Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5425117 | Surface Science | 2007 | 5 Pages |
Abstract
Phthalimide monolayers were prepared on silicon (1Â 1Â 1) by the reaction of hydrogen-terminated silicon surfaces with vinylphthalimide. The hydrolysis reaction of phthalimide on silicon surfaces was performed in a methylamine solution to prepare amino-terminated monolayers. A series of reactions to prepare amino-terminated monolayers was investigated with attenuated total reflectance infrared spectroscopy and atomic force microscopy. This work provides a simple method to prepare amino-terminated organic monolayers act as anchor layers to immobilize functional molecules such as dyes, DNA and proteins.
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Physical Sciences and Engineering
Chemistry
Physical and Theoretical Chemistry
Authors
Masato Ara, Motohiro Tsuji, Hirokazu Tada,