Issue 2, 2009

Supramolecular chemistry of π-extended analogues of TTF and carbon nanostructures

Abstract

The shrewd combination of complementary electroactive molecular fragments through weak, non-covalent forces can be exploited to construct stimuli-responsive assemblies or to achieve self-ordered arrays of electron donor and/or acceptor moieties to be utilized in optoelectronic devices. Among the electron donors, tetrathiafulvalene (TTF) has been particularly fashionable in this field. Comparatively, the supramolecular chemistry of its π-extended analogues was severely underdeveloped. Herein we present a summary of some recent results in the exploration of the non-covalent chemistry of π-extended analogues of tetrathiafulvalene.

Graphical abstract: Supramolecular chemistry of π-extended analogues of TTF and carbon nanostructures

Article information

Article type
Perspective
Submitted
18 Sep 2008
Accepted
14 Nov 2008
First published
16 Dec 2008

New J. Chem., 2009,33, 228-234

Supramolecular chemistry of π-extended analogues of TTF and carbon nanostructures

E. M. Pérez, B. M. Illescas, M. Á. Herranz and N. Martín, New J. Chem., 2009, 33, 228 DOI: 10.1039/B816272G

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