Synthesis, structure and palladium coordination of ambiphilic, pyridine- and phosphine-tethered N-boryl imine ligands
We describe here the synthesis and structural characterization of two new classes of ambiphilic, N-boryl imine ligands, wherein boron is associated with a Lewis basic imine nitrogen. These ligands can be easily generated in two steps from the corresponding pyridinyl- and phosphinyl-tethered aldehyde...
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Veröffentlicht in: | Dalton transactions : an international journal of inorganic chemistry 2019-04, Vol.48 (17), p.5766-5772 |
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container_title | Dalton transactions : an international journal of inorganic chemistry |
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creator | Lorenzini, Fabio Lagueux-Tremblay, Pierre-Louis Kayser, Laure V Anderson, Ethan Arndtsen, Bruce A |
description | We describe here the synthesis and structural characterization of two new classes of ambiphilic, N-boryl imine ligands, wherein boron is associated with a Lewis basic imine nitrogen. These ligands can be easily generated in two steps from the corresponding pyridinyl- and phosphinyl-tethered aldehydes. 11B NMR analysis suggests the association of the Lewis acidic boron to either the pyridine unit or via intermolecular acid/base interactions with the imine. Both of these ligands can coordinate to palladium, and their structures were confirmed by X-ray crystallography. |
doi_str_mv | 10.1039/c8dt05100c |
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subjects | Aldehydes Boron Crystallography Ligands Nitrogen NMR Nuclear magnetic resonance Palladium Structural analysis Synthesis |
title | Synthesis, structure and palladium coordination of ambiphilic, pyridine- and phosphine-tethered N-boryl imine ligands |
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