Blueshift in Trifurcated Hydrogen Bonds: A Tradeoff between Tetrel Bonding and Steric Repulsion

Abstract

We have quantum chemically investigated the origin of the atypical blueshift of the H−C bond stretching frequency in the hydrogen-bonded complex X−•••H3C−Y (X, Y=F, Cl, Br, I), as compared to the corresponding redshift occurring in Cl−•••H3N and Cl−•••H3C−H, using relativistic density functional theory (DFT) at ZORA-BLYP-D3(BJ)/QZ4P. Previously, this blueshift was attributed, among others, to the contraction of the H−C bonds as the H3C moiety becomes less pyramidal. Herein, we provide quantitative evidence that, instead, the blueshift arises from a direct and strong X−•••C interaction of the HOMO of A− with the backside lobe on carbon of the low-lying C−Y antibonding σ* LUMO of the H3C−Y fragment. This X−•••C bond, in essence a tetrel bond, pushes the H atoms towards a shorter H−C distance and makes the H3C moiety more planar. The blueshift may, therefore, serve as a diagnostic for tetrel bonding.