Synthesis characterization and evaluation of symmetrical and unsymmetrical chalcogenides of 2 3 thienyl and ferrocenyl carbaldehyde

dc.contributor.guideMehta, S. K.
dc.coverage.spatialChemistry
dc.creator.researcherHarjit Singh
dc.date.accessioned2024-05-08T06:59:41Z
dc.date.available2024-05-08T06:59:41Z
dc.date.awarded2017
dc.date.completed2016
dc.date.registered2010
dc.description.abstractOrganochalcogen compounds have proved as valuable synthetic reagents in organic synthesis and convenient models for studying fundamental problems in theoretical chemistry. Apart from synthetic applications, organochalcogen compounds are finding potential applications in electronic industry as organic conductors and as precursors for semiconducting materials. In addition, these compounds are biologically important because of their antioxidant properties together with several applications in medical imaging. Synthesis of alkyl, aryl and heteroaryl is well documented in the literature and has proved highly useful to chemists, but curiously the chemistry of 2/3-methylthiophene and methylferrocene has virtually remained under developed probably due to lack of convenient synthetic methods for these compounds. The present work primarily deals with the synthesis characterization and evaluation of symmetrical and unsymmetrical chalcogenides of 2/3-thienyl and ferrocenyl carbaldehyde. newline
dc.description.note
dc.format.accompanyingmaterialCD
dc.format.dimensions-
dc.format.extent212p.
dc.identifier.urihttp://hdl.handle.net/10603/563154
dc.languageEnglish
dc.publisher.institutionDepartment of Chemistry
dc.publisher.placeChandigarh
dc.publisher.universityPanjab University
dc.relation-
dc.rightsuniversity
dc.source.universityUniversity
dc.subject.keywordChalcogenides
dc.subject.keywordFerrocenyl carbaldehyde
dc.subject.keywordOrganochalcogen
dc.subject.keywordThienyl
dc.titleSynthesis characterization and evaluation of symmetrical and unsymmetrical chalcogenides of 2 3 thienyl and ferrocenyl carbaldehyde
dc.title.alternative
dc.type.degreePh.D.

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