Recent Advances in Catalyst Design for Carboxylation Using CO2 as the C1 Feedstock

IF 3.8 3区 化学 Q2 CHEMISTRY, PHYSICAL Catalysts Pub Date : 2023-11-30 DOI:10.3390/catal13121489
Sagarkumar Rajendrakumar Shah, N. J. Mazumdar, Ander Centeno-Pedrazo, D. Deka, N. Artioli, H. Manyar
{"title":"Recent Advances in Catalyst Design for Carboxylation Using CO2 as the C1 Feedstock","authors":"Sagarkumar Rajendrakumar Shah, N. J. Mazumdar, Ander Centeno-Pedrazo, D. Deka, N. Artioli, H. Manyar","doi":"10.3390/catal13121489","DOIUrl":null,"url":null,"abstract":"Carbon dioxide is ideal for carboxylation reactions as a renewable and sustainable C1 feedstock and has significant recognition owing to its low cost, non-toxicity, and high abundance. To depreciate the environmental concentration of CO2, which causes the greenhouse gas effect, developing new catalytic protocols for organic synthesis in CO2 utilization is of great importance. This review focuses on carboxylation reactions using CO2 as a C1 feedstock to synthesize value-added functionalized carboxylic acids and their corresponding derivatives via catalytically generated allyl metal intermediates, photoredox catalysis, and electrocatalysis with a focus on recent developments and opportunities in catalyst design for carboxylation reactions. In this article, we describe recent developments in the carboxylation of C–H bonds, alkenes, and alkynes using CO2 as the C1 source for various reactions under different conditions, as well as the potential direction for the further development of CO2 utilization in organic synthesis.","PeriodicalId":9794,"journal":{"name":"Catalysts","volume":"16 1","pages":""},"PeriodicalIF":3.8000,"publicationDate":"2023-11-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Catalysts","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.3390/catal13121489","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Carbon dioxide is ideal for carboxylation reactions as a renewable and sustainable C1 feedstock and has significant recognition owing to its low cost, non-toxicity, and high abundance. To depreciate the environmental concentration of CO2, which causes the greenhouse gas effect, developing new catalytic protocols for organic synthesis in CO2 utilization is of great importance. This review focuses on carboxylation reactions using CO2 as a C1 feedstock to synthesize value-added functionalized carboxylic acids and their corresponding derivatives via catalytically generated allyl metal intermediates, photoredox catalysis, and electrocatalysis with a focus on recent developments and opportunities in catalyst design for carboxylation reactions. In this article, we describe recent developments in the carboxylation of C–H bonds, alkenes, and alkynes using CO2 as the C1 source for various reactions under different conditions, as well as the potential direction for the further development of CO2 utilization in organic synthesis.
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
以二氧化碳为 C1 原料进行羧化的催化剂设计最新进展
二氧化碳作为一种可再生和可持续的 C1 原料,是羧化反应的理想原料,并因其低成本、无毒性和高丰度而得到广泛认可。为了降低导致温室气体效应的二氧化碳在环境中的浓度,开发新的利用二氧化碳进行有机合成的催化方案具有重要意义。本综述侧重于以二氧化碳为 C1 原料的羧化反应,通过催化生成的烯丙基金属中间体、光氧化催化和电催化合成高附加值的功能化羧酸及其相应衍生物,重点介绍羧化反应催化剂设计方面的最新进展和机遇。在本文中,我们将介绍在不同条件下以 CO2 为 C1 源进行各种反应的 C-H 键、烯烃和炔烃羧化反应的最新进展,以及在有机合成中进一步开发 CO2 利用的潜在方向。
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
Catalysts
Catalysts CHEMISTRY, PHYSICAL-
CiteScore
6.80
自引率
7.70%
发文量
1330
审稿时长
3 months
期刊介绍: Catalysts (ISSN 2073-4344) is an international open access journal of catalysts and catalyzed reactions. Catalysts publishes reviews, regular research papers (articles) and short communications. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
期刊最新文献
Dehydration of Isopropanol over Silica-Supported Heteropoly Acids A Kinetic Model of Furfural Hydrogenation to 2-Methylfuran on Nanoparticles of Nickel Supported on Sulfuric Acid-Modified Biochar Catalyst Comparative Study of Supported Ni and Co Catalysts Prepared Using the All-in-One Method in the Hydrogenation of CO2: Effects of Using (Poly)Vinyl Alcohol (PVA) as an Additive Editorial: Special Issue Entitled “Development of g-C3N4-Based Photocatalysts: Environmental Purification and Energy Conversion” Structure Robustness of Highly Dispersed Pt/Al2O3 Catalyst for Propane Dehydrogenation during Oxychlorination Regeneration Process
×
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