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Synthesis and Photophysical Properties of Tetra- and Octasubstituted Phosphorous Oxide Triazatetrabenzcorrole Photosensitizers
The synthesis of phosphorous oxide triazatetrabenzcorroles (TBC) tetra- (9, 11) or octa- (13) substituted on the ring with halogenated functional groups is reported. The complexes are not aggregated in dimethylsulfoxide (DMSO) and show solubility in solvents such as pyridine. The Q band absorption s...
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Formato: | Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2266970/ https://www.ncbi.nlm.nih.gov/pubmed/18354726 http://dx.doi.org/10.1155/2008/498916 |
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author | Antunes, Edith M. Nyokong, Tebello |
author_facet | Antunes, Edith M. Nyokong, Tebello |
author_sort | Antunes, Edith M. |
collection | PubMed |
description | The synthesis of phosphorous oxide triazatetrabenzcorroles (TBC) tetra- (9, 11) or octa- (13) substituted on the ring with halogenated functional groups is reported. The complexes are not aggregated in dimethylsulfoxide (DMSO) and show solubility in solvents such as pyridine. The Q band absorption spectra of the complexes are red-shifted compared to unsubstituted PTBC. The latter complex shows a large triplet lifetime (1.7 milliseconds), higher than for MPc derivatives. The chlorinated derivatives show good triplet yields (Φ(T)∼ 0.46 and 0.36) and relatively long lifetimes (256 and 452 microseconds), respectively, for 11 and 13. |
format | Text |
id | pubmed-2266970 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-22669702008-03-19 Synthesis and Photophysical Properties of Tetra- and Octasubstituted Phosphorous Oxide Triazatetrabenzcorrole Photosensitizers Antunes, Edith M. Nyokong, Tebello Met Based Drugs Research Article The synthesis of phosphorous oxide triazatetrabenzcorroles (TBC) tetra- (9, 11) or octa- (13) substituted on the ring with halogenated functional groups is reported. The complexes are not aggregated in dimethylsulfoxide (DMSO) and show solubility in solvents such as pyridine. The Q band absorption spectra of the complexes are red-shifted compared to unsubstituted PTBC. The latter complex shows a large triplet lifetime (1.7 milliseconds), higher than for MPc derivatives. The chlorinated derivatives show good triplet yields (Φ(T)∼ 0.46 and 0.36) and relatively long lifetimes (256 and 452 microseconds), respectively, for 11 and 13. Hindawi Publishing Corporation 2008 2008-03-03 /pmc/articles/PMC2266970/ /pubmed/18354726 http://dx.doi.org/10.1155/2008/498916 Text en Copyright © 2008 E. M. Antunes and T. Nyokong. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Antunes, Edith M. Nyokong, Tebello Synthesis and Photophysical Properties of Tetra- and Octasubstituted Phosphorous Oxide Triazatetrabenzcorrole Photosensitizers |
title | Synthesis and Photophysical Properties of Tetra- and Octasubstituted Phosphorous Oxide Triazatetrabenzcorrole Photosensitizers |
title_full | Synthesis and Photophysical Properties of Tetra- and Octasubstituted Phosphorous Oxide Triazatetrabenzcorrole Photosensitizers |
title_fullStr | Synthesis and Photophysical Properties of Tetra- and Octasubstituted Phosphorous Oxide Triazatetrabenzcorrole Photosensitizers |
title_full_unstemmed | Synthesis and Photophysical Properties of Tetra- and Octasubstituted Phosphorous Oxide Triazatetrabenzcorrole Photosensitizers |
title_short | Synthesis and Photophysical Properties of Tetra- and Octasubstituted Phosphorous Oxide Triazatetrabenzcorrole Photosensitizers |
title_sort | synthesis and photophysical properties of tetra- and octasubstituted phosphorous oxide triazatetrabenzcorrole photosensitizers |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2266970/ https://www.ncbi.nlm.nih.gov/pubmed/18354726 http://dx.doi.org/10.1155/2008/498916 |
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