Volume 34, Issue 1 p. 69-73
Communication

Detailed Optimization of Polycondensation Reaction via Direct C–H Arylation of Ethylenedioxythiophene

Koutarou Yamazaki

Tsukuba Research Center for Interdisciplinary Materials Science (TIMS), Graduate School of Pure and Applied Science, University of Tsukuba, 1‐1‐1 Tennodai, Tsukuba 305‐8573, Japan

Search for more papers by this author
Junpei Kuwabara

Tsukuba Research Center for Interdisciplinary Materials Science (TIMS), Graduate School of Pure and Applied Science, University of Tsukuba, 1‐1‐1 Tennodai, Tsukuba 305‐8573, Japan

Search for more papers by this author
Takaki Kanbara

Corresponding Author

Tsukuba Research Center for Interdisciplinary Materials Science (TIMS), Graduate School of Pure and Applied Science, University of Tsukuba, 1‐1‐1 Tennodai, Tsukuba 305‐8573, Japan

Tsukuba Research Center for Interdisciplinary Materials Science (TIMS), Graduate School of Pure and Applied Science, University of Tsukuba, 1‐1‐1 Tennodai, Tsukuba 305‐8573, Japan.Search for more papers by this author
First published: 12 October 2012
Citations: 71

Abstract

The polycondensation reaction of 3,4‐ethylenedioxythiophene with 2,7‐dibromo‐9,9‐dioctylfluorene via Pd‐catalyzed direct arylation gives poly[(3,4‐ethylenedioxythiophene‐2,5‐diyl)‐(9,9‐dioctylfluorene‐2,7‐diyl)]. The reaction conditions are optimized in terms of the Pd precatalysts, reaction time, and carboxylic acid additives. The combination of 1 mol% Pd(OAc)2 and 1‐adamantanecarboxylic acid as an additive is the optimized catalytic system, and it yields the corresponding polymer with a molecular weight of 39 400 in 89% yield. The polycondensation reaction, followed by an end‐capping reaction, effectively provides a linear polymer without Br terminals.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.