Hybrid organic-inorganic quaternary ammonium organosilane functionalized mesoporous thin films

被引:24
作者
Wong, EM
Markowitz, MA
Qadri, SB
Golledge, S
Castner, DG
Gaber, BP
机构
[1] USN, Res Lab, Ctr Biomol Sci & Engn, Lab Mol Interfacial Interact, Washington, DC 20375 USA
[2] USN, Res Lab, Div Mat Sci & Technol, Surface Modificat Branch, Washington, DC 20375 USA
[3] Univ Washington, ESCA & Surface Anal Ctr Biomed Problems, Dept Bioengn, Seattle, WA 98195 USA
[4] Univ Washington, ESCA & Surface Anal Ctr Biomed Problems, Dept Chem Engn, Seattle, WA 98195 USA
关键词
D O I
10.1021/jp014201g
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Quaternary ammonium functionalized mesoporous thin films were prepared by spin casting mixtures of bis-(triethoxysilyl)ethane hexaethoxydisilethylene with a series of quaternary ammonium functionalized organosilanes that primarily differed only in the length of the hydrocarbon segment: N-trimethoxysilylpropyl-N,N,N-trimethylammonium chlorides N,N-didecyl-N-methyl-(3-trimethoxysilyi-propyl)ammonium chloride; tetradecyldimethyl-(3-trimethoxysilyl-propyl)ammonium chlorides and octadecyldimethyl-(3-trimethoxysilyl-propyl)ammonium chloride. X-ray diffraction revealed that the films formed with the longest hydrocarbon segment ( 18 carbons) did not exhibit an ordered structure, while the remainder of the films exhibited p6mm pore ordering. These films remained ordered following surfactant extraction and calcination, with some film shrinkage occurring following either procedure. The d-spacing of the films,vas found to decrease linearly with increasing length of the ammonium chloride hydrocarbon segment. As determined by XPS studies, the longer hydrocarbon chain length organosilanes (n greater than or equal to 10) were also found to incorporate more efficiently into the films than the shorter chain material.
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页码:6652 / 6658
页数:7
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