Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9070
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dc.contributor.authorRawat, Kuber Singhen_US
dc.contributor.authorPathak, Biswarupen_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-21T11:30:55Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-21T11:30:55Z-
dc.date.issued2018-
dc.identifier.citationRawat, K. S., & Pathak, B. (2018). Flexible proton-responsive ligand-based mn(i) complexes for CO2 hydrogenation: A DFT study. Physical Chemistry Chemical Physics, 20(18), 12535-12542. doi:10.1039/c7cp08637gen_US
dc.identifier.issn1463-9076-
dc.identifier.otherEID(2-s2.0-85046963485)-
dc.identifier.urihttps://doi.org/10.1039/c7cp08637g-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/9070-
dc.description.abstractA series of flexible proton-responsive group substituted N^N-bidentate ligand based Mn(i) complexes have been studied for base free CO2 hydrogenation. We show here that proton responsive ligands play a critical role in base free CO2 hydrogenation. Our calculated reaction free energy barrier values for heterolytic H2 cleavage show that such flexible proton-responsive ligands require a very low activation energy (∼3 kcal mol-1) barrier. Such flexible proton responsive ligands improve the strong dihydrogen (H⋯H) bonding, which in turn improves heterolytic H2 cleavage - an important step for base free CO2 hydrogenation. Therefore, we believe that such flexible proton responsive ligand-substituted metal complexes can be promising for base free CO2 hydrogenation reactions. © the Owner Societies 2018.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.sourcePhysical Chemistry Chemical Physicsen_US
dc.titleFlexible proton-responsive ligand-based Mn(i) complexes for CO2 hydrogenation: A DFT studyen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Chemistry

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