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All-Atom Molecular Dynamics Simulations of the Temperature Response of Poly(glycidyl ether)s with Oligooxyethylene Side Chains Terminated with Alkyl Groups
oleh: Erika Terada, Takuya Isono, Toshifumi Satoh, Takuya Yamamoto, Toyoji Kakuchi, Shinichiro Sato
Format: | Article |
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Diterbitkan: | MDPI AG 2023-05-01 |
Deskripsi
Recently, experimental investigations of a class of temperature-responsive polymers tethered to oligooxyethylene side chains terminated with alkyl groups have been conducted. In this study, aqueous solutions of poly(glycidyl ether)s (PGE) with varying numbers of oxyethylene units, poly(methyl(oligooxyethylene)<sub>n</sub> glycidyl ether) (poly(Me(EO)<sub>n</sub>GE)), and poly(ethyl(oligooxyethylene)<sub>n</sub> glycidyl ether) (poly(Et(EO)<sub>n</sub>GE) (<i>n</i> = 0, 1, and 2) were investigated by all-atom molecular dynamics simulations, focusing on the thermal responses of their chain extensions, the recombination of intrapolymer and polymer–water hydrogen bonds, and water-solvation shells around the alkyl groups. No clear relationship was established between the phase-transition temperature and the polymer-chain extensions unlike the case for the coil–globule transition of poly(<i>N</i>-isopropylacrylamide). However, the temperature response of the first water-solvation shell around the alkyl group exhibited a notable correlation with the phase-transition temperature. In addition, the temperature at which the hydrophobic hydration shell strength around the terminal alkyl group equals the bulk water density (<inline-formula><math xmlns="http://www.w3.org/1998/Math/MathML" display="inline"><semantics><mrow><msub><mi>T</mi><mrow><mi mathvariant="normal">CRP</mi></mrow></msub></mrow></semantics></math></inline-formula>) was slightly lower than the cloud point temperature (<inline-formula><math xmlns="http://www.w3.org/1998/Math/MathML" display="inline"><semantics><mrow><msub><mi>T</mi><mrow><mi mathvariant="normal">CLP</mi></mrow></msub></mrow></semantics></math></inline-formula>) for the methyl-terminated poly(Me(EO)<sub>n</sub>GE) and slightly higher for the ethyl-terminated poly(Et(EO)<sub>n</sub>GE). It was concluded that the polymer-chain fluctuation affects the relationship between <inline-formula><math xmlns="http://www.w3.org/1998/Math/MathML" display="inline"><semantics><mrow><msub><mi>T</mi><mrow><mi mathvariant="normal">CRP</mi></mrow></msub></mrow></semantics></math></inline-formula> and <inline-formula><math xmlns="http://www.w3.org/1998/Math/MathML" display="inline"><semantics><mrow><msub><mi>T</mi><mrow><mi mathvariant="normal">CLP</mi></mrow></msub></mrow></semantics></math></inline-formula>.