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Synthesis and properties of novel type I photosensitizer polycyclic amide
Herein, we have designed and synthesized a novel type-I photosensitizer (PhPA) via Rh-catalyzed oxidative cyclization of diacetoxyterephthalamide with alkynes. The photoelectric properties, photosensitivity and photodegradation process of PhPA have been systematically investigated. The remarkable fl...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
RSC
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10334370/ https://www.ncbi.nlm.nih.gov/pubmed/37441256 http://dx.doi.org/10.1039/d3na00341h |
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author | Wang, Kui Ye, Tao Du, Haoyang Jin, Xiangyu Yi, Xiaofen Gao, Huiying Zhang, Yuan Dong, Wei Liu, Shihui Guan, Jing Lin, Feng Xia, Debin |
author_facet | Wang, Kui Ye, Tao Du, Haoyang Jin, Xiangyu Yi, Xiaofen Gao, Huiying Zhang, Yuan Dong, Wei Liu, Shihui Guan, Jing Lin, Feng Xia, Debin |
author_sort | Wang, Kui |
collection | PubMed |
description | Herein, we have designed and synthesized a novel type-I photosensitizer (PhPA) via Rh-catalyzed oxidative cyclization of diacetoxyterephthalamide with alkynes. The photoelectric properties, photosensitivity and photodegradation process of PhPA have been systematically investigated. The remarkable fluorescence quenching effect (Φ(PL) < 0.01) of PhPA suggests that the intersystem crossing from the singlet excited state to the reactive triplet state is enhanced by the enlarged conjugated backbone. Additionally, the ability of superoxide radical (O(2)(−)˙) generation was confirmed by electron paramagnetic resonance spectroscopy. Finally, the mechanism of PhPA photo-oxidative degradation via the structure of two metabolites is proposed. |
format | Online Article Text |
id | pubmed-10334370 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | RSC |
record_format | MEDLINE/PubMed |
spelling | pubmed-103343702023-07-12 Synthesis and properties of novel type I photosensitizer polycyclic amide Wang, Kui Ye, Tao Du, Haoyang Jin, Xiangyu Yi, Xiaofen Gao, Huiying Zhang, Yuan Dong, Wei Liu, Shihui Guan, Jing Lin, Feng Xia, Debin Nanoscale Adv Chemistry Herein, we have designed and synthesized a novel type-I photosensitizer (PhPA) via Rh-catalyzed oxidative cyclization of diacetoxyterephthalamide with alkynes. The photoelectric properties, photosensitivity and photodegradation process of PhPA have been systematically investigated. The remarkable fluorescence quenching effect (Φ(PL) < 0.01) of PhPA suggests that the intersystem crossing from the singlet excited state to the reactive triplet state is enhanced by the enlarged conjugated backbone. Additionally, the ability of superoxide radical (O(2)(−)˙) generation was confirmed by electron paramagnetic resonance spectroscopy. Finally, the mechanism of PhPA photo-oxidative degradation via the structure of two metabolites is proposed. RSC 2023-06-29 /pmc/articles/PMC10334370/ /pubmed/37441256 http://dx.doi.org/10.1039/d3na00341h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Wang, Kui Ye, Tao Du, Haoyang Jin, Xiangyu Yi, Xiaofen Gao, Huiying Zhang, Yuan Dong, Wei Liu, Shihui Guan, Jing Lin, Feng Xia, Debin Synthesis and properties of novel type I photosensitizer polycyclic amide |
title | Synthesis and properties of novel type I photosensitizer polycyclic amide |
title_full | Synthesis and properties of novel type I photosensitizer polycyclic amide |
title_fullStr | Synthesis and properties of novel type I photosensitizer polycyclic amide |
title_full_unstemmed | Synthesis and properties of novel type I photosensitizer polycyclic amide |
title_short | Synthesis and properties of novel type I photosensitizer polycyclic amide |
title_sort | synthesis and properties of novel type i photosensitizer polycyclic amide |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10334370/ https://www.ncbi.nlm.nih.gov/pubmed/37441256 http://dx.doi.org/10.1039/d3na00341h |
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