Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/2694
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dc.contributor.authorKaur, Gurpreet-
dc.contributor.authorChoudhury, A.R.-
dc.date.accessioned2020-12-04T09:41:52Z-
dc.date.available2020-12-04T09:41:52Z-
dc.date.issued2017-
dc.identifier.citationJournal of Materials Chemistry C, 5(31), pp. 21820-21827en_US
dc.identifier.otherhttps://doi.org/10.1039/C7TC02250F-
dc.identifier.urihttps://pubs.rsc.org/en/content/articlelanding/2017/tc/c7tc02250f#!divAbstract-
dc.identifier.urihttp://hdl.handle.net/123456789/2694-
dc.descriptionOnly IISERM authors are available in the record.-
dc.description.abstractFour new Ir(III) complexes with the general formula [IrHCl(C^N)(PPh3)2] containing different conjugated Schiff base ligands (C^N) have been synthesized and characterized by 1H, 13C, and 31P NMR, HRMS, and IR spectra and one of them by single crystal X-ray diffraction. Their photophysical properties in solution and in the solid state have been analyzed and three main practical results have been obtained: (i) a dual fluorescent and phosphorescent emissive complex in solution, (ii) successful acid/base sensing in the solid state and (iii) quantitative CO2 detection. Quantum chemical calculations have been employed to assign the character of the lowest excited states. A plausible explanation for the observed aggregation induced enhanced emission (AIEE) is given, based on the restriction of intramolecular motions due to the effect of intermolecular C–H⋯π and C–H⋯Cl type interactions upon aggregation.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectIridium(iii)en_US
dc.subjectDual emissionen_US
dc.subjectAggregationen_US
dc.titleDual emission and multi-stimuli-response in iridium(iii) complexes with aggregation-induced enhanced emission: applications for quantitative CO2 detectionen_US
dc.typeArticleen_US
Appears in Collections:Research Articles

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