Zinc terpyridine benzoate complex and preparation conditions
A technology of zinc benzoate and terpyridine, which is applied in the field of fluorescent solid materials, can solve the problems that there is no logical theory, long-wave zinc organic coordination polymer fluorescent materials are rare, etc., and achieves high crystal purity, high thermal stability, Simple operation effect
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Embodiment 1
[0030] Embodiment 1 Zinc complex [Zn(tpb) of the present invention 2 ](Htpb) 2 preparation of
[0031] a) Weigh raw materials according to the following molar ratio, Htpb: Zn(NO 3 ) 2 :DMF:H 2 O: HNO 3 The molar ratio is 1:2:516:8888:18, as for the 50mL glass beaker, mix and stir for 0.5 hours;
[0032] b) Transfer the mixture obtained in step a) into a 25mL reactor, and react at 140°C for 3 days;
[0033] c) Naturally cooled to room temperature, yellow crystals were observed, filtered, washed with DMF and water successively, and naturally dried to obtain the target product.
[0034] Use Perkin-Elmer2400 elemental analyzer to conduct elemental analysis on the C, H, and N elements of the target product, calculated value (%): C, 71.93; H, 4.02; N, 11.18; actual measured (%): C, 71.87; H, 4.03; N, 11.21.
[0035] Use Nicolet Impact 410FTIR spectrometer, with KBr as substrate, at 400-4000cm -1 Infrared analysis of the target product within the range, FT-IR (KBr,cm -1 ):3...
Embodiment 2
[0040] Embodiment 2 Zinc complex [Zn(tpb) of the present invention 2 ](Htpb) 2 preparation of
[0041] a) Weigh raw materials according to the following molar ratio, Htpb: Zn(NO 3 ) 2 :DMF:H 2 O: HNO 3 The molar ratio is 1:1:516:8888:12, placed in a 50mL glass beaker, mixed and stirred for 1 hour;
[0042] b) Transfer the mixture obtained in step a) into a 25mL reactor, and react at 130°C for 3 days;
[0043] c) Naturally cooled to room temperature, light yellow crystals were observed, filtered, washed with DMF and water successively, and dried naturally to obtain the target product.
[0044] Carry out elemental analysis, infrared, fluorescence, X-ray powder diffraction characterization to target product with the condition of embodiment 1, result is similar to embodiment 1, the target product that embodiment 2 makes is identical with the target product that embodiment 1 makes, The purity of the sample is high, the results are shown in Figure 5 .
[0045] Repeat this ...
Embodiment 3
[0046] Embodiment 3 Zinc complex [Zn(tpb) of the present invention 2 ](Htpb) 2 preparation of
[0047] a) Weigh raw materials according to the following molar ratio, Htpb: Zn(NO 3 ) 2 :DMF:H 2 O: HNO 3 The molar ratio is 1:1:774:7778:15, placed in a 50mL glass beaker, mixed and stirred for 0.5h;
[0048] b) Transfer the mixture obtained in step a) into a 25mL reactor, and react at 140°C for 2 days;
[0049] c) Naturally cooled to room temperature, light yellow crystals were observed, filtered, washed with DMF and water successively, and dried naturally to obtain the target product.
[0050] Carry out elemental analysis, infrared, fluorescence, X-ray powder diffraction characterization to target product with the condition of embodiment 1, result is similar to embodiment 1, the target product that embodiment 3 makes is identical with the target product that embodiment 1 makes, The purity of the sample is high, the results are shown in Figure 5 .
[0051] Repeat this em...
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