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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/123456789/14068
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dc.contributor.authorPant, Debi D.-
dc.date.accessioned2024-02-02T16:20:44Z-
dc.date.available2024-02-02T16:20:44Z-
dc.date.issued1992-03-
dc.identifier.urihttps://www.sciencedirect.com/science/article/abs/pii/002223139290057G-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/14068-
dc.description.abstractThe excited state dynamics of quinine sulphate (QS), quinidine (Qd) and 6-methoxyquinoline (6MQ) has been studied as a function of pH in steady state and nanosecond time resolved fluorescence experiments. The solvent relaxation process is a dominant process for all the molecules studied, irrespective of pH. Moreover, 6MQ undergoes a proton transfer reaction in the excited state at pH 7 whereas QS and Qd do not exhibit excited state protonation.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectPhysicsen_US
dc.subjectpH dependenceen_US
dc.subjectSpectroscopyen_US
dc.titleTime resolved fluorescence spectroscopy of quinine sulphate, quinidine and 6-methoxyquinoline: pH dependenceen_US
dc.typeArticleen_US
Appears in Collections:Department of Physics

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