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Hybrid Molecular Magnets Obtained by Insertion of Decamethylmetallocenium Cations into Layered, Bimetallic Oxalate Complexes: [Z III Cp* 2 ][M II M III (ox) 3 ] (Z III =Co, Fe; M III =Cr, Fe; M II =Mn, Fe, Co, Cu, Zn; ox=oxalate; Cp*=pentamethylcyclopentadienyl)
Author(s) -
Coronado Eugenio,
GalánMascarós JoséRamón,
GómezGarcía CarlosJosé,
Ensling Jürgen,
Gütlich Philipp
Publication year - 2000
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/(sici)1521-3765(20000204)6:3<552::aid-chem552>3.0.co;2-u
Subject(s) - paramagnetism , chemistry , crystallography , isostructural , ferromagnetism , bimetallic strip , antiferromagnetism , magnetization , mössbauer spectroscopy , oxalate , monoclinic crystal system , inorganic chemistry , crystal structure , condensed matter physics , metal , magnetic field , physics , organic chemistry , quantum mechanics
Paramagnetic and diamagmetic [Z III Cp] + organometallic complexes were used as “templating” cations to prepare a series of hybrid layered magnets based on bimetallic oxalate complexes (see figure). These salts show spontaneous magnetization below T c , corresponding to the presence of ferro‐, ferri‐, or canted antiferromagnetism. The effects of the paramagnetic and ferromagnetic sublattices on the magnetic properties of these compounds were studied by magnetic measurements, and by ESR and Mössbauer spectroscopy.

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