Synthesis and characterization of luminescent metal–organic frameworks for the selective recognition of Cu2+ cation and Tryptophan

Abstract

Three metal-organic frameworks (MOFs), namely, [Mn(CPP)2(H2O)]n (I), [Cd(CPP)2(H2O)]n (II) and {[Zn2(CPP)2(CO3)]·(ClO4)·(H2O)2}n (III) (HCPP = 4'-(4-(4-carboxylphenoxy)-2,2':6′,2′-terpyridine), were successfully achieved under hydrothermal conditions. The as-synthesized coordination polymers have been characterized by IR spectroscopy, elemental analyses and single crystal X-ray diffraction. Single-crystal X-ray diffraction analyses indicate that compounds Ⅰ and Ⅱ display isomorphous and isostructural, in which the central metal ions present distorted octahedral configurations. Ⅰ and Ⅱ feature fascinating 3D frameworks based on π⋯π and CH⋯π interactions between the pyridine rings appertaining CPP− ligands, while compound Ⅲ possesses a 3D net interlinked via C-H⋯π interactions between the phenyl rings belonging to the CPP− ligands. In their 3D frameworks, the {MnN3O3}, {CdN3O3} and {ZnO2N3}–{ZnO2N3} building units are observed, respectively. Luminescent properties of coordination polymer Ⅱ and Ⅲ demonstrate that they may be acted as fluorescent sensors toward Cu2+ cation and Tryptophan, respectively. Furthermore, investigations on magnetic property reveal that coordination polymer Ⅰ presents antiferromagnetic coupling.