The synthesis, electrochemistry and mesogenic properties of novel tetrathia
fulvalenyl- and ferrocenyl-triphenylenes are described. In all cases the ju
xtaposition of the hexa-alkyloxytriphenylene with a tetrathiafulvalene or f
errocene unit failed to give rise to derivatives displaying a discotic meso
phase. Solution electrochemistry of derivatives 7 and 13 has revealed an in
teraction occurs between the dicationic state of the TTF moiety and the tri
phenylene nucleus. (C) 2000 Elsevier Science Ltd. All rights reserved.