Manganese(II) and cobalt(II) complexes based on pyridyl diimide: in situ ligand formation, crystal structures, and sorption properties

摘要

Two complexes, namely {[Mn(L-1)(2)(H2O)(2)]center dot 0.5H(2)O} (n) (1) and {[Co(L-2)(H2O)(2)]center dot 4H(2)O} (n) (2), (L-1,1,3-dioxo-2-pyridin-3-ylmethyl-6-[(pyridin-3-ylmethyl)-carbamoyl]-2,3-dihydro-1H-isoindole-5-carboxylic acid; L-2,2,5-bis-[(pyridine-3-yl methyl)-carbamoyl]-terephthalic acid), were synthesized and characterized by elemental analysis, IR spectroscopy, thermogravimetric analysis, and X-ray single-crystal structure analysis. The ligands HL1 and HL2 were formed in situ by the hydrolysis of N,N'-bis(3-pyridylmethyl)-pyromellitic diimide (L). Apparently, Mn2+ acts as an asymmetric catalyst, such that a new asymmetric pyridinecarboxylate derivative ligand L-1 is formed, while Co2+ acts as a symmetric catalyst, giving the pyridinedicarboxylate derivative ligand L-2. Complex 1 has a 1D double-chain structure, in which the adjacent chains are arranged in parallel arrays through pi center dot center dot center dot pi interactions, resulting in a 2D supramolecular framework. Complex 2 has a grid (4,4)-sql net structure in an edge-to-edge arrangement through hydrogen bonds between adjacent layers, forming a 3D supramolecular framework containing 1D channels to accommodate water guest molecules. The thermal stabilities of both complexes and ethanol adsorption properties of complex 2 were investigated.