A kind of binuclear cadmium organic framework complex and its preparation method and application
A technology for organic frameworks and complexes, applied in the field of binuclear cadmium organic framework complexes and their preparation, can solve the problems that have not been reported, and achieve the effect of simple preparation method, low cost and high yield
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Embodiment 1
[0018] Example 1. [Cd 2 (cpima)(Hcpimda)(H 2 O)] n preparation method
[0019] 1) Weigh 0.05mmol H 3 cpimda with 0.1 mmol CdCl 2· 2.5H 2 O was placed in a 20ml Teflon tube, and 10ml H was added 2 O and 2ml CH 3 CN, then the polytetrafluoroethylene tube was sealed in a stainless steel reaction kettle, the temperature was controlled at 160 ° C 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 obtained cadmium complex The yield was 67%. Elemental analysis: theoretical value (%): C 42.54, H 3.45, N 6.48; experimental value (%): C 42.49, H 3.43, N 6.40.
Embodiment 2
[0020] Example 2. [Cd 2 (cpima)(Hcpimda)(H 2 O)] n crystal structure of
[0021] Select a single crystal of appropriate size under a microscope, use X-ray diffraction, use Bruker Smart Apex II detector to monochromatize Mo-Kα rays through graphite monochromator, scan mode ω, and collect diffraction data at room temperature. All diffraction data were subjected to semi-empirical absorption correction using the SADABS program after SAINT reduction. The crystal structure was solved by SHELXL-97 direct method. The detailed crystal determination data are shown in Table 1; the crystal structure is as figure 1 As shown, Cd(II) adopts hexa- and hepta-coordination modes.
[0022] Table 1 Crystallographic data of the complexes
[0023]
[0024]
Embodiment 3
[0025] Example 3. [Cd 2 (cpima)(Hcpimda)(H 2 O)] n phase analysis of
[0026] 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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