光致变色
荧光
光化学
部分
费斯特共振能量转移
材料科学
螺吡喃
超分子化学
聚合物
单体
共价键
超分子聚合物
纳米技术
化学
有机化学
分子
复合材料
物理
量子力学
作者
Jia Tang,Xiaoling Zhang,Zhong Lin,Chonghua Zhang,Peisheng Zhang,Rongjin Zeng,Si Wu,Xudong Chen,Jian Chen
标识
DOI:10.1021/acsami.2c19227
摘要
Photoswitchable fluorescent materials are desirable for many applications because their emission signals can be easily modulated on demand. In this study, novel photoswitchable multistate fluorescent supramolecular polymers (PMFSPs) were prepared via host-guest interactions under a facile ultrasonication strategy. In the system, photochromic fluorescent diarylethylene monomer (SDTE, donor) and adamantane-containing monomer (BAC) were covalently combined into the backbone of the guest polymer (P1) via radical copolymerization. Meanwhile, the host moiety (CDSP, acceptor) was synthesized by covalent incorporation of photochromic spiropyran dye (SPCOOH) with β-cyclodextrin. By adjusting the stimulation wavelength and utilizing photoinduced fluorescence resonance energy transfer (FRET), the supramolecular polymers can undergo reversible tristate fluorescence switching among none, red, and green. In addition, due to the high contrast, rapid photoresponsiveness and prominent photoreversibility of the prepared PMFSPs, we demonstrated that they have great potential in advanced anti-counterfeiting and multilevel information encryption.
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