Rare earth organic coordination polymers adopting imidazolium cation as template, preparation method and application thereof
A technology of imidazolium cations and coordination polymers, which is applied in the fields of compounds containing Group 3/13 elements of the periodic table, organic chemistry, chemical instruments and methods, etc., can solve the problems of very few coordination polymers and achieve environmental friendliness. , the effect of high yield and novel structure
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Embodiment 1
[0052] {(Him)[Sm(ip) 2 (H 2 O)]} n Synthesis
[0053] Sm(NO 3 ) 3 ·6H 2 O (0.5mmol, 231mg), isophthalic acid (0.5mmol, 83mg), and imidazole (1mmol, 68mg) were dissolved in 20ml of distilled water, stirred evenly, and the pH value of the reaction system was adjusted to 8-9 with sodium hydroxide solution, Then add it into the reaction kettle, heat up, and react at 150°C for 120 hours, gradually lower the temperature, cool to room temperature, filter, wash with water, and dry to obtain blocky yellow 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 method and the least square method, and...
Embodiment 2
[0057] {(Him)[Eu(ip) 2 (H 2 O)]} n Synthesis
[0058] Will Eu 2 o 3 (0.25mmol, 88mg), isophthalic acid (3.75mmol, 623mg), and imidazole (3.75mmol, 255mg) were dissolved in 30ml of distilled water and 20ml of methanol, stirred evenly, and the pH value of the reaction system was adjusted with sulfuric acid solution=5~6 , and then added to the reaction kettle, heated up, reacted at 130 ° C for 240 hours, gradually lowered the temperature, cooled to room temperature, filtered, washed with water, dried to obtain block light yellow 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 method and...
Embodiment 3
[0062] {(Him)[Gd(ip) 2 (H 2 O)]} n Synthesis
[0063] GdCl 3 '6H 2 O (0.5mmol, 186mg), isophthalic acid (1.0mmol, 166mg), and imidazole (0.5mmol, 34mg) were dissolved in 9ml of distilled water and 6ml of ethanol, stirred evenly, and the pH value of the reaction system was adjusted with triethylamine=9 ~10, then added to the reaction kettle, heated up, and reacted at 80°C for 10 hours, then gradually lowered the temperature, cooled to room temperature, filtered, washed with water, and 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 method and the le...
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