Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/2053
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dc.contributor.authorReddy, J S-
dc.contributor.authorAnand, V G-
dc.date.accessioned2015-09-15T03:02:38Z-
dc.date.available2015-09-15T03:02:38Z-
dc.date.issued2008-
dc.identifier.citationJournal of the American Chemical Society 130(12):3718-3719;26 Mar 2008en_US
dc.identifier.issn0002-7863-
dc.identifier.urihttp://ir.niist.res.in:8080/jspui/handle/123456789/2053-
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 20 pi systems displays planarity for each macrocycle and even in their supramolecular arrangement due to C-H center dot center dot F-C interactions.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectPorphyrinsen_US
dc.titlePlanar meso pentafluorophenyl core modified isophlorinsen_US
dc.typeArticleen_US
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