Organic semiconductor material containing naphthalene, anthracene, dibenzothiophene sulfone units and preparation method and application thereof
A technology of benzothiophene sulfone and organic semiconductors, which is applied in the field of organic semiconductor materials and its preparation, and can solve problems such as low luminous efficiency, unstable devices, and weak luminous intensity
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[0032] The embodiment of the present invention also provides a method for preparing the above-mentioned organic semiconductor material containing naphthalene, anthracene, and dibenzothiophene sulfone units. For the process flow of this method, please refer to figure 1 . The organic semiconductor material containing naphthalene, anthracene and dibenzothiophene sulfone units comprises the following steps:
[0033] S1: respectively provide compound A and compound B represented by the following structural formula, wherein, R is F, cyano, aldehyde or nitro,
[0034]
[0035] S2: In an oxygen-free environment and in the presence of organometallic catalysts and organic solvents, compounds A and B are subjected to a Suzuiki coupling reaction to obtain a naphthalene, anthracene, and dibenzothiophene sulfone represented by the general formula (I) unit of organic semiconducting material,
[0036]
[0037] Specifically, in step S1 of the above-mentioned method for preparing organi...
Embodiment 1
[0048] The organic semiconductor material of the present embodiment naphthalene, anthracene, dibenzothiophene sulfone unit is the organic compound 2,7-bis(10-(6-cyano-naphthalene-2- Base) anthracene-9-yl) dibenzothiophene sulfone (CNDNAFSO) and preparation method thereof, its structural formula is as follows I 1 Shown:
[0049]
[0050] The preparation steps of above-mentioned CNDNAFSO are as follows:
[0051] S11: respectively provide compound A and compound B represented by the following structural formula,
[0052]
[0053] Wherein, the specific preparation steps of compound A, namely 2,7-dibromodibenzothiophene sulfone are: dissolving 4 mmol of dibenzothiophene sulfone in 30 ml of concentrated H 2 SO 4 8.2mmol NBS was added at room temperature, and the reaction was stirred. After 24 hours of reaction, the reaction liquid was poured into water, filtered with suction, washed with water and methanol, and the solid was collected, and then the solid was recrystallized ...
Embodiment 2
[0062] The organic semiconductor material of the present embodiment naphthalene, anthracene, dibenzothiophene sulfone unit is the organic compound 2,7-bis(10-(6-formyl-naphthalene-2- Base) anthracene-9-yl) dibenzothiophene sulfone (CHODNAFSO) and preparation method thereof, its structural formula is as follows I 2 Shown:
[0063]
[0064] The preparation steps of above-mentioned CHODNAFSO are as follows:
[0065] S21: respectively provide compound A and compound B represented by the following structural formula,
[0066]
[0067] Wherein, the method for obtaining compound A, that is, 2,7-dibromodibenzothiophene sulfone is the same as step S11 of Example 1;
[0068] S22: Preparation of 2,7-bis(10-(6-formyl-naphthalene-2-yl)anthracen-9-yl)dibenzothiophene sulfone (CHODNAFSO), whose chemical reaction formula is as follows:
[0069]
[0070] The specific preparation process is: the above-mentioned compound A (2,7-dibromodibenzothiophene sulfone) 3mmol, compound B ((10-...
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