1-olefin stereoblock polymer wax, and a process for the preparation thereof

Claim 2

A stereoblock polymer wax comprising units derived from a 1-olefin of the formula RCH═CH 2 in which R denotes an alkyl radical having 1 to 28 carbon atoms, having alternating isotactic sequences with an opposed configuration and having a length of 3 or more monomer units in the molecular chain, having saturated chain ends, having a molecular weight distribution M w /M n of from 1.8 to 3.0 and having a viscosity number of from 2 to 60 cm 3 /g.

Claim 3

A process for the preparation of a 1-olefin stereoblock polymer wax as claimed in claim 1, by polymerizing a 1-olefin of the formula R--CH═CH 2 in which R is an alkyl radical having 1 to 28 carbon atoms, in one or more steps at a temperature of from -50° to 200° C., at a pressure of from 0.5 to 120 bar, in solution, in suspension or in the gas phase, in the presence of a catalyst comprising a transition metal compound and an aluminoxane, which comprises carrying out the polymerization in the presence of a catalyst whose transition metal compound is a metallocene compound of the formula I ##STR8## in which R 1 and R 2 are identical or different and denote a halogen atom, C 1 -C 10 -alkyl, C 6 -C 10 -aryl, C 2 -C 10 alkenyl, C 7 -C 40 -arylalkyl, C 7 -C 40 -alkylaryl or C 8 -C 40 alkenylaryl, R 3 and R 4 are identical or different and denote a substituted cyclopentadienyl radical, where this radical contains one or more centers of chirality and has been produced by reacting an alkali metal cyclopentadienide with a chiral alcohol, and Me is titanium, zirconium or hafnium, and has been pre-activiated before the polymerization for 5 minutes to 60 minutes at a temperature of from -78° to 100° C. using an aluminoxane of the formula II ##STR9## for the linear type or one of the formula III ##STR10## for the cyclic type, where, in the formulae II and III, R 5 denotes methyl, ethyl or isobutyl and n is an integer from 5 to 40, and where the activator is likewise an aluminoxane of the formula II or III, and hydrogen is present in the 1-olefin:H 2 molar ratio of from 3 to 3000.

Claim 4

The process as claimed in claim 2, wherein the 1-olefin is propylene.

Claim 5

The process as claimed in claim 2, wherein the metallocene compound is a compound of zirconium.

Claim 6

The process as claimed in claim 2, wherein the metallocene compound is bis-(neomenthylcyclopentadienyl)zirconium dichloride, bis-(neoisomenthylcyclopentadienyl)zirconium dichloride or bis-(cis-myrtanylcyclopentadienyl)zirconium dichloride.