Fluorination of naphthalimide–cyanostilbene derivatives to achieve dual-state emission luminogens with strong fluorescence in highly polar environments for bioimaging-Reference-Cited by-同舟云学术

Fluorination of naphthalimide–cyanostilbene derivatives to achieve dual-state emission luminogens with strong fluorescence in highly polar environments for bioimaging

Published:2023 Issue:29 Volume:11 Page:6859-6867
ISSN:2050-750X
Container-title:Journal of Materials Chemistry B
language:en
Short-container-title:J. Mater. Chem. B

Author:

Shi Qiusi¹,Ni Yingyong¹,Yang Longmei¹,Kong Lin¹^ORCID,Gu Peiyang²^ORCID,Wang Chengyuan¹^ORCID,Zhang Qichun³^ORCID,Zhou Hongping¹^ORCID,Yang Jiaxiang¹^ORCID

Affiliation:

1. School of Chemistry and Chemical Engineering, Anhui Province Key Laboratory of Chemistry for Inorganic/Organic Hybrid Functionalized Materials, Key Laboratory of Structure and Functional Regulation of Hybrid Materials of Ministry of Education, Anhui University, 111 Jiulong Road, Hefei, 230601, China

2. Jiangsu Key Laboratory of Advanced Catalytic Materials & Technology, School of Petrochemical Engineering, Changzhou University, Changzhou, 213164, China

3. Department of Materials Science and Engineering, Department of Chemistry & Center of Super-Diamond and Advanced Films (COSDAF), City University of Hong Kong, Kowloon, Hong Kong SAR, China

Abstract

Fluorination of naphthalimide–cyanostilbene derivatives to achieve dual-state emission luminogens with good environmental stability of fluorescence in solution and two-photon absorption (2PA) properties for cell-imaging with lipid droplet targeting.

Funder

National Natural Science Foundation of China

City University of Hong Kong

State Key Laboratory of Supramolecular Structure and Materials

Jilin University

Publisher

Royal Society of Chemistry (RSC)

Subject

General Materials Science,Biomedical Engineering,General Chemistry,General Medicine

Link

http://pubs.rsc.org/en/content/articlepdf/2023/TB/D3TB01034A

Reference44 articles.