Spin Trapping of Au-H Intermediate in the Alcohol Oxidation by Supported and Unsupported Gold Catalysts

被引:225
作者
Conte, Marco [1 ]
Miyamura, Hiroyuki [2 ]
Kobayashi, Shu [2 ]
Chechik, Victor [1 ]
机构
[1] Univ York, Dept Chem, York YO10 5DD, N Yorkshire, England
[2] Univ Tokyo, Grad Sch Pharmaceut Sci, Bunkyo Ku, Tokyo 1130033, Japan
基金
英国工程与自然科学研究理事会;
关键词
POLYMER-INCARCERATED PALLADIUM; SELECTIVE AEROBIC OXIDATION; LIQUID-PHASE OXIDATION; RUTHENIUM CATALYSTS; ACTIVE CATALYST; FREE-RADICALS; HYDROGENATION; ALDEHYDES; PLATINUM; NANOPARTICLES;
D O I
10.1021/ja809883c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Electron paramagnetic resonance (EPR) spectroscopy and spin trapping were used to explore the mechanism of alcohol oxidation over gold catalysts. Reaction of secondary alcohols with supported and unsupported gold catalysts (e.g., Au/CeO2, polymer-incarcerated Au nanoparticles, PPh3-protected Au nanoparticles) in the presence of spin traps led to the formation of a hydrogen spin adduct. Using isotope labeling, we confirmed that the hydrogen in the spin adduct originates from the cleavage of the C-H bond in the alcohol molecule. The formation of the hydrogen spin adduct most likely results from the abstracting of hydrogen from the Au surface by a spin trap. These results thus strongly suggest intermediate formation Au-H species during alcohol. This was further confirmed by carrying out gold-catalyzed alcohol oxidation in the absence of oxygen, with nitroxides as hydrogen abstractors. The support (e.g., metal oxides) can activate oxygen and act as an H abstractor from the gold surface and hence lead to a faster recovery of the activity. Peroxyl radicals were also observed during alcohol oxidation, consistent with a free-radical autoxidation mechanism. However, this mechanism is likely to be a minor side reaction, which does not lead to the formation of an appreciable amount of oxidation products.
引用
收藏
页码:7189 / 7196
页数:8
相关论文
共 84 条
[11]  
2-A
[12]   APPLICATIONS OF EPR TO A STUDY OF THE HYDROGENATION OF ETHENE AND BENZENE OVER A SUPPORTED PD CATALYST - DETECTION OF FREE-RADICALS ON A CATALYST SURFACE [J].
CARLEY, AF ;
EDWARDS, HA ;
MILE, B ;
ROBERTS, MW ;
ROWLANDS, CC ;
HANCOCK, FE ;
JACKSON, SD .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1994, 90 (21) :3341-3346
[13]   Thermal stability of 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) and related N-alkoxyamines [J].
Ciriano, MV ;
Korth, HG ;
van Scheppingen, WB ;
Mulder, P .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (27) :6375-6381
[14]   Supported gold nanoparticles from quantum dot to mesoscopic size scale:: Effect of electronic and structural properties on catalytic hydrogenation of conjugated functional groups [J].
Claus, P ;
Brückner, A ;
Mohr, C ;
Hofmeister, H .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (46) :11430-11439
[15]   Heterogeneously catalysed hydrogenation using gold catalysts [J].
Claus, P .
APPLIED CATALYSIS A-GENERAL, 2005, 291 (1-2) :222-229
[16]   Reactions of the ''stable'' nitroxide radical TEMPO. Relevance to ''living'' free radical polymerizations and autopolymerization of styrene [J].
Connolly, TJ ;
Scaiano, JC .
TETRAHEDRON LETTERS, 1997, 38 (07) :1133-1136
[17]   Gold supported on a mesoporous CeO2 matrix as an efficient catalyst in the selective aerobic oxidation of aldehydes in the liquid phase [J].
Corma, A ;
Domine, ME .
CHEMICAL COMMUNICATIONS, 2005, (32) :4042-4044
[18]   Supported gold nanoparticles as catalysts for organic reactions [J].
Corma, Avelino ;
Garcia, Hermenegildo .
CHEMICAL SOCIETY REVIEWS, 2008, 37 (09) :2096-2126
[19]   Gold catalysts open a new general chemoselective route to synthesize oximes by hydrogenation of α,β-unsaturated nitrocompounds with H2 [J].
Corma, Avelino ;
Serna, Pedro ;
Garcia, Hermenegildo .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2007, 129 (20) :6358-+
[20]   Chemoselective hydrogenation of nitro compounds with supported gold catalysts [J].
Corma, Avelino ;
Serna, Pedro .
SCIENCE, 2006, 313 (5785) :332-334