Isomerization effect of triphenylamine-acridine derivatives on excited-state modification, photophysical property and electroluminescence performance-Reference-Cited by-同舟云学术

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Isomerization effect of triphenylamine-acridine derivatives on excited-state modification, photophysical property and electroluminescence performance

Published:2017-11 Issue: Volume:146 Page:558-566
ISSN:0143-7208
Container-title:Dyes and Pigments
language:en
Short-container-title:Dyes and Pigments

Author:

Zhou Changjiang,Zhang Tingke,Zhang Shitong,Liu Haichao,Gao Yu,Su Qing,Wu Qiaolin,Li Weijun,Chen Jiangshan,Yang Bing

Funder

National Natural Science Foundation of China

National Key Basic Research and Development Program of China

Open Project Foundation of the State Key Laboratory of Luminescence and Applications

Postdoctoral Innovation Talent Support Project

Publisher

Elsevier BV

Subject

Process Chemistry and Technology,General Chemical Engineering

Reference42 articles.

1. Acridine: a versatile heterocyclic nucleus;Kumar;Acta Pol Pharm,2012

2. Structure-activity relationships for the antileishmanial and antitrypanosomal activities of 1′-substituted 9-anilinoacridines;Gamage;J Med Chem,1997

3. Synthesis of 9-acridinyl sulfur derivatives: sulfides, sulfoxides and sulfones. Comparison of their activity on tumour cells;Santelli-Rouvier;Eur J Med Chem,2004

4. Synthesis and antileishmanial activity of 6-mono-substituted and 3,6-di-substituted acridines obtained by acylation of proflavine;Di Giorgio;Eur J Med Chem,2007

5. Optical thin film polymeric sensors for the determination of aqueous chloride, bromide and iodide ions at high pH, based on the quenching of fluorescence of two acridinium dyes;Geddes;Dyes Pigments,2000

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