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Polymer, composition for organic electroluminescent element, organic electroluminescent element, organic EL display device, organic EL lighting, and manufacturing method for organic electroluminescent element

專(zhuān)利號(hào)
US12133453B2
公開(kāi)日期
2024-10-29
申請(qǐng)人
Mitsubishi Chemical Corporation(JP Tokyo)
發(fā)明人
Yanjun Li; Tomokazu Umemoto; Hideki Gorohmaru; Koichiro Iida; Kouji Adachi
IPC分類(lèi)
H01L51/50; C08G73/02; C09K11/06; H10K85/10; H10K50/11; H10K50/15; H10K50/17; H10K71/00; H10K71/12; H10K85/60
技術(shù)領(lǐng)域
group,ring,polymer,aromatic,preferably,formula,layer,or,compound,in
地域: Tokyo

摘要

Provided are: a highly durable polymer having a high hole-injection/transport capacity; and a composition for an organic electroluminescent element, which contains the polymer. The polymer contains a repeating unit represented by the following Formula (1) or a repeating unit represented by the following Formula (2) (wherein, Ar1 and Ar2 each represent an aromatic hydrocarbon group optionally having a substituent, or an aromatic heterocyclic group optionally having a substituent; X represents —C(R7)(R8)—, —N(R9)—, or —C(R11)(R12)—C(R13)(R14)—; R1 and R2 as well as R3 and R6 each independently represent an alkyl group optionally having a substituent; R4 and R5 each independently represent an alkyl group optionally having a substituent, an alkoxy group optionally having a substituent, or an aralkyl group optionally having a substituent; and R7 to R9 and R11 to R14 each independently represent hydrogen, an alkyl group optionally having a substituent, an aralkyl group optionally having a substituent, or an aromatic hydrocarbon group optionally having a substituent).

說(shuō)明書(shū)

Bis(triphenylphosphine)palladium (II) dichloride (0.052 g, 0.073 mmol) was added thereto, and the resultant was stirred at 65° C. for 3 hours. Water was added to this reaction solution, which was subsequently extracted with toluene. The resulting organic layer was dried over anhydrous magnesium sulfate and then partially purified with activated earth. The thus obtained partial purification product was further purified by column chromatography (developer: hexane/methylene chloride=75/25), whereby the compound 25 (4.8g, yield: 76.0%) was obtained.

[Synthesis of Compound 27]

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Subsequently, the compound 25 (4.6 g, 5.13 mmol), the compound 26 (2.2 g, 6.67 mmol), potassium carbonate (2.1 g, 15.4 mmol), toluene (24 ml), ethanol (8 ml), and water (8 ml) were added to a flask, and this system was sufficiently purged with nitrogen and heated to 60° C. Tetrakis(triphenylphosphine)palladium (0) (0.18 g, 0.154 mmol) was added thereto, and the resultant was stirred at 85° C. for 3.5 hours. Water was added to this reaction solution, which was subsequently extracted with toluene. The resulting organic layer was dried over anhydrous magnesium sulfate and then partially purified with activated earth. The thus obtained partial purification product was further purified by column chromatography (developer: hexane/methylene chloride=60/40), whereby the compound 27 (3.9 g, yield: 74.9%) was obtained.

[Synthesis of Compound 28]

權(quán)利要求

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