Rare earth coordination polymer taking 2, 2'-bipyridyl as template as well as preparation method and application thereof
A coordination polymer, ‐bipyridine technology, applied in the field of rare earth complex materials, can solve the problem of less preparation of rare earth coordination polymers, and achieve the effects of easy large-scale industrial production, novel structure and high yield
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Embodiment 1
[0045] Example 1 {(bpy) 0.5 [Dy 3 (ip) 4 (phen) 4 (H 2 O)]·2H 2 O} n The preparation method one
[0046] Dy(NO 3 ) 3 ·6H 2 O (0.5mmol, 288mg), isophthalic acid (0.5mmol, 83mg), 1,10-phenanthroline (1mmol, 198mg) were dissolved in 12ml of distilled water, stirred evenly, and the pH value of the reaction system was adjusted with pyridine= 8-9, then added to the reaction kettle, heated up, reacted at 160°C for 168 hours, cooled down, cooled to room temperature, filtered, washed with water, dried to obtain massive light green crystals. The resulting crystals were monochromated with graphite molybdenum target MoKa rays on the Rigaku RAXIS-RAPID single crystal X-ray diffractometer of Japan Rigaku Corporation. Diffraction data were collected at 293(2)K in ω-scan mode. The initial structure of the crystal was solved by the direct method using the SHELX-97 program, and then the coordinates of all non-hydrogen atoms were obtained by the difference Fourier synthesis method an...
Embodiment 2
[0047] Example 2 {(bpy) 0.5 [Dy 3 (ip) 4 (phen) 4 (H 2 O)]·2H 2 O} n The preparation method two
[0048] Will Dy 2 o 3 (0.25mmol, 93mg), isophthalic acid (3.75mmol, 623mg), 1,10-phenanthroline (3.75mmol, 743mg) were dissolved in 40ml distilled water and 10ml ethanol, stirred evenly, adjusted the reaction system with hydrochloric acid pH value = 6-7, then added to the reaction kettle, heated up, reacted at 80°C for 120 hours, cooled down, cooled to room temperature, filtered, washed with water, dried to obtain massive light green crystals. The resulting crystals were monochromated with graphite molybdenum target MoKα rays on the Rigaku RAXIS-RAPID single crystal X-ray diffractometer of Japan Rigaku Corporation. Diffraction data were collected at 293(2)K in ω-scan mode. The initial structure of the crystal was solved by the direct method using the SHELX-97 program, and then the coordinates of all non-hydrogen atoms were obtained by the difference Fourier synthesis met...
Embodiment 3
[0049] Example 3 {(bpy) 0.5 [Dy 3 (ip) 4 (phen) 4 (H 2 O)]·2H 2 O} n The preparation method three
[0050] Will Dy 2 (SO 4 ) 3 ·8H 2 O (0.5mmol, 379mg), isophthalic acid (.0mmol, 166mg), 1,10-phenanthroline (0.5mmol, 99mg) were dissolved in 10ml of distilled water and 5ml of methanol, stirred evenly, and washed with sodium hydroxide solution Adjust the pH value of the reaction system to 7~8, then add it to the reaction kettle, heat up, and react at 130°C for 240 hours, then gradually lower the temperature, cool to room temperature, filter, wash with water, and dry to obtain blocky light green crystals . The resulting crystals were monochromated with graphite molybdenum target MoKα rays on the Rigaku RAXIS-RAPID single crystal X-ray diffractometer of Japan Rigaku Corporation. Diffraction data were collected at 293(2)K in ω-scan mode. The initial structure of the crystal was solved by the direct method using the SHELX-97 program, and then the coordinates of all non...
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