Control of polymer topology through late-transition-metal catalysis

被引:84
作者
Guan, ZB [1 ]
机构
[1] Univ Calif Irvine, Dept Chem, Irvine, CA 92697 USA
关键词
polymer topology; catalysis; chain walking; dendrimers; hyperbranched; late-transition-metal catalysts;
D O I
10.1002/pola.10969
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
In this article, recent examples are reviewed of late-transition-metal catalysis applied to polymer topology control. By the judicious selection or design of late-transition-metal catalysts, polymers with a broad range of topologies, including linear, short-chain-branched, hyperbranched, dendritic, and cyclic topologies, have been successfully synthesized. A distinctive advantage of the catalyst approach is that polymers with complex topologies can be prepared in one pot from simple commercial monomers. A fundamental difference of the catalyst approach with respect to other approaches is that the polymer topology is controlled by the catalysts instead of the monomer structure. In our own laboratory, we have successfully used two strategies to control the polymer topology with late-transition-metal catalysts. In the first strategy, hyperbranched polymers are prepared by the direct free-radical polymerization of divinyl monomers through control of the competition between propagation and chain transfer with a cobalt chain-transfer catalyst. In the second strategy, polyethylene topology is successfully controlled by the regulation of the competition between propagation and chain walking with the Brookhart Pd-II-alpha-bisimine catalyst. (C) 2003 Wiley Periodicals, Inc.
引用
收藏
页码:3680 / 3692
页数:13
相关论文
共 99 条
[1]   Self-assembly of [n]rotaxanes bearing dendritic stoppers [J].
Amabilino, DB ;
Ashton, PR ;
Balzani, V ;
Brown, CL ;
Credi, A ;
Frechet, JMJ ;
Leon, JW ;
Raymo, FM ;
Spencer, N ;
Stoddart, JF ;
Venturi, M .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (48) :12012-12020
[2]   Synthetic carbohydrate dendrimers .1. A convergent synthesis of carbohydrate-containing dendrimers [J].
Ashton, PR ;
Boyd, SE ;
Brown, CL ;
Jayaraman, N ;
Nepogodiev, SA ;
Stoddart, JF .
CHEMISTRY-A EUROPEAN JOURNAL, 1996, 2 (09) :1115-1128
[3]  
Ballauff M, 2001, TOP CURR CHEM, V212, P177
[4]   Synthesis of branched polyolefins using a combination of homogeneous metallocene mimics [J].
Barnhart, RW ;
Bazan, GC ;
Mourey, T .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (05) :1082-1083
[5]   CHAIN DIMENSIONS IN DILUTE POLYMER-SOLUTIONS - A LIGHT-SCATTERING AND VISCOMETRIC STUDY OF MULTIARMED POLYISOPRENE STARS IN GOOD AND THETA-SOLVENTS [J].
BAUER, BJ ;
FETTERS, LJ ;
GRAESSLEY, WW ;
HADJICHRISTIDIS, N ;
QUACK, GF .
MACROMOLECULES, 1989, 22 (05) :2337-2347
[6]   Controlled synthesis of hyperbranched polymers by slow monomer addition to a core [J].
Bharathi, P ;
Moore, JS .
MACROMOLECULES, 2000, 33 (09) :3212-3218
[7]   An "endless" route to cyclic polymers [J].
Bielawski, CW ;
Benitez, D ;
Grubbs, RH .
SCIENCE, 2002, 297 (5589) :2041-2044
[8]   Hyperbranched aryl polycarbonates derived from A2B monomers versus AB2 monomers [J].
Bolton, DH ;
Wooley, KL .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2002, 40 (07) :823-835
[9]   A modular approach toward functionalized three-dimensional macromolecules:: From synthetic concepts to practical applications [J].
Bosman, AW ;
Vestberg, R ;
Heumann, A ;
Fréchet, JMJ ;
Hawker, CJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (03) :715-728
[10]   STEREOSPECIFIC OLEFIN POLYMERIZATION WITH CHIRAL METALLOCENE CATALYSTS [J].
BRINTZINGER, HH ;
FISCHER, D ;
MULHAUPT, R ;
RIEGER, B ;
WAYMOUTH, RM .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 1995, 34 (11) :1143-1170