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.
Authors
- Yun Lü (ORCID: https://orcid.org/0000-0002-3511-6041)
- John W. Sager
- A. T. Austin
- Lauren Phan
Institutions
- Southern Illinois University Edwardsville (US)
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
Funders
- National Institutes of Health
- National Institute of General Medical Sciences