Issue 36, 2015

A versatile and efficient synthesis of bithiophene-based dicarboxaldehydes from a common synthon

Abstract

Bithiophene dicarboxaldehydes are promising electron-rich building blocks for the development of arylene vinylene-based organic semiconductors, but their use has been limited due to their synthetic inaccessibility. To facilitate the facile synthesis of these compounds we have prepared a novel functional bithiophene, namely 2,2′-(3,3′-dibromo-[2,2′-bithiophene]-5,5′-diyl)bis(5,5-dimethyl-1,3-dioxane) in two high yielding steps from 3,3′,5,5′-tetrabromo-2,2′-bithiophene. This synthon is readily transformed into variety of bithiophene-based dicarboxaldehydes, also in high yields. The use of these functional molecules in the synthesis of arylene vinylene-linked donor–acceptor copolymers is demonstrated by the synthesis of two copolymers with electron deficient benzobisazoles.

Graphical abstract: A versatile and efficient synthesis of bithiophene-based dicarboxaldehydes from a common synthon

Supplementary files

Article information

Article type
Paper
Submitted
06 Jun 2015
Accepted
24 Jul 2015
First published
07 Aug 2015

Org. Biomol. Chem., 2015,13, 9462-9470

A versatile and efficient synthesis of bithiophene-based dicarboxaldehydes from a common synthon

A. Bhuwalka, J. F. Mike, J. J. Intemann, A. Ellern and M. Jeffries-EL, Org. Biomol. Chem., 2015, 13, 9462 DOI: 10.1039/C5OB01135C

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements