may vary in mo- lecular weight and/or molecular weight distribution and/or melting point and/or level of crystallinity, and/or glass transition temperature and/or other factors. For copolymers the polymers may differ in ratios of comonomers if the dif- ferent polymerization catalysts polymerize the monomers pre- sent at different relative rates. The polymers produced are useful as molding and extrusion resins and in films as for packaging. They may have advantages such as improved melt processing, toughness and improved low temperature proper- ties.

Hydrogen or other chain transfer agents such as silanes (for example trimethylsilane or triethylsilane) may be used to lower the molecular weight of polyolefin produced in the polymerization process herein. It is preferred that the amount of hydrogen present be about 0.01 to about 50 mole percent of the olefin present, preferably about 1 to about 20 mole percent. When liquid monomers (olefins) are pres- ent, one may need to experiment briefly to find the relative amounts of liquid monomers and hydrogen (as a gas). If both the hydrogen and monomer (s) are gaseous, their relative con- centrations may be regulated by their partial pressures.

In the Examples, all pressures are gauge pressures.

Branching was determined by 1H NMR, taking the total of the

methyl carbon atoms as the number of branches. Branching is uncorrected for end groups. The following abbreviations are used: BINAP-see compound (XI) dba-dibenzylideneacetone EtOAc-ethyl acetate EtOH-ethanol Mn-number average molecular weight Mp-melting point NEt3-triethylamine PDI-weight average molecular weight/number average molecular weight PhCl-chlorobenzene RT-room temperature THF-tetrahydrofuran Tm-melting point Examples 1-11 Preparation of 2-Anilinotropones General Procedure A-The Conversion of 2-Triflatotropone to 2-Anilinotropones with Liquid Anilines A Schlenk tube, flame-dried in vacuo, was placed under an Ar atmosphere on a vacuum line. The tube was charged with Pd2 (dba) 3 (5 mg, 0.005 mmol), rac-BINAP (7 mg, 0.01 mmol), Cs2CO3 (456 mg, 1.4 mmol), and 2-triflatotropone (254 mg, 1.0 mmol). Toluene (2 mL) was added followed by the appropriate aniline (1.2 mmol). The Schlenk tube was sealed and heated to 80°C for approximately 12 h. The reaction mixture was allowed to cool to RT, filtered through a pad of silica gel with the aid of ethyl ether (100 mL), and concentrated to afford the crude product. Purification was effected via flash column chromatography on silica gel.

General Procedure B-The Conversion of 2-Triflatotropone to 2-Anilinotropones with Solid Anilines A Schlenk tube, flame-dried in vacuo, was placed under an Ar atmosphere on a vacuum line. The tube was charged with Pd2 (dba) 3 (5 mg, 0.005 mmol), rac-BINAP (7 mg, 0.01 mmol), Cs2CO3 (456 mg, 1.4 mmol), 2-triflatotropone (254 mg,

1.0 mmol), and the appropriate aniline (1.2 mmol). Toluene (2 mL) was added and the Schlenk tube was sealed and heated to 80°C for approximately 12 h. The reaction mixture was allowed to cool to RT, filtered through a pad of silica gel with the aid of ethyl ether (100 mL), and concentrated to afford the crude product. Purification was effected via flash column chromatography on silica gel.

The individual Examples 1-11 below give the aniline used to produce the corresponding 2-anilinotropone (substi- tution patter on the phenyl rings remained the same).

Example 1 General procedure A was used to convert 2,6- dimethylaniline (148 pl, 1.2 mmol) to the desired product in 15 h. Purification via flash column chromatography (eluants 3: 2 hexane: ether) afforded 201 mg (90% yield) of an orange solid. Mp: 76-78°C. 1H NMR (250 MHz, CDC13) : 8. 40 (bs, 1 H); 7.32 (m, 2 H); 7.18 (m, 3 H); 7.08 (t, J = 10. 5 Hz, 1 H); 6.73 (m, 1 H); 6.22 (d, J = 10. 5 Hz, 1 H); 2.15 (s, 6 H). 13C NMR (100 MHz, CDC13) : 6 176. 6,154.6,137.3,136.3, 136.2,135.1,129.9,128.7,127.8,123.5,109.6,18.0.

Anal. Calcd for CisHigNO : C, 79.97; H, 6.71; N, 6.22. Found: C, 79.92; H, 6.71; N, 6.05.

Example 2 General procedure A was used to convert 2,6-di-i- propylaniline (227 pl, 1.2 mmol) to the desired product in 14 h. Purification via flash column chromatography (eluants 2: 1 hexane: ether) afforded 242 mg (86% yield) of an orange solid. Mp: 86-88°C. 1H NMR (200 MHz, CDC13) : 8 8.42 (bs, 1 H); 7.43-7.24 (m, 5 H); 7.06 (t, J = 10.2 Hz, l H); 6.71 (m, 1 H); 6.26 (d, J = 10.2 Hz, 1 H); 2.90 (m, 2 H); 1.15 (d, J = 7.0 Hz, 6 H); 1.11 (d, J = 7.0 Hz, 6 H). 13C NMR (100 MHz, CDC13) : 6 176.5,156.4,146.9,137.5,136.2,132.5, 130.0,128.9,124.4,123.6,110.4,28.6,24.6,23.4. Anal.

Calcd for C1gH23NO : C, 81.10; H, 8.24; N, 4.98. Found: C, 81.15; H, 8.20; N, 4.94.

Example 3 General procedure A was used to convert 2-t- butylaniline (187 pl, 1.2 mmol) to the desired product in 16 h. Purification via flash column chromatography (eluants 3: 1 hexane: ether) afforded 221 mg (88% yield) of an orange solid. Mp: 92-94°C. 1H NMR (250 MHz, CDC13) : 8 8.80 (bs, 1 H); 7.53 (m, 1 H); 7.35-7.25 (m, 4 H); 7.20 (m, 1 H); 7.10 (d, J = 10.2 Hz, 1 H); 6.75 (m, 2 H); 1.37 (3,9 H). 13C NMR (100 MHz, CDC13) : 8 176.8,155.2,146.8,137.5,136.8,136.2, 130.0,128.6,127.7,127.3,127.2,123.7,110.8,35.1,30.5.

Anal. Calcd for Cl7HlgNO : C, 80.59; H, 7.56; N, 5.53. Found: C, 80.34; H, 7.52; N, 5.51.

Example 4 General procedure A was used to convert 2-t-butyl-6- methylaniline (196 mg, 1.2 mmol) to the desired product in 15.5 h. Purification via flash column chromatography (elu- ants 2: 1 hexane: ether) afforded 97 mg (36% yield) of an or- ange solid. Mp: 115-117°C. 1H NMR (200 MHz, CDC13) : 6 8.69 (bs, 1 H); 7.41-7.18 (m, 5 H); 7.09 (t, J = 10.2 Hz, 1 H); 6.73 (m, 1 H); 6.17 (d, J = 10.2 Hz, 1 H); 2.06 (s, 3 H); 1.32 (s, 9 H). 23C NMR (100 MHz, CDC13) : 6 176.7,155.2, 148.4,137.6,135.1,130.0,129.5,127.9,125.4,123.6, 111.0,35.5,31.1,18.6. Anal. Calcd for Cl8H2lNO : C, 80.86; H, 7.92; N, 5.24. Found: C, 80.61; H, 7.93; N, 5.14.

Example 5 General procedure B was used to convert 2,6- dichloroaniline (194 mg, 1.2 mmol) to the desired product in 14.5 h. Purification via flash column chromatography (elu- ants 2: 1 hexane: ether) afforded 200 mg (75% yield) of an or- ange solid. Mp: 63-65°C. 1H NMR (200 MHz, CDC12) : 6 8.48 (bs, 1 H); 7.47 (d, J = 8.0 Hz, 2 H) ; 7.37 (m, 2 H); 7.26 (t, J = 8.0 Hz, 1 H); 7.13 (t, J = 10.2 Hz, 1 H); 6.83 (m, 1 H); 6.29 (d, J = 10.2 Hz, 1 H). 13C NMR (100 MHz, CDC13) : 8 177.1,152.4,137.5,135.7,134.0,133.5,131.7,129.0, 128.7,125.3,111.3. Anal. Calcd for C13HgNOCl2 : C, 58.67; H, 3.41; N, 5.26. Found: C, 58.78; H, 3.46; N, 5.22.

Example 6 General procedure B on half the scale with the modifi- cation of 12 mg (0.0125 mmol) Pd2dba3 and 16 mg (0.025 mmol) rac-BINAP was used to convert 2,6-dibromoaniline (151 mg, 0.60 mmol) to the desired product in 15 h. Purification via flash column chromatography (eluants 2: 1 hexane: ether) af- forded 122 mg (69% yield) of an orange solid. Mp: 73-75°C.

1H NMR (200 MHz, CDC13) : 8 8.49 (bs, 1 H); 7.68 (d, J = 8. 0 Hz, 2 H); 7.35 (m, 2 H); 7.12 (m, 2 H); 6.83 (m, 1 H); 6.27 (d, J = 10.2 Hz, 1 H). 13C NMR (100 MHz, CDC13) : 6 177.1, 152.5,137.6,136.3,135.4,133.0,131.9,129.9,125.3, 124.4,111.3. Anal. Calcd for C13H_gNOBr2 : C, 43.98; H, 2.56; N, 3.95. Found: C, 43.88; H, 2.61; N, 3.88.

Example 7 General procedure B was used to convert 2,3,4,5,6- pentafluoroaniline (220 mg, 1.2 mmol) to the desired product in 15.5 h. Purification via flash column chromatography (eluants 2: 1 hexane: ether) afforded 256 mg (84% yield) of a green solid. The compound was isolated as a hydrate. Mp: 156-158°C. 1H NMR (400 MHz, CDC13) : 8 8.19 (bs, 1 H); 7.38 (dd, J = 8.2,11.8 Hz, 1 H); 7.32 (d, J = 11.0 Hz, 1 H); 7.15 (t, J = 10.2 Hz, 1 H); 6.87 (t, J = 9.0 Hz, 1 H); 6.49 (dt, J = 2.6,10.0 Hz, 1 H); 2.14 (s, 2 H, coordinated H2O).

13C NMR (100 MHz, CDC13) : 8 177.2,151.6,143.0 (dm, J = 250 Hz), 139.7 (dm, J = 253 Hz), 138.1 (dm, J = 253 Hz), 137.7, 135.2,132.5,126.4,113.7 (dt, J = 3. 8,14.2 Hz), 111.6.

9F NMR (376 MHz, CDC13) : 5-144. 5 (m),-157.31 (m),-161.87 (m). Anal. Calcd for C13H6NOF5 : C, 54.36; H, 2.11; N, 4.88.

Found: C, 54.31; H, 2.18; N, 4.81.

Example 8 General procedure A was used to convert 3,5- bistrifluoromethylaniline (188 pl, 1.2 mmol) to the desired product in 15.5 h. Purification via flash column chromatog- raphy (eluants 2: 1 hexane: ether) afforded 313 mg (89% yield) of a green solid. Compound was isolated as a hydrate. 1H NMR (400 MHz, CDC13) : b 8.87 (bs, 1 H); 7.75 (s, 2 H); 7.66 (s, 1 H); 7.38 (dd, J = 8.5,11.8 Hz, 1 H); 7.31 (d, J =

11.8 Hz, 1 H); 7.20 (m, 2 H); 6.89 (m, 1 H) ; 2. 15 (s, 2.7 H, coordinated H20). 13C NMR (100 MHz, CDC13): 6 117. 5,151.7, 140.8,137.8,135.4,132.9 (q, J = 33.5 Hz), 132.3,126.6, 122.9 (q, J = 271 Hz), 122.7, (d, J = 2.9 Hz), 117.9 (t, J = 3.4 Hz), 111. 1. 19F NMR (376 MHz, CDCl3) : 6-63. 6 (s).

Example 9 General procedure B was used to convert 2,6- diphenylaniline (294 mg, 1.2 mmol) to the desired product in 16.5 h. Purification via flash column chromatography (elu- ants 2: 1 hexane: ether) afforded 127 mg (37% yield) of a yel- low solid.

Example 10 General procedure A was used to convert 2,6- difluoroaniline (129 µl, 1.2 mmol) to the desired product in 19 hours. Purification via flash column chromatography (eluants 2: 1 hexane: ether) afforded 219 mg (94% yield) of a yellow solid. 1H NMR (400 MHz, CDC13) : # 8.30 (bs, 1 H); 7.35 (m, 2 H); 7.25 (m, 1 H); 7.16 (t, J = 10.2 Hz, 1 ; 7.05 (m, 2 H); 6.84 (m, 1 H); 6.55 (dt, J = 2.5,10.2 Hz, 1 H). 13C NMR (100 MHz, CDCl3) : 6 177.0,159.0 (d, J = 4.6 Hz), 156.5 (d, J = 4.6 Hz), 137.3,135.5,131.6,127.3 (t, J = 9. 6 Hz), 125.2,115.5 (t, J = 15.6 Hz), 112.1 (m), 111.4.

9F NMR (376 MHz, CDCl3) : 8-116. 6 (s). Anal. calcd for C13H9NOF2 : C, 66.93; H, 3.89; N, 6.01. Found: C, 66.66; H, 3.90; N, 5.97.

Example 11 General procedure A was used to convert 2-methyl-6- trifluoromethylaniline (630 µl, 3.6 mmol) to the desired product in 14.5 hours. Purification via flash column chro- matography (eluants 2: 1 hexane: ether) afforded 781 mg (93 % yield). 1H NMR (400 MHz, CDC13) : 8 8. 50 (bs, 1 H); 7.64 (d, J = 7. 8 Hz, 1 H); 7.55 (d, J = 7.6 Hz, 1 H); 7.41 (at, J = 7.8 Hz, 1 H); 7.33 (m, 2 H); 7.07 (at, J = 10.2 Hz, 1 H); 6.77 (m, 1 H); 6.14 (d, J = 10.1 Hz, 1 H) ; 2. 17 (s, 3 H). 13C NMR (100 MHz, CDCl3) : # 176.8,154.2,138.6,137.4,135.8,134.9, 134.5,131.1,128.4 (q, J = 29.6 Hz), 127.6,124.8 (q, J = 5.2 Hz), 124.4,123.3 (q, J = 272 Hz), 110.5,17.7.31p NMR

(377 MHz, C6D6) : 8-62. 2. Anal. calcd for C15Hl2NOF3 : C, 64.51; H, 4.33; N, 5. 02. Found: C, 64.23; H, 4.24; N, 4.87.

Example 12 General procedure A was used to convert 2-methylaniline (384 pL, 3.6 mmol) to the desired product in 14.5 hours.

Purification via flash column chromatography (eluants 2: 1 hexane: ether) afforded 561 mg (89% yield). 1H NMR (400 MHz, CDC13) : 6 8.57 (bs, 1 H); 7.40-7. 30 (m, 3 H); 7.30-7. 21 (m, 3 H); 7.12 (dd, J = 10,10.4 Hz, 1 H); 6.77 (m, 1 H); 6.71 (d, J = 10.4 Hz, 1 H); 2.21 (s, 3 H). 13C NMR (100 MHz, CDC13) : 6 176.5,154.5,137.5,136.5,136.2,134.6,131.4, 130.2,127.1,126.1,124.2,110.6,17.8. Anal. calcd for C14Hl3NO : C, 79.59; H, 6.20; N, 6.63. Found: C, 79.62; H, 6.17; N, 6.62.

Examples 13-22 General Procedure for the Synthesis of Na Salts of 2- Anilinotropones: To a side arm flask in a glovebox was added NaH (1.2 equiv). The flask was removed from the glovebox and placed on a vacuum line under argon. THF (5-10 mL) was added to the flask, and the flask was cooled with an ice water bath. Slow addition of the 2-anilinotropone (1 equiv) as a solution in THF (3 mL) resulted in vigorous bub- bling. When bubbling ceased, the flask was removed from the ice water bath and allowed to warm to rt. After 2 h, the solution was cannula filtered away from the remaining NaH, and the residual NaH was washed with THF (3 mL). The THF was removed in vacuo to produce essentially a quantitative yield of the desired salt as its THF adduct. The amount of THF incorporated varied with different salts and was deter- mined by lH NMR.

Example 13 Na Salt of 2- (2, 6-diisopropylanilino) tropone: The gen- eral procedure was employed with 1.28 g (4.5 mmol) anilino- tropone and 120 mg (5 mmol) NaH. The salt was isolated with 1 equiv of THF. 1H NMR (250 MHz, C6D6) : b 7.18-7.04 (m, 3 H); 6.6-6.4 (m, 3 H); 6.32 (dd, J = 8.0,12.2 Hz, 1 H); 6.02 (dt, J = 3.2,7.8 Hz, 1 H); 3.36 (THF); 2.94 (m, 2 H);

1.26 (THF); 1.14 (d, j = 7. 0 Hz, 6 H); 1. 00 (d, J = 7 Hz, 1 H). 13C NMR (100 MHz, C6D6) : 5 177.6,165.8,148.7,139.0, 134.4,133.5,124.2,123.5,121.2,118.4,117.9,68.0,28.2, 25.6,24.9,23.9.

Example 14 Na Salt of 2- (2, 6-dimethylanilino) tropone: The general procedure was employed with 405 mg (1.8 mmol) anilinotropone and 50 mg (2 mmol) NaH. The salt was isolated with 2.18 equiv of THF. 1H NMR (400 MHz, C6D6) : 8 7.05 (m, 2 H); 6.92 (m, 1 H); 6.58-6.33 (m, 4 H); 6.05 (m, 1 H); 3.40 (THF); 1.94 (s, 6 H); 1.31 (THF).

Example 15 Na Salt of 2- (2-t-butylanilino) tropone: The general procedure was employed with 462 mg (1.8 mmol) anilinotropone and 50 mg (5 mmol) NaH. The salt was isolated with 1.5 equiv of THF. 1H NMR (250 MHz, C6D6) : 8 7.42 (d, J = 8.0 Hz, 1 H); 6.98 (m, 1 H); 6.66 (m, 2 H); 6.45 (m, 3 H); 6.04 (at, J = 9.0 Hz, 1 H); 3.44 (THF); 1.37 (THF); 1.29 (s, 9 H).

Example 16 Na Salt of 2- (2-t-butyl-6-methylanilino) tropone: The general procedure was employed with 303 mg (1.14 mmol) ani- linotropone and 31 mg (1.3 mmol) NaH. The salt was isolated with 1.16 equiv of THF. 1H NMR (400 MHz, C6D6) : 8 7.33 (d, J = 7. 6 Hz, 1 H); 7.07 (d, J = 7.6 Hz, 1 H); 6.94 (at, J = 7.6 Hz, 1 H); 6.52 (m, 2 H); 6.39 (m, 2 H); 6.04 (m, 1 H); 3.40 (THF); 1.97 (s, 3 H); 1.30 (s, 9 H + THF).

Example 17 Na Salt of 2- (2, 6-diphenylanilino) tropone: The general procedure was employed with 352 mg (1.0 mmol) anilinotropone and 28 mg (1.2 mmol) NaH. The salt was isolated with 0.55 equiv of THF. 1H NMR (400 MHz, C6D6) : 8 7.28 (d, J = 7.6 Hz, 2 H); 7.19 (d, J = 6.8 Hz, 2 H); 7.04 (t, J = 7.6 Hz, 1 H); 6.81 (m, 6 H); 6.63 (d, J = 11.6 Hz, 1 H); 6.44 (m, 2 H); 6.08 (at, J = 9.0 Hz, 1 H); 6.00 (d, J = 10.4 Hz, 1 H); 3.52 (THF); 1.39 (THF).

Example 18 Na Salt of 2- (2-methyl-6-trifluoromethylanilino)- tropone: The general procedure was employed with 688 mg (2.5 mmol) anilinotropone and 71 mg (2.95 mmol) NaH. The salt was isolated with 1 equiv of THF. 1H NMR (400 MHz, C6D6) 8 7.39 (d, J = 7.6 Hz, 1 H); 7.06 (d, J = 7.6 Hz, 1 H); 6.70 (at, J = 7.6 Hz, 1 H); 6.57 (m, 2 H); 6.45 (dd, J = 8.2, 11.6 Hz, 1 H); 6.28 (d, J = 11.6 Hz, 1 H); 6.08 (at, J = 8.8 Hz, 1 H); 3.46 (THF); 1.88 (s, 3 H); 1.33 (THF).

Example 19 Na Salt of 2- (2, 6-dichloroanilino) tropone: The general procedure was employed with 658 mg (2.5 mmol) anilinotropone and 71 mg (2.95 mmol) NaH. The salt was isolated with 1.6 equiv of THF. 1H NMR (400 MHz, C6D6) : 6 7.08 (d, J = 8.0 Hz, 2 H); 6.73 (d, J = 10.4 Hz, 1 H); 6.59 (at, J = 10. 2 Hz, 1 H); 6.51 (m, 1 H); 6.39 (m, 2 H); 6.11 (at, J = 9.2 Hz, 1 H); 3.50 (THF); 1.35 (THF).

Example 20 Na Salt of 2- (2, 6-dibromoanilino) tropone: The general procedure was employed with 721 mg (2.0 mmol) anilinotropone and 58 mg (2.44 mmol) NaH. The salt was isolated with 1 equiv of THF. 1H NMR (400 MHz, C6D6) : 5 7.26 (m, 2 H); 6.74 (m, 1 H); 6.61 (m, 1 H); 6.50 (m, 1 H); 6.35 (d, J = 11.2 Hz, 1 H); 6.23 (m, 1 H); 6.14 (m, 1 H); 3.51 (THF); 1.33 (THF).

Example 21 Na Salt of 2- (2-methylanilino) tropone: The general pro- cedure was employed with 508 mg (2.4 mmol) anilinotropone and 69 mg (2.9 mmol) NaH. The salt was isolated with 0.89 equiv of THF. 1H NMR (400 MHz, C6D6) : 8 7.11 (m, 2 H); 6.93 (m, 1 H); 6.64-6.45 (m, 4 H); 6.41 (dd, J = 8.6,11.4 Hz, 1 H); 6.08 (at, J = 9. 0 Hz, 1 H); 3.46 (THF); 1.89 (s, 3 H); 1.32 (THF).

Example 22 Na Salt of 2- (2, 3,4,5,6-pentafluoroanilino) tropone: The general procedure was employed with 581 mg (1.9 mmol) anilinotropone and 100 mg (4.2 mmol) NaH. The salt was iso-

lated with no excess THF. 1H NMR (400 MHz, d6-acetone) : 8 6.85 (at, H = 10.2 Hz, 1 H); 6.73 (d, J = 10 Hz, 1 H); 6.69 (at J = 11.4 Hz, 1 H); 6.19 (d, J = 11.2 Hz, 1 H); 6.14 (at, J = 9.2 Hz, 1 H).

Examples 23-32 General Procedure for the Synthesis of Ni Complexes: To a flame dried Schlenk flask in a glovebox were added the so- dium salt of a 2-anilinotropone-THF (1 equiv) and (Ph3P) 2Ni (Ph) (Cl) (1 equiv). The flask was removed from the glovebox, was placed on a vacuum line under Ar, and was cooled to-30°C with a dry ice/acetone bath. THF (-15 mL) was added to the flask, which was allowed to warm to RT over 1 h. The reaction was allowed to stir at ambient tempera- ture for 1 h. THF was removed in vacuo and the crude reac- tion mixture dissolved in toluene (-15 mL). Cannula trans- fer onto a pad of Celite was followed by filtration under Ar. The Celite@ pad was washed with toluene (3x5 mL), and the solvent volume was reduced to 3-5 mL. Pentane (50 mL) was added, and the Schlenk flask was placed in a-30°C freezer overnight. Solvent was removed from the precipitate via cannula filtration, and the residual solid was washed with pentane (3 X 10 mL). Drying in vacuo produces the de- sired nickel complex.

Example 23 2- (2, 6-Diisopropylanilino) tropone Ni Complex (VIII): The general procedure was employed with 201 mg (0.54 mmol) of the sodium salt and 372 mg (0.54 mmol) of (Ph3P) 2Ni (Ph) (Cl) to afford 241 mg (67%) of the desired com- plex as a yellow-orange solid. 1H NMR (400 MHz, C6D6) : 8 7.63 (m, 6 H); 7.08 (d, J = 7.0 Hz, 2 H); 6.98 (m, 12 H); 6.76 (d, J = 10.4 Hz, 1 H); 6.58 (at, J = 9.9 Hz, 1 H).

6.53 (d, J = 11.5 Hz, 1 H); 6.45-6.33 (m, 4 H); 6.13 (at, J = 9.4 Hz, 1 H); 3.82 (sept, J = 6. 8 Hz, 2 H); 1.32 (d, J = 6.8 Hz, 6 H); 1.09 (d, J = 6.8 Hz, 6 H). 13C NMR (100 MHz, C6D6) : 6 180.2 (d, J = 7.6 Hz), 169.6 148.9 (d, J = 45 Hz), 144.4,142.3,138.1 (d, J = 2.2 Hz), 134.6 (d, J = 10.5 Hz), 133.1,132.0,131.6,129.9 (d, J = 1.9 Hz), 125.9,125.5 (d, J = 2 Hz), 123.7,122.2,121.7,121.3,121.1,29.0,25.9, 23.9.31P NMR (162 MHz, C6D6) : 6 28.9. Anal. calcd for C43H42NOPNi : C, 76.12; H, 6.24; N, 2.06. Found: C, 75.83; H, 6.24; N, 1.98.

Example 24 2- (2, 6-dimethylanilino) tropone Ni Complex: The general procedure was employed with 172 mg (0.54 mmol) of the sodium salt and 372 mg (0.54 mmol) of (Ph3P) 2Ni (Ph) (Cl) to afford 190 mg (57%) of the desired complex as a yellow-orange solid. 1H NMR (400 MHz, CD2Cl2) : 6 7. 54 (m, 6 H); 7.39 (m, 3 H); 7.28 (m, 6 H); 7.21 (d, J = 8 Hz, 2 H); 7.09 (dd, J = 10,10.6 Hz, 1 H); 6.99 (m, 2 H); 6.94 (d, J = 10.6 Hz, 1 H); 6.71 (d, J = 10.7 Hz, 1 H); 6.63 (at, J = 9.5 Hz, 1 H); 6.56 (t, J = 8 Hz, 1 H); 6.22 (m, 2 H); 6.14 (m, 2 H); 2.21 (s, 6 H). 13C NMR (100 MHz, CD2Cl2) : # 179.9 (d, J = 7. 2 Hz), 167.7,150.3 (d, J = 44.5 Hz), 146.4,136.9 (d, J = 1. 8 Hz), 134.7,134.6 (d, J = 10.7 Hz), 134.3,131.8 (d, J = 1. 9 Hz), 131.4,130.1,128.2 (d, J = 9.7 Hz), 127.7,124.8 (d, J = 2.6 Hz), 124.3,122.0,121.1,120.5,117.7,18.3. 31P NMR (162 MHz, C6D6) : 8 29.03. Anal. calcd for C39H34NOPNi : C, 75.26; H, 5.51; N, 2.25. Found: C, 75.49; H, 5.57; N, 2.38.

Example 25 2- (2-t-Butylanilino) tropone Ni Complex: The general procedure was employed with 201 mg (0.53 mmol) of the sodium salt and 372 mg (0.54 mmol) of (Ph3P) 2Ni (Ph) (Cl) to afford 195 mg (57%) of the desired complex as a yellow-orange solid. 1H NMR (400 MHz, CD2Cl2) : 7. 47 (m, 6 H); 7.38 (m, 3 H); 7.28 (m, 6 H); 7.18 (dd, J = 1. 4,8 Hz, 1 H); 7.11 (bs, 1 H); 6.95 (at, J = 10.2 Hz, 1 H); 6.81 (m, 2 H); 6.72 (m, 1

H); 6.55 (M, 2 H); 6.46 (d, J = 9.4 Hz, 1 H); 6.42 (dd, J = 1.6,7.7 Hz, 1 H); 6.23 (m, 2 H); 6.07 (bs, 1 H); 1.51 (s, 9 H). 13C NMR (100 MHz, CD2C12) : 8 179.9 (d, J = 7.5 Hz), 169. 1,151.3 (d J = 45 Hz), 146.9,142.3,138.4 (broad), 137.8 (broad), 134.8,134.6 (d, J = 10.5 Hz), 133.7,131.9, 131.5,130.1 (d, J = 1.9 Hz), 128.9,128.8,128.2 (d, J = 9.7 Hz), 126.3,125.1 (broad), 124.2,121.6,120.9,120.7, 120.5,36.4,32.8.31P NMR (162 MHz, CD2C12) : 5 29.34.

Anal. calcd for C41H38NOPNi : C, 75.71; H, 5. 89; N, 2.15.

Found: C, 75. 76; H, 5. 92; N, 2.19.

Example 26 2- (2-t-Butyl-6-methylanilino) tropone Ni Complex: The general procedure was employed with 219 mg (0.59 mmol) of the sodium salt and 409 mg (0. 59 mmol) of (Ph3P) 2Ni (Ph) (Cl) to afford 185 mg (47%) of the desired complex as a yellow- orange solid. 1H NMR (400 MHz, C6D6) : 8 7.63 (m, 6 H); 7.23 (bs, 1 H); 7.15 (m, 1 H); 6.98 (m, 10 H); 6.81 (m, 2 H); 6.75 (d, J = 10.4 Hz, 1 H); 6.58 (at, J = 10 Hz, 1 H); 6.48 (m, 2 H); 6.41 (m, 3 H); 6.11 (at, J = 9.0 Hz, 1 H); 2.46 (s, 3 H); 1.69 (s, 9 H). 13C NMR (100 MHz, CDzCl2) : 8 179. 8 (d, J = 7.3 Hz), 168.1,149.3 (d, J = 45.3 Hz), 145.6, 142.1,138.3 (broad), 137.2 (broad), 134.7,134.5 (d, J = 10.5 Hz), 133.9,133.1,131.9,131.4,130.1,128.2 (d, J = 9.9 Hz), 128.1,127.1,124.9 (broad), 124.4,121.7,121.1, 120.4,119.7,36.9,33.3,19.6.31P NMR (162 MHz, CD2C12) : 8 29.02. Anal. calcd for C42H40NOPNi : C, 75.92; H, 6.07; N, 2.11. Found: C, 75.75; H, 6.11; N, 2.15.

Example 27 2- (2, 6-Diphenylanilino) tropone Ni Complex: The general procedure was employed with 225 mg (0.55 mmol) of the sodium salt and 380 mg (0.55 mmol) of (Ph3P) 2Ni (Ph) (Cl) to afford 220 mg (54%) of the desired complex as a yellow-orange solid. Compound was isolated with 0.33 eq of toluene. 1H NMR (400 MHz, C6D6) : 6 7. 95 (d, J = 7.6 Hz, 4 H); 7.49 (m, 6 H); 7.20 (m, 6 H); 7.13 (m, 6 H); 6.98 (8 H + toluene); 6.77 (d, J = 11.6 Hz, 1 H); 6.55 (m, 2 H); 6.4 (m, 4 H); 6.02 (m, 1 H); 2.09 (toluene). 13C NMR (100 MHz, CD2Cl2) : b 179.6 (d,

J = 7.5 Hz), 168.9,148.0 (d, J = 45.1 Hz), 144.6,140.8, 138.3 (d, J = 2.7 Hz), 137.0,134.8,134.5 (d, J = 10.6 Hz), 133.8,131.8,131.3,130.5,130.2,130.0 (d, J = 1.9 Hz), 129. 3,128.5,128.1 (d, J = 9.8 Hz), 127. 7,127.0,125.6, 125.2,124.9 (d, 1.9 Hz), 122.0,121.2,121.1,120.5,21.5.

31P NMR (162 MHz, C6D6) : 8 29.03. Anal. calcd for C49H38NOPNi0. 33 toluene : C, 79.3; H, 5.27; N, 1.80. Found : C, 79.24; H, 5.37; N, 1.77.

Example 28 2- (2-Methyl-6-trifluoromethylanilino) tropone Ni Com- plex: The general procedure was employed with 192 mg (0.51 mmol) of the sodium salt and 357 mg (0.51 mmol) of (Ph3P) 2Ni (Ph) (Cl) to afford 205 mg (59%) of the desired com- plex as a yellow-orange solid. H NMR (400 MHz, CD2C12) : 8 7.49 (m, 6 H); 7.37 (m, 3 H) ; 7.27 (m, 7 H); 7.04 (d, J = 9.9 Hz, 1 H); 6.96 (m, 2 H); 6.86 (m, 2 H); 6.63 (d, J = 10.6 Hz, 1 H); 6.55 (m, 2 H); 6.17 (m, 3 H); 6.05 (m, 1 H); 2.17 (s, 3 H). 13C NMR (100 MHz, CD2Cl2) : spectrum is diffi- cult to interpret due to extensive F coupling; 8 180.1 (d, J = 7. 3 Hz), 168.0,149.4 (d, J = 46.0 Hz), 146.4,138.1, 136.8,135.2,134.8,134.6 (d, J = 10.6 Hz), 134.4,134.0, 131.8,131.3,130.1 (d J = 2.5 Hz), 128.2 (d, J = 9.7 Hz), 126.2,125.1 (broad), 124.8,124.7 (broad), 124.5 (q, J = 5.6 Hz), 124.3,123.5,122.4,121.9,121.1,118.9,18.2.31p NMR (162 MHz, CD2Cl2) : 8 29.37. Anal. calcd for: C, 69.25; H, 4.62; N, 2.07. Found C39H31NOPNiF3 : C, 69.15; H, 4.57; N, 2.10.

Example 29 2- (2, 6-Dichloroanilino) tropone Ni Complex: The general procedure was employed with 200 mg (0.50 mmol) of the sodium salt and 344 mg (0.50 mmol) of (Ph3P) 2Ni (Ph) (Cl) to afford 250 mg (75%) of the desired complex as a yellow-orange solid. 1H NMR (400 MHz, C6D6) : 8 7.54 (m, 6 H); 7.39 (m, 3 H); 7.29 (m, 6 H); 7.09 (dt, J = 1.0,10.2 Hz, 1 H); 6.96 (m, 5 H); 6.72 (d, J = 10. 8 Hz, 1 H); 6.70 (d, J = 8.1 Hz, 1 H); 6.63 (at, J = 9.5 Hz, 1 H); 6.23 (at, J = 9.5 Hz, 1 H); 6.23 (m, 2 H) ; 6.14 (m, 2 H). 13C NMR (100 MHz, CD2Cl2) : 8

180.2 (d, J = 6.8 Hz), 167.7,149.9 (d, J = 45. 3 Hz), 144.2, 137.1 (d, J = 1.7 Hz), 135.5,134.8,134.7 (d, J = 10.6 Hz), 131.7,131.3,130.2 (d, J = 2 Hz), 128.2 (d, J = 9.7 Hz), 128.1,125.6,124.9 (d, J = 2.1 Hz), 123.2,122.9,121.4, 117.8.31P NMR (162 MHz, CD2Cl2) : 6 29. 13. Anal. calcd for C37H28NOPNiCl2 : C, 67.00; H, 4.26; N, 2.11. Found: C, 66.95; H, 4.37; N, 2.15.

Example 30 2- (2, 6-Dibromoanilino) tropone Ni Complex: The general procedure was employed with 220 mg (0.49 mmol) of the sodium salt and 341 mg (0.49 mmol) of (Ph3P) 2Ni (Ph) (Cl) to afford 315 mg (85%) of the desired complex as a yellow-orange solid. 1H NMR (400 MHz, MHz, CD2Cl2) : 8 7.54 (m, 6 H); 7.39 (m, 3 H); 7.28 (m, 6 H); 7.21 (d, J = 8.0 Hz, 2 H); 7.09 (m, 1 H); 7.00 (m, 2 H); 6.94 (d, J = 10.4 Hz, 1 H); 6.72 (d, J = 10.8 Hz, 1 H); 6.63 (at, J = 9.4 Hz, 1 H); 6.56 (t, J = 8.0 Hz, 1 H); 6.22 (m, 2 H); 6.14 (t, J = 7. 2 Hz, 2 H). 13C NMR (100 MHz, CD2Cl2) : 8 180.2 (d, J = 6.8 Hz), 167.3,149.6 (d, = 45.7 Hz), 146.5,137.4,135.5,134.8,134.7 (d, J = 10.6 Hz), 132.0,131.7,131.3,130.2 (d, J = 1.6 Hz), 128.2 (d, J = 9. 8 Hz), 126.4,124.9 (d, J = 2 Hz), 123.2,123.0,122.3, 121.4,118.0.31P NMR (162 MHz, CD2Cl2) : 8 29.03. Anal. calcd for C37H28NOPNiBr2 : C, 59.08; H, 3.75; N, 1.86. Found: C, 59.35; H, 3.82; N, 1.90.

Example 31 2- (2-Methylanilino) tropone Ni Complex: The general pro- cedure was employed with 100 mg (0.34 mmol) of the sodium salt and 234 mg (0.34 mmol) of (Ph3P) 2Ni (Ph) (Cl) to afford 105 mg (51%) of the desired complex as a yellow-orange solid. 1H NMR (400 MHz, CD2Cl2) : 8 7. 50 (m, 6 H); 7.39 (m, 3 H) ; 7. 28 (m, 6 H); 6.98 (dt, J = 1. 0,10.2 Hz, 1 H); 6.87- 6.67 (m, 6 H); 6.59 (d, J = 10.4 Hz, 1 H); 6.53 (dd, J = 1. 3,7.6 Hz, 1 H); 6.49 (at, J = 9.5 Hz, 1 H); 6.27 (d, J = 11. 6 Hz, 1 H); 6.18 (m, 2 H); 6.06 (bs, 1 H); 2.19 (s, 3 H).

13C NMR (100 MHz, CD2Cl2) : 8 179.9 (d, J = 7.5 Hz), 168.5, 151.6 (d, J = 44.4 Hz), 147.8,138.0 (broad), 137.1 (broad), 134.7,134.6 (d, J = 10.6 Hz), 134.1,132.1,131.9,131.5,

130. 1 (d, J = 2.3 Hz), 130. 0,128.2 (d, J = 9.7 Hz), 126. 3, 126.2,125.0 (broad), 124.2,122.0,121.0,120.8,118.6, 17.9.31p NMR (162 MHz, CD2Cl2) : 8 29.43. Anal. calcd for C38H32NOPNi : C, 75.02; H, 5.30; N, 2.30. Found: C, 74.12; H, 5.33; N, 2.31.

Example 32 2- (2, 3,4,5,6-Pentafluoroanilino) tropone Ni Complex: The general procedure was employed with 136 mg (0.44 mmol) of the sodium salt and 308 mg (0.44 mmol) of (Ph3P) 2Ni (Ph) (Cl) to afford 169 mg (57%) of the desired complex as a yellow- orange solid. 1H NMR (400 MHz, CD2Cl2) : b 7.52 (m, 6 H); 7.39 (m, 3 H); 7.30 (m, 6 H); 7.18 (dt, J = 0.9,10.25 Hz, 1 H); 7.06 (m, 1 H); 6.87 (d, J = 7.2 Hz, 2 H); 6.80 (d, J = 10.8 Hz, 1 H); 6.74 (at, J = 9.6 Hz, 1 H); 6.50 (d, J = 11. 2 Hz, 1 H); 6.36 (t, J = 7.15 Hz, 1 H); 6.28 (m, 2 H). 13C NMR (100 MHz, CD2Cl2) : spectrum difficult to interpret due to ex- tensive F coupling. 8 180.8 (d, J = 6.5 Hz), 169.1,152.2 (d, J = 45.5 Hz), 136.8,136.2,135.4,134.6 (d, J = 10.7 Hz), 132.3 (m), 131.4,131.0,130.3 (d, J = 1.9 Hz), 128.9 (m), 128.3 (d, J = 9. 8 Hz), 125.5 (d, J = 2.5 Hz), 124.5, 124.3,122.0,118.0. 31P NMR (162 MHz, CD2Cl2) : 8 29.71.19F NMR (377 MHz, CD2Cl2) : 8-147. 73 (m),-163.75 (t, J = 22.6 Hz),-166.52 (m). Anal. calcd for C37H25NOPNiF5 : C, 64.94; H, 3.68; N, 2.05. Found: C, 64.45; H, 3.90; N, 2.31.

Example 33 Bistropone Ni Complex from 2- (2, 6-diisopropylanilino)- tropone: To a flame dried Schlenk flask in a glovebox were added the sodium salt of the 2-anilinotropone-THF (377 mg, 0.90 mmol)) and (DME) NiBr2 (139 mg, 0.45 mmol). The flask was removed form the glovebox and placed on a vacuum line under Ar. Et20 (20 mL) was added to the flask, and the reac- tion was allowed to stir at room temperature for 15 h. The crude reaction mixture was filtered through filter paper and condensed to produce 240 mg (88%) of a red-brown solid. 1H NMR (400 MHz, C6D6) : 8 7.29-7. 21 (m, 6 H); 6.26-6.18 (m, 8 H); 5.92 (m, 2 H); 4.18 (sept, J = 6.8 Hz, 4 H); 1.74 (d, J = 6.8 Hz, 12 H); 1.19 (d, J = 6.8 Hz, 12 H). 13C NMR (100

MHz, C6D6) : 6 180. 4,168. 9,143.6,141.1,134.6,133.8, 126.7,124.0,122.8,120.7,119.3,29.2,24.5,24.1. Anal. calcd for C38H42N202Ni : C, 73.67; H, 7.16; N, 4.50. Found: C, 74.10; H, 7.25; N, 4.39.

Examples 34-40 Polymerizations of Ethylene with (VIII) A 1000 mL Parr@ autoclave was heated under vacuum up to 110°C, was cooled, and was backfilled with ethylene. The autoclave was charged with toluene (190 mL), was degassed with ethylene (3 X 1.38 MPa), and was pressurized with eth- ylene to 2.76 MPa for the reaction. The stirring motor was engage, and the reactor was allowed to equilibrate at the desired temperature for 10 min. In a glove box, a Schlenk flask was charged with the catalyst. The Schlenk flask was removed from the glove box and was placed on a vacuum line under Ar. The catalyst was dissolved in toluene (10 mL) and was cannula transferred into the autoclave which had been vented. The autoclave was sealed and was pressurized to 2.76 MPa. At the appropriate time, the reactor was vented, and the polymer was isolated via filtration and was dried in a vacuum oven. Variations in time, temperature, solvent, and catalyst loading were employed to generate the data in Table 2.

Examples 41-80 Unless otherwise noted, the"catalyst" (Ni compound) was (VIII).

General Procedure for High Pressure (Above Atmospheric) Ethylene Polymerizations. A 1000 mL Parr autoclave was heated under vacuum up to 110°C and then was cooled to the desired reaction temperature and backfilled with ethylene.

The autoclave was charged with solvent (190 mL), degassed with ethylene (2 X 1.38 MPa), and pressurized with ethylene to 1.38 MPa. The stirring motor was engaged, and the reac- tor allowed to equilibrate at the desired temperature for approximately 10 min. In a glovebox, a side arm flask was charged with the catalyst. The flask was removed from the glovebox and placed on a vacuum line under Ar. The catalyst

was dissolved in 10 mL toluene and cannula transferred into the vented autoclave with stirring motor off. The autoclave was sealed and pressurized to the desired level, and the stirring motor was reengaged. After the prescribed reaction time, the stirring motor was stopped, the reactor was vented, and the polymer isolated via precipitation from methanol and dried in a vacuum oven. This procedure was em- ployed with modifications in time, temperature, ethylene pressure, and solvent. For the additive studies, 170 mL of toluene and 20 mL of the respective additive were used in place of the 190 mL toluene mentioned above. For the stud- ies with excess PPh3, both the catalyst and PPh3 were added in the same 10 mL toluene.

Procedure for Ethylene Polymerization at 1 atm. In a glovebox, a side arm flask was charged with the catalyst (7.6 pmol). The flask was removed from the glovebox and placed on a vacuum line under argon. Toluene (40 mL) was added to flask, and the flask was placed in an 80°C oil bath. After 10 min, the flask was evacuated and backfilled with ethylene 3 times and left open to ethylene for the du- ration of the polymerization. After 2 h, the reaction was cooled to RT and poured into 200 mL stirred MeOH. After stirring 12 h, an oil had separated out on the bottom. The solvent was decanted and the residual oil dissolved in hex- ane. This solution was filtered through a pad of silica gel with additional hexane, and the solvent was removed in vacuo to yield polymer.

Some of these polymerization runs are reported under different example numbers in the tables. They are repeated to illustrate the effect of different variables on the po- lymerization. Table 3 shows the effect of temperature, Ta- ble 4 the effect of ethylene pressure, Table 5 the effect of catalyst loading, Table 6 the effect of various additives, and Table 7 the effect of various solvents. Table 8 shows the effect of varying the substitution on the phenyl ring derived from the aniline and the column labeled"Ar"gives that substitution pattern.

Examples 81-82 1-Hexene Polymerizations with (VIII) A Schlenk flask in a glove box was charged with the catalyst. The flask was removed from the glove box and was placed on a vacuum line under Ar. Toluene and 1-hexene were added to a separate flask, and the flask was placed in an oil bath at the appropriate temperature and was allowed to equilibrate for 10 min. The catalyst was dissolved in tolu- ene (0.50 mL) and was cannula transferred into the tolu- ene/1-hexene solution. The solution was allowed to stir for the prescribed time, and the solvent and excess 1-hexene were removed to yield the crude polymer. Further purifica- tion was effected via filtration of a hexane solution of the polymer through a pad of Celite and removal of the solvent in vacuo. These conditions were used to generate the data in Table 9.

Table 2 Ex. mol cat Solvent temp time Yield TONa Mn PDI branches/ Tm (x 106) (°C) (h) (g) 100 carbons (°C) 14 3.0 Toluene 40 1.0 0.125 1490 68000 3.57 14 121 15 3.0 Toluene 60 1.0 0.740 8800 151000 2.39 29 102 16 3.0 Toluene 80 1.0 1.14 13600 101000 1.98 48 82 17 10.0 Toluene 40 1.0 1.615 5770 186000 3.67 10 124 18 14.8 Toluene 60b 0.5 13.66 33000 57000 2.80 64 87 19 6.0 CH2Cl2 40 1.0 0.312 1857 86000 4.04 - 116 20 7.6 Hexane 40 1.0 0.527 2480 112000 3.92 - 122 a mol PE/mol cat<BR> b Reaction exotherm to 103 °C.

Table 3a Ex. temp yield TONb Mn PDI Branches per (°C) (g) 1000 carbons 41 40 1. 20 8240 203946 2.81 8 42 60 6. 78 31900 292215 1.97 27 43 80 11. 41 53600 118962 1. 75 49 44 100 4.04 19000 60714 1.85 67

a2.76 MPa E pressure,7.6pmolcatalyst, 1h b mol PE/mol cat Table 4 Ex. ethylene yield TONb Mn PDI Branches per (MPa) (g) 1000 carbons 45C 14 0. 145 980 6700 2. 03 113 46 50 4. 0 27000 49774 1. 68 90 47 100 6. 3 42500 62485 1. 89 76 48 200 9. 2 62120 89637 1. 84 61 49 200d 7. 63 52400 91500 1. 84 61 50 400 7. 1 47800 103908 1. 95 45 51 600 2.6 17500 119571 1.97 41

a5.2 µmol catalyst, 1 h, 80°C. b kg PE/mol catalyst. c7. 6 µmol cat, 40 mL toluene, 2 h. d 10 min run, TOF 8. 8x106 g PE#mol cat-1#h-1.

Table 5a Ex. mol cat yield TONb Mn PDI Branches per Tm (x 106) () 1000 carbons (°C 52 3.0 0.74 8800 151000 2.39 29 102 53 7.6 6.78 31900 292215 1.97 27 54C 14. 8 13. 66 33000 57000 2.80 64 87

aEthylene pressure 2.76 MPa, 60°C, 1 h, b mol PE/mol cat '30 min run, exotherm to 103 °C Table 6 Ex. Solvent additive yield TONb Mn PDI Branches per (mL) (g) 1000 carbons 55 Toluene none 2. 82 19000 189000 1. 81 37 56 Toluene EtOAc(1) 2. 28 15700 192000 1.80 36 57 Toluene H2O (1) 1.40 9600 128000 1. 85 38 58 Hexane H2O (1) 1.48 10200 135000 1. 89 39 59 Toluene EtOH (l) 1.12 7700 131000 1. 88 37 60 Toluene NEt3(1) 2. 74 18800 146000 2.02 38 61 Toluene EtOAc (20) 3.82 26200 163000 1. 92 43 62 Toluene H2O (20) 0. 850 5800 86000 2.31 41 63 Toluene EtOH (20) 0. 160 1100 21000 2.35 48 64 Toluene NEt3 (20) 0.720 5000 87000 1. 54 37

a5.3 µmol catalyst, ethylene pressure 1. 38 MPa, 10 min, (200-X) mL solvent, X=mL addi- tive. b mol PE/mol cat Table 7 Ex. solvent yield TONb Mn PDI Branches per (g) 1000 carbons 65 toluene 2. 82 19000 189000 1. 81 37 66 THF 3.34 22500 146000 1.81 39 67 hexane 2. 59 17400 163000 1. 79 35 68 PhCl 4. 78 32200 182000 1. 90 46 69 PhClb 8. 82 59300 71300 2. 08 67 70 EtOAc 0. 340 2290 66000 4. 01 33

aEthylene pressure 1.38 MPa, 60°C, 10 min, 5. 3 pmol catalyst. bmol PE/mol cat b 80°C Table 8a Ex. Ar Yield TONb Mn PDI Branches per (g) 1000 carbons 71 2, 6-di-i-Pr 7. 63 52400 91500 1. 84 61 72 2, 6-diMe 4. 74 32600 42400 1. 74 61 73 2-CH3-6-CF3 6.0 41200 87900 1.94 59 74 2, 6-diPh 8. 70 59800 94900 1. 77 53 75 2, 6-diCl 3. 40 23400 10000@ 1.96 53 76 2, 6-diBr 3. 46 23800 22300 1. 93 56 77 2-t-Bu-6-CH3 0. 880 6000 115000 2. 02 73 78 2-t-Bu Trace 17600 2. 13 72 79 2-CH3 0. 810? 5600 4700b 2. 41 57 80 pentafluoro 1. 02? 7000 1570b 3. 03 49 aEthylene pressure 1. 38 MPa, 5.2 umol catalyst, 80°C, 10 mm b mol PE/mol cat c determined by'H NMR Table 9 Ex. mol cat Solventa 1-Hexene Temp time yield TO DP branches/ (x 106) (vol %) (°C) (h) (mg) 1000 carbons 81 7.6 Toluene 50 40 3 84 130 21 147 82 7.6 Toluene 50 60 3 127 200 16 152 a Total solution volume 2 mL Example 83 Synthesis of (IX)

To separate flame dried Schlenk flasks in a glove box were added the sodium salt of 2- (2, 6-di-i- propylanilino) tropone*THF made in Example 12 (375 mg, 1.0 mmol), and (TMEDA) Ni (Ph) (Cl) [see E. Wenschub, Z. Chem., vol. 27, p. 448 (1987)] (286 mg, 1.0 mmol). Both flasks were removed from the glove box and placed on a vacuum line under Ar. Toluene (10 mL) was added to each flask, and the flask containing (TMEDA) Ni (Ph) (Cl) was cooled to-40°C (ace- tone/dry ice bath). The toluene solution of the ligand salt was slowly cannula transferred into the precooled flask (10 min). After complete transfer (washed with 5 mL toluene), the reaction was maintained at-40°C for 2 h and then al- lowed to warm to RT over one h. The reaction mixture was cannula transferred onto a pad of Celite and filtered under Ar. The Celite pad was washed with toluene (2 X 10 mL), and the solvent volume was reduced in vacuo to 10 mL. Pentane (50 mL) was added, and the Schlenk flask was placed in a -30°C freezer overnight. Solvent was removed from the pre- cipitate via cannula filtration, and the residual solid was washed with pentane (3 X 5 mL). Drying in vacuo produced 150 mg (30%) of an orange solid. 1H NMR (400 MHz, C6D6) : 8 8.52 (dd, J = 6.6,1.6 Hz, 2 H); 7.32 (dd, J = 8.0,1.2 Hz, 2 H); 7.07 (m, 4 H); 6.76 (t, J = 7.2 Hz, 2 H); 6.67 (m, 2 H); 6.47 (tt, J = 7.6,1.6 Hz, 1 H); 6.37 (d, J = 11.5 Hz, 1 H); 6.27 (ddd, J = 11.6,8.8,1.2 Hz, 1 H); 6.13 (t, J = 9.4 Hz, 1 H); 6.07 (m, 2 H); 3.29 (sept, J = 6.8 Hz, 2 H); 1.39 (d, J = 6.8 Hz, 6 H); 1.10 (d, J = 6.8 Hz, 6 H). 13C NMR (100 MHz, C6D6) : 6 179. 8,170.5,152.6,152.2,144.6,142.7, 137.1,136.0,134.8,132.8,126.3,125.1,123.9,123.3, 122.4,122.1,121.5,120.5,28.8,25.5,23.7.

Example 84 Synthesis of (X)

To a flame dried Schlenk flask in a glovebox were added the sodium salt of 2- (2, 6-di-i-propylanilino) troponenTHF (500 mg, 1.33 mmol) and (TMEDA) Ni (Ph) (Cl) (381 mg, 1.33 mmol). The flask was removed from the glovebox, was placed on a vacuum line under Ar, and was cooled with an ice water bath. Toluene (25 mL) and CH3CN (1.5 mL) were added to the flask, which was removed from the ice water bath after 30 min. The reaction was allowed to stir at ambient temperature for 14.5 h. Initial cannula filtration of the solution was followed by cannula transfer onto a pad of Celite and filtration under Ar. The Celite pad was washed with toluene (20 mL), and the solvent volume was reduced in vacuo to 5 mL. Pentane (50 mL) was added, and the Schlenk flask was placed in a-30°C freezer overnight. Solvent was removed from the precipitate via cannula filtration, and the residual solid was washed with pentane (5 mL). Drying in vacuo produced 90 mg (11%) of a red-brown solid. 1H NMR (400 MHz, C6D6) : 8 7.21-7. 29 (m, 6 H); 6.18-6.26 (m, 8 ; 5.92 (m, 2 H); 4.18 (sept, J = 6.8 Hz, 4 H); 1.74 (d, J = 6.8 Hz, 12 H); 1.19 (d, J-6. 8 Hz, 12 H).