Molecule-based magnets with a fully interlocked three-dimensional structure

Citation
O. Cador et al., Molecule-based magnets with a fully interlocked three-dimensional structure, SYNTH METAL, 122(3), 2001, pp. 559-567
Citations number
37
Categorie Soggetti
Apllied Physucs/Condensed Matter/Materiales Science
Journal title
SYNTHETIC METALS
ISSN journal
03796779 → ACNP
Volume
122
Issue
3
Year of publication
2001
Pages
559 - 567
Database
ISI
SICI code
0379-6779(20010801)122:3<559:MMWAFI>2.0.ZU;2-U
Abstract
This paper concerns the chemistry and the magnetic properties of a family o f compounds with a fully interlocked structure. The general formula is [Etr ad](2)[M-2{Cu(opba)}3].S, with M = Mn2+, Co2+, Mg2+, Ni2+ where Etrad stand s for a radical cation, and opba stands for ortho-phenylenebis(oxamato). Th e structure consists of two interpenetrating graphite-like networks with ed ge sharing hexagons. The magnetic properties of the four compounds have bee n investigated in detail. The Mg2+ derivative behaves as a paramagnet with weak ferromagnetic interactions between Cu2+ and Etrad(+) ions. The three o ther compounds are molecule-based magnets with a spontaneous magnetization below 22.8 K for the Mn2+ derivative, 28 K for the Ni2+ derivative and 37 K for the Co2+ derivative. While the Mn2+ derivative is a soft magnet, the N i2+ and Co2+ derivative display hysteresis loops, with coercive fields high er than 1 kOe depending on the temperature and the size of the particles. T he Ni2+ derivative presents also an inversion of the magnetic poles as the temperature varies under a small external field. For higher field, the magn etization reverses two times. These original results can be properly reprod uced using the molecular-field theory adapted to the system and the magneti c anisotropy. (C) 2001 Elsevier Science B.V. All rights reserved.