Unconventional Parahydrogen-Induced Hyperpolarization Effects in Chemistry and Catalysis: From Photoreactions to Enzymes

IF 13.1 1区 化学 Q1 CHEMISTRY, PHYSICAL ACS Catalysis Pub Date : 2025-04-04 DOI:10.1021/acscatal.4c07870
Andrey N. Pravdivtsev, Ben J. Tickner, Stefan Glöggler, Jan-Bernd Hövener, Gerd Buntkowsky, Simon B. Duckett, Clifford R. Bowers, Vladimir V. Zhivonitko
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Abstract

Nuclear spin hyperpolarization utilizing parahydrogen has the potential for broad applications in chemistry, catalysis, biochemistry, and medicine. This review examines recent chemical and biochemical insights gained using parahydrogen-induced polarization (PHIP). We begin with photoinduced PHIP, which allows the investigation of short-lived and photoactivated catalysis. Next, we review the partially negative line effect, in which distinctive line shape helps to reveal information about rapid exchange with parahydrogen and the role of short-lived catalytic species. The NMR signal enhancement of a single proton in oneH-PHIP is discussed, challenging the underpinning concept of the necessity of pairwise hydrogenation. Furthermore, we examine metal-free PHIP facilitated by frustrated Lewis pair molecular tweezers and radicaloids, demonstrating alternative routes to hydrogenation. Although symmetric molecules incorporating parahydrogen are NMR silent, we showcase methods that reveal hyperpolarized states through post-hydrogenation reactions. We discuss chemical exchange processes that mediate polarization transfer between parahydrogen and a molecular target, expanding the reach of PHIP without synthesizing specialized precursors. We conclude this review by highlighting the role of PHIP in uncovering the H2 activation mechanisms of hydrogenases. By providing a detailed review of these diverse phenomena, we aim to familiarize the reader with the versatility of PHIP and its potential applications for mechanistic studies and chemical analysis.

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化学和催化中非常规对氢诱导的超极化效应:从光反应到酶
利用对氢的核自旋超极化在化学、催化、生物化学和医学等领域具有广泛的应用前景。本文综述了最近利用对氢诱导极化(PHIP)获得的化学和生化见解。我们从光诱导PHIP开始,它允许研究短寿命和光激活的催化。接下来,我们回顾了部分负线效应,其中独特的线形状有助于揭示与对氢的快速交换和短寿命催化物质的作用的信息。讨论了一h - phip中单个质子的核磁共振信号增强,挑战了配对氢化必要性的基本概念。此外,我们研究了由受挫Lewis对分子镊子和自由基促进的无金属PHIP,展示了氢化的替代途径。虽然含有对氢的对称分子是核磁共振沉默的,但我们展示了通过后氢化反应揭示超极化状态的方法。我们讨论了在对氢和分子靶标之间介导极化转移的化学交换过程,在不合成专门前体的情况下扩大了PHIP的范围。我们通过强调PHIP在揭示氢化酶的H2激活机制中的作用来总结这篇综述。通过对这些不同现象的详细回顾,我们旨在使读者熟悉PHIP的多功能性及其在机械研究和化学分析方面的潜在应用。
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来源期刊
ACS Catalysis
ACS Catalysis CHEMISTRY, PHYSICAL-
CiteScore
20.80
自引率
6.20%
发文量
1253
审稿时长
1.5 months
期刊介绍: ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels. The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.
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