Effects of substituent groups on the structures and luminescence properties of 2D/3D CdII complexes with mixed rigid and flexible carboxylate ligands†
Abstract
Three new Cd(II) complexes, [Cd(bic)(adp)0.5] (1), [Cd(mbic)(adp)0.5]·H2O (2) and [Cd(hbic)(adp)0.5]·H2O (3) (Hbic = 1H-benzoimidazole-5-carboxylic acid, Hmbic = 2-methyl-1H-benzoimidazole-5-carboxylic acid, Hhbic = 2-hydroxyethyl-1H-benzoimidazole-5-carboxylic acid, H2adp = adipic acid), have been prepared by the hydrothermal reaction of adp2− with Cd(II) ions in the presence of different benzimidazole carboxylic acids. 1 exhibits a 3D framework constructed from 1D infinite [Cd(COO)]n units which are connected by adp in a trans-(κ2-κ1)-(κ2-κ1)-μ4 mode and bic in a novel trans-(κ1-κ1)-(κ1)-μ3 mode. 2 features an unusual [Cd2(COO)4] paddle-wheel dinuclear secondary building unit (SBU), which is bridged into a 2D sheet by adp in a (κ1-κ1)-(κ1-κ1)-μ4 mode and mbic in a cis-(κ1-κ1)-(κ1)-μ3 mode. For 3, the metal centre is connected into a 1D double chain by hbic in a (κ1)-(κ1-κ1)-μ2 mode, which is further linked by the trans-(κ2-κ1)-(κ2-κ1)-μ4 adp to form a 2D layer architecture. The luminescence properties in the solid state at room temperature of compound 1–3 are almost the same as the free ligand.