Green fluorescent material and preparation method of green fluorescent material
A technology for green fluorescent and fluorescent materials, applied in the field of green fluorescent materials and their preparation, can solve problems such as poor performance and complex preparation process, and achieve the effects of excellent performance, simple preparation process and easy availability of raw materials
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Embodiment 1
[0036] Mix 0.156g of 2,5-furandicarboxylic acid, 0.101g of potassium nitrate and 0.453g of terbium nitrate in a reaction kettle, then add to 50ml of acetonitrile solution, stir for 10 minutes, and then place it in an oven at 120°C. After 48h, cool to obtain colorless massive crystals, which are green fluorescent materials [Tb 3 K 2 (FDA) 4 (NO 3 ) 3 (MeCN) 2 ] n .
[0037] The following instruments and methods were used to characterize the product: 1. Select a crystal with a size of 0.24×0.23×0.22mm3 for single crystal structure analysis. The single crystal diffraction data was collected on a RigakuSCX diffractometer and monochromated with a graphite monochromator. Mok alpha rays 2.32°≤θ≤28.21°. The obtained compound belongs to the monoclinic crystal system, the space group is C2 / c, and the unit cell parameters are approximately α=90°, β=112.17°, and γ=90°. The crystal structure see figure 1 (Drawing using Diamond software).
Embodiment 2
[0039] Mix 0.312g of 2,5-furandicarboxylic acid, 0.202g of potassium nitrate, and 0.906g of terbium nitrate in a reaction kettle, then add it to 100ml of acetonitrile solution, stir for 10 minutes, and then place it in an oven at 120°C. After 48h, cool to obtain colorless massive crystals, which are green fluorescent materials [Tb 3 K 2 (FDA) 4 (NO 3 ) 3 (MeCN) 2 ] n .
[0040] To the [Tb 3 K 2 (FDA) 4 (NO 3 ) 3 (MeCN) 2 ] n Carry out fluorescence test, which produces 24000a.u. intensity of green fluorescence under the irradiation of 370nm incident light, and the fluorescence spectrum curve is as follows figure 2 Shown.
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