The electronic properties of linear π-conjugated systems (LCSs) have acquired a growing
importance in many areas of modern chemistry and physics of condensed matter. At the …

By considering the structures of many salts derived from extended TTF analogues,
relationships between the molecular architecture of the donors with their electrochemical …

Some of the current directions in research on new organic materials based on functionalized
oligoarylenes are reviewed. Particular emphasis is placed upon the use of chemical …

Molecular or polymeric π-electron donors based on the association of tetrathiafulvalene
(TTF) with linear π-conjugated systems are reviewed. Two main classes of materials are …

This review describes the synthesis of 1, 3-and 1, 2-tetrachalcogenafulvalenes, the chemical
transformation of substituents, reactions of the ring system, and the synthesis of polymers …

Push–pull compounds, in which a proaromatic electron donor is conjugated to a 2‐
dicyanomethylenethiazole acceptor, have been prepared, and their properties compared to …

A new series of linearly extended tetrathiafulvalene analogues with thienothiophene and
dithienothiophene π-conjugating spacers has been synthesized. Electronic absorption …

A series of extended tetrathiafulvalene (TTF) derivatives bearing one or two 1, 4‐dithiafulven‐
6‐yl substituents has been prepared. The new compounds present remarkable …

Bridged dithienylethylenes (DTEs) bearing solubilizing alkyl chains at various positions (2−
5) have been synthesized by McMurry dimerization of cyclopenta [b] thiophen-6-ones. In …

Tetrathiafulvalene analogues involving dihexyloxythiophene (1), ethylenedioxythiophene
(2), and bis (3, 4-dihexyloxy-2-thienyl) ethylene (3) as conjugating spacer and diversely …