Synthesis, crystal structure and magnetic properties of coordination compounds of Mn(NCS)2 with the 3-bromopyridine ligand

Abstract

Abstract Reactions of Mn(NCS)2 with 3-bromopyridine in acetonitrile lead to the formation of Mn(NCS)2(3-bromopyridine)4 (1) and Mn(NCS)2(3-bromopyridine)2(MeCN)2 (2) that were characterized by single crystal X-ray diffraction. Compounds 1 and 2 consist of discrete complexes, in which the Mn(II) cations are octahedrally coordinated by two trans-N-bonding thiocyanate anions and four pyridine (1) or two pyridine and two acetonitrile ligands (2). Thermoanalytical measurements on 1 and 2 have shown that upon heating half of the 3-bromopyridine co-ligands from 1 or both acetonitrile ligands from 2 are removed leading to a crystalline phase with the composition [Mn(NCS)2(3-bromopyridine)2] n (3-II). From dry n-butanol a phase with the same composition was obtained (3-I) that corresponds to a polymorphic or isomeric form of 3-II. Crystal structure analysis of 3-I shows that in this form the Mn cations are linked by pairs of anionic ligands into linear chains. The results of magnetic measurements on 3-I show antiferromagnetic interactions along the chains and the analysis of the magnetic susceptibility using the Fisher model for chains gave a J value of −5.76(5) K.