Please use this identifier to cite or link to this item:
http://idr.niser.ac.in:8080/jspui/handle/123456789/1072Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Thomas, Ajesh P. | - |
| dc.contributor.author | Adinarayana, B. | - |
| dc.contributor.author | Srinivasan, A. | - |
| dc.date.accessioned | 2024-12-02T12:07:47Z | - |
| dc.date.available | 2024-12-02T12:07:47Z | - |
| dc.date.issued | 2013-07-11 | - |
| dc.identifier.citation | Thomas, A. P., Sreedevi, K. C. G., Adinarayana, B., Ramakrishnan, S., & Srinivasan, A. (2013). meso-Tetrakis(3,5-dihydroxyphenyl)N-confused porphyrin: influence of polar protic and aprotic solvents in tautomeric existence, exchange and morphology. RSC Advances, 3(38), 16967. | en_US |
| dc.identifier.uri | https://doi.org/10.1039/C3RA42289E | - |
| dc.identifier.uri | http://idr.niser.ac.in:8080/jspui/handle/123456789/1072 | - |
| dc.description.abstract | A hitherto unknown meso-tetrakis(3,5-dihydroxyphenyl)N-confused porphyrin (NCPH) was synthesized and characterized. The typical 3H and 2H tautomeric existence of the N-confused derivative was controlled exclusively by protic and aprotic solvents rather than the established polar and non-polar driving forces. An unprecedented morphological change controlled by two tautomeric forms of NCPH during aggregation was investigated. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | RSC Advances | en_US |
| dc.title | meso-Tetrakis(3,5-dihydroxyphenyl)N-confused porphyrin: influence of polar protic and aprotic solvents in tautomeric existence, exchange and morphology | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | Journal Papers | |
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.