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Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9457
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dc.contributor.authorMobin, Shaikh M.en_US
dc.contributor.authorMisra, Rajneeshen_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-21T11:33:13Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-21T11:33:13Z-
dc.date.issued2012-
dc.identifier.citationGautam, P., Dhokale, B., Mobin, S. M., & Misra, R. (2012). Ferrocenyl BODIPYs: Synthesis, structure and properties. RSC Advances, 2(32), 12105-12107. doi:10.1039/c2ra21964fen_US
dc.identifier.issn2046-2069-
dc.identifier.otherEID(2-s2.0-84871058917)-
dc.identifier.urihttps://doi.org/10.1039/c2ra21964f-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/9457-
dc.description.abstractA set of donor-π-acceptor-π-donor type ferrocenyl substituted BODIPYs were designed and synthesized by the Sonogashira coupling reaction. These compounds exhibit red shifted absorption and poor fluorescence. The electrochemical properties of these compounds exhibit strong donor-acceptor interactions. The crystal structure of 3b exhibits an extensive hydrogen bonded 2-D network. © 2012 The Royal Society of Chemistry.en_US
dc.language.isoenen_US
dc.sourceRSC Advancesen_US
dc.subjectDonor-acceptor interactionen_US
dc.subjectFerrocenylen_US
dc.subjectRed-shifteden_US
dc.subjectSonogashira coupling reactionsen_US
dc.subjectStructure and propertiesen_US
dc.subjectHydrogen bondsen_US
dc.subjectChemical reactionsen_US
dc.titleFerrocenyl BODIPYs: Synthesis, structure and propertiesen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Chemistry

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