Ruthenium(II) complexes derived from 2-phenylthiazoline-4-carboxylic acid: structure and catalytic activity for transfer hydrogenation reaction

被引:8
作者
Denizalti, Serpil [1 ]
Sen, Betul [2 ]
Gokce, Aytac Gurhan [2 ]
Cetinkaya, Bekir [1 ]
机构
[1] Ege Univ, Dept Chem, TR-35100 Bornova, Turkey
[2] Dokuz Eylul Univ, Dept Phys, TR-35160 Buca Izmir, Turkey
关键词
ruthenium complex; thiazoline; transfer hydrogenation; ASYMMETRIC TRANSFER HYDROGENATION; CARBOXYLATE LIGANDS; NITROSYL COMPLEXES; COORDINATION MODE; DIPICOLINIC ACID; REDOX PROPERTIES; AMINO-ACID; KETONES; SUBSTITUTION; ANALOGS;
D O I
10.1002/aoc.3442
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Piano-stool ([(p-cymene)Ru(thz)Cl], 2) and six-coordinated ([Ru(thz)(2)(PPh3)(2)], 3) ruthenium complexes derived from 2-phenylthiazoline-4-carboxylic acid (Hthz, 1) were synthesized for the first time, and fully characterized using conventional methods. Also, the molecular structure of complex 3 was determined using X-ray analysis. These complexes were evaluated as catalysts for transfer hydrogenation of carbonyl compounds in the presence of isopropyl alcohol and (KOBu)-Bu-t. Complex 2 was found to be more active than 3 in transfer hydrogenation. Copyright (c) 2016 John Wiley & Sons, Ltd.
引用
收藏
页码:373 / 377
页数:5
相关论文
共 75 条
  • [1] Ruthenium-Catalyzed Synthesis of Functionalized 1,3-Dienes
    Achard, Mathieu
    Derrien, Nolwenn
    Zhang, Hui-Jun
    Demerseman, Bernard
    Bruneau, Christian
    [J]. ORGANIC LETTERS, 2009, 11 (01) : 185 - 188
  • [2] Nickel Nanoparticles in Hydrogen Transfer Reactions
    Alonso, Francisco
    Riente, Paola
    Yus, Miguel
    [J]. ACCOUNTS OF CHEMICAL RESEARCH, 2011, 44 (05) : 379 - 391
  • [3] [Anonymous], 2011, CRYSALIS PRO SOFTW V
  • [4] Insertion reactions of [M(SR)3(PMe2Ph)2]withCS2 (M= Ru, Os; R = C6F4H-4, C6F5.: X-ray structures of [Ru(S2CSC6F4H-4)2(PMe2Ph)2], trans-thiolates [M(SR)2(S2CSR)(PMe2Ph)2] (M= Ru; R = C6F5 and M= Os; R = C6F4H-4), and trans-thiolate-phosphine [OS(SC6F5)2(S2CSC6F5)(PMe2Ph)2]
    Arroyo, M
    Bernès, S
    Cerón, J
    Rius, J
    Torrens, H
    [J]. INORGANIC CHEMISTRY, 2004, 43 (03) : 986 - 992
  • [5] Unusual coordination mode of thiosemicarbazone ligand. Synthesis, structure, and redox properties of some ruthenium and osmium complexes
    Basuli, F
    Ruf, M
    Pierpont, CG
    Bhattacharya, S
    [J]. INORGANIC CHEMISTRY, 1998, 37 (23) : 6113 - 6116
  • [6] Steric control of the coordination mode of the salicylaldehyde thiosemicarbazone ligand. Syntheses, structures, and redox properties of ruthenium and osmium complexes
    Basuli, F
    Peng, SM
    Bhattacharya, S
    [J]. INORGANIC CHEMISTRY, 1997, 36 (24) : 5645 - 5647
  • [7] EVALUATION OF DESFERRITHIOCIN AND ITS SYNTHETIC ANALOGS AS ORALLY EFFECTIVE IRON CHELATORS
    BERGERON, RJ
    WIEGAND, J
    DIONIS, JB
    EGLIKARMAKKA, M
    FREI, J
    HUXLEYTENCER, A
    PETER, HH
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1991, 34 (07) : 2072 - 2078
  • [8] Synthesis, molecular structure and evaluation of new organometallic ruthenium anticancer agents
    Camm, Kenneth D.
    El-Sokkary, Ahmed
    Gott, Andrew L.
    Stockley, Peter G.
    Belyaeva, Tamara
    McGowan, Patrick C.
    [J]. DALTON TRANSACTIONS, 2009, (48) : 10914 - 10925
  • [9] Carmona D, 1999, CHEM-EUR J, V5, P1544, DOI 10.1002/(SICI)1521-3765(19990503)5:5<1544::AID-CHEM1544>3.0.CO
  • [10] 2-T