TY - JOUR
T1 - Efficient Hydrogenolysis of Alkanes at Low Temperature and Pressure Using Tantalum Hydride on MCM-41, and a Quantum Chemical Study
AU - Polshettiwar, Vivek
AU - Pasha, Farhan Ahmad
AU - De Mallmann, Aimery
AU - Norsic, Sébastien
AU - Thivolle-Cazat, Jean
AU - Basset, Jean-Marie
N1 - KAUST Repository Item: Exported on 2020-10-01
Acknowledgements: The authors thank ESCPE-Lyon, CNRS, and KAUST for financial and logistical support.
PY - 2012/2/10
Y1 - 2012/2/10
N2 - Hydrogenolysis of hydrocarbons is of considerable technological importance for applications such as the hydroprocessing of petrochemical feedstocks to generate high-value and useful chemicals and fuels. We studied the catalytic activity of tantalum hydride supported on MCM-41 for the hydrogenolysis of alkanes at low temperature and low atmospheric pressure in a dynamic reactor. The reactions proceed with good turnover numbers, and the catalyst could be reused for several times, which makes the overall catalytic process sustainable. We derived the plausible mechanism by using DFT calculations and identified the preferred pathways by the analysis of potential energy surface. Our results and the proposed reaction mechanism demonstrate the viability of the "catalyst-by-design" approach. © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
AB - Hydrogenolysis of hydrocarbons is of considerable technological importance for applications such as the hydroprocessing of petrochemical feedstocks to generate high-value and useful chemicals and fuels. We studied the catalytic activity of tantalum hydride supported on MCM-41 for the hydrogenolysis of alkanes at low temperature and low atmospheric pressure in a dynamic reactor. The reactions proceed with good turnover numbers, and the catalyst could be reused for several times, which makes the overall catalytic process sustainable. We derived the plausible mechanism by using DFT calculations and identified the preferred pathways by the analysis of potential energy surface. Our results and the proposed reaction mechanism demonstrate the viability of the "catalyst-by-design" approach. © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
UR - http://hdl.handle.net/10754/562094
UR - http://doi.wiley.com/10.1002/cctc.201100130
UR - http://www.scopus.com/inward/record.url?scp=84857525790&partnerID=8YFLogxK
U2 - 10.1002/cctc.201100130
DO - 10.1002/cctc.201100130
M3 - Article
SN - 1867-3880
VL - 4
SP - 363
EP - 369
JO - ChemCatChem
JF - ChemCatChem
IS - 3
ER -