Variable magnetic interactions in an organic radical system of (m-N-methylpyridinium α-nitronyl nitroxide)⋅X: A possible kagomé antiferromagnet

Kunio Awaga, Tsunehisa Okuno, Akira Yamaguchi, Morikuni Hasegawa, Tamotsu Inabe, Yusei Maruyama, and Nobuo Wada
Phys. Rev. B 49, 3975 – Published 1 February 1994
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Abstract

In this paper we study an organic system of geometrical spin frustration. m-N-methylpyridinium α-nitronyl nitroxide (m-MPYNN+) is a spin-1/2 organic radical. The simple salt, m-MPYNN+ClO4⋅1/3 (acetone), crystallizes in a trigonal P3c1 space group, where the m-MPYNN+ molecules exist as a dimer and the dimer units form a two-dimensional (2D) triangular lattice. One-third of the C1O4 ions are in the organic layer, joining the m-MPYNN+ molecules, and the remainder is between the layers, compensating the excess of positive charge in the organic layers. The single-crystal EPR measurements clearly indicate a 2D Heisenberg character of the magnetic system in it. m-MPYNN+ makes a crystalline solid-solution system, m-MPYNN+⋅(ClO4)xI1x⋅1/3 (acetone) (0≤x≤1), which also belongs to the trigonal system. Both the a and c axes are slightly lengthened with increasing the ratio of the C1O4 ion, x, in the solid solution: The unit-cell volume is increased by 3.2% when x runs from 0 to 1. The temperature dependence of the magnetic susceptibilities of the solid solutions can be well interpreted in terms of a strong ferromagnetic intradimer interaction J1 forming a triplet state and a weak antiferromagnetic interdimer interaction J2 which is expected to give rise to spin frustration among the triplet spin species on each side of the triangles. It is found that J2 quickly weakens with an increase in x, while J1 shows little dependence. There is a possibility that this organic system can be characterized as a spin-1 kagomé antiferromagnet at very low temperatures.

  • Received 16 August 1993

DOI:https://doi.org/10.1103/PhysRevB.49.3975

©1994 American Physical Society

Authors & Affiliations

Kunio Awaga, Tsunehisa Okuno, Akira Yamaguchi, and Morikuni Hasegawa

  • Department of Pure and Applied Sciences, The University of Tokyo, Komaba, Meguro, Tokyo 153, Japan

Tamotsu Inabe

  • Department of Chemistry, Faculty of Science, Hokkaido University, Sapporo 060, Japan

Yusei Maruyama

  • Institute for Molecular Science, Myodaiji, Okazaki 444, Japan

Nobuo Wada

  • Institute of Physics, The University of Tokyo, Komaba, Meguro, Tokyo 153, Japan

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Vol. 49, Iss. 6 — 1 February 1994

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