Frustrated Lewis Pair Reactivity of Bis(1-methyl- <i>ortho-</i> carboranyl)borane

Carboranyl substituted boranes are attractive Lewis acids for frustrated Lewis pair (FLP) chemistry due to their tremendous bulk and high Lewis acidity. In FLP chemistry, secondary boranes are uncommon Lewis acids due to the limited bulk. In this work, we interrogate bis(1-methyl-<i>ortho</i>-carboranyl)borane as a Lewis acid in FLP chemistry that reveals the secondary borane is sufficiently bulky to preclude adduct formation with a variety of Lewis bases and can be applied in bond activation reactions.

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Publication Details

Journal
Inorganic Chemistry
Published
2025-12-01
DOI
https://doi.org/10.1021/acs.inorgchem.5c04710
Primary Topic
Organoboron and organosilicon chemistry
Type
article
Field-Weighted Citation Impact
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article

Frustrated Lewis Pair Reactivity of Bis(1-methyl- ortho- carboranyl)borane

Caleb D. Martin, Kanika Vashisth
Inorganic Chemistry
Organoboron and organosilicon chemistry
article

Frustrated Lewis Pair Reactivity of Bis(1-methyl- ortho- carboranyl)borane

Caleb D. Martin, Kanika Vashisth
article en

Abstract

Carboranyl substituted boranes are attractive Lewis acids for frustrated Lewis pair (FLP) chemistry due to their tremendous bulk and high Lewis acidity. In FLP chemistry, secondary boranes are uncommon Lewis acids due to the limited bulk. In this work, we interrogate bis(1-methyl-<i>ortho</i>-carboranyl)borane as a Lewis acid in FLP chemistry that reveals the secondary borane is sufficiently bulky to preclude adduct formation with a variety of Lewis bases and can be applied in bond activation reactions.

Inorganic ChemistryVol. 64(49)
Baylor University (US)
Openalex Percentile: Top 72%
Organoboron and organosilicon chemistry
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