Supramolecular architectures in CoII and CuII complexes with thiophene-2-carboxylate and 2-amino-4,6-dimethoxypyrimidine ligands

摘要

The coordination chemistry of mixed-ligand complexes continues to be an active area of research since these compounds have a wide range of applications. Many coordination polymers and metal-organic framworks are emerging as novel functional materials. Aminopyrimidine and its derivatives are flexible ligands with versatile binding and coordination modes which have been proven to be useful in the construction of organic-inorganic hybrid materials and coordination polymers. Thiophenecarboxylic acid, its derivatives and their complexes exhibit pharmacological properties. Cobalt(II) and copper(II) complexes of thiophenecarboxylate have many biological applications, for example, as antifungal and antitumor agents. Two new cobalt(II) and copper(II) complexes incorporating thiophene-2-carboxylate (2-TPC) and 2-amino-4,6-dimethoxy-pyrimidine (OMP) ligands have been synthesized and characterized by X-ray diffraction studies, namely (2-amino-4,6-dimethoxypyrimidine-/dV)aquachlorido-(thiophene-2-carboxylato-/cO)cobalt(II) monohydrate, [Co(C5H3O2S)Cl(C6H9-N3O2)(H2O)]H2O, (I), and catewa-poly[copper(II)-tetrakis(/M-thiophene-2-car-boxylato-/c:2O:O/)-copper(II)-(/^-2-amino-4,6-dimethoxypyrimidine-/c:2Af 1:N3)], [Cu2(C5H3O2S)4(C6H9N3O2)]n, (II). In (I), the CoII ion has a distorted tetra-hedral coordination environment involving one O atom from a monodentate 2-TPC ligand, one N atom from an OMP ligand, one chloride ligand and one O atom of a water molecule. An additional water molecule is present in the asymmetric unit. The amino group of the coordinated OMP molecule and the coordinated carboxylate O atom of the 2-TPC ligand form an interligand N — H ? -O hydrogen bond, generating an S(6) ring motif. The pyrimidine molecules also form a base pair [R22(8) motif] via a pair of N—H ? -N hydrogen bonds. These interactions, together with O—H ? -O and O—H ? -Cl hydrogen bonds and jr-jr stacking interactions, generate a three-dimensional supramolecular architecture. The one-dimensional coordination polymer (II) contains the classical paddle-wheel [Cu2(CH3COO)4(H2O)2] unit, where each carboxylate group of four 2-TPC ligands bridges two square-pyramidally coordinated CuII ions and the apically coordinated OMP ligands bridge the dinuclear copper units. Each dinuclear copper unit has a crystallographic inversion centre, whereas the bridging OMP ligand has crystallographic twofold symmetry. The one-dimensional polymeric chains self-assemble via N—H ? -O, it-it and C— H ? -it interactions, generating a three-dimensional supramolecular architecture.