期刊
DALTON TRANSACTIONS
卷 51, 期 12, 页码 4884-4897出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d2dt00018k
关键词
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资金
- Ramon Areces Foundation (Spain)
- Andalusian Regional Government (FQM-346 group) [RTI2018-101611-B-I00]
- Feder Funds
- Instituto Universitario de Investigacion en Quimica Fina y Nanoquimica (IUNAN)
- Servicio Central de Apoyo a la Investigacion (SCAI)
- FPU teaching and research fellowship [FPU17/03981]
A new heterogeneous catalyst with excellent catalytic performance has been synthesized by immobilizing a copper complex on a surface-functionalized ordered mesoporous organosilica. The catalyst showed high conversion and selectivity in the epoxidation reaction.
A new heterogeneous catalyst has been synthesized by immobilization of a copper complex on dipyridyl-pyridazine functionalized periodic mesoporous organosilica (dppz-vPMO). This ordered support was first prepared by a co-condensation reaction between vinyltriethoxysilane and 1,2-bis(trimethoxysilyl)ethane and further post-functionalized through a hetero Diels-Alder reaction with 3,6-di-2-pyridyl-1,2,4,5-tetrazine. Techniques such as XRD, N-2 isotherms, TEM, C-13 NMR, XPS and DRIFT, among others, were employed to characterize the surface functionalized materials. These results have proven the ordered mesostructure of the materials as well as the presence of novel nitrogen-chelating heterocyclic compounds on the pore surface after the post-modification process. Additionally, the successful anchoring of a copper complex on the dipyridyl-pyridazine (dppz) ligands has been confirmed. The resulting material was evaluated as a heterogeneous catalyst in the epoxidation of styrene using tert-butylhydroperoxide (TBHP) as an oxidant. Under the optimized reaction conditions, Cu@dppz-vPMO showed a high styrene conversion (86.0%) and a remarkable selectivity to styrene oxide (41.9%). Indeed, this catalyst provided excellent catalytic results in terms of stability, reaction rate, conversion and selectivity compared to other bipyridine-like copper catalysts.
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