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Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3183
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dc.contributor.authorREDDY, BADDIGAM KIRANen_US
dc.contributor.authorRawson, Jeffen_US
dc.contributor.authorGADEKAR, SANTOSH C.en_US
dc.contributor.authorKgerler, Paulen_US
dc.contributor.authorANAND, V. G.en_US
dc.date.accessioned2019-07-01T05:32:45Z
dc.date.available2019-07-01T05:32:45Z
dc.date.issued2017-06en_US
dc.identifier.citationChemical Communications, 53(58), 8211-8214.en_US
dc.identifier.issn1359-7345en_US
dc.identifier.issn1364-548Xen_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/3183-
dc.identifier.urihttps://doi.org/10.1039/C7CC04050Den_US
dc.description.abstractWe report the first synthesis of a covalent expanded isophlorin dimer from two 24-π doubly S-confused sapphyrin-like pentathiaisophlorins. It exhibits marginal peripheral aromaticity rather than strong global diatropicity or paratropicity and weak intermacrocycle electronic communication. Quantum chemical methods discern that cross-conjugation is responsible for these unusual electronic features.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectNaphthalene-fused dimeren_US
dc.subjectIsophlorinen_US
dc.subjectAromatic macrocyclesen_US
dc.subjectTwo-electron oxidationen_US
dc.subjectNMR spectroscopicen_US
dc.subjectCovalent dimer can existen_US
dc.subject2017en_US
dc.titleA naphthalene-fused dimer of an anti-aromatic expanded isophlorinen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleChemical Communicationsen_US
dc.publication.originofpublisherForeignen_US
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