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   <subfield code="a">Synthesis and Crystal Structure of μ-oxo-bis[(octaethyloxoporphinato)iron(III)] Tetrafluoroborate</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Mozhgan Khorasani-Motlagh, Nasser Safari, Hamid Khavasi, Meissam Noroozifar, Hashem Shahroosvand, Mahtab Biabani]</subfield>
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   <subfield code="a">Exposure of dichloromethane solution of [OEOPFe(BF4)], where OEOP is the monoanion of octaethyloxoporphyrin, to dioxygen results in its transformation into the μ-oxo bridged compound, [(OEOPFe)2O)](BF4)2. The molecular structure of the title compound, [(OEOPFe)2O](BF4)2, was determined by single-crystal X-ray diffraction. It contains a binuclear centrosymmetric [(OEOPFe)2O]2+ cation (the bridging O atom lies on an inversion centre) and two tetrafluoroborate anions. The Fe atom is five-coordinate to four N atoms of the porphyrin ring and to one bridging O atom. The compound is characterized by an average Fe-N bond length of 2.064Å. The Fe-O bond distance is 1.7665(11)Å and the Fe-O-Fe bond angle is 180.0° and the two porphyrin rings are parallel. Crystal data: crystal system, monoclinic, a=8.867(3), b=26.104(9), c=15.748(6)Å, β=105.40(3)°, space group, P21/c, V=3514(2)Å3, Z=2.</subfield>
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