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Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9442
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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.accessioned2022-03-21T11:33:07Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-21T11:33:07Z-
dc.date.issued2013-
dc.identifier.citationSharma, R., Gautam, P., Mobin, S. M., & Misra, R. (2013). β-Substituted ferrocenyl porphyrins: Synthesis, structure, and properties. Dalton Transactions, 42(15), 5539-5545. doi:10.1039/c3dt00003fen_US
dc.identifier.issn1477-9226-
dc.identifier.otherEID(2-s2.0-84875410708)-
dc.identifier.urihttps://doi.org/10.1039/c3dt00003f-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/9442-
dc.description.abstractβ-Substituted ferrocenyl porphyrins were designed and synthesized by the Pd-catalyzed Sonogashira cross-coupling reaction. The UV-vis absorption, emission, and cyclic voltammetric results indicate strong electronic communication between ferrocene and porphyrin. The porphyrin 4a is non-emissive in nature, while 4b and 4c show reduced fluorescence quantum yield. The single crystal X-ray structure of 4b is reported, which shows extensive C-H-π interactions. © 2013 The Royal Society of Chemistry.en_US
dc.language.isoenen_US
dc.sourceDalton Transactionsen_US
dc.subjectCyclic voltammetricen_US
dc.subjectElectronic communicationsen_US
dc.subjectFerrocenesen_US
dc.subjectFerrocenylen_US
dc.subjectFluorescence quantum yielden_US
dc.subjectSingle crystal x-ray structuresen_US
dc.subjectSonogashira cross-coupling reactionen_US
dc.subjectUV-vis absorptionsen_US
dc.subjectOrganometallicsen_US
dc.subjectPorphyrinsen_US
dc.titleβ-Substituted ferrocenyl porphyrins: Synthesis, structure, and propertiesen_US
dc.typeJournal Articleen_US
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