Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/16930
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dc.contributor.advisorMisra, Rajneesh-
dc.contributor.authorKumar, Abhishek-
dc.date.accessioned2025-10-22T15:20:42Z-
dc.date.available2025-10-22T15:20:42Z-
dc.date.issued2025-05-19-
dc.identifier.urihttps://dspace.iiti.ac.in:8080/jspui/handle/123456789/16930-
dc.description.abstractEthynyl bridged ferrocenyl functionalized BODIPY 1 was synthesized via Sonogashira cross-coupling reaction. Tetracyanobutadiene (TCBD) and cyclohexa-2,5-diene-1,4-diylidene-expanded TCBD (DCNQ) incorporated ferrocenyl BODIPYs 2 and 3 were synthesized using [2 + 2] cycloaddition -retroelectrocyclization (CA-RE) reaction, in good yields. BODIPYs 2 and 3 were obtained by reacting BODIPY 1 with strong electron acceptors tetracyanoethylene (TCNE) and tetracyanoquinodimethane (TCNQ) respectively. The electronic absorption spectra and theoretical calculations have been performed using the UV-visible spectrophotometer and density functional theory at B3LYP/6-31+G** level of theory.en_US
dc.language.isoenen_US
dc.publisherDepartment of Chemistry, IIT Indoreen_US
dc.relation.ispartofseriesMS520;-
dc.subjectChemistryen_US
dc.titleDesign and synthesis of β-pyrrole functionalized ferrocenyl BODIPYsen_US
dc.typeThesis_M.Scen_US
Appears in Collections:Department of Chemistry_ETD

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