TY - JOUR
T1 - Hydroformylation of dihydrofurans catalyzed by rhodium complex encapsulated hexagonal mesoporous silica
AU - Khokhar, Munir
AU - Shukla, Ram S.
AU - Jasra, Raksh Vir
N1 - KAUST Repository Item: Exported on 2020-10-01
Acknowledgements: Authors thank Council of Scientific and Industrial Research (CSIR), New Delhi, India, for financial supports for Network Project for the Development of Specialty Inorganic Materials for Diverse Applications.
PY - 2015/5
Y1 - 2015/5
N2 - HRh(CO)(PPh3)3 encapsulated hexagonal mesoporous silica (HMS) is found to be an efficient heterogeneous catalyst for the selective hydroformylation of 2,3-dihydrofuran (2,3DHF) and 2,5-dihydrofuran (2,5DHF). The Rh-complex encapsulated in situ in the organic phase of template inside the pores of HMS was found to act as nano phase reactors. Conversion of 2,3-DHF and 2,5-DHF and selectivity of the corresponding aldehydes were thoroughly investigated by studying the reaction parameters: catalyst amount, substrate concentration, partial as well as total pressure of CO and H2, and temperature. The selectivity for the formation of tetrahydrofuran-2-carbaldehyde (THF-2-carbaldehyde) from the hydroformylation of 2,3-DHF was found to be more than the selectivity of the formation of tetrahydrofuran-3-carbaldehyde (THF-3-carbaldehyde) from 2,5-DHF. The reaction paths are suggested and discussed for the selective formation of the corresponding aldehydes. The catalyst was elegantly separated and effectively recycled for six times.
AB - HRh(CO)(PPh3)3 encapsulated hexagonal mesoporous silica (HMS) is found to be an efficient heterogeneous catalyst for the selective hydroformylation of 2,3-dihydrofuran (2,3DHF) and 2,5-dihydrofuran (2,5DHF). The Rh-complex encapsulated in situ in the organic phase of template inside the pores of HMS was found to act as nano phase reactors. Conversion of 2,3-DHF and 2,5-DHF and selectivity of the corresponding aldehydes were thoroughly investigated by studying the reaction parameters: catalyst amount, substrate concentration, partial as well as total pressure of CO and H2, and temperature. The selectivity for the formation of tetrahydrofuran-2-carbaldehyde (THF-2-carbaldehyde) from the hydroformylation of 2,3-DHF was found to be more than the selectivity of the formation of tetrahydrofuran-3-carbaldehyde (THF-3-carbaldehyde) from 2,5-DHF. The reaction paths are suggested and discussed for the selective formation of the corresponding aldehydes. The catalyst was elegantly separated and effectively recycled for six times.
UR - http://hdl.handle.net/10754/564155
UR - https://linkinghub.elsevier.com/retrieve/pii/S1381116915000424
UR - http://www.scopus.com/inward/record.url?scp=84922539537&partnerID=8YFLogxK
U2 - 10.1016/j.molcata.2015.01.027
DO - 10.1016/j.molcata.2015.01.027
M3 - Article
SN - 1381-1169
VL - 400
SP - 1
EP - 6
JO - Journal of Molecular Catalysis A: Chemical
JF - Journal of Molecular Catalysis A: Chemical
ER -