Compounds and organic electronic devices containing them
A technology of organic electronic devices and compounds, which is applied in the field of organic electronic devices, can solve problems such as insufficiently developed stable and effective materials, and achieve the effects of improving life characteristics, increasing light efficiency, and reducing driving voltage
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment approach
[0070] According to an exemplary embodiment of the specification, Ar 1 For phenyl.
[0071] According to an exemplary embodiment of the specification, Ar 1 For biphenyl.
[0072] According to an exemplary embodiment of the specification, Ar 1 For naphthyl.
[0073] According to an exemplary embodiment of the present specification, L is a substituted or unsubstituted arylene group having 6 to 30 carbon atoms.
[0074] According to an exemplary embodiment of the present invention, L is substituted or unsubstituted phenylene, substituted or unsubstituted biphenylene; substituted or unsubstituted terphenylene; substituted or Unsubstituted naphthylene; substituted or unsubstituted anthracenylene; substituted or unsubstituted phenanthrenylene; substituted or unsubstituted pyrenylene; Fluorenyl.
[0075] According to an exemplary embodiment of the present invention, L is phenylene, biphenylene, terphenylene, naphthylene, anthracenylene, phenanthrene, pyrenylene or fluorenylene....
preparation example 1
[0204] Synthesis of Compound 1
[0205]
[0206] Compound C (7.17g, 22.2mmol) and 4-bromo-N,N'-diphenylaniline (7.17g, 22.2mmol) were completely dissolved in 60ml of xylene, and sodium tert-butoxide (2.56g , 26.6 mmol), and the resulting mixture was stirred while increasing the temperature until the resulting mixture was refluxed. When the mixture started to reflux, bis(tri-tert-butylphosphine)palladium (0.11 g, 0.22 mmol) was slowly added dropwise thereto. After 12 hours, the reaction was terminated, the temperature was lowered to normal temperature, and the resulting product was concentrated under reduced pressure, followed by column purification to prepare 8.68 g of Compound 1.
[0207] MS[M+H] + =576
preparation example 2
[0208] Synthesis of Compound 2
[0209]
[0210] 9.54 g of Compound 2 were prepared by reacting and purifying in the same manner as in Preparation Example 1, except that Compound C (7.17 g, 22.2 mmol) and (4'-bromo-N,N'-diphenyl) were used Biphenyl-4-amine (8.86 g, 22.2 mmol).
[0211] MS[M+H] + =652
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 


