Thermal excitation delayed fluorescence main material based on phosphonic aryl derivatives, preparation method and application thereof
A technology of aryl derivatives and delayed fluorescence, which is applied in the fields of luminescent materials, chemical instruments and methods, semiconductor/solid-state device manufacturing, etc. Effects of Injecting Transport Capabilities, Inhibiting Interactions
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specific Embodiment approach 1
[0059] Embodiment 1: The structural formula of the thermally excited delayed fluorescence host material based on phosphine heteroaryl derivatives in this embodiment is denoted as DPDPA; or denoted as DPDPSA; or Where X=S or O, Y=S or O, when X=Y=S, it is recorded as DPDPS 2 A; when X=S, Y=O, it is recorded as DPDPSOA; when X=Y=O, it is recorded as DPDPO 2 A; or denoted as DPDPP; or denoted as DPDPSP; or Where X=S or O, Y=S or O, when X=Y=S, it is recorded as DPDPS 2 P; when X=S, Y=O, it is recorded as DPDPSOP; when X=Y=O, it is recorded as DPDPO 2 p.
specific Embodiment approach 2
[0060] Specific embodiment two: The preparation method of the thermally excited delayed fluorescence host material based on phosphine heteroaryl derivatives described in specific embodiment one is as follows:
[0061] Add o-dibromoaryl compound, phenylphosphine dichloride, and n-butyllithium into tetrahydrofuran (THF) at a molar ratio of 1:(1~1.5):(2~4), under argon protection Under the condition of -60~-85℃, react for 1~3 hours, then pour into water, extract with dichloromethane to obtain the organic layer, dry the organic layer liquid, directly purify or vulcanize / and oxidize After further purification, a thermally excited delayed fluorescence host material based on phosphine heteroaryl derivatives is obtained; wherein the o-dibromoaryl compound is o-dibromobenzene or 2,3-dibromonaphthalene.
specific Embodiment approach 3
[0062] Specific embodiment three: the difference between this embodiment and specific embodiment two is that the vulcanization process is: adding sulfur powder to the organic layer liquid, stirring and reacting at a temperature of 15-30°C for 0.5-2 hours, Complete vulcanization. Others are the same as in the second embodiment.
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