Trapping of a Terminal Intermediate in the Boron-Mediated Dinitrogen Reduction: Mono‑, Tri‑, and Tetrafunctionalized Hydrazines in Two Steps from N

The addition of chlorotrimethylsilane to a boron-mediated, transition-metal-free N₂ activation reaction leads to the isolation of multiple potassium boryl­(silyl)­hydrazido species, likely trapping products of a terminal dinitrogen complex of boron. One of these silylated N₂ species can be protonate...

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Veröffentlicht in:Journal of the American Chemical Society 2024-04, Vol.146 (16 p.11048-11053), p.11048-11053
Hauptverfasser: Rang, Maximilian, Heinz, Myron, Halkić, Anel, Weber, Marco, Dewhurst, Rian D., Rempel, Anna, Härterich, Marcel, Holthausen, Max C., Braunschweig, Holger
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container_issue 16 p.11048-11053
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container_title Journal of the American Chemical Society
container_volume 146
creator Rang, Maximilian
Heinz, Myron
Halkić, Anel
Weber, Marco
Dewhurst, Rian D.
Rempel, Anna
Härterich, Marcel
Holthausen, Max C.
Braunschweig, Holger
description The addition of chlorotrimethylsilane to a boron-mediated, transition-metal-free N₂ activation reaction leads to the isolation of multiple potassium boryl­(silyl)­hydrazido species, likely trapping products of a terminal dinitrogen complex of boron. One of these silylated N₂ species can be protonated or methylated, providing access to mono- to tetrafunctionalized hydrazines in two steps from N₂ and in the absence of transition metals.
doi_str_mv 10.1021/jacs.4c01818
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subjects boron
methylation
nitrogen
potassium
title Trapping of a Terminal Intermediate in the Boron-Mediated Dinitrogen Reduction: Mono‑, Tri‑, and Tetrafunctionalized Hydrazines in Two Steps from N
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