Miyakoshi Ryo, Shimono Kyohei, Yokoyama Akihiro, Yokozawa Tsutomu
Department of Material and Life Chemistry, Kanagawa University, Rokkakubashi, Kanagawa-ku, Yokohama 221-8686, Japan.
J Am Chem Soc. 2006 Dec 20;128(50):16012-3. doi: 10.1021/ja067107s.
To examine whether catalyst-transfer polycondensation, which affords well-defined polythiophenes, has generality for other conjugated polymers, the synthesis of poly(p-phenylene) (PPP) with various Ni catalysts was investigated. Monomer 1, 1-bromo-4-chloromagnesio-2,5-dihexyloxybenzene, was polymerized with Ni(dppe)Cl2 in the presence of equimolar LiCl to give PPP with a narrow polydispersity. The number-average molecular weight (Mn) of PPP thus obtained increased in proportion to the conversion of 1, indicating that this polymerization also proceeded in a chain-growth polymerization manner. Furthermore, the molecular weight of PPP was controlled by the feed ratio of 1 to the Ni catalyst up to at least Mn = 30000.
为了研究能合成结构明确的聚噻吩的催化转移缩聚反应对其他共轭聚合物是否具有通用性,我们研究了用各种镍催化剂合成聚对亚苯基(PPP)的反应。单体1,1 - 溴 - 4 - 氯镁基 - 2,5 - 二己氧基苯在等摩尔LiCl存在下与Ni(dppe)Cl2聚合,得到了具有窄多分散性的PPP。如此得到的PPP的数均分子量(Mn)与1的转化率成正比增加,这表明该聚合反应也是以链增长聚合方式进行的。此外,PPP的分子量可通过1与镍催化剂的进料比控制,至少在Mn = 30000之前都可以。