Luminescent material of cuprous iodide complex and preparation method thereof
A cuprous iodide-based, luminescent material technology, applied in luminescent materials, copper organic compounds, chemical instruments and methods, etc., can solve the problems of luminous intensity not meeting application requirements, affecting popularization, application and market performance, and expensive prices. , to achieve the effect of good phosphorescence emission performance, low production cost and cheap purification
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Embodiment 1
[0032] Synthesis of Cuprous Iodide-Based Complexes (CuIL) n Single crystal of Ligand L: Weigh 19mg CuI and 20mg Ligand L and dissolve them in 10mL of acetonitrile respectively, gently cover the Ligand L solution on the CuI solution, and after standing for several days, a large number of orange needle-shaped columnar crystals are precipitated. An orange crystal with a size of 0.29mm×0.16mm×0.04mm was selected for X-ray single crystal structure test. The molecular structure of the compound is shown in the attached figure 1 and 2 , and its unit cell packing structure is shown in the attached image 3 .
Embodiment 2
[0034]Weigh 456 mg CuI and 117.7 mg Ligand L (molar ratio 4:1) and dissolve them in 10 mL of acetonitrile respectively, mix the two acetonitrile solutions, and stir to make the coordination reaction fully occur, and the orange color precipitated as the reaction proceeds. Precipitation gradually increased, and finally an orange cloudy solution was formed. The turbid solution obtained from the reaction was filtered, and the obtained precipitate was washed with acetonitrile, and dried in vacuo to obtain a crystalline orange powder product with a yield of 23% (calculated as CuI).
Embodiment 3
[0036] Weigh 114mg CuI and 470.8mg Ligand L (molar ratio 1:4) and dissolve them in 10mL of acetonitrile respectively, mix the two acetonitrile solutions, and stir to make the coordination reaction fully occur, and the orange color precipitated along with the reaction Precipitation gradually increased, and finally an orange cloudy liquid was formed. The turbid solution obtained from the reaction was filtered, the obtained precipitate was washed with acetonitrile, and vacuum-dried to obtain a crystalline orange powder with a yield of 21% (based on ligand L).
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