Reactivity of an <i>Ortho</i>‐Phenylene‐Bridged Al/P Frustrated Lewis Pair toward Small Molecules

Frustrated Lewis pairs (FLPs) as ambiphilic molecules are prone to activate small molecules and are in the focus of interest for many years. Herein, the first ortho ‐phenylene‐bridged Al/P‐based FLP with only one phosphine moiety is presented. The title compound is employed in various reactions with small molecules featuring different functional groups. The Al/P‐based FLP readily forms adducts or activation products and can reversibly activate CO 2 at room temperature.

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Publication Details

Journal
European Journal of Inorganic Chemistry
Published
2025-04-07
DOI
https://doi.org/10.1002/ejic.202500174
Citations
4
Primary Topic
Organoboron and organosilicon chemistry
Type
article
Field-Weighted Citation Impact
3.74

Funders

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article

Reactivity of an Ortho‐Phenylene‐Bridged Al/P Frustrated Lewis Pair toward Small Molecules

Frank Breher, Melina E. A. Dilanas
4 citations
European Journal of Inorganic Chemistry
Organoboron and organosilicon chemistry
3.74
article

Reactivity of an Ortho‐Phenylene‐Bridged Al/P Frustrated Lewis Pair toward Small Molecules

Frank Breher, Melina E. A. Dilanas
article en
4 citations

Abstract

Frustrated Lewis pairs (FLPs) as ambiphilic molecules are prone to activate small molecules and are in the focus of interest for many years. Herein, the first ortho ‐phenylene‐bridged Al/P‐based FLP with only one phosphine moiety is presented. The title compound is employed in various reactions with small molecules featuring different functional groups. The Al/P‐based FLP readily forms adducts or activation products and can reversibly activate CO 2 at room temperature.

European Journal of Inorganic ChemistryVol. 28(14)
Karlsruhe Institute of Technology (DE)
Deutsche Forschungsgemeinschaft, Studienstiftung des Deutschen Volkes
Openalex Percentile: Top 8%
Organoboron and organosilicon chemistry
3.74
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