Facile synthesis of Bidentate Boron Lewis Acids by Pentafluorobenzene Elimination

Abstract The obtained results reveal simple synthetic approach for bidentate boron Lewis acids with the ‐OB(C 6 F 5 ) 2 acid group and aliphatic or aromatic linkers. Computational results showed comparable FIA for the ‐OB(C 6 F 5 ) 2 site in boron bidentate Lewis acids relative to initial B(C 6 F 5 ) 3 . The relative Lewis acid strength of R[OB(C 6 F 5 ) 2 ] 2 (R=C 2 H 4 , p‐C 6 H 4 , m‐C 6 H 4 ) was characterized by Gutman‐Beckett tests. The elimination of pentafluorobenzene by the reaction of R‐OH with B(C 6 F 5 ) 3 can be used for the synthesis of R‐OB(C 6 F 5 ) 2 derivatives and polydentate strong Lewis acids.

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Publication Details

Journal
European Journal of Inorganic Chemistry
Published
2024-11-05
DOI
https://doi.org/10.1002/ejic.202400548
Citations
2
Primary Topic
Organoboron and organosilicon chemistry
Type
article
Field-Weighted Citation Impact
0.50

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article

Facile synthesis of Bidentate Boron Lewis Acids by Pentafluorobenzene Elimination

Mariya A. Kryukova, Anna S. Lisovenko, Igor V. Kazakov, P. I. Kudina
2 citations
European Journal of Inorganic Chemistry
Organoboron and organosilicon chemistry
0.50
article

Facile synthesis of Bidentate Boron Lewis Acids by Pentafluorobenzene Elimination

Mariya A. Kryukova, Anna S. Lisovenko, Igor V. Kazakov, P. I. Kudina
article en
2 citations

Abstract

Abstract The obtained results reveal simple synthetic approach for bidentate boron Lewis acids with the ‐OB(C 6 F 5 ) 2 acid group and aliphatic or aromatic linkers. Computational results showed comparable FIA for the ‐OB(C 6 F 5 ) 2 site in boron bidentate Lewis acids relative to initial B(C 6 F 5 ) 3 . The relative Lewis acid strength of R[OB(C 6 F 5 ) 2 ] 2 (R=C 2 H 4 , p‐C 6 H 4 , m‐C 6 H 4 ) was characterized by Gutman‐Beckett tests. The elimination of pentafluorobenzene by the reaction of R‐OH with B(C 6 F 5 ) 3 can be used for the synthesis of R‐OB(C 6 F 5 ) 2 derivatives and polydentate strong Lewis acids.

European Journal of Inorganic ChemistryVol. 27(36)
St Petersburg University (RU)
Russian Science Foundation
Clean water and sanitation
Openalex Percentile: Top 38%
Organoboron and organosilicon chemistry
0.50
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