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A New Three-dimensional Cd Metal-organic Framework Based on a C-centered Tripodal Flexible Carboxylate and 1,2-Bis(4-pyridyl)ethane Mixed Ligands

A New Three-dimensional Cd Metal-organic Framework Based on a C-centered Tripodal Flexible Carboxylate and 1,2-Bis(4-pyridyl)ethane Mixed Ligands
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摘要 A new MOF {[Cd3(TCOPM)2bpe]·7(H2O)·2DMF}n based on a C-centered tripodal flexible carboxylate ligand and 1,2-bis(4-pyridyl)ethane ligand (HaTCOPM = tris(p-carboxy- phenyl)methane, bpe = 1,2-bis(4-pyridyl) ethane) has been synthesized by the hydrothermal reaction in mixed DMF/H2O solution under 95 ℃. The structure has been determined by single-crystal X-ray diffraction analysis and elemental analysis, IR spectroscopy, and thermogravimetric analysis. Crystal data for the title complex are as follows: triclinic system, space group P/with a = 9.2637(14), b = 13.273(2), c = 14.160(2) A, a = 9.2637(14), β = 13.273(2), γ, = 105.585(2)°, V= 1487.6(4) A3, Mr= 1268.11, Z = 1, F(000) = 628, Dc = 1.416 g/cm3,μ(MoKa) = 1.110 mm^-1, R = 0.0482 and wR = 0.1444 for 5207 observed reflections with I 〉 2σ(I). MOF 1 consists of an infinite 3D network using TCOPM^3- and bpe as mixed bridge ligands. Fluorescence spectrum measurement indicates that MOF 1 shows strong fluorescence emission at 437 nm (λmax) in the solid state at room temperature and realizes tunable emission spectrum through tuning from single to mixed ligand. A new MOF {[Cd3(TCOPM)2bpe]·7(H2O)·2DMF}n based on a C-centered tripodal flexible carboxylate ligand and 1,2-bis(4-pyridyl)ethane ligand (HaTCOPM = tris(p-carboxy- phenyl)methane, bpe = 1,2-bis(4-pyridyl) ethane) has been synthesized by the hydrothermal reaction in mixed DMF/H2O solution under 95 ℃. The structure has been determined by single-crystal X-ray diffraction analysis and elemental analysis, IR spectroscopy, and thermogravimetric analysis. Crystal data for the title complex are as follows: triclinic system, space group P/with a = 9.2637(14), b = 13.273(2), c = 14.160(2) A, a = 9.2637(14), β = 13.273(2), γ, = 105.585(2)°, V= 1487.6(4) A3, Mr= 1268.11, Z = 1, F(000) = 628, Dc = 1.416 g/cm3,μ(MoKa) = 1.110 mm^-1, R = 0.0482 and wR = 0.1444 for 5207 observed reflections with I 〉 2σ(I). MOF 1 consists of an infinite 3D network using TCOPM^3- and bpe as mixed bridge ligands. Fluorescence spectrum measurement indicates that MOF 1 shows strong fluorescence emission at 437 nm (λmax) in the solid state at room temperature and realizes tunable emission spectrum through tuning from single to mixed ligand.
出处 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2015年第12期1915-1921,共7页 结构化学(英文)
基金 Financially supported by the State Key Laboratory of Coordination Chemistry of Nanjing University
关键词 TCOPM bpe FLUORESCENCE MOF TCOPM, bpe, fluorescence, MOF
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  • 1Wang C, Lin W B. Diffusion-controlled luminescence quenching in metal-organic frameworks. J Am Chem Soc, 2011, 133: 4232-4235.
  • 2Kreno L E, Leong K, Omar K F, et al. Metal-organic framework materials as chemical sensors. Chem Rev, 2012, 112: 1105-1125.
  • 3Lu Z Z, Zhang R, Li Y Z, et al. Solvatochromic behavior of a nanotubular metal-organic framework for sensing small molecules. J Am Chem Soc, 2011, 133: 4172-4174.
  • 4Cui J H, Li Y Z, Guo Z J, et al. A porous metal-organic framework based on Zn6O2 clusters: Chemical stability, gas adsorption properties and solvatochromic behavior. Chem Commun, 2013, 49: 555-557.
  • 5Chen B L, Wang L B, Xiao Y Q, et al. A luminescent metal-organic framework with Lewis basic pyridyl sites for the sensing of metal ions. Angew Chem Int Ed, 2009, 48: 508-511.
  • 6Czaja A U, Trukhan N, Muller U. Industrial applications of metal-organic frameworks. Chem Soc Rev, 2009, 38: 1284-1293.
  • 7Lee J Y, Farha O K, Roberts J, et al. Metal-organic framework materials as catalysts. Chem Soc Rev, 2009, 38: 1450-1459.
  • 8Li H, Eddaoudi M, O'keeffe M, et al. Design and synthesis of an exceptionally stable and highly porous metal-organic framework. Nature, 1999, 402: 276-279.
  • 9Hafizovic J, Bj?rgen M, Olsbye U, et al. The inconsistency in adsorption properties and powder XRD data of MOF-5 is rationalized by framework interpenetration and the presence of organic and inorganic species in the nanocavities. J Am Chem Soc, 2007, 129: 3612-3620.
  • 10Yaghi O M, O'Keeffe M, Ockwig N W, et al. Reticular synthesis and the design of new materials. Nature, 2003, 423: 705-714.

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