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Coupling of allenes with mu-alkylidyne ligands in diiron complexes: Synthesis of novel bridging thio- and aminobutadienylidene complexes

机译:亚铁与mu-亚烷基配体在二价铁配合物中的偶联:新型桥联硫代和氨基丁二烯基亚配合物的合成

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摘要

The diiron aminocarbyne complexes [Fe-2{mu-CN(Me)(R)}(mu-CO)(CO)(2)(Cp)(2)](SO3CF3] (R = Xyl, 1a; R = 4-C6H4OMe, 1b; R = Me, 1c; Xyl = 2,6-Me2C6H3) react with allenes of the type CH2=C=CR'R '', in the presence of Me3NO/Et3N, to give the novel butadienylidene complexes [Fe-2{mu-eta(1):eta(3)-C alpha N(R)(Me)-C-beta(H)C gamma C delta(R')(R '')}(mu-CO)(CO)(Cp)(2)] (R = Xyl, R' = R '' = Me, 3a; R = Xyl, R' = Me, R '' = H, 3b; R = Xyl, R' = CO2Et, R '' = H, 3c; R = 4-C6H4OMe, R' = CO2Et, R '' = H, 3d; R = R' = R '' = Me, 3e; R = Me, R' = CO2Et, R '' = H, 3f) in high yields. Analogously, the diiron thiocarbyne complex [Fe-2([mu-CSMe)-(mu-CO)(CO)(2)(Cp)(2)][SO3CF3] (2) reacts with CH2=C=CR'R '', in the presence of Me3NO/Et3N, to afford the compounds [Fe-2{mu-eta(1):eta(3)-C alpha S(Me)C-beta(H)C gamma C delta(R')(R '')}(mu-CO)(CO)(Cp)(2)] (R' = R '' = Me, 4a; R' = CO2Et, R '' = H, 4b; R' = SiMe3, R '' = Me, 4c). Complexes 3-4 exist in solution as mixtures of cis and trans isomers. Compounds 3a and 3e, upon treatment with HSO3CF3, are transformed into the corresponding vinyliminium complexes [Fe-2{mu-eta(1):eta(3)-C-gamma(C delta HMe2)C beta HC alpha N(R)-(Me)}(mu-CO)(CO)(CP)(2)][SO3CF3] (R = Xyl, 5a; R = Me, 5b), in nearly quantitative yields. Conversely, compounds 4a,b undergo methylation (by CH3SO3CF3) at the sulfur to give the cationic complexes [Fe-2{mu-eta(1):eta(3)-C-alpha(SMe2)C-beta(H)C(gamma)C(delta)5(R')(R '')}(mu-CO)(CO)(Cp)(2)][SO3CF3] (R' = R '' = Me, 7a; R' = CO2Et, R '' = H, 7b). Protonation of 3a is not reversible: treating 5a with sodium hydride results in the formation of the 1-metalla-2-amino-cyclopenta-1, 3-dien-5-one species [Fe(Cp)(CO){CN(Me)(Xyl)CHC(CHMe2)C(O)}] (6). The molecular structures of cis-3a, cis-4b, 5a[CF3SO3]center dot CH2Cl2 and 7a[CF3SO3]center dot 0.5CH(2)Cl(2) have been determined by X-ray diffraction studies. (C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008).
机译:二铁氨基卡宾络合物[Fe-2 {mu-CN(Me)(R)}(mu-CO)(CO)(2)(Cp)(2)](SO3CF3](R = Xyl,1a; R = 4 -C6H4OMe,1b; R = Me,1c; Xyl = 2,6-Me2C6H3)在Me3NO / Et3N的存在下与CH2 = C = CR'R''型的异戊烯反应,得到新的丁二烯亚基[ Fe-2 {mu-eta(1):eta(3)-C alpha N(R)(Me)-C-beta(H)CγC delta(R')(R'')}(mu-CO )(CO)(Cp)(2)](R = Xyl,R'= R''= Me,3a; R = Xyl,R'= Me,R''= H,3b; R = Xyl,R' = CO2Et,R''= H,3c; R = 4-C6H4OMe,R'= CO2Et,R''= H,3d; R = R'= R''= Me,3e; R = Me,R'= CO2Et,R''= H,3f)。类似,二铁硫代碳炔络合物[Fe-2([mu-CSMe)-(mu-CO)(CO)(2)(Cp)(2)] [ SO3CF3](2)在Me3NO / Et3N存在下与CH2 = C = CR'R''反应,得到化合物[Fe-2 {mu-eta(1):eta(3)-CαS( Me)C-beta(H)CγC delta(R')(R'')}(mu-CO)(CO)(Cp)(2)](R'= R''= Me,4a; R '= CO2Et,R''= H,4b; R'= SiMe3,R''= Me,4c)。配合物3-4以顺式和反式异构体的混合物形式存在于溶液中。化合物3经HSO3CF3处理后,a和3e转化为相应的乙烯基亚胺络合物[Fe-2 {mu-eta(1):eta(3)-C-γ(C delta HMe2)C beta HC alpha N(R- (Me)}(mu-CO)(CO)(CP)(2)] [SO3CF3](R = Xyl,5a; R = Me,5b),几乎是定量的产量。相反,化合物4a,b在硫上进行甲基化(通过CH3SO3CF3),得到阳离子络合物[Fe-2 {mu-eta(1):eta(3)-C-alpha(SMe2)C-beta(H)C γCδ5(R')(R)}}(mu-CO)(CO)(Cp)(2)] [SO3CF3](R'= R''= Me,7a; R' = CO2Et,R''= H,7b)。 3a的质子化不可逆:用氢化钠处理5a会导致形成1-metalla-2-amino-cyclopenta-1,3-dien-5-one物种[Fe(Cp)(CO){CN(Me )(Xyl)CHC(CHMe 2)C(O)}](6)。通过X射线衍射研究确定了顺式3a,顺式4b,5a [CF3SO3]中心点CH2Cl2和7a [CF3SO3]中心点0.5CH(2)Cl(2)的分子结构。 (C)Wiley-VCH Verlag GmbH&Co.KGaA,69451 Weinheim,德国,2008)。

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