Article ID Journal Published Year Pages File Type
1336619 Polyhedron 2014 5 Pages PDF
Abstract

This paper reports the synthesis, X-ray structure and magnetic characterization of [Mn2Cl(BIP) (HBIMAM)(H2O)5]Cl3·4H2O a novel dinuclear manganese(II) incorporating two related bis(imidazolyl)-based ligands, BIP (3,3-di(2-1H-2-imidazolyl)propanoate) and BIMAM (N-methyldi(1H-2-imidazolyl)methanamine). The metal atoms in the dinuclear entity are bridged by a μ2-η1:η1 carboxylate group (from the propionate arm of the BIP ligand) acting in an anti–anti coordination bridging mode, with an intramolecular Mn⋯Mn distance of 6.47 Å. The coordination around the Mn(II) ions shows a distorted octahedral geometry for both MnClN2O3 and MnN2O4 chromophores. Between the imidazole rings of neighbouring dinuclear units there significant aromatic–aromatic interactions. The propagation of these interactions generates chains of π-stacked dinuclear units, roughly running along the [1 0 0] direction. Magnetic susceptibility measurements in the range 2–300 K show weak antiferromagnetic exchange interactions which were analysed by means of the isotropic S1 = S2 = 5/2 spin-coupled dimer model Hˆ=-2J(Sˆ1·Sˆ2). Finally, the observed magnetic behavior (2J = −0.38(1) cm−1) is compared with that observed in related manganese(II) compounds with single [Mn(μ2-η1:η1-carboxylato)Mn] core.

Graphical abstractA new μ2-η1:η1-carboxylato bridged manganese(II) dinuclear compound with bis(imidazolyl) based ligands is reported. The dinuclear [Mn2Cl(BIP)(HBIMAM)(H2O)5]3+ units form a chain structure through both π⋯π interactions and H-bonds. The observed weak antiferromagnetism is compared with that observed in related manganese(II) compounds with single [Mn(μ2-η1:η1-carboxylato)Mn] bridges. Magnetic properties are discussed on the basis of the interactions network.Figure optionsDownload full-size imageDownload as PowerPoint slide

Related Topics
Physical Sciences and Engineering Chemistry Inorganic Chemistry
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