Abstract
The relationship E(p)vs. ΔG(H-) correlates the applied potential (E(p)) needed to drive organohydride formation with the strength of the hydride donor that is formed: in the absence of kinetic effects E(p)vs. ΔG(H-) should be linear but it would be more energy efficient if E(p) could be shifted anodically using kinetic effects. Biological hydride transfers (HT) performed by cofactors including NADH and lactate racemase do occur at low potentials and functional modeling of those processes could lead to low energy HT reactions in electrosynthesis and to accurate models for cofactor chemistry. Herein we probe the influence of N-alkylation or N-metallation on ΔG(H-) for dihydropyridinates (DHP(-)) and on E(p) of the DHP(-) precursors. We synthesized a series of DHP(-) complexes of the form (pz(2)(H)P(-))E via hydride transfer from their respective [(pz(2)P)E](+) forms where E = AlCl(2)(+), GaCl(2)(+) or Me(+). Relative ΔG(H-) for the (pz(2)(H)P(-))E series all fall within 1 kcal mol(-1), and ΔG(H-) for (pz(2)(H)P)CH(3) was approximated as 47.5 ± 2.5 kcal mol(-1) in MeCN solution. Plots of E(p)vs. ΔG(H-) including [(pz(2)P)E](+) suggest kinetic effects shift E(p) anodically by ∼215 mV.