TY - JOUR
T1 - Nonconventional near-infrared room-temperature phosphorescent materials based on spiropolymer alloy
AU - Ren, Yue
AU - Zhang, Yongfeng
AU - Su, Han
AU - Zhao, Yeyun
AU - Yan, Wenya
AU - Dai, Wenbo
AU - Zhu, Luojie
AU - Wang, Tao
AU - Shi, Jianbing
AU - Zhi, Junge
AU - Tong, Bin
AU - Sun, Peng
AU - Cai, Zhengxu
AU - Dong, Yuping
N1 - Publisher Copyright:
© The Author(s) 2025.
PY - 2025/12
Y1 - 2025/12
N2 - Near-infrared room-temperature phosphorescent (NIR-RTP) materials feature the advantages of large Stokes shift, long emission lifetime, and high penetration ability, and have been broadly applied in bio-medical imaging, fiber optic telecommunication, and night vision-readable display. Developing organic NIR-RTP materials heavily relies on the long-conjugated chemical structures. The large conjugation could result in aggregation caused quenching, complex synthesis, poor processability, and high biological toxicity. Herein, by solution blending poly(iminofuran-spiro-pyrrolone) (PISP) with polystyrene (PS), we construct a nonconventional NIR-RTP polymer alloy without significantly extensive conjugation. The PISP was synthesized via a catalyst-free multicomponent polymerization in air with high molecular weights (up to 41000 g/mol) and decent yields (up to 84%). Although lacking classical luminescent segments and largely extended conjugation, PISPs exhibit the clusterization-triggered cryogenic phosphorescence. More importantly, upon solution blending PISP with PS, the resultant polymer alloy shows a NIR-RTP emission up to 715 nm with a Stokes shift of 375 nm. This work will be of interest for developing luminescent materials for the optoelectronic devices, in vivo imaging, and flexible electronics.
AB - Near-infrared room-temperature phosphorescent (NIR-RTP) materials feature the advantages of large Stokes shift, long emission lifetime, and high penetration ability, and have been broadly applied in bio-medical imaging, fiber optic telecommunication, and night vision-readable display. Developing organic NIR-RTP materials heavily relies on the long-conjugated chemical structures. The large conjugation could result in aggregation caused quenching, complex synthesis, poor processability, and high biological toxicity. Herein, by solution blending poly(iminofuran-spiro-pyrrolone) (PISP) with polystyrene (PS), we construct a nonconventional NIR-RTP polymer alloy without significantly extensive conjugation. The PISP was synthesized via a catalyst-free multicomponent polymerization in air with high molecular weights (up to 41000 g/mol) and decent yields (up to 84%). Although lacking classical luminescent segments and largely extended conjugation, PISPs exhibit the clusterization-triggered cryogenic phosphorescence. More importantly, upon solution blending PISP with PS, the resultant polymer alloy shows a NIR-RTP emission up to 715 nm with a Stokes shift of 375 nm. This work will be of interest for developing luminescent materials for the optoelectronic devices, in vivo imaging, and flexible electronics.
UR - https://www.scopus.com/pages/publications/105024819204
U2 - 10.1038/s41467-025-66035-w
DO - 10.1038/s41467-025-66035-w
M3 - Article
C2 - 41298422
AN - SCOPUS:105024819204
SN - 2041-1723
VL - 16
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 11120
ER -