Effects of different substituents of methyl 5-R-salicylates on the excited state intramolecular proton transfer process-Reference-Cited by-同舟云学术

Effects of different substituents of methyl 5-R-salicylates on the excited state intramolecular proton transfer process

Published:2018 Issue:6 Volume:20 Page:4208-4215
ISSN:1463-9076
Container-title:Physical Chemistry Chemical Physics
language:en
Short-container-title:Phys. Chem. Chem. Phys.

Author:

Li Yongqing¹²³⁴⁵^ORCID,Ma Yanzhen¹²³,Yang Yunfan¹²³,Shi Wei¹²³,Lan Ruifang¹²³,Guo Qiang¹²³⁴⁵

Affiliation:

1. Department of Physics, Liaoning University

2. Shenyang 110036

3. China

4. Lvyuan Institute of Energy & Environmental Science and Technology, Liaoning University

5. Shenyang

Abstract

The proton transfer reaction in methyl 5-R-salicylate is found to be highly sensitive to the presence of specific substituents in resonance with the hydroxyl group, leading to different fluorescence behaviors of methyl 5-R-salicylate with different substituents.

Funder

Natural Science Foundation of Liaoning Province

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Physical and Theoretical Chemistry,General Physics and Astronomy

Link

http://pubs.rsc.org/en/content/articlepdf/2018/CP/C7CP06987A

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1. Tailoring the Excited-State Intramolecular Proton Transfer (ESIPT) Fluorescence of 2-(2'-Hydroxyphenyl)benzoxazole Derivatives

2. Excited state intramolecular proton transfer in 2-acetylindan-1,3-dione