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Ferromagnetic Coupling through Spin Polarization in a Dinuclear Copper( II ) Metallacyclophane
Author(s) -
Fernández Isabel,
Ruiz Rafael,
Faus Juan,
Julve Miguel,
Lloret Francesc,
Cano Joan,
Ottenwaelder Xavier,
Journaux Yves,
Muñoz M. Carmen
Publication year - 2001
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/1521-3773(20010817)40:16<3039::aid-anie3039>3.0.co;2-p
Subject(s) - ferromagnetism , radical , copper , chemistry , metal , cyclophane , molecule , ground state , crystallography , polarization (electrochemistry) , photochemistry , condensed matter physics , crystal structure , physics , organic chemistry , atomic physics
First organic radicals, now metal complexes : A successful extension to metal complexes of a well‐known organic radical approach to ferromagnetism is exemplified by the triplet ground‐state molecule containing two Cu II centers connected by a double m ‐phenylenediamide skeleton of the cyclophane type shown in the scheme.