Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/681
Full metadata record
DC FieldValueLanguage
dc.contributor.authorKumar, Devender-
dc.date.accessioned2016-09-09T15:23:41Z-
dc.date.available2016-09-09T15:23:41Z-
dc.date.issued2015-09-05-
dc.identifier.urihttp://hdl.handle.net/123456789/681-
dc.description.abstractA general method for the synthesis of azo derivatives of active methylene compounds through the in situ generation of arenediazonium salts followed by reacting them with a compound containing active methylene group has been developed. The advantages of these reactions are milder condition, cheaper starting material and simpler execution with high yields apart from many functionalization possibilities. Azo coupling of arenediazonium ion with aliphatic compounds are sensitive reaction so reaction conditions have been optimised by trying different conditions. Azo compound are robust photoswitchable molecules, which can be switched between trans and cis isomers. Due to this photoisomerization, azo molecules will get a significant geometrical change in their molecular structure. Due to the presence of two electron withdrawing groups, few different tautomeric structures are also possible for these systems. Through this work, synthesis, tautomerism and switching behavior have been studied in detail.en_US
dc.description.sponsorshipIISER-Men_US
dc.language.isoenen_US
dc.publisherIISER-Men_US
dc.subjectChemistryen_US
dc.subjectNucleophilesen_US
dc.subjectDiazonium Saltsen_US
dc.titleFurther Exploration on Reactivity of Diazonium Salts with Selective Nucleophiles and Enolatesen_US
dc.typeThesisen_US
Appears in Collections:MS-09

Files in This Item:
File Description SizeFormat 
MS09049.pdf19.86 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.