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1.  Zinc(II) and Nickel(II) Benzoate Complexes from the Use of 1-methyl-4,5-diphenylimidazole 
Two new complexes, [Zn(O2CPh)2(L)2]·2MeOH (1·2MeOH) and [Ni2(O2CPh))4(L)2]·2MeCN (2·2MeCN), have been synthesized and characterized by X-ray analysis in the course of an ongoing investigation of the MII/X−/L [MII = Co, Ni, Cu, Zn; X− = Cl−, Br−, I−, NCS−, NO3−, N3−, PhCO2−; L = 1-methyl-4,5-diphenylimidazole] reaction system, aiming at understanding and assessing the relative strength and the way in which the intermolecular interactions control the supramolecular organization of these compounds. In the mononuclear complex 1·2MeOH, the benzoate ion acts as a monodentate ligand resulting in a distorted tetrahedral N2O2 coordination environment. Complex 2·2MeCN exhibits a dinuclear paddle-wheel structure; each NiII has a square pyramidal NiNO4 chromophore with four benzoate oxygens in the basal plane and the pyridine-type nitrogen atom of one ligand L at the apex. The structure of 1·2MeOH is stabilized by intramolecular π-π interactions between aromatic rings of adjacent 4,5-diphenylimidazole moieties; it is a feature also evidenced in similar compounds of the type [MX2L2].
doi:10.1155/2010/178034
PMCID: PMC2927736  PMID: 20811497
2.  Synthesis and Structural Characterization of a Metal Cluster and a Coordination Polymer Based on the [Mn6(μ4-O)2]10+ Unit 
A new 1-D coordination polymer {[Mn6O2(O2CMe)10(H2O)4]·2.5H2O}∞ (1·2.5H2O)∞ and the cluster [Mn6O2(O2(O2CPh)10 (py)2(MeCN)(H2O)]·2MeCN (2·2MeCN) are reported. Both compounds were synthesized by room temperature reactions of [Mn3(μ3-O)(O2CR)6(L)2(L′)] (R = Me, L = L′ = py, (1·2.5H2O)∞; R = Ph, L = py, L′ = H2O, 2·2MeCN) in the presence of 3-hydroxymethylpyridine (3hmpH) in acetonitrile. The structures of these complexes are based on hexanuclear mixed-valent manganese carboxylate clusters containing the [Mn4IIMn2III(μ4-O)2]10+ structural core. (1·2.5H2O)∞ consists of zigzag chain polymers constructed from [Mn6O2(O2CMe)10(H2O)4] repeating units linked through acetate ligands, whereas 2·2MeCN comprises a discrete Mn6-benzoate cluster.
doi:10.1155/2010/367128
PMCID: PMC2902058  PMID: 20634987
3.  Synthesis and Characterization of a Linear [Mn3(O2CMe)4(py)8]2+ Complex 
Two new compounds that consist of the linear trinuclear manganese(II) cation [Mn3(O2CMe)4(py)8]2+ cocrystallizing with different counteranions (I3−, [1]; ClO4−, [2]) are reported. Complex 1 was prepared from the reaction of [Mn(O2CMe)2] · 4H2O with I2 in MeCO2H/py, whereas complex 2 was isolated from the reaction of [Mn3O(O2CMe)6(py)3] · py with [Mn(ClO4)2] · 6H2O in MeCN/py. The crystal structures of both compounds were determined by single crystal X-ray crystallography. Magnetic susceptibility studies that were performed in microcrystalline powder of 1 in the 2–300 K range revealed the presence of antiferromagnetic exchange interactions that resulted in an S = 5/2 ground spin state.
doi:10.1155/2010/932569
PMCID: PMC2878672  PMID: 20585359

Results 1-3 (3)