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Which future for stereogenic phosphorus? Lessons from P* pincer complexes of iron(ii)
Raffael Huber1, Alessandro Passera1, Antonio Mezzetti1
1Department of Chemistry and Applied Biosciences, ETH Zürich, Wolfgang-Pauli-Str. 10, CH-8093 Zürich, Switzerland. mezzetti@inorg.chem.ethz.ch.
Abstract:
PNP pincer ligands stabilise diamagnetic base metal catalysts, and much effort has been invested in the development of chiral analogues for asymmetric catalysis. Starting from the conformational issues that affect P-stereogenic diphosphines, we extend the analysis to our recently prepared P-stereogenic PNP pincer ligands, which we used in the iron(ii)-catalysed hydrogenation of ketones. Backbone rigidity and size (and shape) of the substituents at phosphorus are pivotal in both bi- and tridentate P-stereogenic ligands, and their interplay is discussed, as well as the contribution (and shortcomings) of DFT calculations to the understanding of the conformational flexibility and enantiodiscrimination.
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