Mono(Silylene)‐Stabilized Borylenes for Small Molecule Activation

Although base-stabilized borylenes are now a decade-old concept, the number of experimentally isolable mono(Lewis base)-stabilized borylenes is scarce. In this work, we have designed a few mono(Lewis base)-stabilized borylenes with silylenes as the Lewis base. Quantum chemical calculations revealed that the designed systems possess appreciable donor and acceptor properties that motivated us to investigate their potential toward the splitting of enthalpically strong E-H bonds (E = H, CH<sub>3</sub>, NHPh) as well as binding of CO and N<sub>2</sub>. All the activation and the binding processes by the proposed borylenes were found to possess either better or comparable activation barriers compared to that obtained for cyclic (alkyl)(amino)carbene-stabilized borylene.

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Publication Details

Journal
Chemistry - A European Journal
Published
2026-01-29
DOI
https://doi.org/10.1002/chem.202503449
Primary Topic
Organoboron and organosilicon chemistry
Type
article
Field-Weighted Citation Impact
0.00

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article

Mono(Silylene)‐Stabilized Borylenes for Small Molecule Activation

Ashwini K. Phukan, Ashim Tamuli
Chemistry - A European Journal
Organoboron and organosilicon chemistry
article

Mono(Silylene)‐Stabilized Borylenes for Small Molecule Activation

Ashwini K. Phukan, Ashim Tamuli
article en

Abstract

Although base-stabilized borylenes are now a decade-old concept, the number of experimentally isolable mono(Lewis base)-stabilized borylenes is scarce. In this work, we have designed a few mono(Lewis base)-stabilized borylenes with silylenes as the Lewis base. Quantum chemical calculations revealed that the designed systems possess appreciable donor and acceptor properties that motivated us to investigate their potential toward the splitting of enthalpically strong E-H bonds (E = H, CH<sub>3</sub>, NHPh) as well as binding of CO and N<sub>2</sub>. All the activation and the binding processes by the proposed borylenes were found to possess either better or comparable activation barriers compared to that obtained for cyclic (alkyl)(amino)carbene-stabilized borylene.

Chemistry - A European Journal
Tezpur University (IN)
Department of Science and Technology, Ministry of Science and Technology, India, Science and Engineering Research Board
Openalex Percentile: Top 72%
Organoboron and organosilicon chemistry
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