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Methyl Groups as Hydrogen Bond Acceptors via Their sp<sup>3</sup>Carbon Atoms

Oliver Loveday, Jorge Echeverría

2021Crystal Growth & Design15 citationsDOIOpen Access PDF

Abstract

We report herein a combined structural and theoretical study of a novel hydrogen bond in which a methyl group, when bound to an electropositive atom E, acts as the acceptor via its carbon atom. A significant number of experimental examples of such interactions have been retrieved from the Cambridge Structural Database, showing a clear trend toward a linear arrangement of the two interacting groups (E–CH3···H–Y) as the interatomic distance shortens. The hydrogen bond has been further investigated by means of different computational techniques in order to assess its strength and nature. We have also unveiled, by means of natural bond orbital analysis, a charge transfer from a σ(E–C) bonding orbital of the methyl group to a σ* antibonding H–Y orbital.

Topics & Concepts

Antibonding molecular orbitalChemistryBond orderCrystallographyHydrogen bondCarbon fibersHydrogen atomAcceptorHydrogenGroup (periodic table)Atom (system on chip)Computational chemistryMolecular orbitalNon-bonding orbitalMolecular orbital diagramBond lengthAtomic orbitalMoleculeMolecular orbital theoryPhysicsMaterials scienceCrystal structureOrganic chemistryCondensed matter physicsQuantum mechanicsElectronComputer scienceComposite numberEmbedded systemComposite materialCrystallography and molecular interactionsMolecular Spectroscopy and StructureCrystal structures of chemical compounds
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