TY - JOUR
T1 - "indanonalkene" Photoluminescence Platform
T2 - Application in Real-Time Tracking the Synthesis, Remodeling, and Degradation of Soft Materials
AU - Feng, Xing
AU - Wu, Tianhong
AU - Sun, Xiaolong
AU - Qian, Xuhong
N1 - Publisher Copyright:
© 2021 American Chemical Society.
PY - 2021/12/29
Y1 - 2021/12/29
N2 - In this Article, we present a strategy to visually track chemically triggered covalent bonding processes in gelation, remodeling, and degradation of soft materials, i.e., hydrogels, based on a new photoluminescence platform. Initially in the development of photoluminophors named "indanonalkenes", turn-on emission can be tracked and quantified in the optical reaction between a conjugate acceptor and amine derivatives. On this basis, fluorescence enhancement and mechanical changes were recorded during the gelation process through amine-thiol exchanges under organic and aqueous conditions. Next in macromolecular remodeling, we realized a stimulus-induced transformation of one architecture into another one, exploiting the orthogonality of chemical covalent bonding that could be visualized using luminescence. Furthermore, the hydrogel network can be degraded to release the coupling partner induced by ethylene diamine, and the process can be monitored using fluorescence changes and quantified through gel permeation chromatography, while the released components can be utilized again to regenerate a new hydrogel. In addition, the photographic images provide alternatives to fluorescence spectra and can be digitally processed to quantify the macroscopic changes, resulting in a photographic imaging approach. The real-time observation and quantification of chemically triggered polymeric formation, morphology, and degradation through luminescence in spatial and time scales herald a new generation of "smart"materials.
AB - In this Article, we present a strategy to visually track chemically triggered covalent bonding processes in gelation, remodeling, and degradation of soft materials, i.e., hydrogels, based on a new photoluminescence platform. Initially in the development of photoluminophors named "indanonalkenes", turn-on emission can be tracked and quantified in the optical reaction between a conjugate acceptor and amine derivatives. On this basis, fluorescence enhancement and mechanical changes were recorded during the gelation process through amine-thiol exchanges under organic and aqueous conditions. Next in macromolecular remodeling, we realized a stimulus-induced transformation of one architecture into another one, exploiting the orthogonality of chemical covalent bonding that could be visualized using luminescence. Furthermore, the hydrogel network can be degraded to release the coupling partner induced by ethylene diamine, and the process can be monitored using fluorescence changes and quantified through gel permeation chromatography, while the released components can be utilized again to regenerate a new hydrogel. In addition, the photographic images provide alternatives to fluorescence spectra and can be digitally processed to quantify the macroscopic changes, resulting in a photographic imaging approach. The real-time observation and quantification of chemically triggered polymeric formation, morphology, and degradation through luminescence in spatial and time scales herald a new generation of "smart"materials.
UR - https://www.scopus.com/pages/publications/85121654233
U2 - 10.1021/jacs.1c09895
DO - 10.1021/jacs.1c09895
M3 - 文章
C2 - 34905350
AN - SCOPUS:85121654233
SN - 0002-7863
VL - 143
SP - 21622
EP - 21629
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 51
ER -