Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9437
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dc.contributor.authorMargani, Rameshen_US
dc.contributor.authorMobin, Shaikh M.en_US
dc.contributor.authorMisra, Rajneeshen_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-21T11:33:03Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-21T11:33:03Z-
dc.date.issued2013-
dc.identifier.citationSharma, R., Margani, R., Mobin, S. M., & Misra, R. (2013). Ferrocenyl substituted calixarenes: Synthesis, structure and properties. RSC Advances, 3(17), 5785-5788. doi:10.1039/c3ra00146fen_US
dc.identifier.issn2046-2069-
dc.identifier.otherEID(2-s2.0-84875774325)-
dc.identifier.urihttps://doi.org/10.1039/c3ra00146f-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/9437-
dc.description.abstractA set of ferrocenyl substituted calix[4]arenes were designed and synthesized by the Pd-catalyzed Sonogashira cross coupling reaction. The photophysical and electrochemical data show a substantial electronic interaction between the ferrocene unit and the calixarene core. Calixarenes 5a-5c are non-emissive in nature and the absorption maxima of 5a-5c exhibit a red shifted absorption. The calixarene core exhibits a cone conformation, which was confirmed by 1H NMR and X-ray crystallography. The crystal packing of 5a exhibits a C-H-π bonded 2-D network. © 2013 The Royal Society of Chemistry.en_US
dc.language.isoenen_US
dc.sourceRSC Advancesen_US
dc.subjectAbsorption maximaen_US
dc.subjectCone conformationsen_US
dc.subjectCrystal packingsen_US
dc.subjectElectrochemical dataen_US
dc.subjectElectronic interactionsen_US
dc.subjectFerrocene unitsen_US
dc.subjectSonogashira cross-coupling reactionen_US
dc.subjectStructure and propertiesen_US
dc.subjectOrganometallicsen_US
dc.subjectX ray crystallographyen_US
dc.subjectPhenolsen_US
dc.titleFerrocenyl substituted calixarenes: Synthesis, structure and propertiesen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Chemistry

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