The locations of triphenylamine and tetraphenylethene on a cyclohexyl ring define a luminogen as an AIEgen or a DSEgen-Reference-Cited by-同舟云学术

The locations of triphenylamine and tetraphenylethene on a cyclohexyl ring define a luminogen as an AIEgen or a DSEgen

Published:2022 Issue:15 Volume:10 Page:6078-6084
ISSN:2050-7526
Container-title:Journal of Materials Chemistry C
language:en
Short-container-title:J. Mater. Chem. C

Author:

Zhang Yuzhu¹,Ding Aixiang²^ORCID,Guo Shengmei¹,He Felicia³,Kong Lin¹,Duan Rui-Huan²^ORCID,Yang Jiaxiang¹^ORCID

Affiliation:

1. College of Chemistry and Chemical Engineering, Key Laboratory of Structure and Functional Regulation of Hybrid Materials (Anhui University), Ministry of Education, Photoelectric Conversion Energy Materials and Devices Key Laboratory of Anhui Province, Anhui University, Hefei, 230061, P. R. China

2. College of Chemistry and Chemical Engineering, Xinyang Normal University, Xinyang, 464000, P. R. China

3. Department of Biomedical Engineering, Case Western Reserve University, 10900 Euclid Avenue, Cleveland, OH, 44106, USA

Abstract

Luminogens with distinct photophysical properties were synthesized by attaching TPE and TPA on a saturated cyclohexyl ring in an isolated fashion, demonstrating the effectiveness of the concept of “aryl isolation” in engineering AIEgens and DSEgens.

Funder

National Natural Science Foundation of China

Anhui Department of Education

Education Department of Henan Province

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/TC/D2TC00350C

Reference64 articles.

1. Recent advances in organic luminescent materials with narrowband emission