Redox Potential Tuning in Bio-relevant Heterocycles via (Anti)Aromaticity Modulated H-Bonding (AMHB)

Hydrogen bonds are arguably the most important non-covalent interactions in chemistry and biology, and their strength and directionality have been elegantly exploited in the rational design of complex structures. We recently noted that the variable responses of cyclic pi-systems upon H-bond formation reciprocally lead to modulations of the H-bonds' strengths, a phenomenon that we dubbed (anti)aromaticity-modulated hydrogen bonding (AMHB) [J. Am. Chem. Soc. 2016, 138, 3427-3432]. Species that switch from aromatic to antiaromatic or vice versa upon changing pi-electron counts should be oppositely stabilized by the AMHB effects, so their redox potentials should be significantly "tuned" by H-bond formation. Herein, using quantum chemical simulations, we explore the effects of these H-bond induced pi-electron polarizations on the redox potentials of (anti)aromatic heterocycles. The systems chosen for this study have embedded amide groups and amidine moieties capable of forming two-point H-bonds in their cyclic pi-systems. Thus, as the 4-electron and 6-electron pi-systems in redox-capable monocycles (e.g., quinones) can be differentially stabilized, their redox potentials can be modulated by H-bond formation by as much as 6 kcal/mol (258 mV for one electron transfer). In fused rings, the connectivity patterns are as important as the pi-electron counts. Extending these ideas to flavin, a biologically relevant case, we find that H-bonding patterns like those found in its crystals can vary its redox potential by up to 1.3 kcal/mol.