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Metal chlorides supported on chiral mesoporous silica (MClx/CMS) as highly active Lewis acid catalyst for the selective hydroamination of cyclohexene
•A series of metal chlorides are impregnated on the CMS (MClx/CMS).•The MClx nanoparticles (∼10nm) are strongly attached on the CMS support.•All MClx/CMS catalysts have Lewis acidity with different strengths and amounts.•ZnCl2/CMS has the strongest Lewis acidity.•The catalysts show catalytic synergi...
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Published in: | Journal of the Taiwan Institute of Chemical Engineers 2014-07, Vol.45 (4), p.1435-1442 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | •A series of metal chlorides are impregnated on the CMS (MClx/CMS).•The MClx nanoparticles (∼10nm) are strongly attached on the CMS support.•All MClx/CMS catalysts have Lewis acidity with different strengths and amounts.•ZnCl2/CMS has the strongest Lewis acidity.•The catalysts show catalytic synergistic effect in hydroamination reaction.•The catalysts can be easily separated after reaction and are recyclable.
Metal chlorides supported on chiral mesoporous silica (MClx/CMS) as solid acid catalysts were prepared, characterized and their catalytic performance in hydroamination of cyclohexene was evaluated. A series of MClx/CMS catalysts were prepared by wet impregnation with various types of metal chlorides (NiCl2, CuCl2, AlCl3, CoCl2, FeCl3, ZnCl2) on CMS support and further heat treated at mild temperature. The supported catalysts showed catalytic synergistic effect (∼60% of conversion) and 100% selectivity in hydroamination of cyclohexene under mild reaction condition (60°C). Furthermore, the influence of reaction parameters and supports on activity of the catalyst was also investigated. The MClx/CMS catalysts can be recovered for reuse for several runs with little reactivity loss (∼5%) and easily handled under the described reaction conditions. |
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ISSN: | 1876-1070 1876-1089 |
DOI: | 10.1016/j.jtice.2013.12.011 |