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dc.contributor.authorThomas, Ajesh P-
dc.contributor.authorGowri Sreedevi, K C-
dc.contributor.authorAdinarayana, B-
dc.contributor.authorRamakrishnan, S-
dc.contributor.authorSrinivasan, A-
dc.date.accessioned2016-10-24T09:58:13Z-
dc.date.available2016-10-24T09:58:13Z-
dc.date.issued2013-07-
dc.identifier.citationRSC Advances, 2013, 3, 16967-16972en_US
dc.identifier.urihttp://hdl.handle.net/123456789/2483-
dc.description.abstractA hitherto unknown meso-tetrakis(3,5-dihydroxyphenyl)N-confused porphyrin (NCPH) was synthesized and characterized. The typical 3H and 2H tautomeric existence of the N-confused derivative was controlled exclusively by protic and aprotic solvents rather than the established polar and non-polar driving forces. An unprecedented morphological change controlled by two tautomeric forms of NCPH during aggregation was investigated.en_US
dc.language.isoenen_US
dc.publisherThe Royal Society of Chemistryen_US
dc.subjectPorphyrinen_US
dc.titlemeso-Tetrakis(3,5-dihydroxyphenyl)N-confused porphyrin: Influence of polar protic and aprotic solvents in tautomeric existence, exchange and morphologyen_US
dc.typeArticleen_US
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