Maeda Yasushi, Kubota Tomoyuki, Yamauchi Hideo, Nakaji Tadashi, Kitano Hiromi
Department of Applied Chemistry and Biotechnology, University of Fukui, Fukui 910-8507, Japan.
Langmuir. 2007 Oct 23;23(22):11259-65. doi: 10.1021/la7016006. Epub 2007 Sep 22.
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
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。