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首页> 外文期刊>Journal of Organometallic Chemistry >Synthesis, molecular structures, Mossbauer and electrochemical investigation of ferrocenyltelluride derivatives: (Fc(2)Te(2))Fe(CO)(3)I-2 [(CO)(3)IFe(mu-TeFc)](2), CpFe(CO)(2)TeFc, CpFe(CO)(2)TeX(2)Fc (X = Br, I) and CpFe(CO)(2)(mu-TeFc)Fe(CO)(3)I-2
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Synthesis, molecular structures, Mossbauer and electrochemical investigation of ferrocenyltelluride derivatives: (Fc(2)Te(2))Fe(CO)(3)I-2 [(CO)(3)IFe(mu-TeFc)](2), CpFe(CO)(2)TeFc, CpFe(CO)(2)TeX(2)Fc (X = Br, I) and CpFe(CO)(2)(mu-TeFc)Fe(CO)(3)I-2

机译:二茂铁基碲化物衍生物的合成,分子结构,Mossbauer和电化学研究:(Fc(2)Te(2))Fe(CO)(3)I-2 [(CO)(3)IFe(mu-TeFc)](2) ,CpFe(CO)(2)TeFc,CpFe(CO)(2)TeX(2)Fc(X = Br,I)和CpFe(CO)(2)(mu-TeFc)Fe(CO)(3)I -2

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摘要

Depending on the ratio of the starting reagents, the interaction of [FcTeI] with Fe(CO)(5) gave complex (Fc(2)Te(2))Fe(CO)(3)I-2 (1) bearing an Fc(2)Te(2) ligand, or a dimeric complex [(CO)(3)IFe(mu-TeFc)](2) (2). An interaction of equimolar amounts of [CpFe(CO)(2)](2) and Fc(2)Te(2) under the thermal conditions in toluene afforded CpFe(CO)(2)TeFc (3). Complex 3 can be easily halogenated at the Te center by elemental bromine and iodine to give monomeric CpFe(CO)(2)TeX(2)Fc (X = Br (4), I (5)). Complex 5 can be prepared alternatively via formal insertion of [FcTeI] into Fc-I bond of CpFe(CO)(2)I. Complex 3 readily substitutes one carbonyl in Fe(CO)(4)I-2 to give the adduct CpFe(CO)(2)(mu-TeFc)Fe(CO)(3)I-2 (6). (C) 2014 Elsevier B.V. All rights reserved.
机译:取决于起始试剂的比例,[FcTeI]与Fe(CO)(5)的相互作用产生复合物(Fc(2)Te(2))Fe(CO)(3)I-2(1) Fc(2)Te(2)配体或二聚体复合物[(CO)(3)IFe(mu-TeFc)](2)(2)。在甲苯中的热条件下,等摩尔量的[CpFe(CO)(2)](2)和Fc(2)Te(2)的相互作用提供了CpFe(CO)(2)TeFc(3)。配合物3可以很容易地在Te中心被元素溴和碘卤化,得到单体CpFe(CO)(2)TeX(2)Fc(X = Br(4),I(5))。可以通过将[FcTeI]正式插入CpFe(CO)(2)I的Fc-1键中来制备复合物5。配合物3可以很容易地在Fe(CO)(4)I-2中取代一个羰基,得到加合物CpFe(CO)(2)(mu-TeFc)Fe(CO)(3)I-2(6)。 (C)2014 Elsevier B.V.保留所有权利。

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