首页> 外文期刊>Organometallics >Nitrogen-nitrogen bond cleavage of hydrazine derivatives by a trinuclear pentahydride complex of ruthenium, (Cp ' Ru)(3)(mu-H)(3)(mu(3)-H)(2) (Cp ' = eta(5)-C5Me5)
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Nitrogen-nitrogen bond cleavage of hydrazine derivatives by a trinuclear pentahydride complex of ruthenium, (Cp ' Ru)(3)(mu-H)(3)(mu(3)-H)(2) (Cp ' = eta(5)-C5Me5)

机译:钌(Cp'Ru)(3)(mu-H)(3)(mu(3)-H)(2)的三核五氢化物络合物裂解肼衍生物的氮-氮键(Cp'= eta(5 )-C5Me5)

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摘要

The reaction of (Cp'Ru)(3)(mu-H)(3)(mu(3)-H)(2) (1) with a monosubstituted hydrazine such as methylhydrazine and phenylhydrazine results in the exclusive formation of the nonsymmetrically capped bis(mu(3)-imido) complex (Cp'Ru)(3)(mu(3)-NR)(mu(3)-NH)(mu-H) (2, R = Me; 3, R = Ph) as a result of cleavage of the nitrogen-nitrogen bond. In contrast to the reaction with monosubstituted hydrazine, the reaction of 1 with 1,2-diphenylhydrazine predominantly yields the monocapped imido complex (Cp'Ru)(3)(mu(3)-NPh)(mu-H)(3) (4), due to the steric hindrance between the Cp' groups surrounding the reaction site of 1 and the incoming bulky 1,2-diphenylhydrazine. Kinetic studies were carried out to elucidate the reaction mechanism and proved that the methylhydrazine molecule was captured by the Ru-3 site from the more nucleophilic -NHMe terminus rather than the less bulky -NH2 terminus. Molecular structures of 2-4 and (Cp'Ru)(3)(mu(3)-NH)(2)(mu-H) (6) have been determined by means of X-ray diffraction studies. [References: 52]
机译:(Cp'Ru)(3)(mu-H)(3)(mu(3)-H)(2)(1)与诸如甲基肼和苯肼的单取代肼的反应导致不对称的排他性形成封端的双(mu(3)-亚氨基)络合物(Cp'Ru)(3)(mu(3)-NR)(mu(3)-NH)(mu-H)(2,R = Me; 3,R =)是氮-氮键断裂的结果。与单取代肼的反应相反,1与1,2-二苯肼的反应主要产生单封端的亚氨基配合物(Cp'Ru)(3)(mu(3)-NPh)(mu-H)(3)( 4),由于围绕1的反应位点的Cp'基团与进入的庞大的1,2-二苯肼之间存在空间位阻。进行了动力学研究以阐明反应机理,并证明了甲基肼分子被Ru-3位点从亲核性更大的-NHMe末端而不是体积较小的-NH2末端捕获。已经通过X射线衍射研究确定了2-4和(Cp'Ru)(3)(mu(3)-NH)(2)(mu-H)(6)的分子结构。 [参考:52]

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