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 |
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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 |
format | Article |
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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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