固体硫酸薄膜の表面分子水素の識別
Suzanne B Couling1, Karen L Nash, John Fletcher
1Department of Chemistry, University of York, Heslington, York YO1 5DD, UK.
Journal of the American Chemical Society
|October 23, 2003
まとめ
イオン硫酸の表面にある安定した分子水素は,アンモニアと反応する. この反応は,枯渇まで急速に発生し,その後,表面ヒドロニウムイオンを含む,より遅い,拡散制限プロセスが続きます.
科学分野:
- 大気化学 大気化学
- 表面科学とは,地表科学である.
背景:
- イオン硫酸水素は,凝縮した薄膜に安定した分子水素を形成する.
- これらの表面水素は化学反応に影響を与えます.
研究 の 目的:
- アモニアとイオン酸硫黄酸水素との相互作用における表面分子水素の役割を調査する.
- 関連する反応機構を明らかにする.
主な方法:
- 赤外線スペクトロスコーピーは,赤外線スペクトロスコーピーを用います.
- 二次イオン質量スペクトロメトリ
主要な成果:
- 安定した分子水素は,イオン硫酸水素の表面で特定されました.
- アンモニアは,この地表の種と,その枯渇まで急速に反応した.
- アンモニアと表面ヒドロニウムイオン (H3O+) の間で,より遅い,拡散制限反応が観察されました.
結論:
- 表面の分子水素は,アンモニアの重要な反応部位である.
- 反応動力学は,急速な表面反応と,より遅い拡散制御プロセスの両方によって影響を受けます.
関連する概念動画
Acid-Catalyzed Hydration of Alkenes
Alkenes react with water in the presence of an acid to form an alcohol. In the absence of acid, hydration of alkenes does not occur at a significant rate, and the acid is not consumed in the reaction. Therefore, alkene hydration is an acid-catalyzed reaction.
Alkynes to Aldehydes and Ketones: Acid-Catalyzed Hydration
Introduction
Analogous to alkenes, alkynes also undergo acid-catalyzed hydration. While the addition of water to an alkene gives an alcohol, hydration of alkynes produces different products such as aldehydes and ketones.
Analogous to alkenes, alkynes also undergo acid-catalyzed hydration. While the addition of water to an alkene gives an alcohol, hydration of alkynes produces different products such as aldehydes and ketones.
Preparation and Reactions of Sulfides
Sulfides are the sulfur analog of ethers, just as thiols are the sulfur analog of alcohol. Like ethers, sulfides also consist of two hydrocarbon groups bonded to the central sulfur atom. Depending upon the type of groups present, sulfides can be symmetrical or asymmetrical. Symmetrical sulfides can be prepared via an SN2 reaction between 2 equivalents of an alkyl halide and one equivalent of sodium sulfide.
Acid Halides to Carboxylic Acids: Hydrolysis
Hydrolysis of acid halides is a nucleophilic acyl substitution reaction in which acid halides react with water to give carboxylic acids. The reaction occurs readily and does not require acid or a base catalyst.
As shown below, the mechanism involves a nucleophilic attack by water at the carbonyl carbon to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen π bond along with the departure of a halide ion. A final proton transfer step yields carboxylic acid...
As shown below, the mechanism involves a nucleophilic attack by water at the carbonyl carbon to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen π bond along with the departure of a halide ion. A final proton transfer step yields carboxylic acid...


