MOSSBAUER STUDY OF A NOVEL BINUCLEAR FE(II/III) DELOCALIZED-VALENCE COMPOUND

被引:11
作者
DING, XQ [1 ]
BOMINAAR, EL [1 ]
BILL, E [1 ]
WINKLER, H [1 ]
TRAUTWEIN, AX [1 ]
DRUEKE, S [1 ]
CHAUDHURI, PH [1 ]
WIEGHARDT, K [1 ]
机构
[1] RUHR UNIV BOCHUM, LEHRSTUHL ANORG CHEM 1, W-4630 BOCHUM, GERMANY
来源
HYPERFINE INTERACTIONS | 1990年 / 53卷 / 1-4期
关键词
D O I
10.1007/BF02101058
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
In this paper, we briefly summarize the main conclusions of the Mössbauer analysis of [L2Fe2(μ-OH)3] (ClO4)2·2CH3OH·2H2O with L=N,N',N"-trimethyl-1,4,7-triazacyclononane, a novel dimeric iron compound, which possesses a central exchange-coupled delocalized-valence Fe(II/III) unit. The complete delocalization of the excess electron in the dimeric iron center is concluded from the indistinguishability of the two iron sites in Mössbauer spectroscopy. The magnetic Mössbauer spectra imply a system spin St=9/2 for the dimer in its ground state. The values for hyperfine and spin-Hamiltonian parameters, obtained from simulations of the Mössbauer spectra, are δ=0.74 mms-1, ΔEQ=-2.14 mms-1, A⊥=-10.6 T, A∥=-13.5 T and D=1.8 cm-1. The system spin St=9/2 is interpreted to be a consequence of double-exchange coupling. © 1990 J.C. Baltzer AG, Scientific Publishing Company.
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页码:311 / 315
页数:5
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