Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9310
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dc.contributor.authorMisra, Rajneeshen_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-21T11:32:14Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-21T11:32:14Z-
dc.date.issued2015-
dc.identifier.citationMisra, R., & Gautam, P. (2015). Meso-tetrakis(ferrocenylethynylphenyl) porphyrins: Synthesis and properties. Journal of Organometallic Chemistry, 776, 83-88. doi:10.1016/j.jorganchem.2014.11.006en_US
dc.identifier.issn0022-328X-
dc.identifier.otherEID(2-s2.0-84949116838)-
dc.identifier.urihttps://doi.org/10.1016/j.jorganchem.2014.11.006-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/9310-
dc.description.abstractWe report the synthesis of meso-tetrakis(ferrocenylethynylphenyl) porphyrins P1, P2 and the zinc derivative ZnP2. The photophysical and electrochemical properties of these porphyrins show substantial donor-acceptor interaction. The computational studies reveal that the para-linkage of the ferrocenyl unit in porphyrin P1 provides better π-conjugation compared to meta-linkage in porphyrin P2, which results in low HOMO-LUMO gap and red shifted absorption. The porphyrin P2 and ZnP2 show better thermal stability compared to the porphyrin P1. ©2014 Elsevier B.V. All rights reserved.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.sourceJournal of Organometallic Chemistryen_US
dc.subjectOrganometallicsen_US
dc.subjectComputational studiesen_US
dc.subjectDonor-acceptor interactionen_US
dc.subjectDonor-acceptorsen_US
dc.subjectElectrochemicalen_US
dc.subjectFerrocenesen_US
dc.subjectHOMO-LUMO gapsen_US
dc.subjectPara-linkageen_US
dc.subjectPhotophysicalen_US
dc.subjectPorphyrinsen_US
dc.titleMeso-tetrakis(ferrocenylethynylphenyl) porphyrins: Synthesis and propertiesen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Chemistry

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