Raquel Andreu, Joaquín Barberá, Javier Garín, Jesús Orduna, José Luis Serrano, Teresa Sierra, Philippe Leriche, Marc Sallé, Amédée Riou, Michel Jubault and Alain Gorgues
The synthesis and characterization of a series of tetrathiafulvalenes (1–3) bearing a different number of 4′-cyanobiphenyl-4-yloxy side groups is reported. Compound 3 exhibits a nematic and a smectic A mesophase. In the smectic A phase a peculiar local biaxial order due to the unconventional molecular structure is proposed. A charge-transfer salt derived from 3, namely 3·I5 , also shows mesogenic behaviour.
, a= 5.072(2); b= 12.081(3); c= 51.773(13)Å;
α= 87.04(2); β= 87.27(3); γ= 78.05(2)°, V= 3097.5(1.5)Å3, Z= 4,
Dc= 1.40 g cm–3, λ(Mo-Kα)= 0.71073 Å. 11438 reflections
(2<θ<25°) were collected at 298 K, 2098 with I > 3 σ(I) used in
the refinements, 305 refined parameters. R= 0.20, Rw= 0.24;;
(b) This X-ray structure has been presented at the ICSM'96, Utah
(USA), July 1996: R. Andreu, J. Barbeá, J. Garín, J. Orduna, J. L. Serrano, T. Sierra, P. Leriche, M. Sallé, A. Riou, M> Jubault and A. Gorgues, Synth. Met., 1997, 86, 1869 Search PubMed.