An octahedral coordination complex of iron(VI)

被引：245
作者：
Berry, John F.
Bill, Eckhard
Bothe, Eberhard
George, Serena DeBeer
Mienert, Bernd
Neese, Frank
Wieghardt, Karl
机构：
[1] Max Planck Inst Bioanorgan Chem, D-45470 Mulheim, Germany
[2] Stanford Univ, Stanford Synchrotron Radiat Lab, Stanford, CA 94309 USA
来源：
SCIENCE | 2006年 / 312卷 / 5782期
关键词：
D O I：
10.1126/science.1128506
中图分类号：
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号：
07 ; 0710 ; 09 ;
摘要：
The hexavalent state, considered to be the highest oxidation level accessible for iron, has previously been found only in the tetrahedral ferrate dianion, FeO42-. We report the photochemical synthesis of another Fe(VI) compound, an octahedrally coordinated dication bearing a terminal nitrido ligand. Mossbauer and x-ray absorption spectra, supported by density functional theory, are consistent with the octahedral structure having an Fe=N triple bond of 1.57 angstroms and a singlet d(xy)(2) ground electronic configuration. The compound is stable at 77 kelvin and yields a high-spin spin Fe(III) species upon warming.
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页码：1937 / 1941
页数：5
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