Competing Intramolecular vs. Intermolecular Hydrogen Bonds in Solution

International Journal of Molecular Sciences

Peter I. Nagy¹ 

[1]Center for Drug Design and Development, the University of Toledo, Toledo, OH 43606-3390, USA

[2] E-Mail

关键词: conformations;    tautomerism;    aqueous solution;    continuum solvent;    Monte Carlo;    relative free energies;    solute dimerization;   

DOI  :  10.3390/ijms151119562

来源: mdpi

【 摘 要 】

A hydrogen bond for a local-minimum-energy structure can be identified according to the definition of the International Union of Pure and Applied Chemistry (IUPAC recommendation 2011) or by finding a special bond critical point on the density map of the structure in the framework of the atoms-in-molecules theory. Nonetheless, a given structural conformation may be simply favored by electrostatic interactions. The present review surveys the in-solution competition of the conformations with intramolecular vs. intermolecular hydrogen bonds for different types of small organic molecules. In their most stable gas-phase structure, an intramolecular hydrogen bond is possible. In a protic solution, the intramolecular hydrogen bond may disrupt in favor of two solute-solvent intermolecular hydrogen bonds. The balance of the increased internal energy and the stabilizing effect of the solute-solvent interactions regulates the new conformer composition in the liquid phase. The review additionally considers the solvent effects on the stability of simple dimeric systems as revealed from molecular dynamics simulations or on the basis of the calculated potential of mean force curves. Finally, studies of the solvent effects on the type of the intermolecular hydrogen bond (neutral or ionic) in acid-base complexes have been surveyed.

【 授权许可】

CC BY   
© 2014 by the authors; licensee MDPI, Basel, Switzerland.