Institute for Advanced Study Shenzhen University, Nanshan District Shenzhen, Guangdong, 518060, P. R. China.
Frontier Chemistry Center Faculty of Engineering Hokkaido University, N13 W8, Sapporo, 060-8628, Japan.
Chem Rec. 2016 Aug;16(4):2161-83. doi: 10.1002/tcr.201600034. Epub 2016 Jul 18.
In contrast to the conventional group transfer polymerization (GTP) using a catalyst of either an anionic nucleophile or a transition-metal compound, the organocatalyzed GTP has to a great extent improved the living characteristics of the polymerization from the viewpoints of synthesizing structurally well-defined acrylic polymers and constructing defect-free polymer architectures. In this article, we describe the organocatalyzed GTP from a relatively personal perspective to provide our colleagues with a perspicuous and systematic overview on its recent progress as well as a reply to the curiosity of how excellently the organocatalysts have performed in this field. The stated perspectives of this review mainly cover five aspects, in terms of the assessment of the livingness of the polymerization, limit and scope of applicable monomers, mechanistic studies, control of the polymer structure, and a new GTP methodology involving the use of tris(pentafluorophenyl)borane and hydrosilane.
与使用阴离子亲核试剂或过渡金属化合物的传统基团转移聚合(GTP)相比,从合成结构明确的丙烯酸聚合物和构建无缺陷聚合物结构的角度来看,有机催化的 GTP 在很大程度上改善了聚合的聚合特性。在本文中,我们将从相对个人的角度描述有机催化的 GTP,为我们的同事提供对其最新进展的清晰而系统的概述,并回答有机催化剂在该领域表现出色的好奇心。本综述的观点主要涵盖五个方面,即聚合的活度评估、适用单体的限制和范围、机理研究、聚合物结构的控制以及涉及使用三(五氟苯基)硼烷和硅烷的新 GTP 方法学。