R. Tamura et al., MOLECULAR AND CRYSTAL-STRUCTURE AND PROPERTIES OF TE-CONTAINING P-TERPHENOQUINONE ANALOGS, Molecular crystals and liquid crystals science and technology. Section A, Molecular crystals and liquid crystals, 278, 1996, pp. 139-150
p-Terphenoquinone analogues containing a quinonoid type of tellurophen
e skeleton in the central position have been prepared with a view to d
eveloping a new type of organic photoconductive materials having ampho
teric redox properties. X-ray structure analysis showed that each mole
cule exhibited an asymmetric boat conformation owing to the bent struc
ture of the whole ring system and the opposite twisting of two termina
l rings. The molecular packing manner in the crystals depends on the s
ubstituents on the terminal quinonoid rings. These compounds were elec
trically amphoteric and afforded radical cation salts and CT complexes
by electrochemical or chemical oxidation or by the reaction with an a
ppropriate electron acceptor, respectively. Preliminary experimental r
esults on the photoconductive properties of the neutral compound along
with the electrical and magnetic properties of the radical cation sal
ts and CT complexes are described.