低温S-S、S-O和S-C键转移连续流动模式下的氢解

IF 2 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY
Andrey M. Chibiryaev, Ivan V. Kozhevnikov, Oleg N. Martyanov
{"title":"低温S-S、S-O和S-C键转移连续流动模式下的氢解","authors":"Andrey M. Chibiryaev,&nbsp;Ivan V. Kozhevnikov,&nbsp;Oleg N. Martyanov","doi":"10.1007/s41981-025-00353-4","DOIUrl":null,"url":null,"abstract":"<div><p>The hydroconversion of model organosulfur compounds with different formal oxidation states of sulfur (thiophene, dimethyl disulfide, dimethyl sulfoxide, dimethyl sulfone, sulfolane, and dimethyl sulfate) was mimicked under transfer hydrogenation (TH) reaction conditions in supercritical methanol and isopropanol. The reactions were carried out in a continuous flow reactor at 250 °C and 350 °C. At 350 °C, only dimethyl disulfide and dimethyl sulfoxide underwent complete or nearly complete conversion within 5 min of contact time, mainly by reductive cleavage of S–S, S–O, and S–C bonds to form dimethyl sulfide MeSMe and methyl mercaptan MeSH.</p><h3>Graphical Abstract</h3><p>Description</p><p>Simple organosulfur compounds with different formal oxidation states of sulfur in their molecules were studied in high-temperature transfer hydrogenation reaction with supercritical methanol and isopropanol in continuous flow mode.</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":630,"journal":{"name":"Journal of Flow Chemistry","volume":"15 2","pages":"131 - 136"},"PeriodicalIF":2.0000,"publicationDate":"2025-04-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"High-temperature S–S, S–O, and S–C bond transfer hydrogenolysis by lower alcohols in continuous flow mode\",\"authors\":\"Andrey M. Chibiryaev,&nbsp;Ivan V. Kozhevnikov,&nbsp;Oleg N. Martyanov\",\"doi\":\"10.1007/s41981-025-00353-4\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The hydroconversion of model organosulfur compounds with different formal oxidation states of sulfur (thiophene, dimethyl disulfide, dimethyl sulfoxide, dimethyl sulfone, sulfolane, and dimethyl sulfate) was mimicked under transfer hydrogenation (TH) reaction conditions in supercritical methanol and isopropanol. The reactions were carried out in a continuous flow reactor at 250 °C and 350 °C. At 350 °C, only dimethyl disulfide and dimethyl sulfoxide underwent complete or nearly complete conversion within 5 min of contact time, mainly by reductive cleavage of S–S, S–O, and S–C bonds to form dimethyl sulfide MeSMe and methyl mercaptan MeSH.</p><h3>Graphical Abstract</h3><p>Description</p><p>Simple organosulfur compounds with different formal oxidation states of sulfur in their molecules were studied in high-temperature transfer hydrogenation reaction with supercritical methanol and isopropanol in continuous flow mode.</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>\",\"PeriodicalId\":630,\"journal\":{\"name\":\"Journal of Flow Chemistry\",\"volume\":\"15 2\",\"pages\":\"131 - 136\"},\"PeriodicalIF\":2.0000,\"publicationDate\":\"2025-04-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Flow Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s41981-025-00353-4\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Flow Chemistry","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s41981-025-00353-4","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

摘要

在超临界甲醇和异丙醇的转移加氢(TH)反应条件下,模拟了不同形式氧化态硫(噻吩、二甲基二硫化物、二甲基亚砜、二甲基砜、砜烷和硫酸二甲酯)的模型有机硫化合物的加氢转化。反应在250℃和350℃的连续流反应器中进行。在350℃下,只有二甲基二硫化物和二甲基亚砜在5 min的接触时间内发生完全或接近完全的转化,主要是通过S-S、S-O和S-C键的还原裂解形成二甲基硫化物MeSMe和甲基硫醇MeSH。摘要用超临界甲醇和异丙醇在连续流模式下进行高温转移加氢反应,研究了分子中硫形态氧化态不同的简单有机硫化合物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

High-temperature S–S, S–O, and S–C bond transfer hydrogenolysis by lower alcohols in continuous flow mode

High-temperature S–S, S–O, and S–C bond transfer hydrogenolysis by lower alcohols in continuous flow mode

The hydroconversion of model organosulfur compounds with different formal oxidation states of sulfur (thiophene, dimethyl disulfide, dimethyl sulfoxide, dimethyl sulfone, sulfolane, and dimethyl sulfate) was mimicked under transfer hydrogenation (TH) reaction conditions in supercritical methanol and isopropanol. The reactions were carried out in a continuous flow reactor at 250 °C and 350 °C. At 350 °C, only dimethyl disulfide and dimethyl sulfoxide underwent complete or nearly complete conversion within 5 min of contact time, mainly by reductive cleavage of S–S, S–O, and S–C bonds to form dimethyl sulfide MeSMe and methyl mercaptan MeSH.

Graphical Abstract

Description

Simple organosulfur compounds with different formal oxidation states of sulfur in their molecules were studied in high-temperature transfer hydrogenation reaction with supercritical methanol and isopropanol in continuous flow mode.

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
Journal of Flow Chemistry
Journal of Flow Chemistry CHEMISTRY, MULTIDISCIPLINARY-
CiteScore
6.40
自引率
3.70%
发文量
29
审稿时长
>12 weeks
期刊介绍: The main focus of the journal is flow chemistry in inorganic, organic, analytical and process chemistry in the academic research as well as in applied research and development in the pharmaceutical, agrochemical, fine-chemical, petro- chemical, fragrance industry.
×
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