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在氢终止的硅(111)上进行热接枝时,Si-O-C相对于Si-C键的优先形成。

Preferential formation of Si-O-C over Si-C linkage upon thermal grafting on hydrogen-terminated silicon (111).

作者信息

Khung Yit Lung, Ngalim Siti Hawa, Meda Laura, Narducci Dario

机构信息

Department of Materials Science, University of Milan-Bicocca, Via R. Cozzi 55, 20125 Milan (Italy), Fax: (+39) 02-6448-5400.

出版信息

Chemistry. 2014 Nov 10;20(46):15151-8. doi: 10.1002/chem.201403014. Epub 2014 Sep 26.

Abstract

In a stringent and near oxygen-free environment, Si-H surfaces were introduced to a trifluoroalkyne, an alcohol-derivatized alkyne, as well as an equal mixture of both alkynes at a temperature of 130 °C. Contact angle measurements, high-resolution X-ray photoelectron spectroscopy (XPS), and angle-resolved XPS were performed to examine the system. Si-H surfaces were found to have a strong preference towards the formation of Si-O-C rather than Si-C bonds when the alcohol and alkyne reactivities were compared.

摘要

在一个严格且近乎无氧的环境中,将硅氢(Si-H)表面在130°C的温度下与三氟炔烃、醇衍生化炔烃以及这两种炔烃的等量混合物接触。通过测量接触角、进行高分辨率X射线光电子能谱(XPS)和角分辨XPS来研究该体系。当比较醇和炔烃的反应活性时,发现硅氢表面强烈倾向于形成硅氧碳(Si-O-C)键而非碳硅(Si-C)键。

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