Numéro |
J. Phys. IV France
Volume 114, April 2004
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Page(s) | 455 - 458 | |
DOI | https://doi.org/10.1051/jp4:2004114106 |
J. Phys. IV France 114 (2004) 455
DOI: 10.1051/jp4:2004114106
Interaction and aggregation of TTF oligomers towards supramolecular chemistry
M. Iyoda1, 1, M. Hasegawa1, K. Hara1, J. Takano1, E. Ogura1 and Y. Kuwatani11 Department of Chemistry, Graduate School of Science, Tokyo Metropolitan University, Hachioji, Tokyo 192-0397, Japan
Abstract
Dimeric and oligomeric TTFs have an inherent
multi-functionality. Thus, radical salts derived from bi-TTF and its
derivatives show high conductivities, reflecting either the enhancement of
dimensionality or the control of stoichiometry. In the case of TTF
oligomers, supramolecular structures can be constructed using association of
TTFs. Thus, quarter-TTF adopts a zigzag structure, and its tetracation forms
a helical structure through the intramolecular
-dimer formation of the
terminal radical cations. Poly(tetrathiafulvalenylethynyl)benzenes dimerize
in solutions, and tetrathiafulvalenylacetylene macrocycles containing TTF
and hexadehydro[12]annulene units show interesting properties such as
solvatochromism, electrochromism, sandwitch complex formation, and
electrical conductivities.
Key words. TTF dimers - TTF oligomers - quarter TTF -
dimensionality - supramolecular structure -
poly(tetrathiafulvalenylethynyl)benzenes - tetrathiafulvalenylacetylene
macrocycles.
© EDP Sciences 2004