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Correction: Near-infrared metal agents assisting precision medicine: from strategic design to bioimaging and therapeutic applications

Chonglu Li ab, Yida Pang b, Yuling Xu b, Mengjiao Lu c, Le Tu b, Qian Li d, Amit Sharma e, Zhenzhong Guo *a, Xiangyang Li *c and Yao Sun *b
aHubei Province Key Laboratory of Occupational Hazard Identification and Control, School of Medicine, School of Public Health, Wuhan University of Science and Technology, Wuhan 430065, China. E-mail: zhongbujueqi@hotmail.com
bNational Key Laboratory of Green Pesticide, College of Chemistry, Central China Normal University, Wuhan 430079, China. E-mail: sunyaogbasp@ccnu.edu.cn
cNational Key Laboratory of Green Pesticide, Key Laboratory of Green Pesticide and Agricultural Bioengineering, Ministry of Education, Guizhou University, Guiyang 550025, China. E-mail: xyli1@gzu.edu.cn
dNHC Key Laboratory of Nuclear Medicine, Jiangsu Key Laboratory of Molecular Nuclear Medicine, Jiangsu Institute of Nuclear Medicine, Wuxi 214063, China
eCSIR-Central Scientific Instruments Organisation, Sector-30C, Chandigarh 160030, India

Received 5th July 2023 , Accepted 5th July 2023

First published on 12th July 2023


Abstract

Correction for ‘Near-infrared metal agents assisting precision medicine: from strategic design to bioimaging and therapeutic applications’ by Chonglu Li et al., Chem. Soc. Rev., 2023, 52, 4392–4442, https://doi.org/10.1039/D3CS00227F.


The authors regret that there were errors in some of the molecular structures in Fig. 5 (compound 19), Fig. 9 (compound 43), Fig. 11 (compounds 51 and 54), Fig. 12 (compound 56) and Fig. 15 (compounds 74 and 76) in the original article. The corrected figures are shown here. None of the conclusions in the paper are affected by these corrections.
image file: d3cs90060f-f5.tif
Fig. 5 Chemical structures and maximum absorption/emission wavelengths of NIR-I Pt(II) polypyridine complexes (15–21).

image file: d3cs90060f-f9.tif
Fig. 9 Chemical structures and maximum absorption/emission wavelengths of NIR-I MMCs containing fluorophore ligands (39–46).

image file: d3cs90060f-f11.tif
Fig. 11 Chemical structures and maximum absorption/emission wavelengths of NIR-II MMCs containing porphyrin ligands (49–54).

image file: d3cs90060f-f12.tif
Fig. 12 Chemical structures and maximum absorption/emission wavelengths of NIR-II MMCs containing fluorophore ligands (55–57).

image file: d3cs90060f-f15.tif
Fig. 15 Chemical structures and maximum absorption/emission wavelengths of NIR-I MOCs (72–77) containing fluorophores.

The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.


Footnote

Equally contributed.

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