Structural and Electronic Properties of Iron(0) PNP Pincer Complexes.

Abstract

In the present work we have prepared and fully characterized several Fe(0) complexes of the type [Fe(PNP)(CO)2] treating Fe(II) complexes [Fe(PNP)(Cl)2] with KC8 in the presence of carbon monoxide. While complexes [Fe(PNPNMe‐iPr)(CO)2], [Fe(PNPNEt‐iPr)(CO)2] adopt a trigonal bipyramidal geometry, the bulkier and more electron rich [Fe(PNPNH‐tBu)(CO)2] is closer to a square pyramidal geometry. Mössbauer spectra showed isomer shifts very close to 0 and similar to those reported for Fe(I) systems. Quadrupole splitting values range between 2.2 and 2.7 mm s−1 both in experiments and DFT calculations, while those of Fe(I) complexes are much smaller (∼0.6 mm s−1).