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A dinuclear cobalt(ii) complex of calix[8]arenes exibiting strong magnetic anisotropy
Author(s) -
Sarah Petit,
Guillaume Pilet,
Dominique Luneau,
Liviu F. Chibotaru,
Liviu Ungur
Publication year - 2007
Publication title -
dalton transactions
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.98
H-Index - 184
eISSN - 1477-9234
pISSN - 1477-9226
DOI - 10.1039/b708926k
Subject(s) - cobalt , monoclinic crystal system , crystallography , triethylamine , chemistry , tetrahedral molecular geometry , coordination sphere , crystal structure , inorganic chemistry , organic chemistry
The solvothermal reaction of cobalt(II) acetate with p-tert-butylcalix[8]arene (calix) and triethylamine affords the compound (Et3NH)2 [CoII2(calix)2] (.2Et3NH) that shows a hydrogen bond bridged dinuclear complex [CoII2(calix)2]2- () with cobalt(II) ions in a tetrahedral geometry. The compound crystallises in the monoclinic, space group P2(1)/n with cell parameters a=14.89(1) A, b=20.90(2) A, c=30.87(4) A, beta=102.57(7) degrees, V=9376(16) A3, Z=2. The magnetic studies together with ab initio calculations are evidence of an important role of the geometry of the second coordination sphere of carbon and hydrogen atoms around the CoO4 core in quantifying the zero field splitting on cobalt sites. This results in strong magnetic anisotropies with a negative axial component on the cobalt fragments.

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