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dc.contributor.authorGowri Sreedevi, K C-
dc.contributor.authorAjesh P Thomas-
dc.contributor.authorRamakrishnan, S-
dc.contributor.authorSalini, P S-
dc.contributor.authorDerry Holaday, M G-
dc.contributor.authorReddy, M L P-
dc.contributor.authorSrinivasan, A-
dc.date.accessioned2013-06-13T08:25:15Z-
dc.date.available2013-06-13T08:25:15Z-
dc.date.issued2012-
dc.identifier.citationOrganic and Biomolecular Chemistry 10(18):3600-3605;2012en_US
dc.identifier.urihttp://hdl.handle.net/123456789/444-
dc.description.abstractSynthesis, spectral and structural characterization of a pyrroloindolizine derivative having structural similarity with calix[2]pyrrole is described. Here, two pyrrole rings are connected with two meso-carbon atoms having an N,α-linkage and an α,β-linkage to afford the smallest analogue in the calixpyrrole family. Detailed NMR spectroscopic studies along with single crystal X-ray analysis confirm the assigned structure of the moleculeen_US
dc.language.isoenen_US
dc.publisherRSC Publishingen_US
dc.subjectPorphyrinoidsen_US
dc.subjectCalix[2]pyrroleen_US
dc.subjectNMR spectroscopic studiesen_US
dc.subjectAnion Bindingen_US
dc.subjectBinuclear Subphthalocyanineen_US
dc.subjectCalixpyrroIesen_US
dc.subjectBoronen_US
dc.subjectIsomersen_US
dc.subjectCrystalen_US
dc.title4,4,9,9-Tetraphenyl pyrroloindolizine: a structural analogue of calix[2] pyrroleen_US
dc.typeArticleen_US
Appears in Collections:2012

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