Lee Jason Albert, Luscombe Christine K
Department of Chemistry, University of Washington, Seattle, Washington 98195-1700, United States.
Department of Materials Science and Engineering, University of Washington, Seattle, Washington 98195-2120, United States.
ACS Macro Lett. 2018 Jul 17;7(7):767-771. doi: 10.1021/acsmacrolett.8b00429. Epub 2018 Jun 11.
Direct arylation polymerization (DArP) has gained interest in materials chemistry as a method to synthesize conjugated polymers with minimal use of harsh reagents and additional steps. Traditional DArP conditions do not readily yield ideal polymerization characteristics, including chain-growth and low dispersities. It would be of great utility to advance DArP methodology to become competitive with traditional conjugated polymerization techniques. We have developed conditions for a dual-catalytic Ag-Pd system for the synthesis of poly(3-hexylthiophene) (P3HT) that exhibits chain-growth kinetics, low dispersities, and catalyst chain association by Pd. Specifically, the presence of Ag-carboxylate additives plays a beneficial role in the polymerization as a C-H activating agent, while PEPPSI-iPr is used as the Pd source for C-C coupling. The addition of pyridine is necessary to inhibit Pd-mediated C-H activation in the interest of catalyst orthogonality, which can lower dispersities.
直接芳基化聚合(DArP)作为一种在合成共轭聚合物时尽量少用苛刻试剂和减少额外步骤的方法,已在材料化学领域引起关注。传统的DArP条件不易产生理想的聚合特性,包括链增长和低分散性。改进DArP方法使其能与传统共轭聚合技术竞争将具有很大的实用性。我们已经开发出一种用于合成聚(3-己基噻吩)(P3HT)的双催化Ag-Pd体系的条件,该体系表现出链增长动力学、低分散性以及通过Pd实现的催化剂链缔合。具体而言,羧酸银添加剂的存在作为C-H活化剂在聚合中发挥有益作用,而PEPPSI-iPr用作C-C偶联的Pd源。为了实现催化剂的正交性以降低分散性,添加吡啶对于抑制Pd介导的C-H活化是必要的。