Spontaneous Adsorption on a Hydrophobic Surface Governed by Hydrogen Bonding

被引:13
作者
Dang, Fuquan [1 ]
Hasegawa, Takeshi [2 ]
Biju, Vasudevanpillai [1 ]
Ishikawa, Mitsuru [1 ]
Kaji, Noritada [3 ]
Yasui, Takao [3 ]
Baba, Yoshinobu [1 ,3 ]
机构
[1] Natl Inst Adv Ind Sci & Technol, Hlth Technol Res Ctr, Takamatsu, Kagawa 7610395, Japan
[2] Tokyo Inst Technol, Dept Chem, Meguro Ku, Tokyo 152855, Japan
[3] Nagoya Univ, Grad Sch Engn, Dept Appl Chem, Chikusa Ku, Nagoya, Aichi 4648603, Japan
关键词
BETA-D-MALTOSIDE; MOLECULAR-ORIENTATION; CHIPS; REFLECTION; CELLULOSE;
D O I
10.1021/la900850u
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Spontaneous adsorption from solution onto solid surface is a common phenomenon in nature, but the force that governs adsorption is still a matter of considerable debate. (1,2) We found that surfactants and cellulose adsorb from solution onto a poly(methyl methacrylate) (PMMA) surface in an ordered and cooperative way governed by hydrogen bonding. The glucose rings of n-dodecyl-beta-D-maltoside (DDM) and hydroxyethylcellulose (HEC) stand perpendicular to the surface, H-bond to the surface COOMe groups with their C=O and Me-O bonds parallel to the surface, and form a tight monolayer. The non-H-bonded COOMe groups orient their C=O bonds perpendicular to the surface. In contrast, the glucose rings of hydrophobically modified hydroxyethylcellulose (HMHEC) lie flat with the side chains perpendicular to the surface and H-bond to the perpendicular-oriented C=O groups. The non-H-bonded COOMe groups orient their C=O bonds parallel but Me-O bonds near-perpendicular to the surface for stabilizing HMHEC. The current work provides a detailed picture of how surface-active molecules interact with a solid surface and self-assemble into greatly different architectures.
引用
收藏
页码:9296 / 9301
页数:6
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