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首页> 外文期刊>Zeitschrift fur Naturforschung, B. A Journal of Chemical Sciences >Synthesis and reactions with CO and C2H4 of cobalt(I) complexes containing trimethylphosphine and chelating o-diphenylphosphanylphenolate ligands
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Synthesis and reactions with CO and C2H4 of cobalt(I) complexes containing trimethylphosphine and chelating o-diphenylphosphanylphenolate ligands

机译:含三甲基膦和螯合邻二苯基膦酰基酚盐配体的钴(I)配合物的合成及与CO和C2H4的反应

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摘要

In tetracoordinate cobalt(I) halide compounds CoX(Ph2P<^>OH)(PMe3)(2)(X = Cl, Br) o-phosphanylphenols Ph2P<^>OH are coordinated as phosphane ligands. In the presence of base chelating anions Ph2P<^>O- give rise to pentacoordinate complexes Co(Ph2P<^>O)(PMe3)(3). Molecular structures are presented for both types of compounds. The five-membered chelate ring in Co(Ph2P<^>O)(PMe3)(3) is resistant to protonation, and ring-opening is not observed in the presence of CO or C2H4 Replacing one of the trimethylphosphanes by one of the pi-acceptor ligands affords fluxional complex molecules which upon cooling attain definite ground-state geometries out of a multitude of possible isomers. [References: 19]
机译:在四配位钴(I)卤化物中,CoX(Ph 2 P OH)(PMe 3)(2)(X = Cl,Br)邻膦基苯酚Ph 2 P OH被配位为膦配体。在碱螯合阴离子的存在下,Ph 2 P 6 O-产生五配位配合物Co(Ph 2 P 6 O)(PMe 3)(3)。给出了两种化合物的分子结构。 Co(Ph2P ^ O)(PMe3)(3)中的五元螯合环具有抗质子化作用,并且在存在CO或C2H4的情况下未观察到开环,其中一个pi取代了一个三甲基膦-受体配体提供了通量复杂的分子,其在冷却时从多种可能的异构体中获得确定的基态几何形状。 [参考:19]

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