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通过 B(CF3)催化的氧化硅表面硅氧烷化反应制备有机单层膜。

Organic Monolayers by B(CF)-Catalyzed Siloxanation of Oxidized Silicon Surfaces.

机构信息

Laboratory of Organic Chemistry, Wageningen University and Research , Stippeneng 4, 6708 WE Wageningen, The Netherlands.

Department of Chemical and Materials Engineering, King Abdulaziz University , Jeddah, Saudi Arabia.

出版信息

Langmuir. 2017 Mar 7;33(9):2185-2193. doi: 10.1021/acs.langmuir.7b00110. Epub 2017 Feb 23.

Abstract

Inspired by the homogeneous catalyst tris(pentafluorophenyl) borane [B(CF)], which acts as a promotor of Si-H bond activation, we developed and studied a method of modifying silicon oxide surfaces using hydrosilanes with B(CF) as the catalyst. This dedihydrosiloxanation reaction yields complete surface coverage within 10 min at room temperature. Organic monolayers derived from hydrosilanes with varying carbon chain lengths (C-C) were prepared on oxidized Si(111) surfaces, and the thermal and hydrolytic stabilities of the obtained monolayers were investigated in acidic (pH 3) medium, basic (pH 11) medium, phosphate-buffered saline (PBS), and deionized water (neutral conditions) for up to 30 days. DFT calculations were carried out to gain insight into the mechanism, and the computational results support a mechanism involving silane activation with B(CF). This catalyzed reaction path proceeds through a low-barrier-height transition state compared to the noncatalyzed reaction path.

摘要

受均相催化剂三(五氟苯基)硼烷 [B(CF)] 激活 Si-H 键作用的启发,我们开发并研究了一种使用 B(CF) 作为催化剂的硅烷化反应来修饰氧化硅表面的方法。在室温下,该反应在 10 分钟内即可实现完全的表面覆盖。我们在氧化的 Si(111)表面上制备了具有不同碳链长度 (C-C) 的硅烷衍生的有机单层,并在酸性 (pH 3)、碱性 (pH 11)、磷酸盐缓冲盐水 (PBS) 和去离子水 (中性条件) 中对所得单层的热稳定性和水解稳定性进行了长达 30 天的研究。我们进行了 DFT 计算以深入了解该反应机制,计算结果支持了涉及 B(CF) 激活硅烷的反应机制。与非催化反应路径相比,该催化反应路径通过低能垒过渡态进行。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99dc/5343549/d9e2d6202343/la-2017-00110d_0007.jpg

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