Tris(acetylacetonato)iron(III)

Fe(acac)3 is prepared by treating freshly precipitated Fe(OH)3 with acetylacetone. :Fe(OH)3 + 3 HC5H7O2 → Fe(C5H7O2)3 + 3 H2O ==Structure and properties==

Fe(acac)3 is an octahedral complex with six equivalent Fe-O bonds with bond distances of about 2.00 Å. The regular geometry is consistent with a high-spin Fe3+ core with sp3d2 hybridization. As the metal orbitals are all evenly occupied the complex is not subject to Jahn-Teller distortions and thus adopts a D3 molecular symmetry. In contrast, the related metal acetylacetonate Mn(acac)3 adopts a more distorted octahedral structure. The 5 unpaired d-electrons also result in the complex being paramagnetic, with a magnetic moment of 5.90 μB. Fe(acac)3 possesses helical chirality. The Δ- and Λ-enantiomers slowly inter-convert via Bailar and Ray–Dutt twists. The rate of interconversion is sufficiently slow to allow its enantiomers to be partially resolved. In diethyl ether solution, at ambient temperature, the half-life of racemisation is 3.3 minutes. ==Reactions==

Fe(acac)3 has been examined as a precatalyst and reagent in organic chemistry, although the active iron-containing species is usually unidentified in these processes. In one instance, Fe(acac)3 was shown to promote cross-coupling a diene to an olefin. Fe(acac)3 catalyzes the dimerization of isoprene to a mixture of 1,5-dimethyl-1,5-cyclooctadiene and 2,5-dimethyl-1,5-cyclooctadiene. : Fe(acac)3 also catalyzes the ring-opening polymerization of 1,3-benzoxazine.{{cite journal : ==References==