氢键
小角X射线散射
预聚物
聚氨酯
超分子化学
材料科学
聚合物
高分子化学
化学
超分子聚合物
化学工程
散射
结晶学
复合材料
分子
有机化学
晶体结构
光学
物理
工程类
作者
Xiaopei Li,Junyu Li,Wanyuan Wei,Fan Yang,Mengjiao Wu,Qin Wu,Titi Xie,Yulan Chen
出处
期刊:Macromolecules
[American Chemical Society]
日期:2021-01-25
卷期号:54 (3): 1557-1563
被引量:24
标识
DOI:10.1021/acs.macromol.0c02622
摘要
The chemiluminescent mechanophore, 1,2-dioxetane (Ad), is incorporated into the backbone of a polyurethane-based prepolymer, which is further end-capped with dimerizable strong hydrogen bonding units, ureidopyrimidinone and pyrimidinedione (UPy, DHB-2) or hydrogen bonding free unit (EtOH). Mechanical, optomechanical measurements, and small-angle/wide-angle X-ray scattering (SAXS/WAXS) analyses of these end-functionalized polyurethanes have demonstrated that the difference in the strength of hydrogen bonding interactions led to different degrees of chain orientation in the bulk, and consequently, different levels of mechano-activation of Ad with distinguishable mechanochemiluminescence intensity. This study not only offers a straightforward way to enhance the mechanochemiluminescence of Ad containing polymers by tailoring the supramolecular interactions between different macromers but also deepens our understanding of the correlations between chain orientation behavior, magnitudes of hydrogen bonding interactions, and the activation of mechanophores.
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