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Immobilization of a Rh complex derived from the Wilkinson's catalyst on activated carbon and carbon nanotubes

机译:将衍生自威尔金森氏催化剂的Rh络合物固定在活性炭和碳纳米管上

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摘要

A Rh complex, derived from the Wilkinson's catalyst [RhCl(PPh3)3], has been immobilized on activated carbon and carbon nanotubes through a linear organic molecule (6-amino-1 -hexanol), covalently bonded to the support. This molecule acts as a linker in order to keep the complex apart of the support surface and to mimic its environment in homogeneous phase. The catalysts have been tested in the hydrogenation of cyclohexene. The hybrid catalyst prepared with the activated carbon is as active as the homogeneous Wilkinson's catalyst, while the catalyst prepared with nanotubes is noticeably more active. Negligible leaching is observed and the catalysts are recyclable. The positive effect of the support has been attributed to the confinement of the active species inside the pores, and thus, the structure and the pore size of the support have an outstanding role in the catalytic behaviour of the hybrid catalyst. The structure of the carbon nanotubes leads to hybrid catalysts with a noticeably enhanced catalytic activity.
机译:衍生自威尔金森催化剂[RhCl(PPh3)3]的Rh络合物已通过共价键合到载体上的线性有机分子(6-氨基-1-己醇)固定在活性炭和碳纳米管上。该分子起着连接剂的作用,以使复合物与载体表面分开,并在均相中模拟其环境。已经在环己烯的氢化中测试了催化剂。用活性炭制备的杂化催化剂与均相威尔金森氏催化剂一样有活性,而用纳米管制备的催化剂则活性更高。观察到可忽略的浸出并且催化剂是可回收的。载体的积极作用归因于孔内活性物质的限制,因此,载体的结构和孔径在杂化催化剂的催化行为中具有突出的作用。碳纳米管的结构导致杂化催化剂具有明显增强的催化活性。

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