Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/9459
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dc.contributor.authorSHUKLA, PRAGATIen_US
dc.contributor.authorAMBHORE, MADAN D.en_US
dc.contributor.authorANAND, V. G.en_US
dc.date.accessioned2025-04-15T06:43:30Z-
dc.date.available2025-04-15T06:43:30Z-
dc.date.issued2024-04en_US
dc.identifier.citationChemical Science, 15(16), 6022-6027.en_US
dc.identifier.issn2041-6520en_US
dc.identifier.issn2041-6539en_US
dc.identifier.urihttps://doi.org/10.1039/D3SC05251Fen_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/9459-
dc.description.abstractPlanar 44π and 46π core-modified decaphyrins with ten thiophene units have been synthesized from short thiophene oligomers. They have been structurally characterized by single crystal X-ray diffraction with further support from spectroscopic analysis and quantum chemical calculations. Our analysis revealed diradicaloid characteristics for 46π species in contrast to the closed shell property of the 44π congener. Further, 44π and 46π undergo reversible two-electron chemical oxidation, as observed by spectro-electrochemical measurements.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectExpanded Porphyrinen_US
dc.subject2024en_US
dc.titleOpen shell (4n + 2)π and closed shell 4nπ planar core-modified decaphyrinsen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleChemical Scienceen_US
dc.publication.originofpublisherForeignen_US
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