Cover Feature: Diarylformamides as a Safe Reservoir and Room Temperature Source of Ultra-Pure CO in the Context of a ‘Green’ rWGS Reaction (ChemSusChem 22/2024)

IF 7.5 2区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY ChemSusChem Pub Date : 2024-11-25 DOI:10.1002/cssc.202482202
Royel Hurtado, Lisha Lou, Lukas Klerner, Iman Dindarloo Inaloo, Frank W. Heineman, Sjoerd Harder, Günter Schmid, Romano Dorta
{"title":"Cover Feature: Diarylformamides as a Safe Reservoir and Room Temperature Source of Ultra-Pure CO in the Context of a ‘Green’ rWGS Reaction (ChemSusChem 22/2024)","authors":"Royel Hurtado,&nbsp;Lisha Lou,&nbsp;Lukas Klerner,&nbsp;Iman Dindarloo Inaloo,&nbsp;Frank W. Heineman,&nbsp;Sjoerd Harder,&nbsp;Günter Schmid,&nbsp;Romano Dorta","doi":"10.1002/cssc.202482202","DOIUrl":null,"url":null,"abstract":"<p><b>The Cover Feature</b> shows how the solvent-free catalytic decarbonylation of diarylformamides affords very pure CO and makes them ideal solid-state reservoirs/vectors of CO. The recovered diarylamines are readily formylated back to the formamides with formic acid/triethylamine azeotrope on 30–100 g scales. More information can be found in the Research Article by I. Dindarloo Inaloo, R. Dorta and co-workers.\n <figure>\n <div><picture>\n <source></source></picture><p></p>\n </div>\n </figure>\n </p>","PeriodicalId":149,"journal":{"name":"ChemSusChem","volume":"17 22","pages":""},"PeriodicalIF":7.5000,"publicationDate":"2024-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cssc.202482202","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemSusChem","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cssc.202482202","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

The Cover Feature shows how the solvent-free catalytic decarbonylation of diarylformamides affords very pure CO and makes them ideal solid-state reservoirs/vectors of CO. The recovered diarylamines are readily formylated back to the formamides with formic acid/triethylamine azeotrope on 30–100 g scales. More information can be found in the Research Article by I. Dindarloo Inaloo, R. Dorta and co-workers.

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
封面专题:二酰甲酰胺作为 "绿色 "rWGS 反应背景下超纯 CO 的安全储备和室温来源(ChemSusChem 22/2024)
封面特写展示了二芳基甲酰胺的无溶剂催化脱羰基反应如何产生纯度极高的一氧化碳,并使其成为理想的一氧化碳固态贮存器/载体。用甲酸/三乙胺共沸物将回收的二芳基甲胺甲酰化成甲酰胺,规模为 30-100 克。更多信息可参阅 I. Dindarloo Inaloo、R. Dorta 及合作者的研究文章。
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
ChemSusChem
ChemSusChem 化学-化学综合
CiteScore
15.80
自引率
4.80%
发文量
555
审稿时长
1.8 months
期刊介绍: ChemSusChem Impact Factor (2016): 7.226 Scope: Interdisciplinary journal Focuses on research at the interface of chemistry and sustainability Features the best research on sustainability and energy Areas Covered: Chemistry Materials Science Chemical Engineering Biotechnology
期刊最新文献
Front Cover: Quantitative Analysis and Manipulation of Alkali Metal Cations at the Cathode Surface in Membrane Electrode Assembly Electrolyzers for CO2 Reduction Reactions (ChemSusChem 22/2024) Cover Feature: Diarylformamides as a Safe Reservoir and Room Temperature Source of Ultra-Pure CO in the Context of a ‘Green’ rWGS Reaction (ChemSusChem 22/2024) Cover Feature: Microplastics in Cosmetics: Open Questions and Sustainable Opportunities (ChemSusChem 22/2024) Cover Feature: Biomass-Derived, Target Specific, and Ecologically Safer Insecticide Active Ingredients (ChemSusChem 22/2024) Advances and Challenges in the Development of Immobilized Enzymes for Batch and Flow Biocatalyzed Processes.
×
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