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首页> 外文期刊>Journal of Organometallic Chemistry >Chemical behaviour of alkyl imido cyclopentadienyl niobium and tantalum(V) complexes in insertion processes. X-ray crystal structures of [MCpCl(NAr){eta(2)-C(Me)=NAr}] (Ar=2,6-Me2C6H3; M = Nb, Cp=eta(5)-C5H4SiMe3; M = Ta, Cp = eta(5)-C5Me5) and [Ta(e
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Chemical behaviour of alkyl imido cyclopentadienyl niobium and tantalum(V) complexes in insertion processes. X-ray crystal structures of [MCpCl(NAr){eta(2)-C(Me)=NAr}] (Ar=2,6-Me2C6H3; M = Nb, Cp=eta(5)-C5H4SiMe3; M = Ta, Cp = eta(5)-C5Me5) and [Ta(e

机译:烷基亚氨基环戊二烯基铌和钽(V)配合物在插入过程中的化学行为。 [MCpCl(NAr){eta(2)-C(Me)= NAr}]的X射线晶体结构(Ar = 2,6-Me2C6H3; M = Nb,Cp = eta(5)-C5H4SiMe3; M = Ta ,Cp = eta(5)-C5Me5)和[Ta(e

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摘要

Pure imido eta(2)-iminoacyl derivatives [MCpX(NAr) {eta(2)-C(R)=NAr}] (Ar = 2,6-Me2C6H3; M = Nb, Cp = eta(5)-C5H4SiMe3 = Cp', X = Cl, R = Me, 1; X = Me, R = NMe2, 2; Me, 3; X = R = CH2SiMe3, 4; CH2CMe3, 5; CH2Ph, 6; M = Ta, Cp = eta(5)-C5Me5 = Cp*, X = Cl, R = Me, 7; CH2SiMe3, 8; CH2CMe2Ph, 9; CH2CMe3, 10; CH2C6H5, 11; 2-(CH2NMe2)C6H4, 12; NMe2, 13; X = R = CH2SiMe3, 14; CH2CMe2Ph, 15; CH2CMe3, 16; CH2C6H5, 17; C6H5, 18) can be prepared by reaction of chloro alkyl or dialkyl imido complexes MCpXR(NAr) with 1 equivalent of 2,6-Me2C6H3NC. Reaction of alkyl methyl imido complexes TaCp*RMe(NAr) with 1 equivalent of isocyanide 2,6-Me2C6H3NC takes place with migration of alkyl or methyl group, leading to the formation of a mixture of methyl eta(2)-alkyliminoacyl [TaCp*Me(NAr){eta(2)-C(R)=NAr}] (Ar = 2,6-Me2C6H3; R = CH2SiMe3, 19; CH2Ph, 21; CH2CMe2Ph, 23; CH2CMe3, 25; C6H5, 27; 2-(CH2NMe2)C6H4, 29; NMe2, 30) and alkyl eta(2)-methyliminoacyl [TaCp*R(NAr){eta(2)-C(Me)=NAr}] (Ar = 2,6-Me2C6H3; R = CH2SiMe3, 20; CH2Ph, 22; CH2CMe2Ph, 24; CH2CMe3, 26; C6H5, 28) complexes. Alkyl imido derivatives also react with CO to give alkyl eta(2)-acyl [TaCp*X(NAr){eta(2)-C(R)=O}] (Ar = 2,6-Me2C6H3; X = R = CH2SiMe3, 31; CH2CMe2Ph, 32; CH2CMe3, 33; CH2Ph, 34), chloro eta(2)-acyl (X = Cl, R = CH2CMe2Ph, 35; NMe2, 36) and methyl eta(2)-acyl (X = Me, R = CH2CMe2Ph, 37; CH2CMe3, 38) complexes. Dinuclear ene diolate complexes [{TaCp*X(NAr)}(2){mu-eta(2)-OC(R)=C(R)O}] (Ar = 2,6-Me2C6H3; X = Cl, R = CH2CMe3, 39; X = Me, R = 2-(CH2NMe2)C6H4, 40) are formed by reaction of the chloro and methyl alkyl imido derivatives with carbon monoxide, whereas using [TaCp*XR(NAr)] (Ar = 2,6-Me2C6H3; X = Cl, R = CH2CMe3,; X = R = Ph) a different sequence of reactions takes place leading finally to oxo eta(2)-iminoacyl complexes [TaCp*X(O){eta(2)-C(R)=NAr}] (X = Cl, R=CH2CMe3, 41; X = R = Ph, 42). All compounds were characterised by NMR (H-1,C-13) spectroscopy and IR measurements. The molecular structures of 1, 7 and 37 were studied by X-ray diffraction methods and are discussed. (C) 2000 Published by Elsevier Science S.A. All rights reserved. [References: 93]
机译:纯亚胺基eta(2)-亚氨基酰基衍生物[MCpX(NAr){eta(2)-C(R)= NAr}](Ar = 2,6-Me2C6H3; M = Nb,Cp = eta(5)-C5H4SiMe3 = Cp',X = Cl,R = Me,1; X = Me,R = NMe2,2; Me,3; X = R = CH2SiMe3,4; CH2CMe3,5; CH2Ph,6; M = Ta,Cp = eta (5)-C5Me5 = Cp *,X = Cl,R = Me,7; CH2SiMe3,8; CH2CMe2Ph,9; CH2CMe3,10; CH2C6H5,11; 2-(CH2NMe2)C6H4,12; NMe2,13; X = R = CH2SiMe3,14; CH2CMe2Ph,15; CH2CMe3,16; CH2C6H5,17; C6H5,18)可以通过氯烷基或二烷基亚氨基配合物MCpXR(NAr)与1当量的2,6-Me2C6H3NC反应制备。烷基甲基亚氨基配合物TaCp * RMe(NAr)与1当量的异氰酸酯2,6-Me2C6H3NC的反应是随着烷基或甲基的迁移而发生的,导致形成甲基eta(2)-烷基亚氨基酰基[TaCp * Me(NAr){eta(2)-C(R)= NAr}]](Ar = 2,6-Me2C6H3; R = CH2SiMe3,19; CH2Ph,21; CH2CMe2Ph,23; CH2CMe3,25; C6H5,27; 2 -(CH2NMe2)C6H4,29; NMe2,30)和烷基eta(2)-甲基亚氨基酰基[TaCp * R(NAr){eta(2)-C(Me)= NAr}](Ar = 2,6-Me2C6H3; R = CH2SiMe3,20; CH2Ph,22; CH2CMe2Ph,24; CH2CMe3,26; C6H5,28)配合物。烷基亚氨基衍生物还与CO反应生成烷基eta(2)-酰基[TaCp * X(NAr){eta(2)-C(R)= O}](Ar = 2,6-Me2C6H3; X = R = CH2SiMe3,31; CH2CMe2Ph,32; CH2CMe3,33; CH2Ph,34),氯eta(2)-酰基(X = Cl,R = CH2CMe2Ph,35; NMe2,36)和甲基eta(2)-酰基(X = Me,R = CH 2 CMe 2 Ph,37; CH 2 CMe 3,38)络合物。双核烯二醇盐配合物[{TaCp * X(NAr)}(2){mu-eta(2)-OC(R)= C(R)O}](Ar = 2,6-Me2C6H3; X = Cl,R = CH2CMe3,39; X = Me,R = 2-(CH2NMe2)C6H4,40)是由氯和甲基烷基亚氨基衍生物与一氧化碳反应形成的,而使用[TaCp * XR(NAr)](Ar = 2 ,6-Me2C6H3; X = Cl,R = CH2CMe3 ,; X = R = Ph)不同的反应顺序发生,最终导致oxo eta(2)-亚氨基酰基复合物[TaCp * X(O){eta(2) -C(R)= NAr}](X = Cl,R = CH 2 CMe 3,41; X = R = Ph,42)。所有化合物均通过NMR(H-1,C-13)光谱和IR测量表征。用X射线衍射方法研究了1、7和37的分子结构并进行了讨论。 (C)2000,Elsevier Science S.A.保留所有权利。 [参考:93]

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