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Preparation and structural characterization of chloro- and alkyl-isocyanidoniobocene compounds. Synthesis of the 1st dicyclopentadienylniobium species containing iminoacyl groups

机译:氯-和烷基-异氰基异戊二烯化合物的制备和结构表征。含亚氨基酰基的第一双二环戊二烯基铌物种的合成

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摘要

The reduction of the niobocene complexes Nb(η5-C5H3RR′)2Cl2 (R = H, R′ = SiMe3 (I); R = R′ = SiMe3 (II)) with one equivalent of (1%) sodium amalgam in the presence of an isocyanide ligand R″NC yields Nb(η5-5H3RR′)2Cl(CNR″) (R = H, R′ = SiMe3, R″ = Cy = cyclohexyl (III); tBu (IV); Ph (V); 2,6-Me2C6H3 (VI), and R = R′ = SiMe3, R″ = Cy (VII), tBu (VIII)). Reactions of III and V with LiMe and LiCH2SiMe3 give the thermally stable iminoacyl compounds [Nb(η5-C5H4SiMe3)2-(CRNR′)]n(R = Me, R′ = Cy (IX); R = CH2SiMe3, R′ = Cy (X) and R = Me, R′ = Ph (XII)), through spontaneous insertion of the isocyanide ligand into the alkyl-niobium bond. Insertion of t-BuNC into the metal-alkyl bond in IV was not observed, and only the alkyl isocyanide derivative Nb(η5-C5H4SiMe3)2(Me)(CNtBu) (XI) was isolated. The compounds were characterized by IR and NMR spectroscopy.
机译:在存在下用一当量(1%)的钠汞齐还原铌茂金属配合物Nb(η5-C5H3RR')2Cl2(R = H,R'= SiMe3(I); R = R'= SiMe3(II))异氰酸酯配体R” NC的产率为Nb(η5-5H3RR')2Cl(CNR”)(R = H,R'= SiMe3,R''= Cy =环己基(III); tBu(IV); Ph(V); 2,6-Me2C6H3(VI),并且R = R'= SiMe3,R''= Cy(VII),tBu(VIII))。 III和V与LiMe和LiCH2SiMe3的反应得到热稳定的亚氨基酰基化合物[Nb(η5-C5H4SiMe3)2-(CRNR')] n(R = Me,R'= Cy(IX); R = CH2SiMe3,R'= Cy(X)和R = Me,R'= Ph(XII)),是通过将异氰酸酯配体自发插入烷基-铌键来实现的。未观察到将t-BuNC插入IV的金属-烷基键中,仅分离了烷基异氰化物衍生物Nb(η5-C5H4SiMe3)2(Me)(CNtBu)(XI)。通过IR和NMR光谱对化合物进行表征。

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