二氧化碳间接加氢的贱金属催化剂

IF 3.3 Q2 CHEMISTRY, MULTIDISCIPLINARY ACS Organic & Inorganic Au Pub Date : 2023-07-24 DOI:10.1021/acsorginorgau.3c00023
Jagrit Grover, Suman Maji, Chitrala Teja, Shaeel A. Al Thabaiti*, Mohamed Mokhtar M. Mostafa, Goutam K. Lahiri* and Debabrata Maiti*, 
{"title":"二氧化碳间接加氢的贱金属催化剂","authors":"Jagrit Grover,&nbsp;Suman Maji,&nbsp;Chitrala Teja,&nbsp;Shaeel A. Al Thabaiti*,&nbsp;Mohamed Mokhtar M. Mostafa,&nbsp;Goutam K. Lahiri* and Debabrata Maiti*,&nbsp;","doi":"10.1021/acsorginorgau.3c00023","DOIUrl":null,"url":null,"abstract":"<p >We herein report a novel Mn-SNS-based catalyst, which is capable of performing indirect hydrogenation of CO<sub>2</sub> to methanol <i>via</i> formylation. In this domain of CO<sub>2</sub> hydrogenation, pincer ligands have shown a clear predominance. Our catalyst is based on the SNS-type tridentate ligand, which is quite stable and cheap as compared to the pincer type ligands. The catalyst can also be recycled effectively after the formylation reaction without any significant change in efficiency. Various amines including both primary and secondary amines worked well under the protocol to provide the desired formylated product in good yields. The formed formylated amines can also be reduced further at higher pressures of hydrogen. As a whole, we have developed a protocol that involves indirect CO<sub>2</sub> hydrogenation to methanol that proceeds <i>via</i> formylation of amines.</p>","PeriodicalId":29797,"journal":{"name":"ACS Organic & Inorganic Au","volume":null,"pages":null},"PeriodicalIF":3.3000,"publicationDate":"2023-07-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.acs.org/doi/epdf/10.1021/acsorginorgau.3c00023","citationCount":"0","resultStr":"{\"title\":\"Base Metal Catalyst for Indirect Hydrogenation of CO2\",\"authors\":\"Jagrit Grover,&nbsp;Suman Maji,&nbsp;Chitrala Teja,&nbsp;Shaeel A. Al Thabaiti*,&nbsp;Mohamed Mokhtar M. Mostafa,&nbsp;Goutam K. Lahiri* and Debabrata Maiti*,&nbsp;\",\"doi\":\"10.1021/acsorginorgau.3c00023\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >We herein report a novel Mn-SNS-based catalyst, which is capable of performing indirect hydrogenation of CO<sub>2</sub> to methanol <i>via</i> formylation. In this domain of CO<sub>2</sub> hydrogenation, pincer ligands have shown a clear predominance. Our catalyst is based on the SNS-type tridentate ligand, which is quite stable and cheap as compared to the pincer type ligands. The catalyst can also be recycled effectively after the formylation reaction without any significant change in efficiency. Various amines including both primary and secondary amines worked well under the protocol to provide the desired formylated product in good yields. The formed formylated amines can also be reduced further at higher pressures of hydrogen. As a whole, we have developed a protocol that involves indirect CO<sub>2</sub> hydrogenation to methanol that proceeds <i>via</i> formylation of amines.</p>\",\"PeriodicalId\":29797,\"journal\":{\"name\":\"ACS Organic & Inorganic Au\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":3.3000,\"publicationDate\":\"2023-07-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.acs.org/doi/epdf/10.1021/acsorginorgau.3c00023\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Organic & Inorganic Au\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acsorginorgau.3c00023\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Organic & Inorganic Au","FirstCategoryId":"1085","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsorginorgau.3c00023","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

摘要

我们在此报道了一种新型的基于Mn-SNS的催化剂,该催化剂能够通过甲酰化将CO2间接氢化为甲醇。在CO2加氢的这一领域,钳型配体显示出明显的优势。我们的催化剂基于SNS型三齿配体,与钳形配体相比,它非常稳定且便宜。催化剂也可以在甲酰化反应后有效地再循环,而效率没有任何显著变化。包括伯胺和仲胺的各种胺在该方案下工作良好,以高产率提供所需的甲酰化产物。形成的甲酰化胺也可以在更高的氢气压力下进一步还原。总的来说,我们已经开发了一个方案,该方案涉及通过胺的甲酰化进行的间接CO2氢化为甲醇。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

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
Base Metal Catalyst for Indirect Hydrogenation of CO2

We herein report a novel Mn-SNS-based catalyst, which is capable of performing indirect hydrogenation of CO2 to methanol via formylation. In this domain of CO2 hydrogenation, pincer ligands have shown a clear predominance. Our catalyst is based on the SNS-type tridentate ligand, which is quite stable and cheap as compared to the pincer type ligands. The catalyst can also be recycled effectively after the formylation reaction without any significant change in efficiency. Various amines including both primary and secondary amines worked well under the protocol to provide the desired formylated product in good yields. The formed formylated amines can also be reduced further at higher pressures of hydrogen. As a whole, we have developed a protocol that involves indirect CO2 hydrogenation to methanol that proceeds via formylation of amines.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
ACS Organic & Inorganic Au
ACS Organic & Inorganic Au 有机化学、无机化学-
CiteScore
4.10
自引率
0.00%
发文量
0
期刊介绍: ACS Organic & Inorganic Au is an open access journal that publishes original experimental and theoretical/computational studies on organic organometallic inorganic crystal growth and engineering and organic process chemistry. Short letters comprehensive articles reviews and perspectives are welcome on topics that include:Organic chemistry Organometallic chemistry Inorganic Chemistry and Organic Process Chemistry.
期刊最新文献
Unraveling Chlorite Oxidation Pathways in Equatorially Heteroatom-Substituted Nonheme Iron Complexes t-Butyl and Trimethylsilyl Substituents in Nickel Allyl Complexes: Similar but Not the Same The Persistence of Hydrogen Bonds in Pyrimidinones: From Solution to Crystal Anion-Exchange Membrane Oxygen Separator Electronic Coupling in Triferrocenylpnictogens
×
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