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dc.contributor.authorChakraborty, Shamik-
dc.date.accessioned2024-09-14T07:05:21Z-
dc.date.available2024-09-14T07:05:21Z-
dc.date.issued2023-05-
dc.identifier.urihttps://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/cphc.202300124-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/15585-
dc.description.abstractAmong the conglomeration of hydrogen bond donors, the C−H group is prevalent in chemistry and biology. In the present work, CHCl3 has been selected as the hydrogen bond donor and are X(CH3)2 are the hydrogen bond acceptors. Formation of C−H⋅⋅⋅X hydrogen bond under the matrix isolation condition is confirmed by the observation of red-shift in the C−H stretching frequency of CHCl3 and comparison with the simulated spectra. Stabilisation energy of all the three complexes is almost equal although the observed red-shift for the C−H⋅⋅⋅O complex is less compared to the C−H⋅⋅⋅S/Se complexes. The nature and origin of the hydrogen bond have been delineated using Natural Bond Orbital, Atoms in Molecules, Non-Covalent Interaction analyses, and Energy Decomposition Analysis. Charge transfer is found to be proportional to the observed red-shift. This work provides the first impression of C−H⋅⋅⋅Se hydrogen bond and its comparison with C−H⋅⋅⋅O/S hydrogen bond interaction under experimental condition.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectChemistryen_US
dc.subjectConglomerationen_US
dc.subjectHydrogen bonden_US
dc.titleAn Experimental Exploration of C−H⋅⋅⋅X Hydrogen Bond in [CHCl3−X(CH3)2] Complexes (X=O, S, and Se)en_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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