Interaction of Fe(III) with herbicide-carboxylato ligands – Di-, tri- and tetra-nuclear compounds: Structure and magnetic behavior

The iron complexes with the phenoxyalkanoic acids 3,4-D, 2,3-D and 2,4,5-T in the presence or not of a nitrogen donor heterocyclic ligand, phen, were prepared and characterized. Interaction of Fe(III) with phenoxyalkanoic acids and phen leads to dinuclear neutral complexes while the absence of phen favours trinuclear cationic or tetranuclear neutral forms. The crystal structure of hexakis(2,3-dichlorophenoxyacetato)tris(methanol)oxotri-iron(III) chloride–methanol(1/3), [Fe3O(2,3-D)6(MeOH)3]Cl · 3MeOH (2), and tetrakis(dimethyl-sulfoxide)octakis(2,4,5-trichlorophenoxyacetato)dioxotetra-iron(III) methanol(1/2)–water(1/1)–dimethylsulfoxide(1/0.8), {[Fe4O2(2,4,5-T)8(dmso)4] · 2MeOH · H2O · 0.8dmso} (3), have been determined and refined by least-squares methods using three-dimensional Mo Kα data.Magnetic data of the trimer show antiferromagnetic interaction. The ground state of the system is S = 1/2 with a small percentage of S = 5/2 paramagnetic impurity ρ = 0.7%. For the tetramer, the magnetic data suggest antiferromagnetically coupled system with S = 0 ground state, while for the dimer, {[Fe2OCl2(3,4-D)2(phen)2] · H2O · 3.5MeOH} a very strong antiferromagnetic exchange interaction between the two ions has been observed. The fitting results give an exchange interaction of J = 254.1 cm−1, with S = 0 ground state with a small amount of paramagnetic S = 5/2 impurity (ρ = 0.3%).

Interaction of Fe(III) with phenoxyalkanoic acids and phen leads to dinuclear neutral complexes while the absence of phen favours trinuclear cationic or tetranuclear neutral forms. The magnetic behavior of all nuclearities show antiferromagnetic exchange interaction with the ground state of the binuclear and tetranuclear compounds S = 0 and for the trinuclear one S = 1/2.Figure optionsDownload as PowerPoint slide