Citation: Yi DING, Peiyu LIAO, Jianhua JIA, Mingliang TONG. Structure and photoluminescence modulation of silver(Ⅰ)-tetra(pyridin-4-yl)ethene metal-organic frameworks by substituted benzoates[J]. Chinese Journal of Inorganic Chemistry, ;2025, 41(1): 141-148. doi: 10.11862/CJIC.20240393 shu

Structure and photoluminescence modulation of silver(Ⅰ)-tetra(pyridin-4-yl)ethene metal-organic frameworks by substituted benzoates

Figures(4)

  • 1, 1, 2, 2-Tetra(pyridin-4-yl)ethene (TEPE) was chosen as a bridging ligand to assemble with Ag(Ⅰ) ions to form the cationic frameworks. And, the pentafluoro-benzoate anions (PFB-) and the benzoate (Bz-) anions as guests were introduced respectively to generate two new coordination compounds: [Ag(TEPE)(H2O)](PFB)·7H2O·3EtOH (1) and [Ag(TEPE)](Bz)·4H2O·2EtOH (2). The compositions and structures of complexes 1 and 2 were characterized using the thermogravimetric analysis, IR spectra, and single-crystal X-ray diffraction analysis. 1 possesses a 2D brick-like coordination layer structure with the classical hcb topology, each Ag(Ⅰ) center is coordinated with an aqua ligand and three N atoms from three TEPE ligands respectively, forming the distorted tetrahedral coordination geometry. The PFB- guests are distributed between the 2D layers to form diverse interactions with the main framework. 2 presents a 3D coordination network structure with the sqc8116 topology, in which each Ag(Ⅰ) center is coordinated in a tetrahedral geometry with four N atoms from four TEPE ligands respectively, and Bz- guests are located at the larger channels along the c-axis. Interestingly, two complexes showed the characteristic fluorescent properties regulated by photoactive guests. Excited by UV light, 1 exhibited a red emission while 2 showed a blue emission.
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