Cited by 67Molecular Sensors and Ion DetectionSulfur Compounds in BiologyLuminescence and Fluorescent Materials

Flexible Designing Strategy to Construct Activatable NIR-II Fluorescent Probes with Emission Maxima beyond 1200 nm

Dou, Kun, Feng, Wenqi, Fan, Chen, Cao, Yu, Xiang, Yunhui, Liu, Zhihong·2021·Analytical Chemistry

Abstract

Activatable second near-infrared (NIR-II) fluorescent probes that can be lighted up by specific targets have attracted great attention because of their high specificity and resolution, which hold great promise in deep-tissue imaging. However, such probes were relatively rarely reported so far, and the emission maximum is still limited (mainly located at 900–1000 nm). To solve the problem, herein, we proposed a flexible strategy to modulate the emission wavelength of NIR-II fluorescent probes, and four proof-of-concept probes ( WH-1, WH-2, WH-3, and WH-4 ) based on D−π-A molecular skeleton were obtained. These probes can be activated by H 2 S and the emission maximum located from 925 to 1205 nm, which was attributed to the cooperation of elongating the π-conjugated system and enhancing the electron-donating ability of the donor region. In these probes, WH-3 exhibited the combination of long excitation/emission (925/1140 nm) and moderate quantum yield as well as high sensitivity toward H 2 S, enabling us to track and image H 2 S in vivo with high contrast. We expected that such a molecular design strategy will become an important approach to developing activatable NIR-II fluorescent probes with long emission.

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Crossref · 10.1021/acs.analchem.0c04990

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Authors
Dou, K., Feng, W., Fan, C., Cao, Y., Xiang, Y., & Liu, Z.
Affiliations
  • Wuhan University (CN)
  • Hubei University (CN)
Corresponding author
Liu, Zhihong
Venue
Analytical Chemistry
Published
2021-02-12
Volume
93
Issue
8
Pages
4006-4014
ISSN
  • 0003-2700 (ISSN-L)
  • 1520-6882
OpenAlex
W3128399770
Cited by
67
References
44
Citations by year
2026: 6 · 2025: 11 · 2024: 12 · 2023: 9 · 2022: 23 · 2021: 6
FWCI
4.56
Type
journal article
Language
en
Open access
closed
Locations
  • Analytical Chemistry (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Lanzhou University (201907)
  • National Natural Science Foundation of China (21625503)
Topics
  • Physical Sciences › Chemistry › Spectroscopy › Molecular Sensors and Ion Detection
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Sulfur Compounds in Biology
  • Physical Sciences › Materials Science › Materials Chemistry › Luminescence and Fluorescent Materials
Keywords
activatable fluorescent probes, hydrogen sulfide detection, deep tissue imaging, in vivo imaging, extended π-conjugation, electron-donating ability, quantum yield

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