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
相关论文
共 30 条
[1]   Engineering atomic and molecular nanostructures at surfaces [J].
Barth, JV ;
Costantini, G ;
Kern, K .
NATURE, 2005, 437 (7059) :671-679
[2]   Characterization of interactions in aqueous solutions of hydroxyethylcellulose and its hydrophobically modified analogue in the presence of a cyclodextrin derivative [J].
Beheshti, N ;
Bu, H ;
Zhu, KZ ;
Kjoniksen, AL ;
Knudsen, KD ;
Pamies, R ;
Cifre, JGH ;
de la Torre, JG ;
Nyström, B .
JOURNAL OF PHYSICAL CHEMISTRY B, 2006, 110 (13) :6601-6608
[3]   Surface modification in microchip electrophoresis [J].
Belder, D ;
Ludwig, M .
ELECTROPHORESIS, 2003, 24 (21) :3595-3606
[4]   INFRARED AND RAMAN SPECTRA OF CELLULOSE FROM CELL WALL OF VALONIA VENTRICOSA [J].
BLACKWELL, J ;
VASKO, PD ;
KOENIG, JL .
JOURNAL OF APPLIED PHYSICS, 1970, 41 (11) :4375-+
[5]   Layer-by-layer self-assembled chitosan/poly(thiophene-3-acetic acid) and organophosphorus hydrolase multilayers [J].
Constantine, CA ;
Mello, SV ;
Dupont, A ;
Cao, XH ;
Santos, D ;
Oliveira, ON ;
Strixino, FT ;
Pereira, EC ;
Cheng, TC ;
Defrank, JJ ;
Leblanc, RM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (07) :1805-1809
[6]   Replica multichannel polymer chips with a network of sacrificial channels sealed by adhesive printing method [J].
Dang, F ;
Shinohara, S ;
Tabata, O ;
Yamaoka, Y ;
Kurokawa, M ;
Shinohara, Y ;
Ishikawa, M ;
Baba, Y .
LAB ON A CHIP, 2005, 5 (04) :472-478
[7]   Hybrid dynamic coating with n-dodecyl β-D-maltoside and methyl cellulose for high-performance carbohydrate analysis on poly(methyl methacrylate) chips [J].
Dang, FQ ;
Kakehi, K ;
Cheng, JJ ;
Tabata, O ;
Kurokawa, M ;
Nakajima, K ;
Ishikawa, M ;
Baba, Y .
ANALYTICAL CHEMISTRY, 2006, 78 (05) :1452-1458
[8]   Characterization of electrophoretic behavior of sugar isomers by microchip electrophoresis coupled with videomicroscopy [J].
Dang, FQ ;
Zhang, LH ;
Jabasini, M ;
Kaji, N ;
Baba, Y .
ANALYTICAL CHEMISTRY, 2003, 75 (10) :2433-2439
[9]   High-performance genetic analysis on microfabricated capillary array electrophoresis plastic chips fabricated by injection molding [J].
Dang, FQ ;
Tabata, O ;
Kurokawa, M ;
Ewis, AA ;
Zhang, LH ;
Yamaoka, Y ;
Shinohara, S ;
Shinohara, Y ;
Ishikawa, M ;
Baba, Y .
ANALYTICAL CHEMISTRY, 2005, 77 (07) :2140-2146
[10]  
Haines A.H., 1976, Adv. Carbohydr. Chem. Biochem, V33, P11, DOI DOI 10.1016/S0065-2318(08)60280-