Numéro |
J. Phys. IV France
Volume 114, April 2004
|
|
---|---|---|
Page(s) | 651 - 653 | |
DOI | https://doi.org/10.1051/jp4:2004114157 |
J. Phys. IV France 114 (2004) 651
DOI: 10.1051/jp4:2004114157
Magnetism in organic radical ion salts based on imidazolyl and benzimidazolyl nitronyl nitroxide
T. Sugano1, 1, S.J. Blundell2, W. Hayes2 and P. Day31 Department of Chemistry, Meiji Gakuin University, Kamikurata, Totsuka, Yokohama 244-8539, Japan
2 Department of Physics, University of Oxford, Clarendon Laboratory, Parks Road, Oxford OX1 3PU, UK
e-mail: stephen.blundell@mansfield.oxford.ac.uk; w.hayes1@physics.ox.ac.uk
3 Royal Institution of Great Britain, 21 Albemarle Street, London W1S 4BS, UK
e-mail: profpday@msn.com
Abstract
Radical ion salts of the neutral organic radicals,
2-imidazolyl nitronyl nitroxide
(2-IMNN) and 2-benz- imidazolyl nitronyl nitroxide (2-BIMNN), and a
diradical cation salt of pyridine-2,6-diylbis(nitronyl nitroxide)
(2,6-PYBNN), were prepared. The radical ion salts of
2-BIMNN, Li
+(2-BIMNN)
and (2-BIMNN)
BF
4-, exhibit strong antiferromagnetic interactions with
exchange coupling constants
J/k = -42 K and -510 K, respectively, while the
2-IMNN salts show Curie-Weiss behaviour with Weiss constants
K for
Li
+(2-IMNN)
and
K for (2-IMNN)
Cl
-, indicating weak interactions. The diradical cation salt
(2,6-PYBNN)
Cl
- shows intramolecular ferromagnetic
interaction with
J/k = +4.7 K and intermolecular antiferromagnetic interaction
with
K, which is remarkably reduced from
J/k = -57 K observed in the
diradical 2,6-PYBNN.
Key words. Magnetism - molecular compounds - radical ion salts.
© EDP Sciences 2004