Polymer life enhancement in oxyanion-catalyzed polymerization

Claim 2

Process of preparing a "living" polymer comprising contacting under polymerization conditions at least one polar acrylic-type alpha olefinic monomer with (i) a tetracoordinate organosilicon, organotin, or organogermanium polymerization initiator having at least one initiating site, (ii) a catalyst which is a salt comprising an oxyanion whose conjugate acid has a pKa (DMSO) of about 5 to about 24, and a suitable cation, characterized by also contacting with (iii) a polymerization life enhancement agent which enhances the duration of "livingness" of the polymerization by increasing the proportion of polymerization events to termination events.

Claim 3

A process of preparing a "living" polymer comprising contacting under polymerization conditions at least one polar acrylic-type alpha olefinic monomer with (i) a tetracoordinate organosilicon, organotin, or organogermanium polymerization initiator having at least one activating substituent or activating diradical attached thereto and optionally having one or more substituents that are inert under polymerizing conditions, (ii) a catayst which is a salt comprising monooxyanion or bioxyanion whose conjugate acid has a pKa(DMSO) of about 5 to about 24, and a suitable cation, characterized by also contacting with (iii) a polymerization life enhancement agent which is selected from the group consisting of acetonitrile and silylated acetonitriles containing 1-3 equivalents of R 3 Si-group per mole of acetonitrile, wherein R is hydrocarbyl of up to 20 carbon atoms, optionally containing one or more ether oxygen atoms within aliphatic segments thereof, and optionally containing one or more functional substituents that are unreactive under polymerizing conditions.

Claim 4

A process of preparing a "living" polymer comprising contacting under polymerization conditions at least one polar acrylic-type alpha olefinic monomer with (i) a tetracoordinate organosilicon, organotin, or organogermanium polymerization initiator having at least one activating substituent or activating diradical attached thereto and optionally having one or more substituents that are inert under polymerizing conditions, (ii) a catayst which is a salt comprising monooxyanion or bioxyanion whose conjugate acid has a pKa(DMSO) of about 5 to about 24, and a suitable cation, characterized by also contacting with (iii) a polymerization life enhancement agent which is selected from the group consisting of acetonitrile and silylated acetonitriles containing 1-3 equivalents of R 3 Si-group per mole of acetonitrile, wherein R is hydrocarbyl of up to 20 carbon atoms, optionally containing one or more ether oxygen atoms within aliphatic segments thereof, and optionally containing one or more functional substituents that are unreactive under polymerizing conditions.

Claim 5

The process of claim 2 wherein the enhancement agent concentration is in the range of about 0.1-1000 moles per mole of catalyst.

Claim 6

The process of claim 3 wherein the enhancement agent concentration is in the range of about 1-200 moles per mole of catalyst.

Claim 7

The process of claim 4 wherein the enhancement agent concentration is in the range of about 5-25 moles per mole of catalyst.

Claim 8

The process of claim 2 wherein the enhancement agent is acetonitrile.

Claim 9

The process of claim 2 wherein the enhancement agent is silylated acetonitrile.

Claim 10

The process of claim 2 wherein said conjugate acid has a pKa(DMSO) of about 6-21.

Claim 11

The process of claim 8 wherein said conjugate acid has a pKa(DMSO) of about 8-18.

Claim 12

The process of claim 2 wherein, in the silylated acetonitrile contains 1 equivalent of R 3 Si-groups per mole of acetonitrile, and R is selected from C 1-4 alkyl groups.

Claim 13

The process of claim 2 wherein, in the silylated acetonitrile contains 3 equivalent of R 3 Si-groups per mole of acetonitrile, and R is selected from C 1-4 alkyl groups.

Claim 14

The process of claim 10 wherein R is a methyl group.