Isomers in the chemistry of iron coordination compounds

被引:2
作者
Melnik, Milan [1 ]
Kohutova, Maria [2 ]
机构
[1] Univ Presov, Fac Humanist & Nat Sci, Dept Ecol, Presov 08116, Slovakia
[2] Comenius Univ, Fac Pharm, Dept Chem Theory Drugs, Bratislava 83232, Slovakia
来源
CENTRAL EUROPEAN JOURNAL OF CHEMISTRY | 2010年 / 8卷 / 05期
关键词
Iron; Complexes; Distortion; Cis; -; trans; Isomers; AXIAL LIGAND ORIENTATION; SPIN-CROSSOVER COMPLEXES; TRANSITION-METAL-COMPLEXES; ELECTRONIC GROUND-STATE; X-RAY-STRUCTURE; CRYSTAL-STRUCTURE; MAGNETIC-PROPERTIES; INTERMEDIATE-SPIN; STRUCTURAL-CHARACTERIZATION; MOLECULAR-STRUCTURES;
D O I
10.2478/s11532-010-0083-2
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The coordination chemistry of iron covers a wide field, as shown by a survey covering the crystallographic and structural data of almost one thousand and three hundred coordination complexes. About 6.7% of these complexes exist as isomers and are summarized in this review. Included are distortion (96.6%) and cis - trans (3.4%) isomers. These are discussed in terms of the coordination about the iron atom, bond length and interbond angles. Distortion isomers, differing only by degree of distortion in Fe-L, Fe-L-Fe and L-Fe-L parameters, are the most common. Iron is found in the oxidation states zero, +2 and +3 of which +3 is most common. The stereochemistry around iron centers are tetrahedral, five - coordinated (mostly trigonal - bipyramid) and six - coordinated. The most common ligands have O and N donor sites.
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页码:965 / 991
页数:27
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