Preparation of polymers from cyclic olefins

Claim 2

Process for preparing a polymer by ring opening polymerization comprising polymerizing a norbornene-type monomer, or a mixture thereof, in presence of an effective amount of at least one organoammonium catalyst, said norbornene-type monomer is characterized by the presence of the norbornene group defined as follows: and said organoammonium catalyst is selected from organoammonium molybdates and organoammonium tungstates that are soluble in said monomer or said monomer mixture.

Claim 3

Process of claim 1 wherein the step of polymerizing said norbornene-type monomer or a mixture thereof is carried out in presence of a hydrocarbon solvent and at least one alkylaluminum halide cocatalyst containing 1 to 12 carbon atoms in the alkyl group, with said organoammonium catalyst being soluble in said hydrocarbon solvent, amount of said organoammonium catalyst is 0.01 to 50 millimoles molybdenum or tungsten per mole of total monomer and the molar ratio of said alkylaluminum halide cocatalyst as aluminum to said organoammonium catalyst as molybdenum or tungsten is in the range of 200:1 to 1:10.

Claim 4

Process of claim 1 wherein said alkylaluminum halide cocatalyst is defined by the following formulas I, II and III: where R is an alkyl group that contains 1 to about 12 carbon atoms and X is a halide; and said organoammonium catalyst is defined by the following formulas IV and V: where each R and R group is independently selected from hydrogen, alkyl and alkylene groups each containing 1 to 20 groups, and cycloaliphatic groups each containing 5 to 16 carbon atoms, the sum of all carbon atoms represented by said R groups is 20 to 72 and the sum of all carbon atoms represented by said R 1 groups is 15 to 54; M is selected from molybdenum (VI) and tungsten (VI); and x and y represent the number of M and O atoms in the molecule.

Claim 5

Process of claim 3 wherein the alkyl group of said alkylaluminum halide cocatalyst contains 2 to 4 carbon atoms and the R and R 1 groups of said organoammonium catalyst are individually selected from alkyl groups.

Claim 6

Process of claim 4 wherein in the formula each R group is selected from alkyl groups each containing 4 to 18 carbon atoms where all R . groups are the same; where three R groups are same each containing 7 to 18 carbon atoms, the remaining R group contains 1 to 18 carbon atoms; whereas where three R groups are the same each containing 4 to 6 carbon atoms, the remaining R radical contains 4 to 18 carbon atoms; where two R groups are same and two R groups are different, the two of the same R groups each contains 12 to 18 carbon atoms whereas the two remaining different R groups each contains 1 to 18 carbon atoms and can be same or different relative to each other; provided that the sum of all of the R radicals is in the range of 25 to 48 carbon atoms, and wherein in the formula 0, M, x and y are defined as above whereas each R is selected from alkyl groups containing 5 to 18 carbon atoms where all R groups are the same; where two R 1 groups are same, or where all R 1 radicals are different, each contains 1 to 18 carbon atoms; provided that the sum of all of the R 1 radicals is in the range of 21 to 42 carbon atoms.

Claim 7

Process of claim 5 wherein said hydrocarbon solvent is selected from aliphatic and cycloaliphatic solvents containing 4 to 18 carbon atoms, aromatic solvents containing 6 to 14 carbon atoms, and substituted hydrocarbons wherein the substituents are inert; and said monomer mixture containing up to about 20% by weight thereof of other polymerizable monomers.

Claim 8

Process of claim 6 wherein said norbornene-type monomer is selected from substituted and unsubstituted 2-norbornenes, dicyclopentadienes, dihydrodicyclopentadienes, trimers of cyclopentadienes, tetracyclododecenes, and mixtures thereof; and the molar ratio of said alkylaluminum halide cocatalyst to said organoammonium catalyst is 5:1 to 2:1.

Claim 9

Process of claim 6 wherein said norbornene-type monomer is selected from monomers, and mixtures thereof, defined by the following formulas VI and VII:

Claim 10

where R and R 1 are independently selected from hydrogen, alkyl groups of 1 to 20 carbon atoms, and saturated and unsaturated hydrocarbon cyclic groups formed by R and R 1 together with the two ring carbon atoms connected thereto containing 4 to 7 carbon atoms; and wherein R 2 and R 3 are independently selected from hydrogen and alkyl groups of 1 to 20 carbon atoms.

Claim 11

where R and R 1 are independently selected from hydrogen, alkyl groups of 1 to 20 carbon atoms, and saturated and unsaturated hydrocarbon cyclic groups formed by R and R 1 together with the two ring carbon atoms connected thereto containing 4 to 7 carbon atoms; and wherein R 2 and R 3 are independently selected from hydrogen and alkyl groups of 1 to 20 carbon atoms.

Claim 12

Process of claim 8 wherein R and R 1 of said norbornene-type monomer are independently selected from hydrogen, alkyl groups of 1 to 3 carbon atoms, and monounsaturated hydrocarbon cyclic groups containing 5 carbon atoms; wherein Rand R 3 are independently selected from hydrogen and alkyl groups containing 1 to 3 carbon atoms.

Claim 13

Process of claim 9 wherein said norbornene-type monomer is selected from norbornene, methyl norbornene, tetracyclododecene, methyl tetracyclododecene, dicyclopentadiene, and mixtures thereof.

Claim 14

ll. Product produced by the process of claim 8.