Evidence for Initiation of Thermal Reactions of Alkenes with Hydrogen-Terminated Silicon by Surface-Catalyzed Thermal Decomposition of the Reactant

被引:18
|
作者
Mischki, Trevor K. [1 ,2 ]
Lopinski, Gregory P. [1 ]
Wayner, Danial D. M. [1 ]
机构
[1] Natl Res Council Canada, Steacie Inst Mol Sci, Ottawa, ON K1A 0R6, Canada
[2] Carleton Univ, Dept Chem, Ottawa, ON K1S 5B6, Canada
关键词
COVALENTLY ATTACHED MONOLAYERS; EXTREMELY MILD ATTACHMENT; ORGANIC MONOLAYERS; ALKYL MONOLAYERS; SI(111) SURFACE; VISIBLE-LIGHT; HYDROSILYLATION; 1-ALKENES; HYBRIDIZATION; DEUTERIUM;
D O I
10.1021/la804210d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
New insights into the mechanism of thermal reactions of alkenes with hydrogen terminated silicon are presented. Scanning tunneling microscopy (STM) imaging at the early stages of the reaction of 1-decene with H/Si(111) at 150 degrees C confirm this reaction occurs via a propagating radical chain mechanism. In addition, evidence is presented for an initiation mechanism involving degradation of hydrocarbon molecules catalyzed by the silanol surface of Schlenk tubes commonly used in carrying out these reactions. Hydrogen-terminated silicon surfaces are found to be unstable in the "inert" solvent dodecane when heated at 150 degrees C in a Pyrex Schlenk tube. By contrast, the surfaces were significantly more stable at the same temperature when reactions were carried out in Teflon (polytetrafluoroethylene or PTFE). The thermal reaction of decene with H/Si(111) was found to proceed more rapidly in Pyrex than in PTFE, consistent with an impurity-based initiation mechanism.
引用
收藏
页码:5626 / 5630
页数:5
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