Abstract
X-ray absorption spectroscopy has been used to characterize the novel nitridoiron(IV) units in two [PhBPR3]Fe(N) complexes (R = iPr and CyCH2) and obtain direct spectroscopic evidence for a very short Fe-N distance. The distance of 1.51-1.55 Å reflects the presence of an Fe≡N triple bond in accord with the observed Fe≡N vibration observed for one of these species (νFeN = 1034 cm-1). This highly covalent bonding interaction results in the appearance of an unusually intense pre-edge peak, whose estimated area of 100(20) units is much larger than those of the related tetrahedral complexes with Fe I-N2-FeI, FeII-NPh2, and FeIII≡NAd motifs, and those of recently described six-coordinate FeV≡N and FeVI≡N complexes. The observation that the FeIV-N distances of two [PhBPR 3]Fe(N) complexes are shorter than the FeIV-O bond lengths of oxoiron(IV) complexes may be rationalized on the basis of the greater π basicity of the nitrido ligand than the oxo ligand and a lower metal coordination number for the Fe(N) complex.
Original language | English (US) |
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Pages (from-to) | 5720-5726 |
Number of pages | 7 |
Journal | Inorganic chemistry |
Volume | 46 |
Issue number | 14 |
DOIs | |
State | Published - Jul 9 2007 |