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首页> 外文期刊>Polyhedron: The International Journal for Inorganic and Organometallic Chemistry >Synthesis and structure of diphenylphosphine derivatives of molybdenocene
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Synthesis and structure of diphenylphosphine derivatives of molybdenocene

机译:钼烯二苯基膦衍生物的合成与结构

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The phosphino molybdenocene complex [Cp2Mo(PPh2H)(2)][BF4](2) (1) (Cp = eta(5)-C5H5) was prepared by reaction of Cp2MoI2 with PPh2 and excess of TlBF4 in NCMe. The monocation [Cp2MoI(PPh2H)](+) (2) as the BF4- or I- salt was synthesised by treatment of Cp2MoI(SPh) with HBF4 followed by addition of PPh2H, or by reaction of Cp2MoI2 with PPh2H, respectively. The indenyl phosphine complex [IndMo(CO)(2)(PPh2H)(2)]BF4 (3) (Ind = eta(5)-C9H7) was prepared by reaction of IndMo(CO)(2)(eta(3)-C3H5) with HBF4 followed by addition of PPh2H. Deprotonation of 1 with dabco led to the formation of the phosphinophosphido molybdenocene [Cp2Mo(PPh2)(PPh2H)][BF4] (4). Treatment of I with two equivalents of LiBu in thf at -30 degreesC formed a thermally unstable complex (5) which could not be isolated. P-31 NMR and protonation to reform 1 support its formulation as CpMo(PPh2)(2). The molecular structures of [Cp2Mo(PPh2H)(2)][BF4](2) and [Cp2MoI(PPh2H)](+) have been determined by single-crystal X-ray diffraction. (C) 2004 Elsevier Ltd. All rights reserved.
机译:通过Cp2MoI2与PPh2和过量的TlBF4在NCMe中的反应制备膦膦钼烯配合物[Cp2Mo(PPh2H)(2)] [BF4](2)(1)(Cp = eta(5)-C5H5)。通过用HBF4处理Cp2MoI(SPh),然后添加PPh2H,或通过使Cp2MoI2与PPh2H反应,分别合成了作为BF4-或I-盐的单阳离子[Cp2MoI(PPh2H)](+)(2)。通过IndMo(CO)(2)(eta(3))反应制备茚基膦络合物[IndMo(CO)(2)(PPh2H)(2)] BF4(3)(Ind = eta(5)-C9H7) -C3H5)与HBF4,然后加入PPh2H。用dabco对1进行质子化导致膦酰基膦基钼烯[Cp2Mo(PPh2)(PPh2H)] [BF4]的形成(4)。在-30℃下用两当量的LiBu处理I时,形成了无法分离的热不稳定配合物(5)。 P-31 NMR和重整1的质子支持其配方为CpMo(PPh2)(2)。 [Cp2Mo(PPh2H)(2)] [BF4](2)和[Cp2MoI(PPh2H)](+)的分子结构已通过单晶X射线衍射确定。 (C)2004 Elsevier Ltd.保留所有权利。

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