TY - JOUR
T1 - Tunable near-infrared piezochromic luminescence by effective substituent modification of D-A structures
AU - Liu, Jianxun
AU - Du, Guoshuai
AU - Liang, Ning
AU - Yang, Li
AU - Feng, Yansong
AU - Chen, Yabin
AU - Yao, Chang Jiang
N1 - Publisher Copyright:
© 2023 The Royal Society of Chemistry.
PY - 2023/5/24
Y1 - 2023/5/24
N2 - Piezochromic luminescent (PCL) materials have attracted extensive research interest due to their potential applications in mechanosensors, ink-free printing, optical data storage, optoelectronic devices, etc. However, there have been few reports on the near-infrared (NIR) piezochromic luminescence of π-conjugated organic materials under external hydrostatic pressure. Herein, we report the design and preparation of five pressure-sensitive AIEgens: TPAM, BTPAM, FTPAM, MTPAM and MOTPAM. These materials exhibit piezochromic luminescence behaviors, whereby their emission colors exhibit significant blue-shifts upon gentle manual grinding due to the phase transition from the crystalline to the amorphous state. With an increase in applied hydrostatic pressure, significant emission red-shifts (up to >200 nm) toward the NIR region were observed with the modification of substituents, attributed to the enhanced intermolecular π-π interactions. The unsubstituted TPAM did not exhibit any red-shifted emission due to the synergistic effect between enhanced intermolecular interactions and molecular configuration deformation during the compression process.
AB - Piezochromic luminescent (PCL) materials have attracted extensive research interest due to their potential applications in mechanosensors, ink-free printing, optical data storage, optoelectronic devices, etc. However, there have been few reports on the near-infrared (NIR) piezochromic luminescence of π-conjugated organic materials under external hydrostatic pressure. Herein, we report the design and preparation of five pressure-sensitive AIEgens: TPAM, BTPAM, FTPAM, MTPAM and MOTPAM. These materials exhibit piezochromic luminescence behaviors, whereby their emission colors exhibit significant blue-shifts upon gentle manual grinding due to the phase transition from the crystalline to the amorphous state. With an increase in applied hydrostatic pressure, significant emission red-shifts (up to >200 nm) toward the NIR region were observed with the modification of substituents, attributed to the enhanced intermolecular π-π interactions. The unsubstituted TPAM did not exhibit any red-shifted emission due to the synergistic effect between enhanced intermolecular interactions and molecular configuration deformation during the compression process.
UR - http://www.scopus.com/inward/record.url?scp=85163769845&partnerID=8YFLogxK
U2 - 10.1039/d3tc01254a
DO - 10.1039/d3tc01254a
M3 - Article
AN - SCOPUS:85163769845
SN - 2050-7526
VL - 11
SP - 8609
EP - 8615
JO - Journal of Materials Chemistry C
JF - Journal of Materials Chemistry C
IS - 25
ER -