Issue 1, 1998

Synthesis and characterisation of telechelic regioregular head-to-tail poly(3-alkylthiophenes)

Abstract

An investigation into the Stille cross-coupling reaction as an alternative synthetic route to regioregular head-to-tail poly(3-alkylthiophenes) is presented. 2-Iodo-3-alkyl-5-tri-n-butylstannylthiophene derivatives were made, isolated and characterised and subsequently used in Pd0 catalysed cross-coupling reactions in different solvents. Short and long chain regioregular poly(3-hexylthiophenes) with over 96% head-to-tail coupling ratios between adjacent thiophene rings were obtained. The materials were analysed by gel permeation chromatography and NMR spectroscopy. Polymers with varying degrees of polymerisation were obtained depending on the conditions used. End group analysis has shown that polymers, functionalised with both iodo and tri-n-butyltin end groups can be obtained under certain reaction conditions. Preliminary homocoupling reactions were also conducted.

Article information

Article type
Paper

J. Mater. Chem., 1998,8, 25-29

Synthesis and characterisation of telechelic regioregular head-to-tail poly(3-alkylthiophenes)

A. Iraqi and G. W. Barker, J. Mater. Chem., 1998, 8, 25 DOI: 10.1039/A706583C

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.

Spotlight

Advertisements