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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/14095
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dc.contributor.authorPant, Debi D.-
dc.date.accessioned2024-02-07T11:17:56Z-
dc.date.available2024-02-07T11:17:56Z-
dc.date.issued2015-06-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0167732215000823-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/14095-
dc.description.abstractAbsorption and fluorescence spectra of dications of cinchonine (C2 +) and cinchonidine (Cd2 +) have been measured at room temperature in solvents of different polarities. Ground and excited state electric dipole moments are determined experimentally using solvatochromic shift method based on bulk solvent properties. Theoretical calculations are done using B3LYP/6-31G(D) and CIS/6-31G(D) levels of theory for ground and excited states, respectively. Both experimental and theoretical studies reveal that excited state dipole moment (μe) values are higher than corresponding ground state dipole moment (μg) value of C2 + and Cd2 +, which is attributed to the higher polarity of excited states compared to the ground state polarity of these molecules.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectPhysicsen_US
dc.subjectSolvatochromic shiften_US
dc.subjectDipole momenten_US
dc.subjectAbsorptionen_US
dc.subjectFluorescenceen_US
dc.subjectCinchonine dicationen_US
dc.subjectCinchonidine dicationen_US
dc.titleSolvent effect on absorption and fluorescence spectra of cinchonine and cinchonidine dications: Estimation of ground and excited state dipole moments by experimental and numerical studiesen_US
dc.typeArticleen_US
Appears in Collections:Department of Physics

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