Author
Listed:
- Zhong-Qiu Li
(Chinese Academy of Sciences
Beijing National Laboratory for Molecular Sciences
Chinese Academy of Sciences
University of Chinese Academy of Sciences)
- Li Meng
(Chinese Academy of Sciences
Renmin University of China)
- Zili Chen
(Renmin University of China)
- Yu-Wu Zhong
(Chinese Academy of Sciences
Beijing National Laboratory for Molecular Sciences
Chinese Academy of Sciences
University of Chinese Academy of Sciences)
Abstract
The preparation of single-crystal polymers with circularly polarized luminesce (CPL) remains a challenging task in chemistry and materials science. Herein, we present the single-crystal-to-single-crystal topochemical photopolymerization of a chiral organic salt to achieve this goal. The in-situ reaction of 1,4-bis((E)-2-(pyridin-4-yl)vinyl)benzene (1) with chiral (+)- or (−)-camphorsulfonic acid (CSA) gives the monomer crystal 1[( + )/( − )-CSA]2 showing yellow CPL with a high luminescent dissymmetry factor |glum| of 0.035 and emission quantum yield Φ of 49.7%. Upon photo-induced topochemical [2 + 2] polymerization, single-crystal polyionic polymers of poly-1[( + )/( − )-CSA]2 are obtained. The single-crystal-to-single-crystal (SCSC) photopolymerization is revealed by in situ powder X-ray diffraction, single-crystal X-ray, optical microscopy, infrared, circular dichroism, and CPL spectroscopic analyzes. Interestingly, the photopolymer crystals show blue and handedness-inverted CPL with |glum| of 0.011 (Φ = 14.2%), with respect to the yellow CPL of the monomer crystal. Furthermore, patterned circularly-polarized photonic heterojunctions with alternate blue and yellow CPL sub-blocks are prepared by a mask-assisted photopolymerization method. Our findings provide a vision for fabricating high-performance CPL-active crystalline polymer materials, paving the way for the further development of photo-response chiral systems.
Suggested Citation
Zhong-Qiu Li & Li Meng & Zili Chen & Yu-Wu Zhong, 2025.
"Endowing single-crystal polymers with circularly polarized luminescence,"
Nature Communications, Nature, vol. 16(1), pages 1-10, December.
Handle:
RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-024-55181-2
DOI: 10.1038/s41467-024-55181-2
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