A julolidine-fused anthracene derivative: synthesis, photophysical properties, and oxidative dimerization

We describe the synthesis and characterization of a julolidine-fused anthracene derivative J-A, which exhibits a maximum absorption of 450 nm and a maximum emission of 518 nm. The fluorescent quantum yield was determined to be 0.55 in toluene. J-A dimerizes in solution via oxidative coupling. Struct...

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Detalles Bibliográficos
Autores principales: Xia, Zeming, Guo, Xiaoyu, Zhu, Yanpeng, Wang, Yonggen, Wang, Jiaobing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Chemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9079783/
https://www.ncbi.nlm.nih.gov/pubmed/35542525
http://dx.doi.org/10.1039/c8ra02205d
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author Xia, Zeming
Guo, Xiaoyu
Zhu, Yanpeng
Wang, Yonggen
Wang, Jiaobing
author_facet Xia, Zeming
Guo, Xiaoyu
Zhu, Yanpeng
Wang, Yonggen
Wang, Jiaobing
author_sort Xia, Zeming
collection PubMed
description We describe the synthesis and characterization of a julolidine-fused anthracene derivative J-A, which exhibits a maximum absorption of 450 nm and a maximum emission of 518 nm. The fluorescent quantum yield was determined to be 0.55 in toluene. J-A dimerizes in solution via oxidative coupling. Structure of the dimer was characterized using single crystal X-ray diffraction.
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spelling pubmed-90797832022-05-09 A julolidine-fused anthracene derivative: synthesis, photophysical properties, and oxidative dimerization Xia, Zeming Guo, Xiaoyu Zhu, Yanpeng Wang, Yonggen Wang, Jiaobing RSC Adv Chemistry We describe the synthesis and characterization of a julolidine-fused anthracene derivative J-A, which exhibits a maximum absorption of 450 nm and a maximum emission of 518 nm. The fluorescent quantum yield was determined to be 0.55 in toluene. J-A dimerizes in solution via oxidative coupling. Structure of the dimer was characterized using single crystal X-ray diffraction. The Royal Society of Chemistry 2018-04-11 /pmc/articles/PMC9079783/ /pubmed/35542525 http://dx.doi.org/10.1039/c8ra02205d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Xia, Zeming
Guo, Xiaoyu
Zhu, Yanpeng
Wang, Yonggen
Wang, Jiaobing
A julolidine-fused anthracene derivative: synthesis, photophysical properties, and oxidative dimerization
title A julolidine-fused anthracene derivative: synthesis, photophysical properties, and oxidative dimerization
title_full A julolidine-fused anthracene derivative: synthesis, photophysical properties, and oxidative dimerization
title_fullStr A julolidine-fused anthracene derivative: synthesis, photophysical properties, and oxidative dimerization
title_full_unstemmed A julolidine-fused anthracene derivative: synthesis, photophysical properties, and oxidative dimerization
title_short A julolidine-fused anthracene derivative: synthesis, photophysical properties, and oxidative dimerization
title_sort julolidine-fused anthracene derivative: synthesis, photophysical properties, and oxidative dimerization
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9079783/
https://www.ncbi.nlm.nih.gov/pubmed/35542525
http://dx.doi.org/10.1039/c8ra02205d
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