Structural, Magnetochemical and Electrochemical Studies of Dinuclear Complexes Containing the [VVO]2, [VIVO]2, CrIII2, MnIII2 and FeIII2 Cores of a Potentially Pentadentate Phenol-Containing Ligand with (O,N,O,N,O)-Donor Atoms

✍ Scribed by Soumen Mukherjee; Thomas Weyhermüller; Eberhard Bothe; Phalguni Chaudhuri

• Publisher: John Wiley and Sons
• Year: 2003
• Tongue: English
• Weight: 214 KB
• Volume: 2003
• Category: Article
• ISSN: 1434-1948
• DOI: 10.1002/ejic.200200594

✦ Synopsis

Abstract

Dinuclear complexes [L~2~Fe^III^~2~] (1), [L~2~Mn^III^~2~] (2a), [L~2~Mn^III^~2~(THF)~2~] (2b), [L~2~Cr^III^~2~] (3), [L(V^IV^O)~2~(OCHMe~2~)] (4) and [L~2~(V^V^O)~2~] (5) with a pentadentate phenol‐containing ligand H~3~L (= C~6~H~2~(CH~3~)(OH){[C(CH~3~)~3~]~2~(OH)NCH}~2~) bearing the N~2~O~3~ donor atoms have been synthesized and the X‐ray structures of 1, 2b, 4 and 5 are reported. The compounds were characterized by IR, UV/Vis and Mössbauer spectroscopy, mass spectrometry, electrochemical and variable‐temperature (2−295 K) magnetic susceptibility measurements. Analysis of the susceptibility data demonstrates antiferromagnetic interactions between the metal centers establishing diamagnetic ground states for complexes 1−4. The electrochemical results suggest the generation of ligand‐centered oxidation processes attributable to the phenoxyl radicals, rather than the formation of unusually high oxidation states at the central metal centers. The ligand H~3~L has the potential to act in a multidentate fashion as evidenced by the X‐ray structures of 2b and 5. In compound 2b the central phenolate oxygen of the p‐cresol ring does not function as a bridging atom between two manganese centers, whereas in 5 the ligand is tetradentate with one noncoordinating nitrogen atom. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003)