H–D Exchange between methane and deuteriated potassium amide supported on alumina

H. Handa, T. Baba, Y. Ono
{"title":"H–D Exchange between methane and deuteriated potassium amide supported on alumina","authors":"H. Handa, T. Baba, Y. Ono","doi":"10.1039/A706059I","DOIUrl":null,"url":null,"abstract":"The H–D exchange reaction between methane and deuteriated potassium amide supported on alumina (KND2/Al2O3), a strongly basic catalyst, has been investigated by FTIR spectroscopy. KND2/Al2O3 was prepared by contacting KNH2/Al2O3 with D2 at 373 K for 30 min. The N–D asymmetric and symmetric bands in KND2 were observed at 2411 and 2343 cm−1. The ND2 bending bands were observed at 1132 cm−1. The H–D exchange reaction between CH4 and KND2 proceeded at room temperature. First, the N–H bands in KNDH were observed at 3210 cm−1. and then KNDH was further converted to KNH2, whose N–H stretching bands were observed at 3238 and 3190 cm−1. The H–D exchange reaction between ethane and KND2/Al2O3 also proceeded at room temperature, but the rate was slower than that between methane and KND2/Al2O3. The lower reactivity of ethane indicates a carbanion mechanism since the acidity (pKa) of ethane (42) is lower than that of methane (40).","PeriodicalId":17286,"journal":{"name":"Journal of the Chemical Society, Faraday Transactions","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"1998-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"11","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the Chemical Society, Faraday Transactions","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1039/A706059I","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 11

Abstract

The H–D exchange reaction between methane and deuteriated potassium amide supported on alumina (KND2/Al2O3), a strongly basic catalyst, has been investigated by FTIR spectroscopy. KND2/Al2O3 was prepared by contacting KNH2/Al2O3 with D2 at 373 K for 30 min. The N–D asymmetric and symmetric bands in KND2 were observed at 2411 and 2343 cm−1. The ND2 bending bands were observed at 1132 cm−1. The H–D exchange reaction between CH4 and KND2 proceeded at room temperature. First, the N–H bands in KNDH were observed at 3210 cm−1. and then KNDH was further converted to KNH2, whose N–H stretching bands were observed at 3238 and 3190 cm−1. The H–D exchange reaction between ethane and KND2/Al2O3 also proceeded at room temperature, but the rate was slower than that between methane and KND2/Al2O3. The lower reactivity of ethane indicates a carbanion mechanism since the acidity (pKa) of ethane (42) is lower than that of methane (40).
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
氧化铝负载的甲烷与氘化钾酰胺之间的H-D交换
采用傅里叶红外光谱研究了强碱性催化剂氧化铝(KND2/Al2O3)负载的甲烷与氘化钾酰胺之间的H-D交换反应。将KNH2/Al2O3与D2在373 K下接触30 min,制得KND2/Al2O3,在2411和2343 cm−1处观察到KND2中的N-D不对称带和对称带。在1132 cm−1处观察到ND2弯曲带。CH4和KND2之间的H-D交换反应在室温下进行。首先,在3210 cm−1处观察到KNDH中的N-H带。KNDH进一步转化为KNH2,在3238和3190 cm−1处观察到KNH2的N-H伸展带。乙烷与KND2/Al2O3之间的H-D交换反应也在室温下进行,但速度比甲烷与KND2/Al2O3之间的反应慢。乙烷(42)的酸度(pKa)低于甲烷(40),表明乙烷的反应活性较低,表明其为碳离子反应机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Very low pressure pyrolysis of phenylacetic acid Photophysics and photoreactivity of substituted thioxanthones Hydrogen bonding Part 44 Thermodynamics of complexation of 3,5-dichlorophenol with ketones and ethers in cyclohexane: the Badger–Bauer relationship IR spectroscopy of small and weakly interacting molecular probes for acidic and basic zeolites Electron transfer in proteins
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1