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

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<sup>+</sup> 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<i>G°</i> relationship in favor of the KIE-DAD relationship, lending strong support to the latter.

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Publication Details

Journal
The Journal of Organic Chemistry
Published
2025-02-13
DOI
https://doi.org/10.1021/acs.joc.4c03080
Citations
3
Primary Topic
Chemical Reactions and Isotopes
Type
article
Field-Weighted Citation Impact
2.37

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article

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

Yun Lü, John W. Sager, A. T. Austin, Lauren Phan
3 citations
The Journal of Organic Chemistry
Chemical Reactions and Isotopes
2.37
article

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

Yun Lü, John W. Sager, A. T. Austin, Lauren Phan
article en
3 citations

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<sup>+</sup> 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<i>G°</i> relationship in favor of the KIE-DAD relationship, lending strong support to the latter.

The Journal of Organic ChemistryVol. 90(8)
Southern Illinois University Edwardsville (US)
National Institutes of Health, National Institute of General Medical Sciences
Openalex Percentile: Top 13%
Chemical Reactions and Isotopes
2.37
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Structural Effects on the Hydride-Tunneling Kinetic Isotope Effects of NADH/NAD<sup>+</sup> Model Reactions: Relating to the Donor–Acceptor Distances — Yun Lü, John W. Sager, et al. · The Journal of Organic Chemistry (2025) | TGRS Research Map | TGRS