22 research outputs found

    Dynamic effects of solvent on the Brönsted α

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    In hydroxylic solvents the primary kinetic isotope effect on reactions which transfer hydride between NAD+ analogues is maximized and constant, and the Brönsted α indicates a critical configuration equally resembling reactants and products. However, in certain polar, aprotic solvents, most notably DMSO, the isotope effect is sharply reduced and the Brönsted a indicates a product-like critical configuration. These changes are attributed to a barrier due to solvent

    The Separation of Polar, Steric, and Resonance Effects by the Use of Linear Free Energy Relationships

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