Amino Imidazoline-2-imine-Chelated Triel Carbenoids as Ligands for Ruthenium Complexes: DFT Studies on Their Activity as Potential Olefin Metathesis Catalysts

We used a computational density functional theory approach to study second-generation Hoveyda–Grubbs-type complexes bearing Tl/Ga/In(AmIm) ligands, focusing on their application as olefin metathesis catalysts. Of these three, the organothallium compound was assessed as the most potent candidate for an efficient catalyst, exhibiting low free energy barriers (14.51 kcal/mol for the rate-determining step of the simplest metathesis process), which suggested its activity, even at low temperatures. This species may potentially catalyze not only the formation of simple olefins but also more sterically hindered ones, including the synthesis of demanding tetra-substituted alkenes.

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Publication Details

Journal
Organometallics
Published
2024-11-19
DOI
https://doi.org/10.1021/acs.organomet.4c00256
Primary Topic
Synthetic Organic Chemistry Methods
Type
article
Field-Weighted Citation Impact
0.00

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article

Amino Imidazoline-2-imine-Chelated Triel Carbenoids as Ligands for Ruthenium Complexes: DFT Studies on Their Activity as Potential Olefin Metathesis Catalysts

Bartosz Trzaskowski, Tymoteusz Basak
Organometallics
Synthetic Organic Chemistry Methods
article

Amino Imidazoline-2-imine-Chelated Triel Carbenoids as Ligands for Ruthenium Complexes: DFT Studies on Their Activity as Potential Olefin Metathesis Catalysts

Bartosz Trzaskowski, Tymoteusz Basak
article en

Abstract

We used a computational density functional theory approach to study second-generation Hoveyda–Grubbs-type complexes bearing Tl/Ga/In(AmIm) ligands, focusing on their application as olefin metathesis catalysts. Of these three, the organothallium compound was assessed as the most potent candidate for an efficient catalyst, exhibiting low free energy barriers (14.51 kcal/mol for the rate-determining step of the simplest metathesis process), which suggested its activity, even at low temperatures. This species may potentially catalyze not only the formation of simple olefins but also more sterically hindered ones, including the synthesis of demanding tetra-substituted alkenes.

OrganometallicsVol. 43(23)
University of Warsaw (PL)
Narodowe Centrum Nauki
Openalex Percentile: Top 85%
Synthetic Organic Chemistry Methods
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