The adsorption and reaction of 2-iodoethanol on Ag(111)

被引:50
作者
Wu, G
Stacchiola, D
Kaltchev, M
Tysoe, WT [1 ]
机构
[1] Univ Wisconsin, Dept Chem, Milwaukee, WI 53211 USA
[2] Univ Wisconsin, Surface Studies Lab, Milwaukee, WI 53211 USA
关键词
alcohols; infrared adsorption spectroscopy; reflection spectroscopy; silver; thermal desorption spectroscopy;
D O I
10.1016/S0039-6028(00)00602-6
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Oxametallacycles have been previously grafted onto Ag(110) by adsorbing 2-iodoethanol to mimic possible intermediates in the catalytic epoxidation of ethylene. Since Ag(111) has been shown to be a good model catalyst for this reaction under realistic pressures of ethylene and oxygen, this work was extended to studying the chemistry of 2-iodoethanol on Ag(111) using temperature-programmed desorption and reflection-absorption infrared spectroscopies. It was found that iodoethanol reacts at relatively low temperatures to form 2-hydroxyethyl species and co-adsorbed iodine. Hydroxyethyl species react above similar to 150 K to eliminate water and evolve equimolar amounts of ethylene. The remaining fragment with stoichiometry C2H4O reacts with the surface to form predominantly oxametallacycles which thermally decompose at similar to 260 K to yield acetaldehyde. A minority species is also identified which thermally decomposes to yield acetaldehyde at similar to 315 K and may be due to an oxametallacycle which adopts a different orientation as a function of temperature and coverage or a 2-hydroxyethylidene species. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:81 / 92
页数:12
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