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红光诱导、铜催化的原子转移自由基聚合。

Red-Light-Induced, Copper-Catalyzed Atom Transfer Radical Polymerization.

机构信息

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

出版信息

ACS Macro Lett. 2022 Mar 15;11(3):376-381. doi: 10.1021/acsmacrolett.2c00080. Epub 2022 Feb 28.

Abstract

Despite advances in photochemical atom transfer radical polymerization (photoATRP), these systems often rely on the use of UV light for the activation/generation of the copper-based catalytic species. To circumvent the problems associated with the UV light, we developed a dual photoredox catalytic system to mediate photoinduced ATRP under red-light irradiation. The catalytic system is comprised of a Cu catalyst to control the polymerization via ATRP equilibrium and a photocatalyst, such as zinc(II) tetraphenylporphine or zinc(II) phthalocyanine, to generate the activator Cu species under red-light irradiation. In addition, this system showed oxygen tolerance due to the consumption of oxygen in the photoredox reactions, yielding well-controlled polymerizations without the need for deoxygenation processes.

摘要

尽管光化学原子转移自由基聚合(photoATRP)取得了进展,但这些体系通常依赖于使用紫外光来激活/生成基于铜的催化物种。为了避免与紫外光相关的问题,我们开发了一种双重光氧化还原催化体系,以在红光照射下介导光诱导 ATRP。该催化体系由 Cu 催化剂组成,通过 ATRP 平衡来控制聚合,以及光催化剂,如锌(II)四苯基卟啉或锌(II)酞菁,在红光照射下生成活化剂 Cu 物种。此外,由于光氧化还原反应中消耗了氧气,该体系具有耐氧性,无需进行脱氧处理即可进行可控聚合。

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