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Correction: Fused ambipolar aza-isoindigos with NIR absorption
Liping
Yao
ab,
Danlei
Zhu
c,
Hailiang
Liao
a,
Sheik
Haseena
d,
Mahesh Kumar
Ravva
d,
Shengyu
Cong
a,
Liuyuan
Lan
a,
Yazhou
Wang
a,
Zhengke
Li
*a,
Lang
Jiang
*c and
Wan
Yue
*a
aState Key Laboratory of Optoelectronic Materials and Technologies, Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education, Guangzhou Key Laboratory of Flexible Electronic Materials and Wearable Devices, School of Materials Science and Engineering, Sun Yat-Sen University, Guangzhou 510275, China. E-mail: lizhengke@mail.sysu.edu.cn; yuew5@mail.sysu.edu.cn
bCollege of Chemistry and Chemical Engineering, Guangxi University for Nationalities, Nanning 530006, P. R. China
cBeijing National Laboratory for Molecular Sciences, Key Laboratory of Organic Solids, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China. E-mail: ljiang@iccas.ac.cn
dDepartment of Chemistry, SRM University-AP, Andhra Pradesh 522502, India
First published on 3rd March 2021
Abstract
Correction for ‘Fused ambipolar aza-isoindigos with NIR absorption’ by Liping Yao et al., Org. Chem. Front., 2021, DOI: 10.1039/d0qo01495h.
In the published paper, one of the double bonds of the chemical structure of the molecules reported was drawn as a single bond in error. The experimental results (notably the 1H NMR and MALDI-TOF data) and our previous work (Chem. Plus. Chem. 2019, 84, 1257–1262) provided enough evidence to support the presence of double bonds. This mistake was caused by negligence and does not have any negative influence on the experimental details, discussion and conclusion of this paper. The table of contents image and Scheme S1 have been updated, while the revised Fig. 1 and Scheme 1 are shown below.
 | ||
| Fig. 1 The chemical structures of modified IID cores. 1a: isoindigo;341b: benzothiophene isoindigo;401c: naphthalene isoindigo;351d: benzothienothiophene isoindigo;371e: benzofuranbenzene isoindigo; 1f: benthiothiobenzene isoindigo;41 and 1g: the chemical structures in this work. | ||
 | ||
| Scheme 1 The synthesis route to the aza-IID derivatives. Reaction conditions: (a) AcOH, CHCl3; yields: 72% (AI-6), 79% (FAI-6), and 83% (AI-7). (b) Hexaethyltriaminophosphine, CH2Cl2; yields: 30% (AIID-12), 18% (FAIID-12), and 44% (AIID-14). | ||
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