Organocalcium pyridine-type polymerization initiators

Claim 2

A polymerization process which comprises reacting under solution polymerization conditions and temperatures a polymerizable monomer with an effective initiating amount of an organocalcium polymerization initiator prepared by the process which comprises contacting substantially pure calcium metal with a pyridine-type compound in a hydrocarbon or ethereal diluent or mixture, in the substantial absence of oxygen and ammonia, wherein said pyridine-type compound is selected from the group consisting of pyridines, bipyridines, and polycyclic fused-ring aromatic compounds wherein at least one of said fused rings is a pyridine ring and the remainder of said rings are carbocyclic rings, wherein the number of carbon atoms of said pyridine-type compound is in the range of 5 to 40, employing a ratio of gram atoms of said calcium metal to moles of said pyridine-type compound in the range of about 1:1 to 25:1, and wherein said polymerizable monomer contains 3 to 20 carbon atoms per molecule and is an α,β-unsaturated nitrile, alkyl, cycloalkyl, and aralkyl ester of acrylic and methacrylic acid, vinyl ketone, vinylpyridine, vinylquinoline, vinylpyrrolidone, or vinyl ester of a hydrocarbon monocarboxylate.

Claim 3

The polymerization process of claim 1 wherein said contacting of said calcium metal with said pyridine-type compound is conducted in said ethereal diluent, and said ethereal diluent contains 2 to 20 carbon atoms and 1 to 4 ether groups per molecule and wherein said contacting is at a temperature in the range of -100° to 200° F.

Claim 4

The polymerization process of claim 2 wherein said pyridine-type compound is 2,2'-bipyridine; 2,3'-bipyridine; 2,4'-bipyridine; 3,3'-bipyridine; 3,4'-bipyridine; 4,4'-bipyridine; quinoline; isoquinoline; acridine; 1,5-phenanthroline; 1,8-phenanthroline; or 4,5-phenanthroline.

Claim 5

The polymerization process of claim 3 wherein said diluent employed in said contacting of said calcium with said pyridine-type compound is tetrahydrofuran; 1,2-dimethoxyethane; or 1,4-dioxane.

Claim 6

The polymerization process of claim 1 wherein said contacting of said calcium metal with said pyridine-type compound process further includes the addition of a promoter in the range of 0.002 to 0.2 mole per gram atom of said calcium metal, and wherein said promoter is a halogen-containing organic compound that reacts substantially immediately to expose fresh surface area calcium metal.

Claim 7

The polymerization process of claim 1 wherein said substantially pure calcium metal has been priorly finely divided by the vaporization thereof.

Claim 8

The polymerization process of claim 2 wherein said polymerizable monomer is selected from the group consisting of acrylonitrile, methacrylonitrile, cinnamonitrile, 2-butene nitrile, 2-octene nitrile, 2-dodecene nitrile, 2-methyl-2-dodecene nitrile, methyl acrylate, ethyl acrylate, butyl acrylate, cyclohexyl acrylate, octyl acrylate, dodecyl acrylate, methyl methacrylate, ethyl methacrylate, butyl methacrylate, cyclohexyl methacrylate, octyl methacrylate, dodecyl methacrylate, benzyl acrylate, benzyl methacrylate, vinyl acetate, vinyl butyrate, vinyl 2-ethyl-hexanoate, vinyl octanoate, vinyl cyclohexanoate, vinyl benzoate, vinyl phenylacetate, vinyl dodecanoate, methyl vinyl ketone, benzyl vinyl ketone, ethyl vinyl ketone, butyl vinyl ketone, octyl vinyl ketone, phenyl vinyl ketone, 1-naphthyl vinyl ketone, 2-ethylhexyl vinyl ketone, cyclohexyl vinyl ketone, cyclododecyl vinyl ketone, 3-methyl-cyclopentyl vinyl ketone, 4-ethylphenyl vinyl ketone, decyl vinyl ketone, 5-cyclopentyl-2-naphthyl vinyl ketone, 2-vinylpyridine, 4-vinylpyridine, 2-methyl-5-vinylpyridine, 4-vinylquinoline, 2-methyl-8-vinylquinoline, 1-vinyl-2-pyrrolidone, 1-vinyl-3,3-dimethyl-2-pyrrolidone, 2-ethylhexyl acrylate, and 2-ethylhexyl methacrylate.

Claim 9

A polymerization process which comprises polymerizing under conditions suitable for solution polymerization in hydrocarbon or etheral diluent or mixture at polymerization temperatures in the range of -100° to 200° F a polymerizable monomer with an organocalcium polymerization initiator, wherein said polymerizable monomer is an α,β-unsaturated nitrile, alkyl, cycloalkyl, and aralkyl ester of acrylic and methacrylic acid, vinyl ketone, vinylpyridine, vinylquinoline, vinylpyrrolidone, or vinyl ester of a hydrocarbon monocarboxylic acid of 3 to 20 carbon atoms per molecule, and wherein said organocalcium initiator is prepared by contacting substantially pure calcium metal with a pyridine-type compound containing 5 to 40 carbon atoms per molecule selected from the group consisting of pyridines, bipyridines, and polycyclic fused-ring aromatic compounds wherein at least one of said fused rings is a pyridine ring and the remainder of said rings are carbocyclic rings, employing a ratio of gram atoms of said calcium metal to moles of said pyridine-type compound in the range of about 1:1 to 25:1, wherein said contacting of said calcium metal with said pyridine-type compound is conducted at a temperature in the range of about -100° to 200° F. in an ethereal or hydrocarbon diluent, in the substantial absence of oxygen and ammonia, and wherein said polymerization process employs a concentration of said organocalcium initiator of about 0.1 to 100 gram millimoles per 100 grams of polymerizable monomer employed.

Claim 10

A polymerization process which comprises polymerizing under conditions suitable for solution polymerization in hydrocarbon or etheral diluent or mixture at polymerization temperatures in the range of -100° to 200° F a polymerizable monomer with an organocalcium polymerization initiator, wherein said polymerizable monomer is an α,β-unsaturated nitrile, alkyl, cycloalkyl, and aralkyl ester of acrylic and methacrylic acid, vinyl ketone, vinylpyridine, vinylquinoline, vinylpyrrolidone, or vinyl ester of a hydrocarbon monocarboxylic acid of 3 to 20 carbon atoms per molecule, and wherein said organocalcium initiator is prepared by contacting substantially pure calcium metal with a pyridine-type compound containing 5 to 40 carbon atoms per molecule selected from the group consisting of pyridines, bipyridines, and polycyclic fused-ring aromatic compounds wherein at least one of said fused rings is a pyridine ring and the remainder of said rings are carbocyclic rings, employing a ratio of gram atoms of said calcium metal to moles of said pyridine-type compound in the range of about 1:1 to 25:1, wherein said contacting of said calcium metal with said pyridine-type compound is conducted at a temperature in the range of about -100° to 200° F. in an ethereal or hydrocarbon diluent, in the substantial absence of oxygen and ammonia, and wherein said polymerization process employs a concentration of said organocalcium initiator of about 0.1 to 100 gram millimoles per 100 grams of polymerizable monomer employed.

Claim 11

The polymerization process of claim 8 wherein said polymerizable monomer is an α,β-unsaturated nitrile, alkyl, cycloalkyl, or aralkyl ester of acrylic or methacrylic acid, vinylpyridine, vinylpyrrolidone, or vinyl ketone.

Claim 12

The polymerization process of claim 9 wherein said polymerizable monomer is 2-vinylpyridine, methyl methacrylate, or methyl vinyl ketone.

Claim 13

The polymerization process of claim 8 wherein sid organocalcium polymerization initiator is prepared in situ during said polymerization process.

Claim 14

The polymerization process according to claim 9 wherein said pyridine-type compound is pyridine or monoalkyl-substituted pyridine wherein said alkyl group contains 1 to 6 carbon atoms.

Claim 15

The polymerization process of claim 6 wherein said diluent employed in said contacting of said calcium with said pyridine-type compound is said hydrocarbon diluent and is aliphatic, cycloaliphatic, or aryl hydrocarbon.

Claim 16

The polymerization process according to claim 7 wherein said pyridine-type compound is pyridine, alkyl-substituted pyridine of up to 6 carbon atoms per alkyl group, unsubstituted bipyridine, alkyl-substituted bipyridine containing up to 6 carbon atoms per alkyl group, quinoline, isoquinoline, 1,10-phenanthroline, acridine, alkyl-substituted quinolines of up to 6 carbon atoms per alkyl group, alkyl-substituted isoquinolines of up to 6 carbon atoms per alkyl group, alkyl-substituted 1,10-phenanthroline of up to 6 carbon atoms per alkyl group, or alkyl-substituted acridine of up to 6 carbon atoms per alkyl group.

Claim 17

The polymerization process according to claim 14 wherein said pyridine-type compound is pyridine, monoalkyl-substituted pyridine of up to 6 carbon atoms in the alkyl group, 2,2'-bipyridine, monoalkyl-substituted 2,2'-bipyridine wherein the alkyl group contains up to 6 carbon atoms, quinoline, isoquinoline, 1,10-phenanthroline, acridine, monoalkyl-substituted quinoline of up to 6 carbon atoms in the alkyl group, monoalkyl-substituted isoquinoline of up to 6 carbon atoms in the alkyl group, monoalkyl-substituted 1,10-phenanthroline of up to 6 carbon atoms in the alkyl group, or monoalkyl-substituted acridine of up to 6 carbon atoms in the alkyl group.

Claim 18

The polymerization process according to claim 7 wherein said pyridine-type compound is benzo[b]-1,5-naphthyridine, pyrido[2,3-g]quinoline, benzo[c][1,8]naphthyridine, phenanthridine, pyrido[2,3-f][1,7]phenanthroline, dibenzo[b,g][1,8]naphthyridine, naphth[1,2-h]isoquinoline, quino[5,6-b][4,7]phenanthroline, naptho-[1,2-b][4,7]phenanthroline, dibenz[b,i]acridine, acridino[1,2-a]acridine, phenaleno-[1,2,3-k,l]acridine, dinaphtho[2,3-c:2',3'-i]phenanthridine, 4-cyclopentyl-6-phenoxy-dinaphth[2,3-a:2,3'-j]acridine, 1-phenyl-5-ethoxy-benzo[c]benz[5,6]acridino[3,4-h]acridine, 2-(4-ethylphenyl)-6-butylthio-benzo[1,2-c:5,4-c']diacridine, 3-phenylthio-7-cyclohexylmethyl-9-(N,N-diethylamino)phenanthro[2,1,10-m,n,a]acridine; 2-benzyl-quino[5,6-b][1,7]phenanthroline; 1-chloro-10-ethoxy-benzo[c][1,7]naphthyridine, 5-bromo-10-ethyl-4,7-phenanthroline; 7-iodo-10-phenylbenzo[c][2,7]naphthyridine; 4-phenylthio-4'-N,N-dibutylamino-2,2'-bipyridine; 4-chloro-4'-bromo-3,3'-bipyridine; 1,4,5,8-tetraphenylacridine, 4-phenylpyridine; 5-methylquinoline; 4,4'-dichloro-2,2'-bipyridine; 3-ethoxy-2,3'-bipyridine; 3-ethoxy-2,3'-bipyridine; 4-cyclohexylisoquinoline; 9-fluoroacridine; 8-bromo-1,5-phenanthroline; 9-iodo-1,8-phenanthroline; pyridine; 2,2'-bipyridine; 2,3'-bipyridine; 2,4'-bipyridine; 3,3'-bipyridine; 3,4'-bipyridine; 4,4'-bipyridine; quinoline; isoquinoline; acridine; 1,5-phenanthroline; 1,8-phenanthroline; or 4,5-phenanthroline.

Claim 19

The polymerization process according to claim 7 wherein said pyridine-type compound is 5-methylquinoline, pyridine, 2,2'-bipyridine, 2,3'-bipyridine; 2,4'-bipyridine, 3,3'-bipyridine; 3,4'-bipyridine; 4,4'-bipyridine, quinoline, isoquinoline, acridine, 1,5-phenanthroline, 1,8-phenanthroline; 4,5-phenanthroline, 2-methylpyridine; 3-methylpyridine; 4-methylpyridine; 2,6-dimethylpyridine; 3,5-dimethylpyridine; 5-methyl-3,4'-bipyridine; 4-methyl-2,2'-bipyridine; 3-methyl-2,2'-bipyridine; 6-tert-butylisoquinoline; 3-methylisoquinoline; 2-hexylquinoline; 4-methylquinoline; 1-methylacridine; 3-hexylacridine; 1,10-phenanthroline; 5,6-diethyl-1,10-phenanthroline; or 4-methyl-1,10-phenanthroline.

Claim 20

The polymerization process according to claim 17 wherein said pyridine-type compound is: pyridine; 2,2'-bipyridine; quinoline; isoquinoline; acridine; 2-methylpyridine; 3-methylpyridine; 4-methylpyridine; 4-methyl-2,2'-bipyridine; 3-methyl-2,2'-bipyridine; 6-tert-butylisoquinoline; 3-methylisoquinoline; 2-hexylquinoline; 4-methylquinoline; 1-methylacridine; 3-hexylacridine; 1,10-phenanthroline; 4-methyl-1,10-phenanthroline.

Claim 21

The polymerization process according to claim 8 wherein said calcium is contacted with said pyridine-type compound at a contacting temperature in the range of about -20 to 125° F in the presence of an ethereal diluent wherein said ethereal diluent contains 2 to 20 carbon atoms per molecule and 1 to 4 ether groups per molecule.

Claim 22

The polymerization process according to claim 19 wherein said ether is diethyl ether, dibutyl ether, methylbutyl ether, phenylmethyl ether, diphenyl ether, cyclohexylmethyl ether, tetrahydrofuran, 1,2-dimethoxyethane, or 1,4-dioxane.

Claim 23

The polymerization process according to claim 8 wherein said initiator-forming reaction conditions include contacting in the temperature range of about -100 to 200° F, in the presence of said hydrocarbon diluent, said calcium metal is employed in the form of a finely divided calcium prepared by a vaporization process, and said contacting is conducted in the substantial absence of oxygen.

Claim 24

The polymerization process according to claim 8 wherein said initiator-forming reaction conditions include the employment during the preparation of the initiator of an organic promoter effective to react to expose fresh calcium surface metal during the preparation of the initiator, said organic promoter is an alkyl or alkylene halogen-containing promoter, and said promoter is employed in the range of about 0.002 to 0.2 mole per gram atom of calcium metal.

Claim 25

The polymerization process according to claim 8 wherein said pyridine-type compound further can contain alkyl, cycloalkyl, aryl, alkoxy, aryloxy, alkylthio, arylthio, N,N-dialkylamino, or combination substituents, wherein the number of carbon atoms in total of said substitutents is 1 to 24.

Claim 26

The polymerization process according to claim 9 wherein said pyridine-type compound is 2,2'-bipyridine, said ethereal diluent is tetrahydrofuran, and said contacting is in the presence of a promotor which is 1,2-dibromoethane.

Claim 27

The polymerization process according to claim 9 wherein said pyridine-type compound is a bipyridine.

Claim 28

The polymerization process according to claim 25 wherein said pyridine-type compound is 2,2'-bipyridine; and said diluent employed in formation of said initiator is said ethereal diluent and is tetrahydrofuran.