Heteroatom-substituted constrained-geometry complexes. Dramatic substituent effect on catalyst efficiency and polymer molecular weight

Citation
J. Klosin et al., Heteroatom-substituted constrained-geometry complexes. Dramatic substituent effect on catalyst efficiency and polymer molecular weight, ORGANOMETAL, 20(13), 2001, pp. 2663-2665
Citations number
32
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
ORGANOMETALLICS
ISSN journal
02767333 → ACNP
Volume
20
Issue
13
Year of publication
2001
Pages
2663 - 2665
Database
ISI
SICI code
0276-7333(20010625)20:13<2663:HCCDS>2.0.ZU;2-2
Abstract
The new constrained-geometry complexes (CGC) [(eta (5)-C9H5X)(SiMe2-t-BU)Ti R2 (X = 2-OEt (1a,b), 2-NMe2 (2a,b), 3-OMe (3a,b), 3-NC4H4 (4a,b); R = Cl, Me) have been synthesized with alkoxy and amino substituents attached to a second and third indenyl position. Four of the new complexes (1a-4a) have b een characterized by single-crystal X-ray analysis. An ethylene-octene copo lymerization study revealed an enormous substituent effect, both on the cat alysts' activity and the molecular weight of produced polymers. The 3-amino -substituted complex 4b exhibits the highest catalytic activity and forms t he highest molecular weight ethylene/octene copolymers that have ever been reported for this class of catalysts.