Circularly Polarized Organic Long‐Persistent Luminescence from Polymer Films Doped with Chiral Cu(I) Complexes

H Hengshan Wei (School of Chemistry South China Normal University Guangzhou 510006 China) S Shihua Qin (School of Chemistry South China Normal University Guangzhou 510006 China) H Huiwen Zeng (School of Chemistry South China Normal University Guangzhou 510006 China) J Jiahui Sun Y Yaohui Liang (School of Chemistry South China Normal University Guangzhou 510006 China) H Huaqing Zhang (Innovative Centre for Flexible Devices (iFLEX), Max Planck-NTU Joint Lab for Artificial Senses, School of Materials Science and Engineering, Nanyang Technological University, 50 Nanyang Avenue, Singapore 639798, Republic of Singapore) H Huili Yang (School of Chemistry South China Normal University Guangzhou 510006 China) C Chunxiong Zheng (School of Chemistry South China Normal University Guangzhou 510006 China) G Guang Shi Z Zhenguo Chi (School of Environmental and Chemical Engineering) Z Zujin Zhao (State Key Laboratory of Luminescent Materials and Devices, and Guangdong Provincial Key Laboratory of Luminescence from Molecular Aggregates) Z Zhan Yang Z Zhu Mao B Bingjia Xu (School of Environmental and Chemical Engineering Wuyi University Jiangmen 529020 China)

Abstract

Abstract The development of polymer materials with circularly polarized organic long‐persistent luminescence (CP‐OLPL) remains challenging yet highly desirable. Herein, a polymer‐based OLPL system is prepared by embedding a Cu(I) complex rac ‐NDP‐CuCl into polymethyl methacrylate, which exhibits a high phosphorescence quantum yield ( Φ phos. ) of 64.0% and an emission duration exceeding 3 h under ambient conditions. Moreover, by simply replacing the racemic guest rac ‐NDP‐CuCl with its enantiomers R ‐NDP‐CuCl and S ‐NDP‐CuCl, polymer‐based luminescent materials with CP‐OLPL properties are successfully developed for the first time. These doped polymer films display Φ phos. values and emission durations comparable to those of the racemic system, along with satisfactory asymmetry factors for both circularly polarized phosphorescence and OLPL, reaching up to 4.79 × 10 −3 at room temperature. In contrast to conventional OLPL systems based on binary donor–acceptor doping, the present design facilitates the formation of intermediate charge‐separated states via photoinduced metal‐to‐ligand charge transfer, which are effectively stabilized and spatially separated within the polar polymer matrix, thereby enabling notable OLPL and CP‐OLPL emissions. These findings provide new insights into the molecular design of ambient OLPL materials and open a promising avenue for developing polymer‐based CP‐OLPL systems.

Article Details

Volume / Issue Vol. 65, Issue 10
Published March 02, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (14)

H

Hengshan Wei

School of Chemistry South China Normal University Guangzhou 510006 China

S

Shihua Qin

School of Chemistry South China Normal University Guangzhou 510006 China

H

Huiwen Zeng

School of Chemistry South China Normal University Guangzhou 510006 China

J

Jiahui Sun

Y

Yaohui Liang

School of Chemistry South China Normal University Guangzhou 510006 China

H

Huaqing Zhang

Innovative Centre for Flexible Devices (iFLEX), Max Planck-NTU Joint Lab for Artificial Senses, School of Materials Science and Engineering, Nanyang Technological University, 50 Nanyang Avenue, Singapore 639798, Republic of Singapore

H

Huili Yang

School of Chemistry South China Normal University Guangzhou 510006 China

C

Chunxiong Zheng

School of Chemistry South China Normal University Guangzhou 510006 China

G

Guang Shi

Z

Zhenguo Chi

School of Environmental and Chemical Engineering

Z

Zujin Zhao

State Key Laboratory of Luminescent Materials and Devices, and Guangdong Provincial Key Laboratory of Luminescence from Molecular Aggregates

Z

Zhan Yang

Z

Zhu Mao

B

Bingjia Xu

School of Environmental and Chemical Engineering Wuyi University Jiangmen 529020 China