Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/15616
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dc.contributor.authorPatra, Soumyadipen_US
dc.contributor.authorKharde, Tushar A.en_US
dc.contributor.authorKalita, Khanindraen_US
dc.contributor.authorSingh, Sanjay Kumaren_US
dc.date.accessioned2025-01-28T10:48:21Z-
dc.date.available2025-01-28T10:48:21Z-
dc.date.issued2025-
dc.identifier.citationPatra, S., Kharde, T. A., Kalita, K., & Singh, S. K. (2025). Ruthenium-Catalyzed Methanol Production from Aqueous Paraformaldehyde and Mechanistic Study. ChemCatChem. Scopus. https://doi.org/10.1002/cctc.202401643en_US
dc.identifier.issn1867-3880-
dc.identifier.otherEID(2-s2.0-85215072242)-
dc.identifier.urihttps://doi.org/10.1002/cctc.202401643-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/15616-
dc.description.abstractA series of water-soluble arene-Ru(II) complexes, [(η6-p-cymene)RuCl(L)]+Cl‒ ([Ru]-7 – [Ru]-12) (L = substituted bis-imidazole methane) exhibited efficient and selective methanol production from paraformaldehyde in water. The findings inferred a crucial role of the ligand in tuning the catalytic performance. A pH-dependent behavior of this series of catalysts was observed, where the amount of base was influential in methanol production from paraformaldehyde. The catalyst [Ru]-7 (L1 = 4,4′-((2-hydroxyphenyl)methylene)bis(2-ethyl-5-methyl-1H-imidazole) was the most efficient among the explored catalysts giving a turnover number (TON) of 1200 at 90 °C. A mechanistic cycle has also been proposed for the catalytic reaction based on the mass and NMR investigations including those using deuterium-labelled molecules. © 2024 Wiley-VCH GmbH.en_US
dc.language.isoenen_US
dc.publisherJohn Wiley and Sons Incen_US
dc.sourceChemCatChemen_US
dc.subjectCatalysisen_US
dc.subjectLigand effecten_US
dc.subjectMethanolen_US
dc.subjectParaformaldehydeen_US
dc.subjectRutheniumen_US
dc.subjectWater-based reactionsen_US
dc.titleRuthenium-Catalyzed Methanol Production from Aqueous Paraformaldehyde and Mechanistic Studyen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Chemistry

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