Tuning the steric hindrance of alkylamines: a predictive model of steric editing of planar amines

Michele Tomasini, Maria Voccia, Lucia Caporaso, Michal Szostak, Albert Poater

Research output: Contribution to journalArticlepeer-review

Abstract

Amines are one of the most prevalent functional groups in chemistry. Perhaps even more importantly, amines represent one of the most ubiquitous moieties within the realm of bioactive natural products and life-saving pharmaceuticals. The archetypal geometrical property of amines is their sp3 hybridization with the lone pair of nitrogen occupying the apex of the pyramid. Herein, we present a blueprint for quantifying the properties of extremely sterically hindered alkylamines. These amines reach planarity around the nitrogen atom due to the excessive steric hindrance, which results in a conformational re-modeling of the amine moiety. Crucially, the steric properties of amines are characterized by the %VBur index, which we show is a general predictive parameter for evaluating the properties of sterically hindered amines. Computational studies on the acidic nature and the reactivity of organometallic Au and Pd complexes are outlined. Density functional theory calculations permit for predictive catalysis, ordering the mapping of extremely hindered tertiary amines by employing artificial intelligence via machine learning. Overall, the study outlines the correlation between the unusual geometry and the key thermodynamic and kinetic properties of extremely hindered alkylamines. The steric hindrance, as quantified by %VBur, is the crucial factor influencing the observed trends and the space required to accommodate sterically hindered tertiary amines.

Original languageEnglish (US)
Pages (from-to)13405-13414
Number of pages10
JournalChemical Science
Volume15
Issue number33
DOIs
StatePublished - Jul 11 2024
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • General Chemistry

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