Organosulfur and Organoselenium Functionalized Benzimidazo[1,2-a]quinolines: From Experimental and Theoretical Photophysics to All-Solution-Processed OLEDs-Reference-Cited by-同舟云学术

Organosulfur and Organoselenium Functionalized Benzimidazo[1,2-a]quinolines: From Experimental and Theoretical Photophysics to All-Solution-Processed OLEDs

Published:2023-08-05 Issue: Volume: Page:
ISSN:1053-0509
Container-title:Journal of Fluorescence
language:en
Short-container-title:J Fluoresc

Author:

da Silva Rodrigo Borges,Coelho Felipe Lange,de Castro Silva Junior Henrique,Germino José Carlos,Atvars Teresa Dib Zambon,Rodembusch Fabiano Severo,Duarte Luís Gustavo Teixeira Alves,Schneider Paulo Henrique

Publisher

Springer Science and Business Media LLC

Subject

Law,Clinical Biochemistry,Spectroscopy,Sociology and Political Science,Social Sciences (miscellaneous),Clinical Psychology,Biochemistry

Link

https://link.springer.com/content/pdf/10.1007/s10895-023-03358-1.pdf

Reference51 articles.

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2. Perin N, Martin-Kleiner I, Nhili R, Laine W, David-Cordonnier MH, Vugrek O, Karminski-Zamola G, Kralj M, Hranjec M (2013) Biological activity and DNA binding studies of 2-substituted benzimidazo[1,2-a]quinolines bearing different amino side chains. MedChemComm 4:1537–1550

3. Perin N, Alić J, Liekens S, Van Aerschot A, Vervaeke P, Gadakh B, Hranjec M (2018) Different positions of amide side chains on the benzimidazo[1,2-a]quinoline skeleton strongly influence biological activity. New J Chem 42:7096–7104

4. Wang YN, Bheemanaboina RRY, Gao WW, Kang J, Cai GX, Zhou CH (2018) Discovery of benzimidazole-quinoline hybrids as new cleaving agents toward drug-resistant pseudomonas aeruginosa DNA. ChemMedChem 13:1004–1017

5. Nandwana NK, Singh RP, Patel OPS, Dhiman S, Saini HK, Jha PN, Kumar A (2018) Design and synthesis of imidazo/benzimidazo[1,2-c]quinazoline derivatives and evaluation of their antimicrobial activity. ACS Omega 3:16338–16346

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