Synthesis of [(3,4,5‐F<sub>3</sub>C<sub>6</sub>H<sub>2</sub>)(4‐<sup><i>n</i></sup>BuC<sub>6</sub>H<sub>4</sub>)<sub>2</sub>C][HCB<sub>11</sub>Cl<sub>11</sub>]: A Much More Soluble Version of the Trityl Cation with Slightly Higher Lewis Acidity

A new triarylmethyl cation (*Tr + ), designed to closely mimic Ph 3 C + in reactivity, has been prepared as a [HCB 11 Cl 11 ] − salt. *Tr + very slightly exceeds the Lewis acidity of Ph 3 C + in chloride and hydride transfer reactions, but possesses two orders of magnitude higher solubility in organic solvents of low polarity.

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Publication Details

Journal
European Journal of Inorganic Chemistry
Published
2025-04-07
DOI
https://doi.org/10.1002/ejic.202500087
Primary Topic
Boron Compounds in Chemistry
Type
article
Field-Weighted Citation Impact
0.00

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article

Synthesis of [(3,4,5‐F3C6H2)(4‐nBuC6H4)2C][HCB11Cl11]: A Much More Soluble Version of the Trityl Cation with Slightly Higher Lewis Acidity

Oleg V. Ozerov, Jack P. Raker
European Journal of Inorganic Chemistry
Boron Compounds in Chemistry
article

Synthesis of [(3,4,5‐F3C6H2)(4‐nBuC6H4)2C][HCB11Cl11]: A Much More Soluble Version of the Trityl Cation with Slightly Higher Lewis Acidity

Oleg V. Ozerov, Jack P. Raker
article en

Abstract

A new triarylmethyl cation (*Tr + ), designed to closely mimic Ph 3 C + in reactivity, has been prepared as a [HCB 11 Cl 11 ] − salt. *Tr + very slightly exceeds the Lewis acidity of Ph 3 C + in chloride and hydride transfer reactions, but possesses two orders of magnitude higher solubility in organic solvents of low polarity.

European Journal of Inorganic ChemistryVol. 28(20)
Texas A&M University (US)
U.S. Department of Energy, Office of Science, Basic Energy Sciences
Openalex Percentile: Top 89%
Boron Compounds in Chemistry
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