Two-dimensional cadmium organic framework coordination compound and preparation method and application thereof
A technology of organic frameworks and complexes, applied in the field of transition metal complexes, achieving the effects of high yield, low cost, and simple preparation methods
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Embodiment 1
[0019] Embodiment 1. Complex of the present invention [Cd (μ 5 -Hcbic)] n preparation method
[0020] Weigh 0.05mmolH 3 cbic with 0.1mmol CdCl 2 2.5H 2 O was placed in a 10ml Teflon tube, and 4ml H was added 2 O and 3ml CH 3 CN, stirred at room temperature for 30 minutes. Then the polytetrafluoroethylene tube was sealed in a stainless steel reaction kettle, the temperature was controlled at 160°C and heated for 72 hours, and it was naturally lowered to room temperature to obtain colorless blocky crystals, which were washed three times with distilled water and dried in vacuum. The yield of the obtained cadmium complex was was 63%. Elemental analysis: theoretical value: C 45.26, H 2.22, N 6.21; experimental value: C 45.35, H 2.17, N 6.29.
Embodiment 2
[0021] Embodiment 2. Complexes of the present invention [Cd (μ 5 -Hcbic)] n crystal structure of
[0022] The crystal structure was determined using the Beijing Synchrotron Radiation 1W2B working line station light source For the incident radiation, the MAR165CCD detector, MARCCD and HKL2000 programs collect and restore the data and unit cell parameters, and use the SHELXL-97 direct method and least square method to correct the coordinates of each atom from the difference Fourier electron density map, and use Lorentz and polarization effect correction, and finally solved the crystal structure ( figure 1 ). C and O atoms are hydrogenated using theory. The detailed crystal determination data are shown in Table 1.
[0023] Crystallographic data of the complexes in Table 1
[0024]
[0025]
Embodiment 3
[0026] Embodiment 3. Complexes of the present invention [Cd (μ 5 -Hcbic)] n phase analysis of
[0027] X-ray powder diffraction such as figure 2 As shown, the experimental diffraction pattern is consistent with the powder diffraction pattern simulated based on the crystal structure, indicating that the crystal sample is homogeneous.
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