Stereoinversion of tetrahedral p-block element hydrides

The potential energy surfaces of 15 tetrahedral p-block element hydrides were screened on the multireference level. It was addressed whether stereoinversion competes against other reactions, such as reductive H2-elimination or hydride loss, and if so, along which pathway the stereomutation occurs. I...

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Main Authors: Sigmund, Lukas M. (Author) , Ehlert, Christopher (Author) , Gryn’ova, Ganna (Author) , Greb, Lutz (Author)
Format: Article (Journal)
Language:English
Published: 20 May 2022
In: The journal of chemical physics
Year: 2022, Volume: 156, Issue: 19, Pages: 1-11
ISSN:1089-7690
DOI:10.1063/5.0090267
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1063/5.0090267
Verlag, lizenzpflichtig, Volltext: https://aip.scitation.org/doi/10.1063/5.0090267
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Author Notes:Lukas M. Sigmund, Christopher Ehlert, Ganna Gryn’ova, and Lutz Greb
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Summary:The potential energy surfaces of 15 tetrahedral p-block element hydrides were screened on the multireference level. It was addressed whether stereoinversion competes against other reactions, such as reductive H2-elimination or hydride loss, and if so, along which pathway the stereomutation occurs. Importantly, stereoinversion transition structures for the ammonium cation (C4v) and the tetrahydridoborate anion (Cs) were identified for the first time. Revisiting methane’s Cs symmetric inversion transition structure with the mHEAT+ protocol revealed an activation enthalpy for stereoinversion, in contrast to all earlier studies, which is 5 kJ mol−1 below the C-H bond dissociation enthalpy. Square planar structures were identified lowest in energy only for the inversion of AlH4−, but a novel stepwise Cs-inversion was discovered for SiH4 or PH4+. Overall, the present contribution delineates essentials of the potential energy surfaces of p-block element hydrides, while structure-energy relations offer design principles for the synthetically emerging field of structurally constrained compounds.
Item Description:Gesehen am 07.07.2022
Physical Description:Online Resource
ISSN:1089-7690
DOI:10.1063/5.0090267