氧化石墨作为钯和铑配合物的载体,作为1-庚烷部分氢化的催化剂

Quiroga Me, L. da, Cagnola Ea, Á. Mastalir, T. Szabó, J. Paredes, L. MartínezBovier, C. Betti
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引用次数: 0

摘要

用氧化石墨(GO)锚定[PdCl 2 (TDA) 2]和[RhCl(TDA) 3] (TDA = nh2 (ch2) 12 ch3),金属载荷为2wt %。采用元素分析(EA)、FTIR、XPS、XRD和原子吸收光谱(AA)等技术进行表征。FTIR和XRD分析表明,这两种配合物主要固定在氧化石墨烯表面。以1-庚烷的部分加氢反应为试验反应,在温和的温度和压力条件下,在半连续过程中评价了这些多相配合物的催化性能。并与相同操作条件下使用威尔金森催化剂的结果进行了比较。AA分析表明,在非均相催化评价过程中,配合物没有浸出。[RhCl(TDA) 3]/GO为最佳催化剂,受电子效应、位阻效应及载体的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Graphite oxide as a support for palladium and rhodium complexes, assessed as catalysts for the partial hydrogenation of 1-heptyne
Graphite oxide (GO) was used to anchor [PdCl 2 (TDA) 2 ] and [RhCl(TDA) 3 ] (TDA = NH 2 (CH 2 ) 12 CH 3 ) with 2wt % of metal load. Elemental analysis (EA), FTIR, XPS, XRD and atomic absorption spectroscopy (AA) were the techniques employed for characterization. FTIR and XRD revealed that both complexes were mainly immobilized on the GO surface. The partial hydrogenation of 1-heptyne was the test reaction to evaluate the catalytic behavior of these heterogenized complexes under mild conditions of temperature and pressure in a semi continuous process. The results were compared with those obtained with the Wilkinson catalyst under the same operational conditions. AA analysis revealed that there is no leaching of the complexes during the heterogeneous catalytic evaluations. [RhCl(TDA) 3 ]/GO was the best catalyst due to electronic and steric effects as well as the influence of the support.
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