Dual fluorescence of a few organic molecules : Intramolecular charge transfer and intramolecular proton transfer

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dc.contributor.authorBehera, Santosh Kumar
dc.date.accessioned2018-05-30T07:11:27Z
dc.date.accessioned2023-10-19T12:09:51Z
dc.date.available2018-05-30T07:11:27Z
dc.date.available2023-10-19T12:09:51Z
dc.date.issued2016
dc.descriptionSupervisor: G. Krishnamoorthyen_US
dc.description.abstractThe thesis reports the investigation of a few organic molecules those undergo intramolecular charge transfer (ICT) or intramolecular proton transfer. The introduction to the thesis is presented first, followed by details of the materials, methods and instrumentation. The mechanism for the dual emission of 2-(4'-N,N-dimethylaminophenyl imidazo[4,5-c]pyridine (DMAPIP-c) is investigated and found that the relay of proton by solvent molecules induces the twisted ICT (TICT) emission in DMAPIP-c. The spectral characteristics of neutral and monocationic (MC) of N,N-dimethylaminophenyl)imidazopyridines (DMAPIPs) in aqueous cucurbit-7-uril (CB-7) are also studied. Both the molecules form a 1:1 complex with CB-7 and pyridoimidzole rings are present inside the cavity. Both double proton transfer and the relay proton transfer induced TICT emissions are also observed in CB-7. The effect of CB-7 on the monocationic equilibrium of DMAPIPs are also explored. All three MCs of DMAPIPs present in the ground state in CB-7. However, the monocationic equilibrium shifts in CB-7 medium. An almost exclusive excited state intramolecular proton transfer (ESIPT) is reported. In the next chapter, an exclusive aggregation induced enhanced tautomer emission of a newly synthesized ESIPT molecule is described.en_US
dc.identifier.otherROLL NO.11612207
dc.identifier.urihttps://gyan.iitg.ac.in/handle/123456789/957
dc.language.isoenen_US
dc.relation.ispartofseriesTH-1702;
dc.subjectCHEMISTRYen_US
dc.titleDual fluorescence of a few organic molecules : Intramolecular charge transfer and intramolecular proton transferen_US
dc.typeThesisen_US
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