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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/123456789/14071
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dc.contributor.authorPant, Debi D.-
dc.date.accessioned2024-02-02T16:35:53Z-
dc.date.available2024-02-02T16:35:53Z-
dc.date.issued1991-02-
dc.identifier.urihttps://www.sciencedirect.com/science/article/abs/pii/1010603091800219-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/14071-
dc.description.abstractSteady state and transient studies of 6-methoxyquinoline (6MQ) were undertaken. 6MQ undergoes a large change of dipole moment on excitation. The low energy absorption band Lb does not change in position with solvent polarity whereas the emission maxima shift towards lower frequencies with broadening of the spectra. The edge excitation red shift, which is associated with the time-dependent red shift of emission, is observed in all polar solvents. The fluorescence decay is monoexponential and is dependent on emission wavelength. The data are explained with the help of the Bakhshiev model of solvent relaxation. The solvent relaxation time τr and the fluorescence lifetime τf increase with the polarity of the solvent. In aqueous solution, 6MQ undergoes a protolytic reaction in the excited state. The rate constant for the proton transfer is 1.2×108 s−1.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectPhysicsen_US
dc.subject6-methoxyquinoline (6MQ)en_US
dc.titleExcited state solvation dynamics of 6-methoxyquinolineen_US
dc.typeArticleen_US
Appears in Collections:Department of Physics

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