Tada Takanori, Hirano Tomohiro, Ute Koichi, Katsumoto Yukiteru, Asoh Taka-Aki, Shoji Tatsuya, Kitamura Noboru, Tsuboi Yasuyuki
Graduate School of Chemical Sciences and Engineering, Hokkaido University , Sapporo 060-0810, Japan.
Department of Chemical Science and Technology, Institute of Technology and Science, The University of Tokushima , Minamijosanjima 2-1, Tokushima 770-8506, Japan.
J Phys Chem B. 2016 Aug 11;120(31):7724-30. doi: 10.1021/acs.jpcb.6b03200. Epub 2016 Jul 27.
The dynamic and static phase separation behavior in aqueous poly(N-isopropylacrylamide) (PNIPAM) solutions is highly sensitive to the tacticity of PNIPAM. We investigated the phase separation dynamics of aqueous solutions of PNIPAM with different tacticities (atactic and syndiotactic-rich types) and found that the phase separation dynamics of syndiotactic-rich PNIPAM was much different from that of atactic-type PNIPAM. First, phase separation in syndiotactic-rich PNIPAM was faster. Second, there was a critical point (Ccp) in the concentration dependence of the phase separation rate: the phase separation accelerated dramatically when the solution concentration was higher than 2.0 wt % (= Ccp). Third, syndiotactic-rich PNIPAM required a higher thermal energy for phase separation compared to atactic PNIPAM. Such behavior can be explained on the basis of the high hydrophobicity of syndiotactic-rich PNIPAM in a dehydrated state and a diffusion-controlled aggregation model. The present study shows that precise control of the stereoregularity will open new channels toward the design and development of stimuli-responsive-polymer-based smart materials.
聚(N-异丙基丙烯酰胺)(PNIPAM)水溶液中的动态和静态相分离行为对PNIPAM的立构规整性高度敏感。我们研究了不同立构规整性(无规和间同立构富集型)的PNIPAM水溶液的相分离动力学,发现间同立构富集型PNIPAM的相分离动力学与无规型PNIPAM有很大不同。首先,间同立构富集型PNIPAM中的相分离更快。其次,在相分离速率的浓度依赖性方面存在一个临界点(Ccp):当溶液浓度高于2.0 wt%(= Ccp)时,相分离急剧加速。第三,与无规PNIPAM相比,间同立构富集型PNIPAM进行相分离需要更高的热能。这种行为可以基于间同立构富集型PNIPAM在脱水状态下的高疏水性以及扩散控制的聚集模型来解释。本研究表明,对立构规整性的精确控制将为基于刺激响应聚合物的智能材料的设计和开发开辟新途径。