几丁质季铵盐磷钨酸盐催化环氧化合物选择性氧化裂解生成醛

IF 2.5 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Tengfei Niu, Xile Xia, Ziyi Wei, Xiao Yu and Zhongjian Tian
{"title":"几丁质季铵盐磷钨酸盐催化环氧化合物选择性氧化裂解生成醛","authors":"Tengfei Niu, Xile Xia, Ziyi Wei, Xiao Yu and Zhongjian Tian","doi":"10.1039/D5NJ02656C","DOIUrl":null,"url":null,"abstract":"<p >The selective cleavage oxidation of epoxide represents a promising strategy for generating value-added chemicals such as aldehyde compounds. However, due to the fast oxidation kinetics of aldehydes, developing a catalytic process with high selectivity remains a challenge. In this work, a chitin quaternary ammonium-composite phosphotungstate catalyst HPW-CT-QAS<small><sub>16</sub></small> has been prepared and found to show remarkable catalytic activity for the selective oxidative cleavage of epoxide using H<small><sub>2</sub></small>O<small><sub>2</sub></small> as the oxidant. Both alkyl epoxide and aromatic epoxide and natural methyl 9,10-epoxystearate can participate well in the reaction affording 100% conversion and up to 97.5% aldehyde selectivity. More importantly, the chitin-based catalyst could be easily recovered and reused at least 5 times without any significant loss in its catalytic activity. These characteristics make the selective oxidative cleavage of epoxide more efficient and environmentally friendly, which may be beneficial for industrial applications.</p>","PeriodicalId":95,"journal":{"name":"New Journal of Chemistry","volume":" 37","pages":" 16180-16186"},"PeriodicalIF":2.5000,"publicationDate":"2025-08-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Selective oxidative cleavage of epoxides to aldehydes by chitin quaternary ammonium phosphotungstate as a recycle catalyst\",\"authors\":\"Tengfei Niu, Xile Xia, Ziyi Wei, Xiao Yu and Zhongjian Tian\",\"doi\":\"10.1039/D5NJ02656C\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The selective cleavage oxidation of epoxide represents a promising strategy for generating value-added chemicals such as aldehyde compounds. However, due to the fast oxidation kinetics of aldehydes, developing a catalytic process with high selectivity remains a challenge. In this work, a chitin quaternary ammonium-composite phosphotungstate catalyst HPW-CT-QAS<small><sub>16</sub></small> has been prepared and found to show remarkable catalytic activity for the selective oxidative cleavage of epoxide using H<small><sub>2</sub></small>O<small><sub>2</sub></small> as the oxidant. Both alkyl epoxide and aromatic epoxide and natural methyl 9,10-epoxystearate can participate well in the reaction affording 100% conversion and up to 97.5% aldehyde selectivity. More importantly, the chitin-based catalyst could be easily recovered and reused at least 5 times without any significant loss in its catalytic activity. These characteristics make the selective oxidative cleavage of epoxide more efficient and environmentally friendly, which may be beneficial for industrial applications.</p>\",\"PeriodicalId\":95,\"journal\":{\"name\":\"New Journal of Chemistry\",\"volume\":\" 37\",\"pages\":\" 16180-16186\"},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2025-08-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"New Journal of Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2025/nj/d5nj02656c\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Journal of Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/nj/d5nj02656c","RegionNum":3,"RegionCategory":"化学","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

环氧化物的选择性裂解氧化代表了一种有前途的策略,以产生增值化学品,如醛化合物。然而,由于醛的快速氧化动力学,开发具有高选择性的催化过程仍然是一个挑战。本研究制备了甲壳素季铵复合磷钨酸盐催化剂HPW-CT-QAS16,并发现该催化剂在H2O2为氧化剂的情况下,对环氧化物的选择性氧化裂解具有显著的催化活性。烷基环氧化物、芳烃环氧化物和天然9,10-环氧硬脂酸甲酯均能很好地参与反应,转化率为100%,醛选择性高达97.5%。更重要的是,甲壳素基催化剂可以很容易地回收和重复使用至少5次,而其催化活性没有明显的损失。这些特点使得环氧化物的选择性氧化裂解更加高效和环保,这可能有利于工业应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Selective oxidative cleavage of epoxides to aldehydes by chitin quaternary ammonium phosphotungstate as a recycle catalyst

Selective oxidative cleavage of epoxides to aldehydes by chitin quaternary ammonium phosphotungstate as a recycle catalyst

The selective cleavage oxidation of epoxide represents a promising strategy for generating value-added chemicals such as aldehyde compounds. However, due to the fast oxidation kinetics of aldehydes, developing a catalytic process with high selectivity remains a challenge. In this work, a chitin quaternary ammonium-composite phosphotungstate catalyst HPW-CT-QAS16 has been prepared and found to show remarkable catalytic activity for the selective oxidative cleavage of epoxide using H2O2 as the oxidant. Both alkyl epoxide and aromatic epoxide and natural methyl 9,10-epoxystearate can participate well in the reaction affording 100% conversion and up to 97.5% aldehyde selectivity. More importantly, the chitin-based catalyst could be easily recovered and reused at least 5 times without any significant loss in its catalytic activity. These characteristics make the selective oxidative cleavage of epoxide more efficient and environmentally friendly, which may be beneficial for industrial applications.

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
New Journal of Chemistry
New Journal of Chemistry 化学-化学综合
CiteScore
5.30
自引率
6.10%
发文量
1832
审稿时长
2 months
期刊介绍: A journal for new directions in chemistry
×
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