Pica Andrea, Graziano Giuseppe
Dipartimento di Scienze Chimiche, Università degli Studi di Napoli Federico II, Complesso Universitario di Monte Sant'Angelo, Via Cintia, 80126 Napoli, Italy.
Dipartimento di Scienze e Tecnologie, Università del Sannio, Via Port'Arsa 11, 82100 Benevento, Italy.
Biophys Chem. 2017 Dec;231:34-38. doi: 10.1016/j.bpc.2017.01.001. Epub 2017 Jan 5.
When methanol is added to water at room temperature and 1atm, poly (N-isopropylacrylamide), PNIPAM, undergoes a coil-to-globule collapse transition. This intriguing phenomenon is called cononsolvency. Spectroscopic measurements have shown that application of high hydrostatic pressure destroys PNIPAM cononsolvency in water-methanol solutions. We have developed a theoretical approach that identifies the decrease in solvent-excluded volume effect as the driving force of PNIPAM collapse on increasing the temperature. The same approach indicates that cononsolvency, at room temperature and P=1atm, is caused by the inability of PNIPAM to make all the attractive energetic interactions that it could be engaged in, due to competition between water and methanol molecules. The present analysis suggests that high hydrostatic pressure destroys cononsolvency because the coil state becomes more compact, and the quantity measuring PNIPAM-solvent attractions increases in magnitude due to the solution density increase, and the ability of small water molecules to substitute methanol molecules on PNIPAM surface.
在室温及1个大气压下,向水中加入甲醇时,聚(N-异丙基丙烯酰胺)(PNIPAM)会发生从线圈状到球状的塌缩转变。这种有趣的现象被称为共溶剂化。光谱测量表明,施加高静水压力会破坏水-甲醇溶液中PNIPAM的共溶剂化。我们开发了一种理论方法,该方法确定溶剂排除体积效应的降低是PNIPAM在温度升高时塌缩的驱动力。同样的方法表明,在室温及P = 1个大气压下,共溶剂化是由于水和甲醇分子之间的竞争,PNIPAM无法进行其本可参与的所有吸引能相互作用而导致的。目前的分析表明,高静水压力会破坏共溶剂化,因为线圈状态变得更加紧凑,并且由于溶液密度增加以及小水分子在PNIPAM表面替代甲醇分子的能力,测量PNIPAM-溶剂吸引力的量在大小上增加。