Please use this identifier to cite or link to this item: https://idr.l2.nitk.ac.in/jspui/handle/123456789/12128
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dc.contributor.authorMohan, M.
dc.contributor.authorPangannaya, S.
dc.contributor.authorSatyanarayan, M.N.
dc.contributor.authorTrivedi, D.R.
dc.date.accessioned2020-03-31T08:38:41Z-
dc.date.available2020-03-31T08:38:41Z-
dc.date.issued2018
dc.identifier.citationChemistrySelect, 2018, Vol.3, 13, pp.3803-3813en_US
dc.identifier.urihttp://idr.nitk.ac.in/jspui/handle/123456789/12128-
dc.description.abstractA series of Schiff base thiophene derivatives, D1 to D9, which exhibits a phenomenon of aggregation-induced emission enhancement (AIEE) have been synthesised and characterized by standard spectroscopic techniques. Multicoloured emission enhancement has been achieved just by introduction of electron donating and withdrawing substituent on the thiophene moiety. Few of the molecules in the series exhibited enhanced fluorescence emission intensity in solvent mixture in comparison with that observed in pure solvent supportive of AIE. Single crystal x-ray diffraction (SCXRD) studies on selected molecules, D6 and D7 of the series revealed the existence of planar structure and a herringbone type of crystal packing arrangement. In specific, molecules D6 and D7, possesses a larger ?-? stacking distance of around 4.866 and 4.636 , which curbs all the non-radiative pathways, in turn leading to AIEE. DFT and TDDFT calculations confirm the structural planarity supportive of SCXRD analysis and the nature of electronic transition correlating well with the experimental results. 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheimen_US
dc.titleMulticoloured Thiophene Based AIEgens: Single Crystal Structure Elucidation, Spectral Behaviour and DFT Studiesen_US
dc.typeArticleen_US
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