Ambient-pressure selective hydrogenation of unsaturated aldehydes and ketones into unsaturated alcohols in the water phase†

IF 3.3 3区 化学 Q2 CHEMISTRY, INORGANIC & NUCLEAR
Tao Wang, Bin Li, Yu Zhang, Shuting Xu, Jun Wang, Jianwei Zheng, Hao Li, Fengjun Zhang and Xiaolong Fang
{"title":"Ambient-pressure selective hydrogenation of unsaturated aldehydes and ketones into unsaturated alcohols in the water phase†","authors":"Tao Wang, Bin Li, Yu Zhang, Shuting Xu, Jun Wang, Jianwei Zheng, Hao Li, Fengjun Zhang and Xiaolong Fang","doi":"10.1039/D4DT03338H","DOIUrl":null,"url":null,"abstract":"<p >A universal and green catalytic system for the hydrogenation of unsaturated aldehydes and ketones into the corresponding alcohols with the C<img>C bonds retained under atmospheric hydrogen pressure in the water phase was realized by <em>N</em>-functionalized amino ligand-stabilized ruthenium complexes (<em>o</em>-PPh<small><sub>2</sub></small>C<small><sub>6</sub></small>H<small><sub>4</sub></small>NHMe)[(CH<small><sub>2</sub></small>NHR)<small><sub>2</sub></small>]RuCl<small><sub>2</sub></small> (R = H, Me, Et) and (<em>o</em>-PPh<small><sub>2</sub></small>C<small><sub>6</sub></small>H<small><sub>4</sub></small>NMe<small><sub>2</sub></small>)[(CH<small><sub>2</sub></small>NHEt)<small><sub>2</sub></small>]RuCl<small><sub>2</sub></small> with wide substrate compatibility and excellent functionality tolerance. The structural synergism between <em>o</em>-PPh<small><sub>2</sub></small>C<small><sub>6</sub></small>H<small><sub>4</sub></small>NHMe and (CH<small><sub>2</sub></small>NHEt)<small><sub>2</sub></small> achieves the enhanced performance, with a positive correlation with the electron density of the amino ligand.</p>","PeriodicalId":71,"journal":{"name":"Dalton Transactions","volume":" 5","pages":" 1791-1796"},"PeriodicalIF":3.3000,"publicationDate":"2025-01-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Dalton Transactions","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/dt/d4dt03338h","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0

Abstract

A universal and green catalytic system for the hydrogenation of unsaturated aldehydes and ketones into the corresponding alcohols with the CC bonds retained under atmospheric hydrogen pressure in the water phase was realized by N-functionalized amino ligand-stabilized ruthenium complexes (o-PPh2C6H4NHMe)[(CH2NHR)2]RuCl2 (R = H, Me, Et) and (o-PPh2C6H4NMe2)[(CH2NHEt)2]RuCl2 with wide substrate compatibility and excellent functionality tolerance. The structural synergism between o-PPh2C6H4NHMe and (CH2NHEt)2 achieves the enhanced performance, with a positive correlation with the electron density of the amino ligand.

Abstract Image

不饱和醛和酮在水相中常压选择性加氢成不饱和醇的研究
采用n功能化氨基配体稳定的钌配合物(o-PPh2C6H4NHMe)[(CH2NHR)2]RuCl2 (R = H, Me, Et)和(o-PPh2C6H4NMe2)[(CH2NHEt)2]RuCl2,具有广泛的底物相容性和优异的功能耐受性,实现了水相常压下不饱和醛和酮加氢成具有保留C=C键的相应醇的绿色催化体系。o-PPh2C6H4NHMe和(CH2NHEt)2之间的结构协同作用使性能得到增强,且与氨基配体的电子密度呈正相关。
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 求助全文
来源期刊
Dalton Transactions
Dalton Transactions 化学-无机化学与核化学
CiteScore
6.60
自引率
7.50%
发文量
1832
审稿时长
1.5 months
期刊介绍: Dalton Transactions is a journal for all areas of inorganic chemistry, which encompasses the organometallic, bioinorganic and materials chemistry of the elements, with applications including synthesis, catalysis, energy conversion/storage, electrical devices and medicine. Dalton Transactions welcomes high-quality, original submissions in all of these areas and more, where the advancement of knowledge in inorganic chemistry is significant.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信