Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Polycyclic aromatic compound, reactive compound, polymer compound, suspension-type polymer compound, and use using same

A polycyclic aromatic compound technology, applied in the field of suspended polymer compounds, can solve problems such as insufficient life, unsuitable main materials, and insufficient stability of aromatic epoxy redox

Pending Publication Date: 2020-12-08
KWANSEI GAKUIN EDUCATIONAL FOUND +1
View PDF45 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the oxidation-reduction stability of the aromatic ring with a small conjugated system is not sufficient, and the life of the device using the molecule having the conventional aromatic ring as the host material is not sufficient.
On the other hand, polycyclic aromatic compounds with extended π-conjugated systems usually have excellent redox stability, but the HOMO-LUMO gap (band gap Eg of the film) or the triplet excitation energy (E T ) are low and are therefore considered unsuitable for host materials

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Polycyclic aromatic compound, reactive compound, polymer compound, suspension-type polymer compound, and use using same
  • Polycyclic aromatic compound, reactive compound, polymer compound, suspension-type polymer compound, and use using same
  • Polycyclic aromatic compound, reactive compound, polymer compound, suspension-type polymer compound, and use using same

Examples

Experimental program
Comparison scheme
Effect test

Embodiment

[1755] Hereinafter, although an Example demonstrates this invention more concretely, this invention is not limited to the said Example. First, a synthesis example of a polycyclic aromatic compound will be described below.

Synthetic example (A1

[1756] Synthesis Example (A1): Synthesis of Compound (1-30)

[1757] [Chemical 437]

[1758]

[1759] Under nitrogen atmosphere, intermediate (I-A) (16.0 g), intermediate (I-B) (12.8 g), dichlorobis[(di-tert-butyl(4-dimethylaminophenyl) phosphino)palladium] (Pd-132, 0.29 g), sodium tert-butoxide (NaOtBu, 5.9 g) and xylene (100 ml) were placed in a flask, and heated at 120° C. for 1 hour. After the reaction, water and ethyl acetate were added to the reaction liquid and stirred, and then the organic layer was separated and washed with water. Then, the organic layer was concentrated to obtain a crude product. The crude product was purified with a silica gel short column (eluent: toluene / heptane=1 / 4 (volume ratio)) to obtain Intermediate (I-C) (22.6 g).

[1760] [Chemical 438]

[1761]

[1762] To a flask containing Intermediate (I-C) (20.0 g) and tert-butylbenzene (90 ml) was added a 1.56M solution of tert-butyllithium in pentane (36.2 ml) at 0°C under nitrogen. After ...

Synthetic example (B1

[1767] Synthesis Example (B1): Synthesis of Compound (1-3001)

[1768] [Chemical 440]

[1769]

[1770] Under a nitrogen atmosphere, 3-bromo-N,N-diphenylaniline (35 g), 4-tert-butylaniline (19.3 g), dichlorobis[(di-tert-butyl (4-tert-butyl) as a palladium catalyst were combined Dimethylaminophenyl)phosphino)]palladium (Pd-132, 76 mg), sodium tert-butoxide (NaOtBu, 15.6 g) and xylene (200 ml) were put into a flask, and heated at 120° C. for 2 hours. After completion of the reaction, water and ethyl acetate were added to the reaction liquid and stirred, and then the organic layer was separated and washed with water. Then, the crude product obtained by concentrating the organic layer was purified with a silica gel short column (eluent: toluene / heptane=1 / 1 (volume ratio)) to obtain an intermediate (I-1) 40g.

[1771] [Chemical 441]

[1772]

[1773] Under a nitrogen atmosphere, intermediate (I-1) (10.0 g), intermediate (I-2) (12.3 g), Pd-132 (0.2 g) as a palladium cataly...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The present invention provides a novel amino-substituted polycyclic aromatic compound, a reactive compound, a polymer compound, a suspension type polymer compound, and a use using same. Specific aminogroups or specific substituents, such as Ra groups and Rb groups, are introduced into a polycyclic aromatic compound in which a plurality of aromatic rings are linked by boron atoms, oxygen atoms, orthe like, thereby increasing options for organic device materials such as organic EL element materials. In addition, by using such a novel amino-substituted polycyclic aromatic compound as a materialfor an organic EL element, it is possible to provide an organic EL element having, for example, excellent light emission efficiency or element life.

Description

technical field [0001] The present invention relates to an amino-substituted polycyclic aromatic compound and its multimer (hereinafter, also collectively referred to as "polycyclic aromatic compound"), and an organic electroluminescence device, organic field effect transistor and organic thin film using the same Solar cells, display devices and lighting devices, reactive compounds, polymer compounds, suspension-type polymer compounds, and uses using the same. In addition, in this specification, an "organic electroluminescence element" may be expressed as an "organic EL (electroluminescence) element" or only as a "element". Background technique [0002] In the past, various studies have been conducted on display devices using light-emitting elements that perform electroluminescence to achieve power saving and thinning. Further, organic electroluminescent elements containing organic materials have been actively used because they are easy to reduce in weight or increase in siz...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
IPC IPC(8): C07F5/02C08G61/02C09D11/03H01L51/00H01L51/54
CPCC07F5/027C08G61/02C09D11/03C08G2261/3247C08G2261/52C08G2261/95H10K85/615H10K85/631H10K85/636H10K85/626H10K85/633H10K85/657H10K85/6576H10K85/6572H10K85/6574Y02E10/549C08G61/12H10K59/00H10K85/322H10K10/00H10K30/00H10K50/11H10K50/15H10K50/16H10K50/17
Inventor 畠山琢次马场大辅小林孝弘大森英史枝连一志
Owner KWANSEI GAKUIN EDUCATIONAL FOUND
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products