可回收多金属氧酸离子液体催化剂在温和条件下选择性裂解木质素β-O-4模型

IF 9.3 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Green Chemistry Pub Date : 2023-03-07 DOI:10.1039/D3GC00087G
Xing Xin, Zheng Li, Manzhou Chi, Mo Zhang, Yuanyuan Dong, Hongjin Lv and Guo-Yu Yang
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引用次数: 0

摘要

在温和的条件下,β-O-4键的高效和选择性裂解是将木质纤维素转化为增值芳香化学品的一个有前途的策略。通过H5PMo10V2O40 (HPMoV)多氧酸与1-甲基-3-(4-磺基丁基)- 1h -咪唑(BMIM-SO3)两性离子的反应,成功构建了可回收型多金属氧酸离子液体(POM-IL)催化剂。该POM-IL催化剂可以在温和均相条件下选择性有效地将各种β-O-4木质素模型转化为芳香酸和酚类。在均匀的反应后溶液中加入乙酸乙酯,可以轻松回收POM-IL催化剂,进行连续五次高稳健性回收试验。通过一系列的机理研究,阐明了主要的催化途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A recoverable polyoxometalate-ionic liquid catalyst for selective cleavage of lignin β-O-4 models under mild conditions†

A recoverable polyoxometalate-ionic liquid catalyst for selective cleavage of lignin β-O-4 models under mild conditions†

The efficient and selective cleavage of the β-O-4 linkage under mild conditions represents a promising strategy to convert lignocellulose to value-added aromatic chemicals. In this work, a recoverable polyoxometalate-ionic liquid (POM-IL) catalyst has been successfully constructed by reacting H5PMo10V2O40 (HPMoV) polyoxoacids with 1-methyl-3-(4-sulfobutyl)-1H-imidazolium (BMIM-SO3) zwitterions. Such a POM-IL catalyst can selectively and effectively convert various β-O-4 lignin models into aromatic acids and phenols under mild homogeneous conditions. Addition of ethyl acetate to the homogeneous post-reaction solution allows the easy recovery of the POM-IL catalyst for successive five recycling tests with high robustness. The dominant catalytic pathway was elucidated by a series of mechanistic studies.

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来源期刊
Green Chemistry
Green Chemistry 化学-化学综合
CiteScore
16.10
自引率
7.10%
发文量
677
审稿时长
1.4 months
期刊介绍: Green Chemistry is a journal that provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998), which defines green chemistry as the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry aims to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. The journal welcomes submissions on all aspects of research relating to this endeavor and publishes original and significant cutting-edge research that is likely to be of wide general appeal. For a work to be published, it must present a significant advance in green chemistry, including a comparison with existing methods and a demonstration of advantages over those methods.
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