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Issue 17, 2019
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Synthesis, structure and palladium coordination of ambiphilic, pyridine- and phosphine-tethered N-boryl imine ligands

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Abstract

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.

Graphical abstract: Synthesis, structure and palladium coordination of ambiphilic, pyridine- and phosphine-tethered N-boryl imine ligands

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Publication details

The article was received on 24 Dec 2018, accepted on 19 Mar 2019 and first published on 20 Mar 2019


Article type: Paper
DOI: 10.1039/C8DT05100C
Citation: Dalton Trans., 2019,48, 5766-5772

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    Synthesis, structure and palladium coordination of ambiphilic, pyridine- and phosphine-tethered N-boryl imine ligands

    F. Lorenzini, P. Lagueux-Tremblay, L. V. Kayser, E. Anderson and B. A. Arndtsen, Dalton Trans., 2019, 48, 5766
    DOI: 10.1039/C8DT05100C

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