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首页> 外文期刊>Journal of Organometallic Chemistry >Synthesis, characterization, reactivity and theoretical studies of ruthenium carbonyl complexes containing ortho-substituted triphenyl phosphanes
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Synthesis, characterization, reactivity and theoretical studies of ruthenium carbonyl complexes containing ortho-substituted triphenyl phosphanes

机译:含邻位取代的三苯基膦的羰基钌配合物的合成,表征,反应性和理论研究

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A series of ruthenium o-phosphane complexes was synthesized and characterized. The reactivity of the prepared complexes was studied by using them as catalysts for the hydroformylation of 1-hexene. The activities depended on the binding mode of the phosphane and on the strength of the ruthenium-phosphane interaction. Strongly coordinated chelating [2-(dimethylamino)phenyl]-(diphenyl) phosphane and [2-(methylthio)phenyl]-(diphenyl) phosphane showed poor activity, while weakly chelated [2-(methoxy)phenyl]-(diphenyl) phosphane and non-chelating phosphanes such as [2-(methyl)phenyl]-(diphenyl) phosphane or [2-(ethyl)phenyl]-(diphenyl) phosphane led to higher activities. (c) 2005 Elsevier B.V. All rights reserved.
机译:合成并表征了一系列钌邻膦烷配合物。通过将它们用作1-己烯加氢甲酰化的催化剂,研究了所制备的配合物的反应性。活性取决于膦的结合模式和钌-膦相互作用的强度。强配位螯合的[2-(二甲氨基)苯基]-(二苯基)膦和[2-(甲硫基苯基)]-(二苯基)膦表现出较弱的活性,而弱螯合的[2-(甲氧基)苯基]-(二苯基)膦非螯合的膦,例如[2-(甲基)苯基]-(二苯基)膦或[2-(乙基)苯基]-(二苯基)膦导致更高的活性。 (c)2005 Elsevier B.V.保留所有权利。

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