Synthesis of a terphenyl-supported aminoborane: an inorganic analogue to styrene

The preparation of an inorganic styrene analogue, Ar Dipp B(H)=NH 2 (Ar Dipp = 2,6-Dipp 2 C 6 H 3 ; Dipp = 2,6- i Pr 2 C 6 H 3 ), supported by a bulky terphenyl ligand is reported. While crystals of Ar Dipp B(H)=NH 2 suitable for X-ray crystallographic analysis could not be obtained, 1 H- 15 N heteronuclear single quantum correlation NMR and computational studies indicate possible B–N double bond character within the BN array. Attempts to induce further dehydrogenation from Ar Dipp B(H)=NH 2 in the presence of various transition metals complexes were unsuccessful.

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Publication Details

Journal
Canadian Journal of Chemistry
Published
2025-04-14
DOI
https://doi.org/10.1139/cjc-2024-0282
Primary Topic
Organoboron and organosilicon chemistry
Type
article
Field-Weighted Citation Impact
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article

Synthesis of a terphenyl-supported aminoborane: an inorganic analogue to styrene

Eike Dornsiepen, Eric Rivard, Samuel Baird, M.J. Ferguson et al.
Canadian Journal of Chemistry
Organoboron and organosilicon chemistry
article

Synthesis of a terphenyl-supported aminoborane: an inorganic analogue to styrene

Eike Dornsiepen, Eric Rivard, Samuel Baird, M.J. Ferguson, Evangeline Dugbenu
article en

Abstract

The preparation of an inorganic styrene analogue, Ar Dipp B(H)=NH 2 (Ar Dipp = 2,6-Dipp 2 C 6 H 3 ; Dipp = 2,6- i Pr 2 C 6 H 3 ), supported by a bulky terphenyl ligand is reported. While crystals of Ar Dipp B(H)=NH 2 suitable for X-ray crystallographic analysis could not be obtained, 1 H- 15 N heteronuclear single quantum correlation NMR and computational studies indicate possible B–N double bond character within the BN array. Attempts to induce further dehydrogenation from Ar Dipp B(H)=NH 2 in the presence of various transition metals complexes were unsuccessful.

Canadian Journal of ChemistryVol. 103(11)
University of Alberta (CA)
Openalex Percentile: Top 94%
Organoboron and organosilicon chemistry
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