Numéro |
J. Phys. IV France
Volume 114, April 2004
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|
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Page(s) | 449 - 453 | |
DOI | https://doi.org/10.1051/jp4:2004114105 |
J. Phys. IV France 114 (2004) 449
DOI: 10.1051/jp4:2004114105
Crystal design of cation-radical salts based on the supramolecular self-organizing arrangement of mellitate anions
T. Inabe1, 1, N. Kobayashi1 and T. Naito11 Division of Chemistry, Graduale School of Science, Hokkaido University, Sapporo 060-0810, Japon
Abstract
Mellitate anions form hydrogen-bonding infinite networks
in the salts with pyridinium cations. The network pattern depends on the
number of deprotonation (
n) from the mellitic acid; for
n = 3, triangular
hydrogen-bond units form a two-dimensional sheet, while for
n = 2, dual
hydrogen-bond units induce one-dimensional belts or two-dimensional grids.
These self-organizing properties have been utilized for the crystal design
of the TTF-type radical cation salts. Crystallization with TMTTF gave two
kinds of crystals. One of the radical cation salt crystals consists of a
channel network of the anions and one-dimensional columns of TMTTF in the
channels. In the other TMTTF salt, the anions with
n = 1 form a
two-dimensional sheet with methanol molecules. The TMTTF radicals are packed
between the sheets with their molecular planes parallel to the anion planes.
Key words. Hydrogen-bond - mellitate anion - crystal design -
radical cation salt - infinite network.
© EDP Sciences 2004