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Low-Valent Iron Mono-Diazadiene Compounds: Electronic Structure and Catalytic Application

机译:价铁单重氮化合物:电子结构和催化应用

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摘要

A series of monodiazadiene diolefin iron compounds, [Fe(trop(2)dad)(L)] (4; L = neutral ligand), has been prepared by one-electron oxidation of the Fe-I species [NaFe-(trop(2)dad)(thf)(3)] (dad = diazadiene; trop = 5H-dibenzo[a,d]-cyclohepten-5-yl). The electronic structures of compounds 4 were investigated by NMR and Mossbauer spectroscopy, single-crystal X-ray diffraction, solid- and liquid-phase magnetic susceptibility measurements, and DFT calculations. Compounds of type 4 with labile ligands L were found to be active (pre)catalysts for the dehydrogenative coupling of (alkyl)amine-boranes. Remarkably high activities were observed, especially for the homogeneous dehydrogenative polymerization of methylamine-borane.
机译:一系列单重氮二烯二烯烃铁化合物[Fe(trop(2)dad)(L)](4; L =中性配体),是通过Fe-I物种[NaFe-(trop( 2)dad)(thf)(3)](dad =二氮杂二烯; trop = 5H-二苯并[a,d]-环庚-5-基)。通过NMR和Mossbauer光谱,单晶X射线衍射,固相和液相磁化率测量以及DFT计算研究了化合物4的电子结构。发现具有不稳定配体L的4型化合物为(烷基)胺-硼烷的脱氢偶联的活性(预)催化剂。观察到非常高的活性,特别是对于甲胺-硼烷的均相脱氢聚合。

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