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Aromatic amine derivative and organic electroluminescence device

a technology of organic electroluminescence and amine, which is applied in the direction of discharge tube luminescnet screens, other domestic articles, organic chemistry, etc., can solve the problems of reducing the lifetime of light emission, increasing the driving voltage of the driving voltage, and reducing the current efficiency of light emission, so as to prolong the lifetime of organic el devices and improve yields

Inactive Publication Date: 2010-01-07
IDEMITSU KOSAN CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0052]The aromatic amine derivative of the present invention hardly causes the crystallization of a molecule and further, it improves yields upon production of the organic EL device, and contributes to prolong the lifetime of the organic EL devices.

Problems solved by technology

Usually, driving or storing the organic EL devices under an environment of elevated temperatures causes adverse influences such as changes of luminescent colors, degradation of current efficiency of light emission, increase of their driving voltage, reduction of lifetime in their light emission, etc.
However, in a compound having a symmetrical structure in a molecule, crystallization is liable to occur upon production of the organic EL device through the formation of a thin film by using those hole transporting materials.
As a result, there arises a problem such as clogging of an outlet of a crucible to be used in vapor deposition or a reduction in yields of the organic EL device due to generation of defects of the thin film resulting from the crystallization.
Accordingly, there arises a problem in that the lifetime is short, because a phenomenon such as decomposition at the time of the vapor deposition or the formation of a nonuniform deposition film is expected to occur.
Patent Documents 6 to 8 disclose about compounds having dibenzofuran structures through an aryl group in monoamines therof, however, the compounds do not sufficiently improve the performance as the organic EL device.
Although Patent Documents 12 to 14 disclose about usages as materials for the organic El, device, the materials do not sufficiently improve the performance as the organic EL device.
However, the lifetime is still insufficient.

Method used

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  • Aromatic amine derivative and organic electroluminescence device
  • Aromatic amine derivative and organic electroluminescence device
  • Aromatic amine derivative and organic electroluminescence device

Examples

Experimental program
Comparison scheme
Effect test

synthesis example 1

Synthesis of Intermediate 1

[0224]Under an argon gas flow, 47 g of 4-bromobiphenyl, 23 g of iodine, 9.4 g of periodic acid dihydrate, 42 ml of water, 360 ml of acetic acid and 11 ml of sulfuric acid were placed into a 1000-ml three-necked flask. After stirring the resultant solution at 65° C. for 30 minutes, the reaction was allowed to proceed at 90° C. for 6 hours. The resultant mixture was poured into iced water, and then filtered. After having been washed with water, the resultant was washed with methanol to obtain 67 g of a white powder. The white powder was identified as Intermediate 1 from the analysis in accordance with Field Desorption Mass Spectrum (hereinafter, FD-MS) because the main peaks of m / z=358 and 360 were shown for C12H8BrI=359.

synthesis example 2

Synthesis of Intermediate 2

[0225]Performing a reaction in the same manner as in Synthesis Example 1 except that 2-bromo-9,9-dimethylfluorene was used instead of 4-bromobiphenyl, 61 g of a white powder was obtained. The white powder was identified as Intermediate 2 from the analysis in accordance with the FD-MS because the main peaks of m / z=398 and 400 were shown for C15H12BrI=399.

synthesis example 3

Synthesis of Intermediate 3

[0226]Providing 150 g (892 mmol) of dibenzofuran and 1 liter of acetic acid into a flask, the inside of the flask was replaced with the nitrogen gas and the resultant mixture was heated and dissolved. After dropping 188 g (1.18 mol) of bromine while sometimes cooling with water, the mixture was stirred under air-cooling for 20 hours. The precipitated crystal was separated by filtration, washed with acetic acid and water sequentially, and was dried under reduced pressure. After refining the resultant crystal with reduced-pressure distillation, it was subjected to re-crystallization with methanol repeatedly several times to obtain 66.8 g (yield:31%) of 2-bromodibenzofran.

[0227]Under the atmosphere of argon gas, 400 ml of anhydrous THF was added to 24.7 g (100 mmol) of 2-bromodibenzofuran, and while stirring at −40° C., a hexane solution of n-butyllithium with 1.6 M concentration in an amount of 63 ml (100 mmol) was further added. The reacted solution was st...

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Abstract

An aromatic amine derivative having a specific structure. An organic electroluminescence device which is composed of one or more organic thin film layers sandwiched between a cathode and an anode, wherein at least one of the organic thin film layers, especially a hole transporting layer, contains the aromatic amine derivative. The aromatic amine derivative has at least one substituted or unsubstituted dibenzofuran skeleton and at least one substituted or unsubstituted terphenylene skeleton. Because the molecules in the aromatic amine derivative hardly crystallize, organic electroluminescence devices improving their production yield and having prolonged lifetime are provided.

Description

TECHNICAL FIELD[0001]The present invention relates to an aromatic amine derivative, a material for an organic electroluminescence (EL) device, and an organic EL device using the same; and more particularly, to an aromatic amine derivative actualizing the organic EL device capable of lengthening a lifetime of the organic EL device by using an aromatic amine derivative having a specific structure as a hole injecting material or a hole transporting material.BACKGROUND ART[0002]An organic EL device is a spontaneous light emitting device which utilizes a phenomenon that a fluorescent substance emits light by energy of recombination of holes injected from an anode and electrons injected from a cathode when an electric field is applied. Since an organic EL device of the laminate type driven under a low electric voltage was reported by C. W. Tang et al. of Eastman Kodak Company [C. W. Tang and S. A. Vanslyke, Applied Physics Letters, Volume 51, Page 913, 1987], many studies have been conduc...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): H01J1/63C07D307/91H10K99/00
CPCC07D307/91C07D407/12H10K85/636H10K85/633H10K85/631H10K85/6574H10K50/14C09K11/06Y10S428/917H10K85/622H10K85/6572H10K85/615
Inventor YABUNOUCHI, NOBUHIRO
Owner IDEMITSU KOSAN CO LTD
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