首页> 外文期刊>Journal of Organometallic Chemistry >Some reactions of the platinum(II) carbene complex cis-dichloro(dimethylaminomethylene)(triphenylphosphine)platinum(II) and the X-ray crystal and molecular structures of the products trans-(CH2,P)-chloro(chloromethyl)(dimethylaminomethylene)(tripheny
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Some reactions of the platinum(II) carbene complex cis-dichloro(dimethylaminomethylene)(triphenylphosphine)platinum(II) and the X-ray crystal and molecular structures of the products trans-(CH2,P)-chloro(chloromethyl)(dimethylaminomethylene)(tripheny

机译:铂(II)卡宾配合物顺-二氯(二甲基氨基亚甲基)(三苯基膦)铂(II)的一些反应以及产物反式-(CH2,P)-氯(氯甲基)(二甲基氨基亚甲基)的X射线晶体和分子结构(三折线

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The reaction of the title complex 1 with excess diazomethane results in the exclusive insertion of a methylene group into the Pt-Cl bond trans to the phosphine ligand, to give the chloromethyl complex 6. The reactions of 1 with the diphosphines, Ph2P(CH2)nPPh(2)(n = 2, dppe, n = 3, dppp), and with the organometallic reagents Ph4Sn, Ph2Hg, or PhSnMe3, can also all be interpreted as proceeding via initial displacement of the chlorine trans to PPh3. The chelating phosphine ligands give equilibrium mixtures of the products [(LL)Pt(CHNMe2)(PPh3)](2 +)2Cl(-) and [(LL)Pt(CHNMe2)Cl]Cl+- (LL = dppe, dppp), and treatment of the mixture [(LL)= dppe] with excess aqueous KPF6 gave [(dppe)Pt(CHNMe2)PPh3)](2+) 2PF(6)(-) (9b). The insertion product (Ph3P)Pt(CHPhNMe2)Cl (11) was isolated from the reaction of 1 with PhSnMe3. This complex undergoes further reaction upon standing in CDCl3 solution, giving various products including benzaldehyde, N,N-dimethylbenzylamine, cis- and trans(Ph3P)Pt(NHMe2)Cl-2, and the new carbene complex cis-(Ph3P)Pt[C(Ph)NMe2]Cl-2 (17). Mechanisms are suggested for the formation of these products. The structures of chloromethyl complex 6 and hexafluorophosphate salt 9b have been determined by X-ray crystallography. (C) 2001 Published by Elsevier Science B.V. [References: 24]
机译:标题配合物1与过量的重氮甲烷的反应导致亚甲基仅插入反式连接至膦配体的Pt-Cl键中,得到氯甲基配合物6。1与二膦Ph2P(CH2)的反应nPPh(2)(n = 2,dppe,n = 3,dppp),并且与有机金属试剂Ph4Sn,Ph2Hg或PhSnMe3一起,也可以全部解释为通过将氯转化为PPh3进行初始取代而进行。螯合膦配体给出了产物[(LL)Pt(CHNMe2)(PPh3)](2 +)2Cl(-)和[(LL)Pt(CHNMe2)Cl] Cl +-(LL = dppe,dppp)的平衡混合物,并用过量的KPF6水溶液处理[(LL)= dppe]混合物,得到[(dppe)Pt(CHNMe2)PPh3)](2+)2PF(6)(-)(9b)。从1与PhSnMe3的反应中分离出插入产物(Ph3P)Pt(CHPhNMe2)Cl(11)。该配合物在CDCl3溶液中放置后会进一步反应,得到各种产物,包括苯甲醛,N,N-二甲基苄胺,顺式和反式(Ph3P)Pt(NHMe2)Cl-2,以及新的卡宾配合物顺式((Ph3P)Pt [ C(Ph)NMe 2] Cl-2(17)。建议了形成这些产物的机制。氯甲基配合物6和六氟磷酸盐9b的结构已经通过X射线晶体学确定。 (C)2001年由Elsevier Science B.V.出版[参考文献:24]

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