Thermally Induced Hydrosilylation at Deuterium-Terminated Silicon Nanoparticles: An Investigation of the Radical Chain Propagation Mechanism

被引:16
|
作者
Holm, Jason [2 ]
Roberts, Jeffrey T. [1 ]
机构
[1] Univ Minnesota, Dept Chem, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Mech Engn, Minneapolis, MN 55455 USA
基金
美国国家科学基金会;
关键词
NORMAL-ALKYL CHAINS; H STRETCHING MODES; POROUS SILICON; INFRARED-SPECTROSCOPY; HYDROGEN; MONOLAYERS; SURFACES; FUNCTIONALIZATION; CHEMISTRY; ALKENES;
D O I
10.1021/la8042236
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Isotopic labeling techniques were employed to study alkene addition to hydrogen- and deuterium-terminated silicon nanoparticles. Deuterium-terminated silicon nanoparticle synthesis is described, as is the characterization of fresh deuterium-terminated particles by transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and in situ Fourier transform infrared spectroscopy (FTIR). Particles were refluxed in pure 1-dodecene and subsequently characterized by FTIR and nuclear magnetic resonance (NMR) spectroscopy. H-1 NMR results showed features consistent with dodecyl-terminated nanoparticles. Infrared absorption spectra of refluxed particles showed strong evidence of new C-D bond formation, which is consistent with a radical chain mechanism for alkene addition by hydrosilylation.
引用
收藏
页码:7050 / 7056
页数:7
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