Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3284
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dc.contributor.authorKumar, Ranjeeten_US
dc.contributor.authorGaurav, Archanaen_US
dc.contributor.authorPAL, SHIVen_US
dc.contributor.authorKumar, Krishnan R.en_US
dc.contributor.authorSridhar, Balasubramanianen_US
dc.contributor.authorTewari, Ashish K.en_US
dc.date.accessioned2019-07-01T05:35:43Z
dc.date.available2019-07-01T05:35:43Z
dc.date.issued2017-04en_US
dc.identifier.citationChemistrySelect, 2(11), 3249-3255.en_US
dc.identifier.issn2365-6549en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3284-
dc.identifier.urihttps://doi.org/10.1002/slct.201700269en_US
dc.description.abstractHerein, we report o‐xylene based symmetrical dimers of 2‐thiopyridine derivative for studies of intramolecular stacking and conformational analysis 1‐3. The conformational analyses of all compounds have been carried out in solid, solution and gaseous states. Interestingly, all compounds showed reverse intramolecular stacked conformation between contiguous rings. Among all, compound 3 has shown polymorphism properties that also shown reverse intramolecular stacked conformation. The polymorphic studies have been achieved through single crystal X‐ray diffraction, intermolecular interactions in their crystal packing, overlay diagram, DSC analysis and Hirshfeld surface analysis.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectReverse Intramolecularen_US
dc.subjectConformational Stabilityen_US
dc.subject2-Thiopyridine Derivativeen_US
dc.subjectConformational analysisen_US
dc.subjectDFT calculationsen_US
dc.subjectHirshfeld surface analysisen_US
dc.subject2017en_US
dc.titleReverse Intramolecular Stacking in o‐Xylene Bridge Symmetrical Dimers of 2‐Thiopyridine Derivative: Assessment of the Conformational Stabilityen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleChemistrySelecten_US
dc.publication.originofpublisherForeignen_US
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