Low-Coordinate Iron(II) Amido Complexes of β-Diketiminates: Synthesis, Structure, and Reactivity

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Abstract
The synthesis, structure, and reactivity of a series of low-coordinate Fe(II) diketiminate amido complexes are presented. Complexes L(R)FeNHAr (R = methyl, tert-butyl; Ar = para-tolyl, 2,6-xylyl, and 2,6-diisopropylphenyl) bind Lewis bases to give trigonal pyramidal and trigonal bipyramidal adducts. In the adducts, crystallographic and (1)H NMR evidence supports the existence of agostic interactions in solid and solution states. Complexes L(R)FeNHAr may be oxidized using AgOTf, and the products L(R)Fe(NHAr)(OTf) are characterized with (19)F NMR spectroscopy, UV/vis spectrophotometry, solution magnetic measurements, elemental analysis, and, in one case, X-ray crystallography. In the structures of the iron(III) complexes L(R)Fe(NHAr)(OTf) and L(R)Fe(OtBu)(OTf), the angles at nitrogen and oxygen result from steric effects and not pi-bonding. The reactions of the amido group of L(R)FeNHAr with weak acids (HCCPh and HOtBu) are consistent with a basic nitrogen atom, because the amido group is protonated by terminal alkynes and alcohols to give free H(2)NAr and three-coordinate acetylide and alkoxide complexes. The trends in complex stability give insight into the relative strength of bonds from three-coordinate iron to anionic C-, N-, and O-donor ligands.