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Isomers in the chemistry of iron coordination compounds

机译:铁配位化合物化学中的异构体

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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.
机译:铁的配位化学涵盖了广阔的领域,如一项涵盖近一千三百种配位配合物的晶体学和结构数据的调查显示。这些复合物中约有6.7%以异构体形式存在,本综述对此进行了概述。其中包括畸变(96.6%)和顺-反(3.4%)异构体。这些是根据铁原子​​,键长和键间角的配位关系进行讨论的。最常见的畸变异构体仅在Fe-L,Fe-L-Fe和L-Fe-L参数的畸变程度上有所不同。发现铁的氧化态为零,+ 2和+3,其中最常见的是+3。铁中心周围的立体化学是四面体,五配位(主要是三角-双锥体)和六配位。最常见的配体具有O和N供体位点。

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