Abstract
Palladium complexes of corrole and sapphyrin were prepared in high yield and fully characterized. The corrole provides a tetradentate/trianionic square planar coordination sphere for Pd-II, charge balanced by pyridinium. Both one and two Pd(II)ions may be accommodated by the pentapyrrolic skeleton of the sapphyrin, and in each case the macrocycle acts as bidentate/monoanionic ligand and the inner-sphere square planar geometry is completed by allyl anions coordinated in an eta(3)fashion. NMR spectroscopy and X-ray crystallography data analyses uncovered the presence of interesting stereoisomers due to the flexibility of the ally ligands and also the pyrrole ring(s) that is/are not involved in metal binding.
Original language | English |
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Pages (from-to) | 9481-9485 |
Number of pages | 6 |
Journal | Chemistry-A European Journal |
Issue number | 43 |
DOIs | |
Publication status | Published - 9 Jul 2020 |
Funding
This research was supported by a grant from the Pazy Foundation.