Structure modulation of metal-organic frameworks via reaction pH: Self-assembly of a new carboxylate containing ligand N-(3-carboxyphenyl)iminodiacetic acid with cadmium(II) and cobalt(II) salts

摘要

Self-assembly of a new carboxylate containing ligand, N-(3-carboxyphenyl)iminodiacetic acid (H3L), with Cd(II) and Co(II) salts under different reaction pH results in the formation of four new coordination polymers, namely [Cd(HL)(H2O)] (1), [Co(HL)(H2O)] (2), [Cd(HL)(H2O)(4)] (3) and [Cd-3(L)(2)(H2O)(9)] center dot 7H(2)O (4). Single crystal X-ray diffraction analysis indicates that I and 2 are isomorphous and isostructural with a 2D wave-like network structure, while 3 has a ID zigzag chain structure. The complexes 1-3 were obtained at low pH (< 7) which makes the ligands only partly deprotonated. However, complex 4, obtained at pH 7 with all the carboxylate groups deprotonated, exhibits a 2D network structure. The results suggest that the reaction pH is one of the key factors in the formation of the coordination architectures. In addition, the photoluminescence properties of the free ligand (H3L) and complexes 1, 3 and 4 were studied in the solid state at room temperature. Moreover, the magnetic property of complex 2 was investigated. (c) 2007 Elsevier Ltd. All rights reserved.