Photoacidity of the N -salicylidene-5-chloroaminopyridine-Reference-Cited by-同舟云学术

Photoacidity of the N -salicylidene-5-chloroaminopyridine

Published:2017-04 Issue: Volume:184 Page:268-272
ISSN:0022-2313
Container-title:Journal of Luminescence
language:en
Short-container-title:Journal of Luminescence

Author:

Barboza Cristina Aparecida,Germino José Carlos,Duarte Luís Gustavo Teixeira Alves,Quites Fernando Junior,Vazquez Pedro Antônio Muniz,Atvars Teresa Dib Zambon

Funder

FAPESP

National Institute of Organic Electronics

CNPq

GRID/UNESP

CENAPAD/SP

Publisher

Elsevier BV

Subject

Condensed Matter Physics,Biochemistry,General Chemistry,Atomic and Molecular Physics, and Optics,Biophysics

Reference54 articles.

1. Tautomerization and solvent effects on the absorption and emission properties of the Schiff base N,N′-bis(salicylidene)-p-phenylenediamine – a TDDFT study;Santhanamoorthi;Mol. Phys.,2010

2. Excited state intramolecular charge transfer suppressed proton transfer process in 4-(Diethylamino)-2-hydroxy-benzaldehyde;Jana;J. Phys. Chem. A,2013

3. Intramolecular proton transfer in 2-(2’-hydroxyphenyl)oxazolo[4,5-b]pyridine: evidence for Tautomer in the ground state;Chipem;Photochem. Photobiol.,2015

4. IR spectroscopy and ab initio calculations on ESIPT in 3-hydroxyfalvone solvated in acetonitrile;Chevalier;Phys. Chem. Chem. Phys.,2012

5. From ultrafast events to equilibrium – uncovering the unusual dynamics of ESIPT reaction: the case of dually fluorescent diethyl-2,5-(dibenzoxazolyl)-hydroquinone;Wnuk;Phys. Chem. Chem. Phys.,2014

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Substituent effect induced the distinctive ESIPT reaction and photophysical property of N-salycilidene-5-chloroaminopyridine;Journal of Molecular Structure;2022-02

2. Near Attack Conformation as Strategy for ESIPT Modulation for White-Light Generation;The Journal of Physical Chemistry C;2020-09-21

3. Photoacidity as a tool to rationalize excited state intramolecular proton transfer reactivity in flavonols;Photochemical & Photobiological Sciences;2018