Low-Coordinate Iron(I) and Manganese(I) Dimers: Kinetic Stabilization of an Exceptionally Short Fe?Fe Multiple Bond

被引:77
作者
Fohlmeister, Lea [1 ]
Liu, Shengsi [2 ,3 ]
Schulten, Christian [1 ]
Moubaraki, Boujemaa [1 ]
Stasch, Andreas [1 ]
Cashion, John D. [4 ]
Murray, Keith S. [1 ]
Gagliardi, Laura [2 ,3 ]
Jones, Cameron [1 ]
机构
[1] Monash Univ, Sch Chem, Melbourne, Vic 3800, Australia
[2] Univ Minnesota, Dept Chem, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Minnesota Supercomp Inst, Minneapolis, MN 55455 USA
[4] Monash Univ, Sch Phys, Melbourne, Vic 3800, Australia
基金
澳大利亚研究理事会;
关键词
density functional calculations; iron; magnesium; manganese; metal-metal interactions; OXIDATION-STATE METALLACYCLES; METAL-METAL DISTANCES; ELECTRONIC-STRUCTURE; MAGNETIC-PROPERTIES; STABLE COMPOUND; COMPLEXES; CHEMISTRY; REACTIVITY; REDUCTION; ANGSTROM;
D O I
10.1002/anie.201203711
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Not just any old iron! The reduction of a bulky guanidinato iron(II) bromide complex yields a three-coordinate iron(I) dimer that possesses the shortest Fe-Fe interaction (2.127 Å) reported to date. Magnetic, Mössbauer, and computational studies show the unprecedented compound to contain two high-spin iron(I) centers with significant multiple-bond character. A related dimer containing a rare example of an unsupported, carbonyl-free Mn-Mn bond is also described. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
引用
收藏
页码:8294 / 8298
页数:5
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