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Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/3130
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dc.contributor.authorRamachandran, G.-
dc.contributor.authorRaman, A.-
dc.contributor.authorEaswaramoorthi, S.-
dc.contributor.authorRathore, R.S.-
dc.contributor.authorSathiyanarayanan, K.-
dc.date.accessioned2020-12-14T10:30:38Z-
dc.date.available2020-12-14T10:30:38Z-
dc.date.issued2014-
dc.identifier.citationRoyal Society of Chemistry, 4(55), pp.29276-29280.en_US
dc.identifier.otherhttps://doi.org/10.1039/C4RA03622K-
dc.identifier.urihttps://pubs.rsc.org/en/content/articlelanding/2014/RA/C4RA03622K#!divAbstract-
dc.identifier.urihttp://hdl.handle.net/123456789/3130-
dc.description.abstractA series of new dimeric tetracyclic dilactam fluorophores (DTDF) consisting of diazabicyclooctane-dione (DBOD) fused to tetrahydronaphthalene (THP) was designed and synthesized from a simple precursor. The monomers showed enhanced emission in THF–water solvent and also benzene-dimer like absorption and fluorescence, originating from the hydrogen-bonding aided self-assembly of dilactams. The crystal structures revealed water-mediated molecular aggregates with several hydrogen-bond bridges formed by water.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectDilactam fluorophoresen_US
dc.subjectDiazabicyclooctane-dioneen_US
dc.subjectFluorophoresen_US
dc.titleFour component domino reaction for the synthesis of highly functionalized dimeric tetracyclic dilactam fluorophores: H-bond aided self-assemblyen_US
dc.typeArticleen_US
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