自愈水凝胶
聚(N-异丙基丙烯酰胺)
反作用坐标
高分子化学
异丙基
低临界溶液温度
相变
肿胀 的
拉曼光谱
聚合物
相(物质)
酰胺
化学
材料科学
体积热力学
动力学
化学工程
物理化学
热力学
共聚物
有机化学
复合材料
物理
光学
工程类
量子力学
作者
Tsung-Yu Wu,Alyssa B. Zrimsek,Sergei V. Bykov,Ryan S. Jakubek,Sanford A. Asher
标识
DOI:10.1021/acs.jpcb.8b00740
摘要
The best-known examples of smart, responsive hydrogels derive from poly( N-isopropylacrylamide) (PNIPAM) cross-linked polymer networks. These hydrogels undergo volume phase transitions (VPTs) triggered by temperature, chemical, and/or environmental changes. PNIPAM hydrogels can undergo more than 50-fold volume changes within ∼1 μs intervals. Studies have tried to elucidate the molecular mechanism of these extraordinarily large responses. Nevertheless, the molecular reaction coordinates that drive the VPT remain unclear. Using visible nonresonance Raman temperature-jump spectroscopy, we determined the molecular ordering of this VPT. The PNIPAM hydrophobic isopropyl and methylene groups dehydrate with time constants of 109 ± 64 and 104 ± 44 ns, initiating the volume collapse of PNIPAM. The subsequent dehydration of the PNIPAM amide groups is significantly slower, as our group previously discovered (360 ± 85 ns). This determination of the ordering of the molecular reaction coordinate of the PNIPAM VPT enables the development of the next generation of super-responsive materials.
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