Diastereomeric half-sandwich Ru(II) cationic complexes containing amino amide ligands. Synthesis, solution properties, crystal structure and catalytic activity in transfer hydrogenation of acetophenone

被引:26
作者
Bacchi, Alessia [1 ]
Pelagatti, Paolo [1 ]
Pelizzi, Corrado [1 ]
Rogolino, Dominga [1 ]
机构
[1] Univ Parma, Dipartimento Chim Gen & Inorgan, I-43100 Parma, Italy
关键词
Ruthenium; Amino amides; Chiral complexes; Configurational stability; Transfer hydrogenation; ESI; ASYMMETRIC TRANSFER-HYDROGENATION; BIOLOGICALLY IMPORTANT LIGANDS; RUTHENIUM(II) ARENE COMPLEXES; TRANSITION-METAL-COMPLEXES; BIFUNCTIONAL CATALYSIS; TRANSFER REDUCTION; AROMATIC KETONES; ALDOL REACTION; L-PROLINAMIDE; IRIDIUM(III);
D O I
10.1016/j.jorganchem.2009.05.010
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The cationic complexes [(eta(6)-arene) Ru(N,O-amino amide) X]Y (arene = p-cymene or indane; N, O-amino amide = (L)-proline amide or (L)-phenylalanine amide; X = Cl or I; Y = Cl, I or PF6) have been synthesised and fully characterized by spectroscopic and analytical methods. In several cases (1a, 3a, 4a, 4b, 5) the metal configuration has been definitively established by X-ray analysis on single crystal. The lability of the metal center in solution has been studied by H-1 NMR and CD techniques. The highest configurational stability has been found in the complexes of the type [(eta(6)-indane)Ru(N,O-proline amide)Cl]Y (4a, b). The complexes 1b, 2a-b, 3b, 4b and 5 are good precatalysts for the transfer hydrogenation of acetophenone in basic i-PrOH, with ee up to 76% at 30 degrees C. An ESI(+)-MS study of pre-catalytic solutions has provided useful information on the catalytic mechanism. (C) 2009 Elsevier B. V. All rights reserved.
引用
收藏
页码:3200 / 3211
页数:12
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