6533b7cefe1ef96bd1257976
RESEARCH PRODUCT
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subject
Halogen bondDenticityHydrogen010405 organic chemistryChemistrychemistry.chemical_elementGeneral ChemistryElectron010402 general chemistry01 natural sciencesBiochemistryCatalysis0104 chemical sciencesCrystallographyCarbenium ionchemistry.chemical_compoundColloid and Surface ChemistryGroup (periodic table)Lewis acids and basesCarbondescription
Tetrel bonding is the noncovalent interaction of group IV elements with electron donors. It is a weak, directional interaction that resembles hydrogen and halogen bonding yet remains barely explored. Herein, we present an experimental investigation of the carbon-centered, three-center, four-electron tetrel bond, [N–C–N]+, formed by capturing a carbenium ion with a bidentate Lewis base. NMR-spectroscopic, titration-calorimetric, and reaction-kinetic evidence for the existence and structure of this species is reported. The studied interaction is by far the strongest tetrel bond reported so far and is discussed in comparison with the analogous halogen bond. The necessity of the involvement of a bidentate Lewis base in its formation is demonstrated by providing spectroscopic and crystallographic evidence that a monodentate Lewis base induces a reaction rather than stabilizing the tetrel bond complex. A vastly decreased Lewis basicity of the bidentate ligand or reduced Lewis acidity of the carbenium ion weaken...
| year | journal | country | edition | language |
|---|---|---|---|---|
| 2018-11-28 | Journal of the American Chemical Society |