Multifrequency high-field EPR study of binuclear Mn(III)Mn(IV) complexes

被引:14
|
作者
Policar, C
Knüpling, M
Frapart, YM
Un, S
机构
[1] Univ Paris 11, Inst Chim Mol Orsay, Chim Inorgan Lab, CNRS URA 420, F-91405 Orsay, France
[2] CNRS, MPIF, Grenoble High Magnet Field Lab, F-38042 Grenoble 9, France
[3] Free Univ Berlin, Inst Phys Expt, D-14195 Berlin, Germany
[4] CEA Saclay, CNRS URA 2096, Sect Bioenerget, Dept Biol Cellulaire & Mol, F-91191 Gif Sur Yvette, France
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 1998年 / 102卷 / 50期
关键词
D O I
10.1021/jp982096d
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The results from a multifrequency high-field EPR study of five di-mu-oxo bridged mixed-valence binuclear Mn(III)Mn(IV) complexes are reported. Spectra were obtained at 9, 95, and 285 GHz. The g anisotropy was unambiguously observable at 285 GHz. Hyperfine and g tensor values were estimated using spectral simulation procedures that cyclically and simultaneously fit the multifrequency data. In all five cases, the g tensors of the mixed-valence complexes were found to be rhombic. The g tensors were analyzed using the vector projection model. Most, but not all, of the g anisotropy originates from the Mn(III) center. The rhombic g tensors result from the low symmetry of the manganese centers. The size of the effective g anisotropy for a given complex was found to be a linear function of the average bond distance between the manganese and axial nitrogens. This relationship can be understood in terms of the influence of tetragonal distortion on the electronic levels of the Mn(III) center. The frequency-dependent line broadening observed in these mixed-valence complexes is explained in terms of the relationship between g anisotropy and structure.
引用
收藏
页码:10391 / 10398
页数:8
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