Volume 2, Issue 11 p. 1477-1482
Full Paper

A Covalently Immobilized Triphenylphosphine Rhodium Complex: Synthesis, Characterization, and Application in Catalytic Olefin Hydrogenation

Lei Wang,

Fachbereich Chemie, Technische Universität Kaiserslautern, Erwin-Schrödinger-Str. Geb. 54, 67663, Kaiserslautern (Germany), Fax: (+49) 631-2054676

Key Laboratory of Surface and Interface Chemistry of Jilin Province, College of Chemistry, Jilin University, Changchun, 130012 (China)

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Prof. Dr. Mingjun Jia,

Key Laboratory of Surface and Interface Chemistry of Jilin Province, College of Chemistry, Jilin University, Changchun, 130012 (China)

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Dr. Sankaranarayanapillai Shylesh,

Fachbereich Chemie, Technische Universität Kaiserslautern, Erwin-Schrödinger-Str. Geb. 54, 67663, Kaiserslautern (Germany), Fax: (+49) 631-2054676

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Thomas Philippi,

Fachbereich Chemie, Technische Universität Kaiserslautern, Erwin-Schrödinger-Str. Geb. 54, 67663, Kaiserslautern (Germany), Fax: (+49) 631-2054676

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Dr. Andreas Seifert,

Technische Universität Chemnitz, Institut für Chemie, Straße der Nationen 62, 09111 Chemnitz (Germany)

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Prof. Dr. Stefan Ernst,

Fachbereich Chemie, Technische Universität Kaiserslautern, Erwin-Schrödinger-Str. Geb. 54, 67663, Kaiserslautern (Germany), Fax: (+49) 631-2054676

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Dr. Anand Pal Singh,

Inorganic and Catalysis Division, National Chemical Laboratory, Dr. Homi Bhabha Road, Pashan, Pune 411 008 (India)

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Prof. Dr. Werner R. Thiel,

Fachbereich Chemie, Technische Universität Kaiserslautern, Erwin-Schrödinger-Str. Geb. 54, 67663, Kaiserslautern (Germany), Fax: (+49) 631-2054676

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First published: 20 August 2010
Citations: 12

Abstract

A trimethoxysilane functionalized triphenylphosphine was coordinated to rhodium(I) and the resulting rhodium complex was covalently bound to a mesoporous SBA-15 support. The catalytic activity of this hybrid material was studied for the hydrogenation of 2-cyclohexen-1-one and compared with the corresponding homogeneous catalyst. According to the 31P-MAS NMR data, the catalytically active species was stable against oxidation; no structural change could be detected after exposing it to air for more than two months. Transmission electron microscopy (TEM) measurements on the used catalyst confirmed that the rhodium species was also stable against reduction to the metal because the formation of rhodium nanoparticles during the catalysis could be excluded. The kinetic curves of the recycled system confirmed that this hybrid catalyst shows excellent activity, selectivity, stability, and reusability, and is truly heterogeneous in the hydrogenation reaction.