Hyperpolarized NMR reveals transient species and elusive routes in acid-catalyzed furfural oxidation at natural isotope abundance†

IF 4.2 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Stefan S. Warthegau, Magnus Karlsson, Pernille Rose Jensen and Sebastian Meier
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引用次数: 0

Abstract

Transient reaction steps often remain elusive to conventional NMR detection. Using hyperpolarized dDNP-NMR with signal enhancements over 30 000, we clarified elusive pathways in biomass upgrading. Both furfural and a lactone deriving from furfural were hyperpolarized using a PEG-400/trityl matrix at natural isotope abundance. Hyperpolarization allowed the detection of elusive reaction species by tracking protonated sites that undergo significant chemical shift changes. Combined with careful choice of the decoupling scheme, hyperpolarized NMR revealed that furfural undergoes Baeyer–Villiger oxidation, while the lactone undergoes epoxidation.

Abstract Image

超极化核磁共振揭示了天然同位素丰度下酸催化糠醛氧化的瞬态物种和难以捉摸的路线。
传统的核磁共振检测往往难以捉摸瞬态反应步骤。利用信号增强超过30000的超极化dDNP-NMR,我们澄清了生物质升级的难以捉摸的途径。糠醛和由糠醛衍生的内酯在PEG-400/三烷基基质中以天然同位素丰度进行超极化。超极化可以通过跟踪质子化位点来检测难以捉摸的反应物种,这些质子化位点经历了显著的化学位移变化。结合解耦方案的精心选择,超极化核磁共振显示糠醛发生Baeyer-Villiger氧化,而内酯发生环氧化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Chemical Communications
Chemical Communications 化学-化学综合
CiteScore
8.60
自引率
4.10%
发文量
2705
审稿时长
1.4 months
期刊介绍: ChemComm (Chemical Communications) is renowned as the fastest publisher of articles providing information on new avenues of research, drawn from all the world''s major areas of chemical research.
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