Organometallic Chemistry Laboratory, RIKEN, 2-1 Hirosawa, Wako, Saitama, 351-0198, Japan.
Advanced Catalysis Research Group, RIKEN Center for Sustainable Resource Science, Saitama, 351-0198, Japan.
Angew Chem Int Ed Engl. 2016 Nov 14;55(47):14812-14817. doi: 10.1002/anie.201609065. Epub 2016 Oct 24.
The simultaneous chain-growth and step-growth polymerization of a monomer is of great interest and importance because it can produce unique macromolecules which are difficult to prepare by other means. However, such a transformation is usually difficult to achieve in one polymerization system because chain-growth polymerization and step-growth polymerization proceed by different reaction mechanisms. Reported here is the simultaneous chain-growth and step-growth polymerization of para- and meta-methoxystyrenes catalyzed by half-sandwich rare-earth alkyl complexes, and the step-growth polymerization proceeds by the C-H polyaddition of anisyl units to vinyl groups. This unprecedented transformation affords a new family of macromolecules containing unique alternating anisole-ethylene sequences. In contrast to para- and meta-methoxystyrenes, ortho-methoxystyrene exclusively undergo syndiospecific, living chain-growth polymerization by continuous C=C bond insertion to give perfect syndiotactic poly(ortho-methoxystyrene) with high molecular weight and narrow polydispersity (rrrr >99 %, M up to 280 kg mol , M /M <1.10).
单体的链式增长和逐步增长聚合同时发生具有重要意义,因为它可以产生独特的大分子,而这些大分子很难通过其他方法制备。然而,由于链式增长聚合和逐步增长聚合通过不同的反应机制进行,因此通常很难在一个聚合体系中实现这种转变。本文报道了在半夹心稀土烷基配合物的催化下,对间位和对位甲氧基苯乙烯进行的同时链式增长和逐步增长聚合,其中逐步增长聚合是通过芳基单元的 C-H 加成到乙烯基上进行的。这种前所未有的转变提供了一类含有独特交替苯甲醚-乙烯序列的新型大分子。与间位和对位甲氧基苯乙烯不同,邻位甲氧基苯乙烯通过连续的 C=C 键插入进行全同立构特异性、活性链式增长聚合,得到高分子量和窄分散性的完美间同立构聚(邻位甲氧基苯乙烯)(rrrr>99%,M 高达 280kgmol,M/M<1.10)。