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dc.contributor.authorAnju, K S-
dc.contributor.authorRamakrishnan, S-
dc.contributor.authorAjesh P Thomas-
dc.contributor.authorSuresh, E-
dc.contributor.authorSrinivasan, A-
dc.date.accessioned2014-04-28T11:05:01Z-
dc.date.available2014-04-28T11:05:01Z-
dc.date.issued2008-
dc.identifier.citationOrganic Letters 10(24):5545-5548;18 Dec 2008en_US
dc.identifier.issn1523-7060-
dc.identifier.urihttp://ir.niist.res.in:8080/jspui/handle/123456789/1372-
dc.description.abstractmeso-Tetraarylporphycenes, structural isomers of meso-tetraarylporphyrins, were synthesized by the acid-catalyzed oxidative coupling reaction for the first time which is an alternative synthetic methodology to the traditional McMurry coupling reaction. The structure of the macrocycle and Ni(II) complex are characterized by single-crystal X-ray diffraction analyses where both form 1-D supramolecular assembly.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectPhotodynamic therapyen_US
dc.subjectPorphyceneen_US
dc.subjectMetalloporphycenesen_US
dc.subjectPorphyrinsen_US
dc.subjectTetraphenylporphyceneen_US
dc.title9,10,19,20-Tetraarylporphycenesen_US
dc.typeArticleen_US
Appears in Collections:2008

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