Abstract
The aerobic reaction of the Schiff-base ligand N-(benzimidazol-2-yl)salicylaldimine (Hbisi) with iron(II) perchlorate in methanol leads to the formation of the remarkable coordination compound [Fe4(μ4-O)(μ-MeO)4(bisi)4](ClO4)2·4MeOH (1), whose single-crystal X-ray structure reveals the presence of a discrete FeIII4(μ4-O) core. Magnetic and Mössbauer studies both show that the exchange interaction within the square tetranuclear iron(III) unit is dominated by the central bridging μ4-oxido ligand, the involvement of the μ-methoxido bridges being negligible.
| Original language | English |
|---|---|
| Pages (from-to) | 2427–2434 |
| Number of pages | 8 |
| Journal | Inorganic Chemistry |
| Volume | 49 |
| Issue number | 5 |
| Early online date | 2 Feb 2010 |
| DOIs | |
| Publication status | Published - 1 Mar 2010 |
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