High-Pressure In Situ NMR Methods for the Study of Reaction Kinetics in Homogeneous Catalysis

被引:18
|
作者
Torres, Alexandre [1 ]
Perez, Nieves Molina [1 ]
Overend, Gillian [1 ]
Hodge, Nicholas [1 ]
Heaton, Brian T. [1 ]
Iggo, Jonathan A. [1 ]
Satherley, John [1 ]
Whyman, Robin [1 ]
Eastham, Graham R. [2 ]
Gobby, Darren [2 ]
机构
[1] Univ Liverpool, Dept Chem, Liverpool L69 7ZD, Merseyside, England
[2] Lucite Int, Wilton Ctr, Wilton TS10 4RF, Redcar, England
来源
ACS CATALYSIS | 2012年 / 2卷 / 11期
关键词
high-pressure NMR; kinetics; hydroformylation; hydroesterification; methoxycarbonylation; RHODIUM CARBONYL CLUSTERS; TOROID CAVITY AUTOCLAVE; METHYL PROPANOATE; ASYMMETRIC HYDROFORMYLATION; HIGH-RESOLUTION; METHOXYCARBONYLATION; COMPLEXES; ETHENE; MONOXIDE; HYDROGENATION;
D O I
10.1021/cs300439n
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
High-pressure NMR methods for the study of the kinetics of gas solution reactions are presented, and the importance/interplay of mass transport and chemical resistances are discussed. For reactions that are slow compared with mass transport, the true reaction kinetics can be obtained and used to confirm that the observed species are relevant to the catalytic reaction. Conversely, the ability to determine the catalyst speciation during the catalytic reaction aids interpretation of the kinetic data. When chemical reaction is fast compared with diffusion across the gas-liquid interface, reaction is shown to occur in the liquid layer; for such a transport-controlled reaction, chemical reaction can increase the concentration gradient across the boundary layer, enhancing diffusion both across the phase boundary and within the liquid layer, resulting in apparent positive orders in catalyst, substrate, or both. These dependencies do not reflect the chemical dependence of the reaction rate on these concentrations.
引用
收藏
页码:2281 / 2289
页数:9
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