Peer-reviewedCC BYCatalysis science & technology
Atmospheric pressure water-gas shift reaction and transfer hydrogenation of ketones using a ruthenium pincer catalyst.
- 1EaStCHEM, School of Chemistry, University of St Andrews North Haugh KY16 9ST St Andrews UK [email protected].
Abstract
We report the use of a Ru-MACHO pincer complex as a catalyst for the homogeneous water-gas shift reaction (WGSR) under atmospheric pressure of CO and at 150 °C, achieving cumulative turnover numbers (TONs) of more than 6000 from the catalyst recycling of a total of 4 runs. This activity was then exploited to reduce ketones to secondary alcohols via transfer hydrogenation using CO and water as a reducing agent. Stoichiometric NMR experiments and DFT calculations were performed to elucidate key organometallic intermediates and the catalytic cycle.
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BibTeX
@article{luk2026atmospheric,
title = {{Atmospheric pressure water-gas shift reaction and transfer hydrogenation of ketones using a ruthenium pincer catalyst.}},
author = {James Luk and Luming Guo and Michael Bühl and Amit Kumar},
journal = {Catalysis science \& technology},
year = {2026},
month = sep,
doi = {10.1039/d6cy01293k},
url = {https://europepmc.org/article/MED/42909389},
note = {CC BY},
}
RIS
TY - JOUR
TI - Atmospheric pressure water-gas shift reaction and transfer hydrogenation of ketones using a ruthenium pincer catalyst.
AU - James Luk
AU - Luming Guo
AU - Michael Bühl
AU - Amit Kumar
PY - 2026
DA - 2026/09/25
JO - Catalysis science & technology
DO - 10.1039/d6cy01293k
UR - https://europepmc.org/article/MED/42909389
AB - We report the use of a Ru-MACHO pincer complex as a catalyst for the homogeneous water-gas shift reaction (WGSR) under atmospheric pressure of CO and at 150 °C, achieving cumulative turnover numbers (TONs) of more than 6000 from the catalyst recycling of a total of 4 runs. This activity was then exploited to reduce ketones to secondary alcohols via transfer hydrogenation using CO and water as a reducing agent. Stoichiometric NMR experiments and DFT calculations were performed to elucidate key organometallic intermediates and the catalytic cycle.
SN - 2044-4753
SN - 2044-4761
ER -