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首页> 外文期刊>Polyhedron: The International Journal for Inorganic and Organometallic Chemistry >Water as hydride source in the reduction of nitrobenzene to aniline catalyzed by cis-[Rh(CO)(2)(2-picoline)(2)] (PF6) in aqueous 2-picoline under CO atmosphere: kinetics study
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Water as hydride source in the reduction of nitrobenzene to aniline catalyzed by cis-[Rh(CO)(2)(2-picoline)(2)] (PF6) in aqueous 2-picoline under CO atmosphere: kinetics study

机译:CO气氛下2-甲基吡啶水溶液中顺式-[Rh(CO)(2)(2-甲基吡啶)(2)](PF6)催化硝基苯还原成苯胺中水的氢化物动力学研究

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The cis-[Rh(CO)(2)(2-picoline)(2)] (PF6) complex is active for the catalytic reduction of nitrobenzene to aniline in aqueous 2-picoline solution under water gas shift reaction conditions. The catalytic activities for this system were studied as functions of the reaction parameters (P(CO), [Rh](tot), and T). The nitrobenzene reduction rate displays a first-order dependence on CO pressure, P(CO), over the range 0-1.9 atm at 80, 100 and 120 degrees C. The kinetics behavior with respect to P(CO) leads to the proposal that addition of CO to the catalytic species precedes the rate-limiting step. The catalytic activity proved to be non-linear in total rhodium concentration, [Rh](tot), over the range 5-60 mM. This observation was interpreted in terms of the presence of active mononuclear and polynuclear rhodium species in the system, the mononuclear species being the more active for nitrobenzene reduction. In situ FT-IR spectroscopic study confirms the presence of rhodium species with terminal and bridging carbonyls. (C) 2000 Elsevier Science Ltd All rights reserved. [References: 24]
机译:顺式-[Rh(CO)(2)(2-甲基吡啶)(2)](PF6)络合物在水煤气变换反应条件下可将硝基苯水溶液中的硝基苯催化还原为苯胺。研究了该系统的催化活性与反应参数(P(CO),[Rh](tot)和T)的关系。硝基苯的还原速率在80、100和120摄氏度下在0-1.9 atm的范围内表现出对CO压力P(CO)的一级依赖性。相对于P(CO)的动力学行为导致提出以下建议:在限速步骤之前先向催化物质中加入CO。在总铑浓度[Rh](tot)中,在5-60 mM范围内,催化活性被证明是非线性的。根据系统中存在的活性单核和多核铑物种来解释该观察结果,单核物种对硝基苯还原的活性更高。 FT-IR光谱原位研究证实了存在带有末端羰基和桥接羰基的铑物种。 (C)2000 Elsevier Science Ltd保留所有权利。 [参考:24]

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