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首页> 外文期刊>Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics >KINETICS AND MECHANISM OF NUCLEOPHILIC SUBSTITUTIONS ON COORDINATED POLYENES AND POLYENYLS .1. REACTIONS OF TERTIARY PHOSPHINES WITH [RU(ETA(5)-C5H5)(ETA(4)-C5H4O)(L)]CF3SO3 (L=CH3CN, BENZONITRILE, THIOUREA, PYRIDINE)
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KINETICS AND MECHANISM OF NUCLEOPHILIC SUBSTITUTIONS ON COORDINATED POLYENES AND POLYENYLS .1. REACTIONS OF TERTIARY PHOSPHINES WITH [RU(ETA(5)-C5H5)(ETA(4)-C5H4O)(L)]CF3SO3 (L=CH3CN, BENZONITRILE, THIOUREA, PYRIDINE)

机译:核聚合物和多核上核亲取代基的动力学和机理.1。叔膦与[RU(ETA(5)-C5H5)(ETA(4)-C5H4O)(L)] CF3SO3(L = CH3CN,苯甲腈,硫脲,吡啶)的反应

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摘要

Complexes of the type [Ru(eta(5)-C5H5)(eta(4)-C5H4O)(L)]CF3SO3 (L = CH3CN (1a), benzonitrile (1b), pyridine (2), thiourea (3)) react with tertiary phosphines to give either 1,1'- or 1,2-disubstituted ruthenocenes depending on the basicity of the entering phosphine and the nature of L. For 1a and 1b, only phosphines with a pK(a) value above 5 substitute on the C5H5 ring while others substitute on the C5H4O ring. For compounds 2 and 3, the two rings are deactivated such that only the most basic phosphines react, and they attack only the C5H4O ring. In some cases of the reactions of 2 and 3, an intermediate is observed in which the monodentate ligand has migrated to the C5H5 ring while the entering nucleophile coordinates to the metal center. The mechanism by which phosphines attack a coordinated C5H4O ring has been established, and detailed kinetic parameters have been obtained. For the reaction of 1a with PPh(3), PPh(2)Me, and P(p-PhOMe)(3) in acetone, the kinetics give a rate law indicating the reversible formation of an intermediate which goes irreversibly to the 1,2-disubstituted ruthenocene product. All three rate constants and their thermal activation parameters have been obtained for each of these reactions. For the P(p-PhOMe)(3) reaction, the volume of activation for each step has also been determined. The reaction of 2 and 3 with PBu(3)(n), PCy(3), PPhMe(2), and PMe(3) in CD3CN give a long-lived intermediate which also goes to the 1,2-disubstituted ruthenocene product. For the intermediates formed from 3, the kinetics of this last step have been studied to determine the rate constants and their thermal activation parameters. In the case of PBu(3)(n), the intermediate formed from 3 has been isolated and an X-ray structure determined, establishing that phosphine attack has occurred at the C5H4O ring. [References: 21]
机译:[Ru(eta(5)-C5H5)(eta(4)-C5H4O)(L)] CF3SO3类型的配合物(L = CH3CN(1a),苄腈(1b),吡啶(2),硫脲(3))与叔膦反应生成1,1'-或1,2-二取代的钌烯,这取决于进入的膦的碱性和L的性质。对于1a和1b,只有pK(a)值大于5的膦才可以在C5H5环上,而其他取代在C5H4O环上。对于化合物2和3,两个环失活,因此只有最碱性的膦反应,它们仅攻击C5H4O环。在2和3反应的某些情况下,观察到一种中间体,其中单齿配体已迁移至C5H5环,而进入的亲核试剂与金属中心协调。已建立了膦类攻击配位的C5H4O环的机理,并获得了详细的动力学参数。对于1a与PPh(3),PPh(2)Me和P(p-PhOMe)(3)在丙酮中的反应,动力学给出了速率定律,表明可逆地形成中间体,该中间体不可逆地变成1, 2-二取代的钌茂金属产品。对于这些反应中的每一个都获得了所有三个速率常数及其热活化参数。对于P(p-PhOMe)(3)反应,还确定了每个步骤的激活量。 2和3与CD3CN中的PBu(3)(n),PCy(3),PPhMe(2)和PMe(3)反应可得到长寿命的中间体,该中间体也可用于1,2-二取代的钌茂金属产品。对于由3形成的中间体,已经研究了这一最后步骤的动力学,以确定速率常数及其热活化参数。在PBu(3)(n)的情况下,已分离出由3形成的中间体并确定了X射线结构,从而确定在C5H4O环上发生了膦攻击。 [参考:21]

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