efficient copolymerizations of ethylene with cyclic olefins [norbornene (NBE)
cyclopentene (CPE)] using nonbridged half-titanocenes of type
Cp
TiCl2(L) (Cp
= cyclopentadienyl group
L = aryloxo
ketimide)-MAO catalyst systems have been summarized. CpTiCl2(N=CtBu2) exhibited both remarkable catalytic activity and efficient NBE incorporation for ethylene/NBE copolymerization: the NBE incorporation by CpTiCl2(X) (X = N=CtBu2
O-2
6-iPr2C6H3; Cp
=Cp
C5Me5
indenyl) was related to the calculated coordination energy after ethylene insertion. (tBuC5H4)TiCl2(N=CtBu) exhibited significant catalytic activities with efficient CPE incorporations in ethylene/CPE copolymerization in the presence of MAO. The polymerization proceeded with exclusive 1
2-CPE incorporation
affording high molecular weight (alternating) copolymers with uniform distributions. Therefore
the cyclopentadienyl fragment (Cp) plays an essential role in terms of both the activity and the efficient cyclic olefin incorporation.
Abstract
Precise
efficient copolymerizations of ethylene with cyclic olefins [norbornene (NBE)
cyclopentene (CPE)] using nonbridged half-titanocenes of type
Cp
TiCl2(L) (Cp
= cyclopentadienyl group
L = aryloxo
ketimide)-MAO catalyst systems have been summarized. CpTiCl2(N=CtBu2) exhibited both remarkable catalytic activity and efficient NBE incorporation for ethylene/NBE copolymerization: the NBE incorporation by CpTiCl2(X) (X = N=CtBu2
O-2
6-iPr2C6H3; Cp
=Cp
C5Me5
indenyl) was related to the calculated coordination energy after ethylene insertion. (tBuC5H4)TiCl2(N=CtBu) exhibited significant catalytic activities with efficient CPE incorporations in ethylene/CPE copolymerization in the presence of MAO. The polymerization proceeded with exclusive 1
2-CPE incorporation
affording high molecular weight (alternating) copolymers with uniform distributions. Therefore
the cyclopentadienyl fragment (Cp) plays an essential role in terms of both the activity and the efficient cyclic olefin incorporation.
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