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Preparation of amino-terminated monolayers via hydrolysis of phthalimide anchored to Si(111)

机译:通过锚固在Si(111)上的邻苯二甲酰亚胺的水解制备氨基端基单层

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摘要

Phthalimide monolayers were prepared on silicon (111) by the reaction of hydrogen-terminated silicon surfaces with vinylphthali-mide. 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.
机译:通过氢封端的硅表面与乙烯基邻苯二甲酰亚胺的反应,在硅(111)上制备邻苯二甲酰亚胺单层。在甲胺溶液中在硅表面上进行邻苯二甲酰亚胺的水解反应,以制备氨基端基单层。用衰减全反射红外光谱和原子力显微镜研究了一系列反应,以制备氨基末端的单分子层。这项工作提供了一种简单的方法来制备氨基末端的有机单分子层,作为固定层来固定功能分子,例如染料,DNA和蛋白质。

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