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铜催化的可控自由基聚合反应(原子转移自由基聚合)的本质特性

Radical Nature of Cu-Catalyzed Controlled Radical Polymerizations (Atom Transfer Radical Polymerization).

作者信息

Matyjaszewski K

机构信息

Carnegie Mellon University, Department of Chemistry, 4400 Fifth Avenue, Pittsburgh, Pennsylvania 15213.

出版信息

Macromolecules. 1998 Jul 28;31(15):4710-7. doi: 10.1021/ma980357b.

Abstract

Copper-catalyzed atom transfer radical polymerization (ATRP) is one of the most robust and precise techniques for controlling radical polymerization. The very good control of molecular weights, polydispersities, functionalities, chain composition, and topologies unusual for radical systems combined with the application of transition metals as catalysts requires more detailed mechanistic studies and proof of the radical nature of active species. The following results are in agreement with the radical nature of ATRP: reverse ATRP, chemoselectivities similar to those for conventional radical polymerization (effect of additives and inhibitors/scavengers, reactivity ratios, transfer coefficients), regioselectivities similar to those for conventional radical polymerization (low proportion of head-to-head units and expected structure of both tail and head end groups), stereoselectivities (tacticities) similar to that in conventional radical polymerization, EPR detection of X-Mtn+1 species resulting from the persistent radical effect, and confirmation of the termination by doubling molecular weights as well as cross-linking with multifunctional initiators and inimers. In addition, it seems that, in most ATRP systems, the contribution of degenerative transfer and reversible formation of organometallic intermediates is small and a halogen atom is transferred in the concerted process rather than in a two-step process with the involvement of radical anions.

摘要

铜催化原子转移自由基聚合(ATRP)是控制自由基聚合最可靠、最精确的技术之一。对于自由基体系而言,能很好地控制分子量、多分散性、官能度、链组成和拓扑结构,同时使用过渡金属作为催化剂,这需要更详细的机理研究以及对活性物种自由基性质的证明。以下结果与ATRP的自由基性质相符:反向ATRP、与传统自由基聚合相似的化学选择性(添加剂和抑制剂/清除剂的影响、竞聚率、转移系数)、与传统自由基聚合相似的区域选择性(头对头单元的低比例以及尾端和头端基团的预期结构)、与传统自由基聚合相似的立体选择性(立构规整度)、通过持久自由基效应产生的X-Mtn+1物种的电子顺磁共振检测,以及通过分子量翻倍以及与多官能引发剂和内单体交联来确认终止反应。此外,在大多数ATRP体系中,退化转移和有机金属中间体可逆形成的贡献似乎很小,并且卤原子是在协同过程中转移的,而不是在涉及自由基阴离子的两步过程中转移。

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