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
相关论文
共 51 条
[1]   Selective C-C bond formation at diiron μ-aminocarbyne complexes [J].
Albano, VG ;
Busetto, L ;
Camiletti, C ;
Castellari, A ;
Monari, M ;
Zanotti, V .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1997, (24) :4671-4676
[2]   Diiron μ-vinyliminium complexes from acetylene insertion into a metal-aminocarbyne bond [J].
Albano, VG ;
Busetto, L ;
Marchetti, F ;
Monari, M ;
Zacchini, S ;
Zanotti, V .
ORGANOMETALLICS, 2003, 22 (06) :1326-1331
[3]   Acetonitrile activation in di-iron μ-carbyne complexes:: synthesis and structure of the cyanomethyl complex [Fe2(μ-CNMe2)(μ-CO)(CO)(CH2CN)(CP)2] [J].
Albano, VG ;
Busetto, L ;
Marchetti, F ;
Monari, M ;
Zanotti, V .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 2002, 649 (1-2) :64-69
[4]   Carbon-carbon bond formation in the reactions of diiron μ-carbyne complexes with 2-thienyllithium, synthesis and structural characterization [J].
Albano, VG ;
Bordoni, S ;
Busetto, L ;
Camiletti, C ;
Monari, M ;
Palazzi, A ;
Prestopino, F ;
Zanotti, V .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1997, (24) :4665-4670
[5]   DINUCLEAR CYANOALKYLIDENE COMPLEXES OF IRON [J].
ALBANO, VG ;
BORDONI, S ;
BRAGA, D ;
BUSETTO, L ;
PALAZZI, A ;
ZANOTTI, V .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 1991, 30 (07) :847-849
[6]   Reactions of acetonitrile di-iron μ-aminocarbyne complexes;: synthesis and structure of [Fe2(μ-CNMe2)(μ-H)(CO)2(Cp)2] [J].
Albano, VG ;
Busetto, L ;
Monari, M ;
Zanotti, V .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 2000, 606 (02) :163-168
[7]   SIR97:: a new tool for crystal structure determination and refinement [J].
Altomare, A ;
Burla, MC ;
Camalli, M ;
Cascarano, GL ;
Giacovazzo, C ;
Guagliardi, A ;
Moliterni, AGG ;
Polidori, G ;
Spagna, R .
JOURNAL OF APPLIED CRYSTALLOGRAPHY, 1999, 32 :115-119
[8]  
[Anonymous], 1998, SMART SAINT SOFTWARE
[9]   Guanidines as neutral monodentate ligands; syntheses and crystal structures of [Co{PhN=C(NHPh)(2)}(2)Cl-2] and [Ag{PhN=C(NHPh)(2)}][SO3CF3] [J].
Bailey, PJ ;
Grant, KJ ;
Pace, S ;
Parsons, S ;
Stewart, LJ .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1997, (22) :4263-4266
[10]   Fischer carbene complexes. A new tool for heterocyclic synthesis [J].
Barluenga, J .
PURE AND APPLIED CHEMISTRY, 2002, 74 (08) :1317-1325