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Correction: Activity-based NIR fluorescent probes based on the versatile hemicyanine scaffold: design strategy, biomedical applications, and outlook
Haidong
Li
ab,
Heejeong
Kim
c,
Feng
Xu
ad,
Jingjing
Han
c,
Qichao
Yao
a,
Jingyun
Wang
ab,
Kanyi
Pu
*ef,
Xiaojun
Peng
*ag and
Juyoung
Yoon
*c
aState Key Laboratory of Fine Chemicals, Dalian University of Technology, 2 Linggong Road, Dalian 116024, China. E-mail: pengxj@dlut.edu.cn
bSchool of Bioengineering, Dalian University of Technology, 2 Linggong Road, Dalian 116024, China
cDepartment of Chemistry and Nano Science, Ewha Womans University, Seoul 03760, Korea. E-mail: jyoon@ewha.ac.kr
dThe Key Laboratory of Laboratory Medicine, Ministry of Education, School of Laboratory Medicine and Life Science, Wenzhou Medical University, Wenzhou 325035, China
eSchool of Chemical and Biomedical Engineering, Nanyang Technological University, 70 Nanyang Drive, 637457, Singapore. E-mail: kypu@ntu.edu.sg
fDivision of Chemistry and Biological Chemistry, School of Physical and Mathematical Sciences, Nanyang Technological University, 21 Nanyang Link, Singapore
gResearch Institute of Dalian University of Technology in Shenzhen, Nanshan District, Shenzhen 518057, China
First published on 21st February 2022
Abstract
Correction for ‘Activity-based NIR fluorescent probes based on the versatile hemicyanine scaffold: design strategy, biomedical applications, and outlook’ by Haidong Li et al., Chem. Soc. Rev., 2022, DOI: 10.1039/d1cs00307k.
In the published article, Fig. 1 was incorrect (structures 3 and 4 are the same); the corrected version is shown below.
 | ||
| Fig. 1 (A) Chemical structures of 7-hydroxycoumarin, fluorescein, and new NIR fluorophore HDs bearing an optically tunable hydroxyl moiety. (B) Representative derivatives (1–6) of NIR fluorophore HDs. | ||
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
| This journal is © The Royal Society of Chemistry 2022 |