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“Hydridic Hydrogen-Bond Donors” Are Not Hydrogen-Bond Donors

Lucas de Azevedo Santos, Pascal Vermeeren, F. Matthias Bickelhaupt, Célia Fonseca Guerra

2024Journal of the American Chemical Society27 citationsDOIOpen Access PDF

Abstract

High Resolution Image Download MS PowerPoint Slide Herein, we dismiss a recent proposal by Civiš, Hobza, and co-workers to modify the IUPAC definition of hydrogen bonds in order to expand the scope from protonic Y–H δ+ to hydridic Y–H δ− hydrogen-bond donor fragments [ J. Am. Chem. Soc. 2023, 145, 8550]. Based on accurate Kohn–Sham molecular orbital (KS-MO) analyses, we falsify the conclusion that interactions involving protonic and hydridic hydrogens are both hydrogen bonds; they are not. Instead, our quantitative KS-MO, energy decomposition, and Voronoi deformation density analyses reveal two fundamentally different bonding mechanisms for protonic Y–H δ+ and hydridic Y–H δ− fragments which go with charge transfer in opposite directions. On one hand, we confirm the IUPAC definition for regular hydrogen bonds in the case of protonic Y–H δ+ fragments. On the other hand, complexes involving Y–H δ− fragments are, in fact, acceptors in other well-known families of Lewis-acid/base interactions, such as halogen bonds, chalcogen bonds, and pnictogen bonds. These mechanisms lead to the same spectroscopic phenomenon in both the Y–H δ+ and Y–H δ− fragments, that is, the redshift in the Y–H stretching frequency, which is, thus, not an exclusive indicator for hydrogen bonding.

Topics & Concepts

ChemistryHydrogen bondLow-barrier hydrogen bondBondHydrogenBond orderSextuple bondPhotochemistryBond lengthOrganic chemistryMoleculeFinanceEconomicsCrystallography and molecular interactionsHydrogen Storage and MaterialsAsymmetric Hydrogenation and Catalysis