Unusual structural types in polynuclear iron chemistry from the use of N,N,N',N'-tetrakis(2-hydroxyethyl)ethylenediamine (edteH4): Fe5, Fe6, and Fe12 clusters

The syntheses, crystal structures, and magnetochemical characterization of five new iron clusters Fe5O2(O2CPh)7(edte)(H2O)] (1), Fe6O2(O2CBut)8(edteH)2] (2), Fe12O4(OH)2(O2CMe)6(edte)4(H2O)2](ClO4)4 (3), Fe12O4(OH)8(edte)4(H2O)2](ClO4)4 (4), and Fe12O4(OH)8(edte)4(H2O)2](NO3)4 (5) (edteH4= N,N,N',N'-tetrakis(2-hydroxyethyl) ethylenediamine) are reported. The reaction of edteH4 with Fe3O(O2CPh)6(H2O)3](NO3) and Fe3O(O2CBut)6(H2O)3](OH) gave 1 and 2, respectively. Complex 3 was obtained from the reaction of edteH4 and NaO2CMe with Fe(ClO4)3, whereas 4 and 5 were obtained from the reaction of edteH4 with Fe(ClO4)3 and Fe(NO3)3, respectively. The core of 1 consists of a Fe4(mu3-O)2]8+ butterfly unit to which is attached a fifth Fe atom by four bridging O atoms. The core of 2 consists of two triangular Fe3(mu3-O)]7+ units linked together by six bridging O atoms. Finally, the cores of 3-5 consist of an Fe12(mu4-O)4(mu-OH)2]26+ unit. Variable-temperature (T) and -field (H) solid-state direct and alternating current magnetization (M) studies were carried out on complexes 1-3 in the 1.8-300 K range. Analysis of the obtained data revealed that 1, 2, and 3-5 possess an S = 5/2, 5, and 0 ground-state spin, respectively. The fitting of the obtained M/N(muB) vs H/T data was carried out by matrix diagonalization, and this gave values for the axial zero-field splitting (ZFS) parameter D of -0.50 cm-1 for 1 and -0.28 cm-1 for 2.