Mixed-Valence Heptanuclear Iron Complexes with Ferromagnetic Interaction

Abstract

Three new Prussian blue analogues, heptanuclear mixed-valence iron complexes of the type [Fe^II(CN)₆{Fe^III(1_–2H)}₆]­Cl₂·<i>n</i>H₂O, were synthesized and structurally and spectrally characterized, and their magnetic properties were investigated (1_–2H corresponds to doubly deprotoned Schiff-base pentadentate ligands <b>1a</b>, <i>N</i>,<i>N</i>′-bis­(2-hydroxybenzylidene)-1,5-diamino-3-azapentane, <b>1b</b>, <i>N</i>,<i>N</i>′-bis­(3-ethoxy-2-hydroxybenzylidene)-1,7-diamino-4-azaheptane, or <b>1c</b>, <i>N</i>,<i>N</i>′-bis­(3-methoxy-2-hydroxybenzylidene)-1,6-diamino-3-azahexane). These compounds were formed by assembling the [Fe­(CN)₆]^4– building block with mononuclear complexes of the [Fe­(1_–2H)­Cl] type. X-ray structure analysis revealed that the complexes adopt a star-like architecture: the Fe­(II) ion lies at the very center, and on its octahedral nodes the Fe­(III) sites are coordinated in the Fe^II–CN–Fe^III manner. The Schiff-base pentadentate ligand moiety 1_–2H coordinates a single Fe­(III) center in two complexes <b>3b</b> and <b>3c</b>. Ligands 1a_–2H in the complex cation of <b>3a</b> adopt an unusual coordination mode: three donor atoms of the same ligand (one O and two N) coordinate one Fe­(III), whereas the remaining N′ and O′ donor atoms coordinate the neighboring Fe­(III) center creating the {Fe­(ON₂)­(N′O′)­N″} chromophore involving two 1a_–2H ligand moieties. Moreover, three Fe­(III) centers are interconnected with three 1a_–2H ligands in such a manner that two {Fe^III₃(1a_–2H)₃} units form two intramolecular rings. Magnetic investigation of the heptanuclear complexes revealed the high-spin state of all six Fe­(III) coordination sites (<i>s</i> = 5/2), while the very central Fe­(II) site is in the low-spin state (<i>s</i> = 0). At low temperature, the ferromagnetic exchange interactions stay evident for all three complexes. Mössbauer spectra of compounds <b>3a</b> and <b>3b</b> revealed a presence of two different doublets for both compounds: the major doublet is related to six Fe­(III) high-spin coordination sites and the minor doublet refers to the low-spin very central Fe­(II)