Synthesis and Photoinduced Processes of Donor-Acceptor Substituted Diarylbutadienes

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dc.contributor.advisor Kanvah, Sriram
dc.contributor.author Agnihotri, Harsha
dc.date.accessioned 2016-01-08T11:58:44Z
dc.date.available 2016-01-08T11:58:44Z
dc.date.issued 2015
dc.identifier.citation Agnihotri, Harsha, (2015). Synthesis and Photoinduced Processes of Donor-Acceptor Substituted Diarylbutadienes (Phd Thesis). Indian Institute of Technology, Gandhinagar, pp. 142 (Acc No: T00097) en_US
dc.identifier.uri https://repository.iitgn.ac.in/handle/123456789/2057
dc.description.abstract Several donor-π-acceptor systems based on diarylpolyene scaffold were synthesized and examined for their fluorescence and photochemical properties. The fluorescence investigations of these dienes reveal weak to strong solvatochromism attributed to intramolecular charge transfer (ICT). The systems containing nitro as acceptor, exhibit very weak quantum yields. Changing the position of nitro group from para, meta or to ortho results in further loss in emission. Interestingly, simple para (or meta) nitro diarylbutadienes show inefficient photoisomerization. However, introduction of a methyl group on the double bond in the same system yields regioselective isomer of methyl substituted double bond. Likewise presence of nitro group at ortho position also yields regioselective isomer of the double bond distal to the aromatic nitro group. Such behaviour is explained by (a) steric effect of methyl group that induces non-planarity and (b) the intramolecular C − H … . O hydrogen bonding that inhibits the isomerization of the proximal double bond. Similar photoisomerization observations were seen with a pyridyl group in place of phenyl ring. NMR and single crystal X-ray data substantiates these observations. Incorporation of suitable donating groups on phenyl ring of an arylpolyene scaffold bearing pyridine as an acceptor reveals remarkable fluorescence properties with strong bathochromic emission shifts. Methylation of pyridine results in a positively charged pyridinium ion which enhances the electron withdrawing ability and show strongly red-shifted emission near ~700nm. Such a strong emission, coupled with water-solubility can have useful applications as fluorescence probes for biological media. en_US
dc.description.statementofresponsibility by Harsha Agnihotri
dc.format.extent 142 p.; col.; ill; 31 cm. + 1 CD-ROM
dc.language.iso en en_US
dc.publisher Indian Institute of Technology Gandhinagar en_US
dc.subject Donor en_US
dc.subject Diarylbutadienes en_US
dc.subject Hydrochloric acid en_US
dc.subject Dimethylformamide en_US
dc.subject Ultraviolet-visible en_US
dc.subject Correlated Spectroscopy en_US
dc.title Synthesis and Photoinduced Processes of Donor-Acceptor Substituted Diarylbutadienes en_US
dc.type Thesis en_US
dc.contributor.department Chemistry
dc.description.degree Ph.D.


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