Since its original discovery over a century ago, the water-gas shift reaction (WGSR) has played a crucial role in industrial chemistry, providing a source of H2 to feed fundamental industrial transformations such as the Haber-Bosch synthesis of ammonia. Although the production of hydrogen remains nowadays the major application of the WGSR, the advent of homogeneous catalysis in the 1970s marked the beginning of a synergy between WGSR and organic chemistry. Thus, the reducing power provided by the CO/H2 O couple has been exploited in the synthesis of fine chemicals; not only hydrogenation-type reactions, but also catalytic processes that require a reductive step for the turnover of the catalytic cycle. Despite the potential and unique features of the WGSR, its applications in organic synthesis remain largely underdeveloped. The topic will be critically reviewed herein, with the expectation that an increased awareness may stimulate new, creative work in the area.
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http://dx.doi.org/10.1002/anie.201601803 | DOI Listing |
Angew Chem Int Ed Engl
December 2024
Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), State Key Laboratory of Chemical Engineering, Haihe Laboratory of Sustainable Chemical Transformations, Tianjin Key Laboratory of Applied Catalysis Science and Engineering, School of Chemical Engineering & Technology, Tianjin University, Tianjin, 300072, P. R. China.
CO hydrogenation to methanol using green hydrogen derived from renewable resources provides a promising method for sustainable carbon cycle but suffers from high selectivity towards byproduct CO. Here, we develop an efficient PdZn-ZnO/TiO catalyst by engineering lattice dislocation structures of TiO support. We discover that this modification orders irregularly arranged atoms in TiO to stabilize crystal lattice, and consequently weakens electronic interactions with supported active phases.
View Article and Find Full Text PDFBiotechnol Biofuels Bioprod
January 2025
Section II: Electrobiotechnology, Institute of Process Engineering in Life Science, Karlsruhe Institute of Technology, 76131, Karlsruhe, Germany.
Background: Parageobacillus thermoglucosidasius is a facultatively anaerobic thermophile that is able to produce hydrogen (H) gas from the oxidation of carbon monoxide through the water-gas shift reaction when grown under anaerobic conditions. The water-gas shift (WGS) reaction is driven by a carbon monoxide dehydrogenase-hydrogenase enzyme complex. Previous experiments exploring hydrogenogenesis with P.
View Article and Find Full Text PDFNanoscale
January 2025
School of Chemistry, Dalian University of Technology, No.2 Linggong Road, Dalian City, Liaoning Province, 116024, P. R. China.
The mechanism and activity of the water-gas shift reaction (WGSR) on single-atom alloy Al/Cu (111) and Cu (111) surfaces were studied using GGA-PBE-D3. Al/Cu (111) exhibited bifunctional active sites, with the Al site being positively charged and the Cu site negatively charged due to electronic interactions. This led to selective adsorption of HO and CO.
View Article and Find Full Text PDFRSC Adv
January 2025
Institute of Molecular Science, Key Laboratory of Chemical Biology and Molecular Engineering of Ministry of Education, Shanxi University Taiyuan 030006 China
CO conversion and reuse technology are crucial for alleviating environmental stress and promoting carbon cycling. Reverse water gas shift (RWGS) reaction can transform inert CO into active CO. Molybdenum carbide (MoC) has shown good performance in the RWGS reaction, and different crystalline phases exhibit distinct catalytic behaviors.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Institute of Materials, China Academy of Engineering Physics, Jiangyou 621908, China.
Solar-driven dry reforming of methane (DRM) offers a milder, more cost-effective, and promising environmentally friendly pathway compared to traditional thermal catalytic DRM. Numerous studies have extensively investigated inexpensive Ni-based catalysts for application in solar-driven DRM. However, these catalysts often suffer from activity loss due to carbon accumulation.
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