Magneto-structural analysis of Iron(III) Keggin polyoxometalates

Identificador:  imarina:5131441

Handle: https://hdl.handle.net/20.500.11797/imarina5131441

Autors:  Bandeira, NAG; Sadeghi, O; Woods, TJ; Zhang, YZ; Schnack, J; Dunbar, K; Nyman, M; Bo, C

Resum:
A computational study and magnetic susceptibility measurements of three homonuclear Fe(III) Keggin structures are herein presented: the [FeO4@Fe12F24(μ−OCH3)12]5− anion (1), the [Bi6{FeO4@Fe12O12(OH)12}(μ-O2CCCl3)12]+ cation (2) and its polymorph [Bi6{FeO4@Fe12O12(OH)10(H2O)2}(μ-O2CCF3)10]3+ (3). These results are contrasted with the exchange interactions present in the previously characterized [Fe6(OH)3Ge2W18O68(OH)6]11− and [H12As4Fe8W30O120(H2O)2]4− anions. The computational analysis shows that the most significant antiferromagnetic spin coupling takes place at the junction between each of the {Fe3O6(OH)3}/{Fe3F6(OCH3)3} framework motifs, a possibility that had been previously discarded in the literature on the basis of the Fe−Fe distances. For all the examined iron(III) Keggin structures, it is found that the magnitude of the magnetic couplings within each structural subunit follows the same trend.