28755-93-3Relevant articles and documents
A convenient procedure for the synthesis of fluoro-iron(III) complexes of common synthetic porphyrinates
Meininger, Daniel J.,Muzquiz, Nicanor,Arman, Hadi D.,Tonzetich, Zachary J.
, p. 416 - 423 (2014)
We report here an improved method for the preparation of fluoro-iron(III) porphyrinate complexes. Treatment of [Fe2(P)2(μ-O)] (P = tetraphenylporphyrinate {TPP}, tetra-p-tolylporphyrinate {TTP}, or octaethylporphyrinate {OEP}) or [Fe(OH)(OH2)(TMP)] (TMP = tetramesitylporphyrinate) with the commercially available fluorinating agent, Et3N·3HF, in dichloromethane affords the desired [FeF(P)] complexes in a straightforward fashion and in good yield while avoiding the use of aqueous hydrofluoric acid. All fluoro-iron(III) complexes have been completely characterized by a series of different spectroscopic techniques including cyclic voltammetry. Reaction of a representative complex, [FeF(OEP)], with various chloride reagents demonstrates that halide exchange with chloride is facile, but only proceeds at an appreciable rate in the presence of proton sources. Unexpectedly, treatment of [FeF(OEP)] with NOBF4 did not to lead formation of an oxidized species, but rather to formation of the {Fe-NO}6 complex, [Fe(NO)(OEP)](BF4).
Iodo(etiohemiporphycenato)iron(III). Unexpected difference in magnetic behavior in solution and solid
Ohgo, Yoshiki,Neya, Saburo,Takahashi, Masashi,Takeda, Masuo,Funasaki, Noriaki,Nakamura, Mikio
, p. 526 - 527 (2003)
Although iodo(etiohemiporphycenato)iron(III) showed an admixed intermediate-spin state (S = 3/2, 5/2) with a major contribution of S = 3/2 in solution, the same complex exhibited the high-spin state (S = 5/2) in the solid phase. Importance of the crystal packing has been pointed out for the formation of the high-spin complex in the solid.
Synthesis and structural determination of new octaethylporphyrin iron(III) complexes containing cyanamide derivatives as axial ligand
Khorasani-Motlagh, Mozhgan,Safari, Nasser,Noroozifar, Meissam,Shahroosvand, Hashem,Patrick, Brian O.
, p. 1260 - 1266 (2009/06/05)
The reactions of heme, [OEPFeCl] where OEP is the dianion of octaethylporphyrin, with phenylcyanamide (pcyd) ligands have been studied. Four new porphyrin complexes, [OEPFe(L)] (L = pcyd (2), 2-Clpcyd (3), 2-Mepcyd (4), 2,4-Me2pcyd (5)), have b