Synthesis and characterization of monomer and dimer complexes of porphyrin iron(III) with bridging phenylcyanamide ligands

Several new mono and dinuclear complexes of [(P)FeIII(L)], in which P is the dianion of tetraphenylporphyrin(TPP) and tetramesitylporphyrin(TMP) and L is the monoanion of 4-azo(phenylcyanamido)benzene (apc) (1) and (2) or dianion 1,4-di cyanamidobenzene (dicyd) (3), (4), (7), (8) and 4,4′-azo-diphenylcyanamide (adpc) (5), (6), (9), (10) have been prepared by the reaction of [(P)FeIIICl] with appropriate thallium salts of phenylcyanamide derivatives. Each of the complexes has been characterized by FT-IR, UV–Vis, 1H NMR, MALDI-TOF and EPR spectroscopic data. In non-coordinating solvents (such as toluene or chloroform) these complexes exhibit 1H NMR spectra that are characteristic of high-spin (S = 5/2) species. The cyanamide group (NCN) of the bridging ligand is coordinated to Fe(III) ions through the nitrile-nitrogen. The iron(III) phenylcyanamide complexes are not reactive toward dioxygen, they convert into [TPPFeIIICl] when treated with HCl. EPR and NMR have shown that in dinuclear complexes weak magnetic interactions take place between two iron(III) paramagnetic centers.

Several new complexes of [(P)FeIII(L)], where P is the dianion of tetraphenylporphyrin and tetramesitylporphyrin and L is the monoanion of 4-azo(phenylcyanamido)benzene (apc) or dianion 1,4-di cyanamidobenzene (dicyd) or 4,4′-azo-diphenylcyanamide (adpc).Figure optionsDownload as PowerPoint slide