Easy and Quantitative Access to Fe(II) and Fe(III) Diarylalkynyl-phosphine Oxides Featuring [Fe(dppe)Cp*] Endgroups: Terminal P=O Functionality Blocks the Dimerisation of the Fe(III) Derivatives
Résumé
A series of paramagnetic di(aryl)alkynylphosphine oxides [PF6] featuring an open-shell [Fe(κ(2)-dppe)(η(5)-C5Me5)](+) endgroup were obtained by oxidation of their neutral Fe(II) parents 3a-c, themselves obtained in a simple and nearly quantitative fashion from the corresponding Fe(II) metallophosphines 1a-c. The new organometallic radicals were characterised by NMR and ESR and were shown to be perfectly stable in solution, in contrast to species such as 1a-b[PF6] which readily dimerise.
Domaines
ChimieOrigine | Fichiers produits par l'(les) auteur(s) |
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