A blue or/and green light-emitting mononuclear copper[i] complex material
A complex, green light technology, used in luminescent materials, compounds of Group 5/15 elements of the periodic table, copper organic compounds, etc.
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Embodiment 1
[0053] This embodiment provides a mononuclear copper [I] complex material emitting blue-green light, and its structural formula is:
[0054] , its preparation method is: in ice-water bath, N 2 Under protection, a solution containing 1 mmol of n-butyllithium (n-BuLi) (concentration: 2.5 mol / L) was added dropwise to tetrahydrofuran containing 1 mmol of carbazole, N 2 The reaction was stirred for 1 hour under protection; then a THF solution containing N,N'-dicyclohexylcarbodiimide (DCC) (1 mmol, 206.3 mg) was added dropwise at low temperature, and stirring was continued for 1 hour at low temperature, and then recovered to room temperature; the solution was then transferred to a solution containing 1 mmol POPCu (MeCN 2 )BF 4 (POPCu(MeCN 2 )BF 4 Synthetic reference: G.J. Kubas, Inorg.Synth., 1979, 19, 90-92) in tetrahydrofuran solution, N 2 Refluxed overnight under protection to finally obtain a yellow-green solution; after drying, the crude product was subjected to column c...
Embodiment 2
[0057] This embodiment provides a mononuclear copper [I] complex material emitting blue-green light, and its structural formula is:
[0058] , the preparation method is basically the same as that in Example 1, except that 1-bromobenzene is reacted with n-butyllithium (n-BuLi) solution, and finally 1.26g (yield 74%) is obtained, which has a wavelength of 350nm The emission spectrum under light excitation is shown in figure 2 Shown, specifically as described in the following reaction process:
[0059] .
Embodiment 3
[0061] This embodiment provides a blue light-emitting mononuclear copper [I] complex material, its structural formula is:
[0062] , its preparation method is basically the same as that in Example 1, the difference is that CH 3 I, then reacted with N,N'-diisopropylcarbodiimide (DIC) (1mmol, 127.13mg) to finally obtain a light yellow solution, after drying, the crude product was subjected to column chromatography, and the stationary phase was silica gel. The mobile phase is a mixture of dichloromethane and petroleum ether (10:1), and finally 0.48g (yield 64%) is obtained. Its emission spectrum under 350nm wavelength light excitation is as follows image 3 shown.
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