Synthesis and catalytic activity of ruthenium(II) complexes containing pyridine-based tridentate triamines ('NNN') and pyridine carboxylate ligands (NO)

被引:30
|
作者
Dayan, Osman [1 ]
Ozdemir, Namik [2 ]
Serbetci, Zafer [3 ]
Dincer, Muharrem [2 ]
Cetinkaya, Bekir [4 ]
Buyukgungor, Orhan [2 ]
机构
[1] Canakkale Onsekiz Mart Univ, Lab Inorgan Synth & Mol Catalysis, TR-17020 Canakkale, Turkey
[2] Ondokuz Mayis Univ, Fac Sci & Art, Dept Phys, TR-55139 Samsun, Turkey
[3] Bingol Univ, Fac Sci & Art, Dept Chem, TR-12000 Bingol, Turkey
[4] Ege Univ, Dept Chem, TR-35100 Izmir, Turkey
关键词
Bidentate NO- donors; Tridentate triamine ligands; Ruthenium complexes; Transfer hydrogenation; ASYMMETRIC TRANSFER HYDROGENATION; TRANSITION-METAL-COMPLEXES; EFFECTIVE CORE POTENTIALS; CRYSTAL-STRUCTURE; MOLECULAR CALCULATIONS; CHIRAL RUTHENIUM; KETONES; CLEAVAGE; CONFIGURATION; DIASTEREOMERS;
D O I
10.1016/j.ica.2012.02.034
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The reaction of [(p-cymene)RuCl2](2) with K[NOa-b] (NO- = 2-picolinate, a or 2-quinaldinate, b) gave neutral [(p-cymene)RuCl(NOa-b)] (1a-b), complexes which were treated with pyridine-based meridional triamine ligands ('NNN') to create complexes of the type [RuCl(NOa-b)('NNN')] (2a: 'N = N-d, NOa(-) = 2-picolinato; 2b: 'N = N-d, NOb- = 2-quinaldinato; 3a: 'N = N-b, NOa- = 2-picolinato; 3b: 'N = N-b, NOb- = 2-quinaldinato; 4a: 'N = N-p, NOa- = 2-picolinato; 4b: 'N = N-p, NOb- = 2-quinaldinato). The new compounds were characterized by elemental analysis, IR and NMR spectroscopy and, 1b was studied by single crystal X-ray diffraction. The complexes 1-4 have been employed as catalysts for the transfer hydrogenation (TH) of acetophenone derivatives to secondary alcohols in the presence of KOH using 2-propanol as a hydrogen source at 82 degrees C. The highest catalytic activity was obtained with 3a. (C) 2012 Elsevier B. V. All rights reserved.
引用
收藏
页码:246 / 253
页数:8
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