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聚(甲基丙烯酸2-(2-甲氧基乙氧基)乙酯)在水中热敏相分离过程中的水合变化

Hydration changes of poly(2-(2-methoxyethoxy)ethyl methacrylate) during thermosensitive phase separation in water.

作者信息

Maeda Yasushi, Kubota Tomoyuki, Yamauchi Hideo, Nakaji Tadashi, Kitano Hiromi

机构信息

Department of Applied Chemistry and Biotechnology, University of Fukui, Fukui 910-8507, Japan.

出版信息

Langmuir. 2007 Oct 23;23(22):11259-65. doi: 10.1021/la7016006. Epub 2007 Sep 22.

Abstract

Hydration changes of poly(2-(2-methoxyethoxy)ethyl methacrylate) (PMoEoEMa) during thermosensitive phase separation in water have been investigated by infrared spectroscopy. The C=O stretching band can be separated into three components assigned to non-hydrated carbonyl groups and singly and doubly hydrogen-bonded carbonyl groups (1728, 1709, and 1685 cm-1, respectively). Relatively large parts of the carbonyl groups (50% in 30 wt % solution) do not form hydrogen bonds even below the transition temperature (Tp) probably because they possess crowded positions near the backbone. The fraction of hydrogen-bonding carbonyl groups decreased during phase separation by approximately 0.2. Among five nu(C-H) bands, the highest- and the lowest-frequency bands (nu(C-H)A and nu(C-H)E) exhibited relatively large red shifts of 8 and 11 cm(-1), respectively. DFT calculations indicate that the formation of a H-bond between the ether oxygen and water leads to blue shifts of nu(C-H) of adjacent alkyl groups and has a larger effect than a direct H-bond to the alkyl groups, namely, C-H...O H-bonds. The fraction of hydrogen-bonding methoxy oxygens estimated from the position of the nu(C-H)A is 1 at Tp. This result indicates that the methoxy oxygens and the carbonyl are more favorably hydrated than the other at Tp, respectively.

摘要

通过红外光谱研究了聚(甲基丙烯酸2-(2-甲氧基乙氧基)乙酯)(PMoEoEMa)在水中热敏相分离过程中的水合变化。C=O伸缩带可分为三个组分,分别归属于非水合羰基以及单氢键合和双氢键合的羰基(分别为1728、1709和1685 cm-1)。即使在转变温度(Tp)以下,相当一部分羰基(30 wt%溶液中为50%)也不形成氢键,这可能是因为它们在主链附近位置拥挤。在相分离过程中,氢键合羰基的比例下降了约0.2。在五个ν(C-H)带中,最高频率和最低频率的带(ν(C-H)A和ν(C-H)E)分别表现出相对较大的8和11 cm-1的红移。密度泛函理论计算表明,醚氧与水之间形成氢键会导致相邻烷基的ν(C-H)发生蓝移,且其影响比烷基直接形成的氢键(即C-H...O氢键)更大。根据ν(C-H)A的位置估算,氢键合甲氧基氧的比例在<Tp时为1,在>Tp时为零。这一结果表明,在<Tp时,甲氧基氧比羰基更易水合,而在>Tp时,羰基比甲氧基氧更易水合。

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