Structural Effects on the Hydride-Tunneling Kinetic Isotope Effects of NADH/NAD+ Model Reactions: Relating to the Donor–Acceptor Distances

IF 3.6 2区 化学 Q1 CHEMISTRY, ORGANIC Journal of Organic Chemistry Pub Date : 2025-02-13 DOI:10.1021/acs.joc.4c03080
Ava Austin, Jessica Sager, Lauren Phan, Yun Lu
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Abstract

Contemporary H-tunneling theories predict that a longer donor–acceptor distance (DAD) corresponds to a larger kinetic isotope effect (KIE). Herein, hydride-tunneling reactions of NADH/NAD+ analogues in acetonitrile were used to examine the KIE–DAD relationship. Reaction pairs of similar tunneling-ready conformations were selected, so that additional factors influencing KIEs would be relatively fixed. Positive results were obtained, with some reaction pairs displaying a reversal of the traditional KIE−Δ relationship in favor of the KIE–DAD relationship, lending strong support to the latter.

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NADH/NAD+模型反应氢化物隧穿动力学同位素效应的结构效应:与供体-受体距离有关
当代h隧穿理论预测较长的供体-受体距离(DAD)对应较大的动力学同位素效应(KIE)。本研究利用NADH/NAD+类似物在乙腈中的氢化物隧穿反应来检验ki - dad关系。选择相似隧道准备构象的反应对,使影响KIEs的附加因素相对固定。得到了积极的结果,一些反应对显示了传统的KIE - ΔG°关系的反转,有利于KIE - dad关系,为后者提供了有力的支持。
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来源期刊
Journal of Organic Chemistry
Journal of Organic Chemistry 化学-有机化学
CiteScore
6.20
自引率
11.10%
发文量
1467
审稿时长
2 months
期刊介绍: Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.
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