Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/1912
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dc.contributor.authorNasare, Roshan-
dc.date.accessioned2022-12-17T05:58:29Z-
dc.date.available2022-12-17T05:58:29Z-
dc.date.issued2022-04-
dc.identifier.urihttp://hdl.handle.net/123456789/1912-
dc.description.abstractPhotoswitchable compounds in general, and azobenzene photoswitches in specific continue to attract significant attention for a wide array of applications. Azoheteroarenes represent a relatively new but less studied type of photoswitch, where one of the aryl rings from the conventional azobenzene has been replaced with a five-membered heteroaromatic ring. Considering their increasing importance in a variety of fields, tuning and understanding the structure-property relationships of them are quite useful. In this regard, we have synthesized azopyrazoles and azoisoxazoles with extended π-conjugation. The aims of this study include the effect of π-conjugation at different position of azopyrazole and azoisoxazole derivatives on the photoswitching, and the thermal stability of their cis-isomers. Through systematic studies, a comparison has been made and the results are presented in this contribution.en_US
dc.language.isoen_USen_US
dc.publisherIISER Mohalien_US
dc.subjectSynthesisen_US
dc.subjectCharactrerizationen_US
dc.subjectphotoswitching studiesen_US
dc.subjectazopyrazoleen_US
dc.subjectazoisoxazoleen_US
dc.titleSynthesis, Charactrerization and photoswitching studies of extended π-conjugated azopyrazole and azoisoxazole derivativesen_US
dc.typeThesisen_US
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