Graduate School of Chemical Sciences and Engineering , Hokkaido University , Sapporo 060-0810 , Japan.
Department of Chemistry, Faculty of Science , Fukuoka University , 8-19-1 Nanakuma , Jonan-ku, Fukuoka 814-0180 , Japan.
Langmuir. 2018 Nov 13;34(45):13690-13696. doi: 10.1021/acs.langmuir.8b02848. Epub 2018 Nov 2.
We studied the dependence on tacticity of the dynamic phase separation behavior of thermoresponsive poly( N, N-diethylacrylamide) (PDEA) in an aqueous solution. Using a laser temperature-jump technique combined with transient photometry, we determined the time constants of the phase separation and found that both atactic and isotactic-rich PDEAs had fast and slow phase separation processes (τ and τ). The fast process (τ) was independent of the tacticity, irrespective of the concentration. On the other hand, the slow process had a strong dependence on the tacticity. We found the slow phase separation process got considerably faster with increasing isotacticity in dilute solutions. This effect due to the tacticity of the PDEA is totally different from that of poly( N-isopropylacrylamide) and can be explained on the basis of the difference between the hydrophobicity of atactic PDEA and that of isotactic-rich PDEA.
我们研究了温敏性聚(N,N-二乙基丙烯酰胺)(PDEA)在水溶液中动态相分离行为对立构规整性的依赖性。利用激光温度跃变技术结合瞬态光度法,我们确定了相分离的时间常数,发现无规和全同规富 PDEA 都具有快速和缓慢的相分离过程(τ和τ)。快速过程(τ)与立构规整性无关,与浓度无关。另一方面,缓慢过程对立构规整性有很强的依赖性。我们发现,在稀溶液中,随着全同规度的增加,缓慢相分离过程明显加快。这种由于 PDEA 的立构规整性引起的效应与聚(N-异丙基丙烯酰胺)完全不同,可以根据无规 PDEA 的疏水性与全同规富 PDEA 的疏水性之间的差异来解释。