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首页> 外文期刊>Inorganica Chimica Acta >Preparation, UV-Vis, IR and 1H NMR spectra, and molecular structure of the complex ion (η~2-carbonato)(α,α,α,α-tetrakis (o-pivalamidophenyl)porphinato)ferrate(III)
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Preparation, UV-Vis, IR and 1H NMR spectra, and molecular structure of the complex ion (η~2-carbonato)(α,α,α,α-tetrakis (o-pivalamidophenyl)porphinato)ferrate(III)

机译:高铁酸盐(III)络合物离子(η〜2-碳原子)(α,α,α,α-四(邻-新戊酰胺基苯基)卟啉)的制备,紫外-可见,IR和1H NMR光谱及分子结构

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摘要

An iron(lIl) porphyrin complex containing a bidentate carbonato axial ligand has been synthesized for the first time and fully characterized by UV-Vis, IR and 1H NMR spectroscopies and X-ray crystallography. Proton NMR data for the isolated species is in accordance with high-spin (S = 5/2) ferric derivative. The crystal structure of the (cryptand-222 )potassium(+) (dihaptocarbonato)(α,α,α,α-terakis(opivalamidophenyl)(porphinato)ferrate(III) chlorobenzene has been determined. This structure confirms the highspinstate of the carbonato derivative and shows that the coordination sphere of the iron atom is strongly affected by the asymmetric bidentate (η~2) mode of the carbonato axial ligand.
机译:含二齿碳原子轴向配体的铁(III)卟啉配合物是首次合成,并通过UV-Vis,IR和1H NMR光谱学和X射线晶体学进行了全面表征。分离出的物质的质子NMR数据与高自旋(S = 5/2)铁衍生物一致。确定了(cryptand-222)钾(+)(二碳杂碳酸盐)(α,α,α,α-叔丁基(opivalamidophenyl)(porphinato)高铁(III))氯苯的晶体结构,该结构证实了碳酸盐的高自旋态并表明碳原子轴向配体的不对称双齿(η〜2)模强烈影响铁原子的配位球。

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