Chemistry

Synthesis, structure, and magnetic properties of a family of Mn(II) compounds with substituted 2-aminopyridinium ions

David J. Carnevale, Nova Southeastern University
Louise N. Dawe, Wilfrid Laurier University
Christopher P. Landee, Clark University
Mark M. Turnbull, Clark University
Jan L. Wikaira, University of Canterbury

Abstract

A family of complexes were made by combining MnX2·nH2O (X = Cl, Br) with 2-amino-3-methylpyridine (3MAP), 2-amino-5-methylpyridine (5MAP) or 2-amino-5-iodopyridine (5IAP) in aqueous acidic conditions. The resulting complexes were (3MAPH)2Cl2.MnCl2(H2O)2 (1), (3MAPH)2Br2.MnBr2(H2O)2 (2), (5IAPH)8 [Mn4Cl10(H2O)8] Cl6 (3) and (5MAPH)2 MnBr4 (4). Complexes 1–3 crystalize in monoclinic space groups (1 = P21/c, 2&3 = P21/n) with chains formed by halide bridged manganese ions. Compound 4 crystalizes in the triclinic space group P-1 with a manganese halide ladder structure formed via short Br…Br contacts. Complexes 1, 2 and 4 were studied through variable temperature magnetic susceptibility measurements, all of which exhibited weak antiferromagnetic interactions (J = ~ – 0.45 to –0.05 K).