Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9332
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dc.contributor.authorMobin, Shaikh M.en_US
dc.contributor.authorMisra, Rajneeshen_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-21T11:32:22Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-21T11:32:22Z-
dc.date.issued2014-
dc.identifier.citationGautam, P., Maragani, R., Mobin, S. M., & Misra, R. (2014). Reversible mechanochromism in dipyridylamine-substituted unsymmetrical benzothiadiazoles. RSC Advances, 4(94), 52526-52529. doi:10.1039/c4ra09921den_US
dc.identifier.issn2046-2069-
dc.identifier.otherEID(2-s2.0-84908235902)-
dc.identifier.urihttps://doi.org/10.1039/c4ra09921d-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/9332-
dc.description.abstractWe report the design and synthesis of push-pull benzothiadiazoles (BTDs) of type D1-π-A-π-D2 and D1-π-A-D2. These BTDs show strong charge transfer interaction. BTD 3 shows reversible mechanochromism with color contrast between yellow (crystalline state) and orange (amorphous state). Photophysical and computational studies reveal that the planar orientation of the pyridyl and BTD unit in 2 results in no change in solid state emission whereas non-planar orientation of the dipyridylamine and BTD unit in 3 results in efficient mechanochromism. This journal is © the Partner Organisations 2014.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.sourceRSC Advancesen_US
dc.subjectBenzothiadiazolesen_US
dc.subjectDipyridylamineen_US
dc.titleReversible mechanochromism in dipyridylamine-substituted unsymmetrical benzothiadiazolesen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Chemistry

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