Issue 6, 2003

The synthesis and characterisation of amphiphilic α,α-linked sexithiophenes with substituents at the terminal α-positions

Abstract

A series of polydisperse amphiphilic α,α-linked sexithiophenes with an oligoethylene oxide substituent at one terminal α-position and a hydrogen atom or a hexyl group at the other have been synthesised via Stille and Suzuki cross coupling reactions. The products have been characterised by a combination of 1H and 13C NMR spectroscopy and detailed MALDI-TOF mass spectrometry.

Graphical abstract: The synthesis and characterisation of amphiphilic α,α-linked sexithiophenes with substituents at the terminal α-positions

Article information

Article type
Paper
Submitted
29 Nov 2002
Accepted
09 Apr 2003
First published
22 Apr 2003

J. Mater. Chem., 2003,13, 1269-1273

The synthesis and characterisation of amphiphilic α,α-linked sexithiophenes with substituents at the terminal α-positions

O. Henze, D. Parker and W. J. Feast, J. Mater. Chem., 2003, 13, 1269 DOI: 10.1039/B211891M

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