pi-Extended Coumarins Derived with Nonhydrolyzable Iminophosphoranes as Two-Photon-Excited Fluorophores

Liang-Yu Hsia, Hsin-Ni Chen, Chun-Hao Chiang, Ming-Yang Hung, Hao-Keng Wei, Chih-Wei Luo, Ming-Yu Kuo, Shun-Yuan Luo*, Chih-Chien Chu*

*此作品的通信作者

研究成果: Article同行評審

7 引文 斯高帕斯(Scopus)

摘要

Novel coumarin-iminophosphorane (IPP) fluorophores that have stable resonance contributions from aza-ylides were formed by using the nonhydrolysis Staudinger reaction. The N=P formation reaction kinetics obey the conventional Staudinger reaction. The absorption and emission profiles of the coumarin-IPP derivatives can be fine-tuned: an electron-donating group at PPh3 enhances absorption and fluorescence, whereas an electron-withdrawing group at C-3 drives absorption and emission peaks toward blue-light wavelengths. Two-photon adsorption, accompanied by anti-Stokes fluorescence, is achieved under near-infrared femtosecond laser excitation.

原文English
頁(從 - 到)9361-9366
頁數6
期刊Journal of Organic Chemistry
85
發行號14
DOIs
出版狀態Published - 17 7月 2020

指紋

深入研究「pi-Extended Coumarins Derived with Nonhydrolyzable Iminophosphoranes as Two-Photon-Excited Fluorophores」主題。共同形成了獨特的指紋。

引用此