Cyclic olefin polymerization and relationships between addition and ring opening metathesis polymerization

被引:58
作者
Tritto, I [1 ]
Boggioni, L [1 ]
Sacchi, MC [1 ]
Locatelli, P [1 ]
机构
[1] CNR, Ist Chim Macromol, I-20133 Milan, Italy
关键词
polymerization; copolymers; cyclic olefin;
D O I
10.1016/S1381-1169(98)00105-8
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Results of our work concerning: (i) the elucidation of the role of the ionic species [(Cp2TiCH3)-C-13](+)[Cl . MAO](-) and of precursors of alkylidene Cp2Ti=CH2 species in addition alkene polymerization, (ii) the synthetical strategies for converting the living active titanacyclobutanes into sigma-titanocene complexes, and (iii) the evidence for the synthesis of polyethylene polynorbornene di-block copolymer are briefly summarized. C-13 NMR spectra of ethylene-norbornene copolymers, prepared with addition catalysts based on ansa-zirconocenes and methylaluminoxane as cocatalyst, and assignments of comonomer pentads in ethylene-norbornene (EN) copolymers are reported. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:139 / 150
页数:12
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