Please use this identifier to cite or link to this item:
http://localhost:8080/xmlui/handle/123456789/1372
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Anju, K S | - |
dc.contributor.author | Ramakrishnan, S | - |
dc.contributor.author | Ajesh P Thomas | - |
dc.contributor.author | Suresh, E | - |
dc.contributor.author | Srinivasan, A | - |
dc.date.accessioned | 2014-04-28T11:05:01Z | - |
dc.date.available | 2014-04-28T11:05:01Z | - |
dc.date.issued | 2008 | - |
dc.identifier.citation | Organic Letters 10(24):5545-5548;18 Dec 2008 | en_US |
dc.identifier.issn | 1523-7060 | - |
dc.identifier.uri | http://ir.niist.res.in:8080/jspui/handle/123456789/1372 | - |
dc.description.abstract | meso-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.iso | en | en_US |
dc.publisher | American Chemical Society | en_US |
dc.subject | Photodynamic therapy | en_US |
dc.subject | Porphycene | en_US |
dc.subject | Metalloporphycenes | en_US |
dc.subject | Porphyrins | en_US |
dc.subject | Tetraphenylporphycene | en_US |
dc.title | 9,10,19,20-Tetraarylporphycenes | en_US |
dc.type | Article | en_US |
Appears in Collections: | 2008 |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
2008_0027.pdf Restricted Access | 434.11 kB | Adobe PDF | View/Open Request a copy |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.