Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/8230
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dc.contributor.authorMISHRA, VISHNUen_US
dc.contributor.authorUDAYA, HOSAHALLI S.en_US
dc.contributor.authorANAND, V. G.en_US
dc.date.accessioned2023-10-20T10:23:40Z
dc.date.available2023-10-20T10:23:40Z
dc.date.issued2023-10en_US
dc.identifier.citationOrganic & Biomolecular Chemistry, 21(38), 7691-7695.en_US
dc.identifier.issn1477-0520en_US
dc.identifier.issn1477-0539en_US
dc.identifier.urihttps://doi.org/10.1039/D3OB01270Ken_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/8230
dc.description.abstractMaximum confusion in porphyrinoids can be achieved by inter-linking heterocycles only through 2,4-connectivity. 20π confused porphycene and 30π expanded porphycene represent examples with the highest number of confused heterocyclic units in a given macrocycle. They significantly differ from the parent 20π porphycene and 30π hexaphyrin in their structural, electronic and redox properties due to the cross conjugation arising from the 2,4-connectivity of the heterocycle. They have been characterized by single crystal X-ray diffraction studies and their aromatic features have been substantiated by quantum chemical calculations.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectISOMERen_US
dc.subject2023-OCT-WEEK1en_US
dc.subjectTOC-OCT-2023en_US
dc.subject2023en_US
dc.titleTetra S-confused porphyrinoidsen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleOrganic & Biomolecular Chemistryen_US
dc.publication.originofpublisherForeignen_US
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