C-N coupling between μ-aminocarbyne and nitrile ligands promoted by tolylacetylide addition to [Fe2{μ-CN(Me)(Xyl)}-(μ-CO)(CO)(NCCMe3)(CP)2][SO3CF3] -: Formation of a novel bridging η1:η2 allene-diaminocarbene ligand

被引:22
作者
Albano, VG
Bordoni, S
Busetto, L
Marchetti, F
Monari, M
Zanotti, V
机构
[1] Univ Bologna, Dipartimento Chim Fis & Inorgan, I-40136 Bologna, Italy
[2] Univ Bologna, Dipartimento Chim G Ciamician, I-40126 Bologna, Italy
关键词
nitrile; carbyne; carbene; allene; diiron complexes; crystal structures;
D O I
10.1016/S0022-328X(03)00501-1
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The reaction of the mu-aminocarbyne complex [Fe-2{mu-CN(Me)(Xyl)}(mu-CO)(CO)(NCCMe3)(CP)(2)][SO3CF3] (2) (Xyl = 2,6-Me2C6H3) with tolylacetylide, followed by treatment with HSO3CF3 affords the complex [Fe-2{mu-eta(1):eta(3)C(Tol)double bondCdouble bondC(CMe3)N(H)CN(Me)(Xyl)}(mu-CO)(CO)(Cp-2)][SO3CF3] (3) (Tol = 4-MeC6H4). The X-ray molecular structure of 3 reveals the peculiar character of the bridging ligand, which exhibits both eta(1):eta(2) allene and aminocarbene nature. The formation of 3 proceeds through several intermediate species, which have been detected by IR spectroscopy. Addition of HSO3CF3 at an early stage of the reaction between 2 and LiCdropCTol leads to the formation of the imine complex [Fe-2{mu-CN(Me)Xyl}(mu-CO)(CO){NHC(CdropCTol)CMe3}(Cp)(2)][SO3CF3] (6) indicating that the first step of the reaction consists in the acetylide addition at the coordinated NCCMe3. The molecular structure of 6 has been elucidated by an X-ray diffraction study. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:37 / 43
页数:7
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