2015) Synthesis and Crystal Structure of a µ-Oxido-Bridged Dinuclear Iron(III) Complex Derived From 3, 5-Dichlorosalicylaldehyde and 4-(2-Aminoethyl)morpholine, Synthesis and Reactivity in Inorganic, Metal-Organic, and Nano-Metal Chemistry, 45:3, 388-391, A m-oxido-bridged dinuclear iron(III) complex, [Fe 2 O(L 1 ) 2 (L 2 ) 2 ], where L 1 and L 2 are the deprotonated forms of 2,4-dichloro-6-[(2-morpholin-4-ylethylimino)methyl]phenol and 3,5-dichlorosalicylaldehyde, respectively, has been prepared and characterized by elemental analysis, infrared spectrum, and single-crystal X-ray determination. The complex crystallizes in the triclinic space group P1, with unit cell dimensions a D 10.670(1) A , b D 11.585(1) A , c D 19.748(2) A , a D 86.766(2) , b D 85.038(2) , g D 73.973(2) , V D 2336.1(4) A 3 , Z D 2, GOOF D 1.019, R 1 D 0.0422, and wR 2 D 0.1024. Structural analysis shows that the iron atoms in the complex are hexacoordinate with a normal Fe-O-Fe bridging angle of 150.84(13) . Each Fe atom is coordinated by the NNO donor atoms of L 1 , OO donor atoms of L 2 , and one bridging O atom. The Fe¢ ¢ ¢Fe distance is 3.467(2) A .