Srinivasan, Alagar ; Reddy, VenkatRam M. ; Jeyaprakash Narayanan, S. ; Sridevi, Bashyam ; Pushpan, Simi K. ; Ravikumar, Murugaeson ; Chandrashekar, Tavarekere K. (1997) Tetrathia- and tetraoxarubyrins: aromatic, core-modified, expanded porphyrins Angewandte Chemie International Edition, 36 (23). pp. 2598-2601. ISSN 1433-7851
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Official URL: http://onlinelibrary.wiley.com/doi/10.1002/anie.19...
Related URL: http://dx.doi.org/10.1002/anie.199725981
Abstract
The remarkably simple synthesis of tetrathia- and tetraoxarubyrins 1 and 2 is achieved by the routes presented here. Spectroscopic, 1H NMR, and electrochemical data suggest that 1, 2, and their protonated derivatives are aromatic 26 π electron systems, and the protonated derivatives form stable complexes in solution with anions such as F-, N3-, and adenosine 5'-monophosphate.
| Item Type: | Article |
|---|---|
| Source: | Copyright of this article belongs to John Wiley and Sons, Inc. |
| Keywords: | Bithiophenes; Porphyrinoids; Rubyrin; Sensitizers |
| ID Code: | 5328 |
| Deposited On: | 18 Oct 2010 08:43 |
| Last Modified: | 27 May 2011 11:47 |
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