TY - JOUR
T1 - Molecular magnets constructed from cyanometalate building blocks
AU - Entley, William R.
AU - Treadway, Christopher R.
AU - Girolami, Gregory S.
N1 - Funding Information:
We thank the Department of Energy under contract DEFG02-02-91ER45439 for support of this research and Quantum Chemicals, E. I. DuPont de Nemours & Co., and Amoco for fellowships to W.R.E.
PY - 1995/11
Y1 - 1995/11
N2 - The properties of magnetic solids constructed from cyanometalate building blocks are reviewed. Most of these solids adopt face-centered cubic lattices in which adjacent metal centers are linked by CN bridges; they are analogues of the long-known inorganic coordination polymer Prussian blue. Ferromagnets, ferrimagnets, and metamagnets can be obtained depending on the building blocks used. The effects of linkage disorder, site vacancies, and the inclusion of metal ions with orbitally degenerate ground states on the magnetic ordering temperature and hysteretic behavior are discussed. Substitution of low-valent early transition metals such as vanadium(II) into the lattice leads to remarkably high magnetic ordering temperatures, in some cases above 200 K. The large exchange couplings in these vanadium-based molecular magnets are attributed to strong -backbonding interactions with the cyanide orbitals.
AB - The properties of magnetic solids constructed from cyanometalate building blocks are reviewed. Most of these solids adopt face-centered cubic lattices in which adjacent metal centers are linked by CN bridges; they are analogues of the long-known inorganic coordination polymer Prussian blue. Ferromagnets, ferrimagnets, and metamagnets can be obtained depending on the building blocks used. The effects of linkage disorder, site vacancies, and the inclusion of metal ions with orbitally degenerate ground states on the magnetic ordering temperature and hysteretic behavior are discussed. Substitution of low-valent early transition metals such as vanadium(II) into the lattice leads to remarkably high magnetic ordering temperatures, in some cases above 200 K. The large exchange couplings in these vanadium-based molecular magnets are attributed to strong -backbonding interactions with the cyanide orbitals.
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U2 - 10.1080/10587259508031851
DO - 10.1080/10587259508031851
M3 - Article
AN - SCOPUS:0029485221
VL - 273
SP - 153
EP - 166
JO - Molecular Crystals and Liquid Crystals
JF - Molecular Crystals and Liquid Crystals
SN - 1542-1406
IS - 1
ER -