Issue 3, 2008

Synthesis and properties of polysilanes with tetrathiafulvalene as pendant group

Abstract

Two polysilanes with tetrathiafulvalene (TTF) as pendant groups were synthesized by reaction of 2-cyanoethyl substituted TTF 1 with (chloromethylphenyl)dimethyl(phenyl)polysilane, or reaction of 4-vinylphenyl-TTF 2 with poly[methylsilane-co-methyl(phenyl)silane]. The structures and properties of TTF-polysilanes and their intermediates were characterized by 1H NMR, mass, GPC, UV/Vis, IR and cyclic voltammetry (CV). The results of UV/Vis and CV of these polysilanes indicated interaction between the TTF moieties and σ-electron delocalized Si–Si chain in the ground states. These polysilanes doped by I2 exhibited high conductivities (10−2 S cm−1).

Graphical abstract: Synthesis and properties of polysilanes with tetrathiafulvalene as pendant group

Article information

Article type
Paper
Submitted
11 Sep 2007
Accepted
19 Nov 2007
First published
04 Dec 2007

New J. Chem., 2008,32, 505-510

Synthesis and properties of polysilanes with tetrathiafulvalene as pendant group

Y. Liu, C. Wang, M. Li, G. Lai and Y. Shen, New J. Chem., 2008, 32, 505 DOI: 10.1039/B713819A

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