Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1338
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dc.contributor.authorREDDY, J. SREEDHARen_US
dc.contributor.authorANAND, V. G.en_US
dc.date.accessioned2018-11-14T09:11:48Z
dc.date.available2018-11-14T09:11:48Z
dc.date.issued2008-02en_US
dc.identifier.citationJournal of the American Chemical Society, 130(12)en_US
dc.identifier.issn0002-7863en_US
dc.identifier.issn1520-5126en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/1338-
dc.identifier.urihttps://doi.org/10.1021/ja710664yen_US
dc.description.abstractIsophlorins and its analogues bridge the structural features between porphyrins and annulenes. Invariably they are known to be unstable but can be stabilized by appropriate substituents in the core and periphery of a macrocycle. Solid-state characterization of these 20π systems displays planarity for each macrocycle and even in their supramolecular arrangement due to C−H···F−C interactions.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectCore Modified Isophlorinsen_US
dc.subjectPorphyrinsen_US
dc.subject2008en_US
dc.titlePlanar Meso Pentafluorophenyl Core Modified Isophlorinsen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleJournal of the American Chemical Societyen_US
dc.publication.originofpublisherForeignen_US
Appears in Collections:JOURNAL ARTICLES

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