1380445-20-4

Usage

Type of compound

2-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolane-2-yl)phenyl-5-(9-phenanthryl)phenyl]-4,6-diphenyl-1,3,5-triazine is a complex organic compound, specifically a triazine derivative.

Elements present

The compound contains carbon (C), hydrogen (H), nitrogen (N), and boron (B) atoms.

Aromatic rings

It is composed of three aromatic rings, which contribute to its stability and structure.

Triazine group

The compound has a nitrogen-containing triazine group (C3H3N3) that connects two of the aromatic rings.

Dioxaborolane group

It features a boron-containing 1,3,2-dioxaborolane group (B2O4) with tetramethyl substituents, which is connected to one of the phenyl groups.

Phenanthryl group

One of the phenyl groups is connected to a 9-phenanthryl group, which is a large, fused aromatic ring system.

Tetramethyl substituents

The dioxaborolane group has four methyl (CH3) groups attached to it, which can influence the compound's reactivity and properties.

Potential applications

2-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolane-2-yl)phenyl-5-(9-phenanthryl)phenyl]-4,6-diphenyl-1,3,5-triazine may have potential applications in materials science, organic synthesis, and pharmaceutical research due to its unique structure and potential reactivity.

Complexity

The presence of phenanthryl and tetramethyl groups, along with the triazine and dioxaborolane groups, makes 2-[3-{(4,4,5,5-tetramethyl-1,3,2-dioxaborolane-2-yl)phenyl}-5-(9-phenanthryl)phenyl]-4,6-diphenyl-1,3,5-triazine highly complex and potentially interesting for further research and development.

Upstream product

• 810681-06-2 3-bromo-5-iodobenzoyl chloride 
• 188815-32-9 3-bromo-5-iodo-benzoic acid 
• 573-17-1 9-bromophenanthrene 
• 1268251-22-4 2-[3-chloro-5-(phenanthrene-9-yl)phenyl]-4,6-diphenyl-1,3,5-triazine 
• 73183-34-3 bis(pinacol)diborane 
• 1073062-42-6 2-(3-bromo-5-chlorophenyl )-4,6-diphenyl-1,3,5-triazine 
• 1073062-59-5 2-(3,5-dibromophenyl)-4,6-diphenyl-1,3,5-triazine 
• 23950-59-6 3,5-dibromobenzoyl chloride 
• 100-47-0 benzonitrile 
• 1268250-99-2 2-(3-bromo-5-(phenanthren-9-yl)phenyl)-4,6-diphenyl-1,3,5-triazine 
• 68572-87-2 9-phenanthrenylboronic acid 

Downstream Products

• 1268250-91-4 2-[3-(2,2'-bipyridin-6-yl)-5-(9-phenanthryl)phenyl]-4,6-diphenyl-1,3,5-triazine 

Relevant academic research and scientific papers

TRIAZINE COMPOUND HAVING CONJUGATED PYRIDYL GROUP

PROBLEM TO BE SOLVED: To provide a triazine compound for an organic electroluminescent element. SOLUTION: Provided is a triazine compound of general formula (1). (In the general formula (1), Ar1 represents a phenyl group, a naphthyl group, or a biphenyl group; Ar2 represents a C10-18 condensed ring aromatic hydrocarbon; and Ar3 represents a C10-24 aromatic hydrocarbon constituted of 2 or more rings, or a C6-23 nitrogen-containing aromatic group constituted of 2 or more rings.) SELECTED DRAWING: Figure 1 COPYRIGHT: (C)2019,JPOandINPIT

PHENANTHROLINE-TRIAZINE COMPOUND AND ORGANIC LIGHT EMITTING DIODE COMPRISING THE SAME

The present invention relates to a phenanthroline-triazine compound, capable of improving driving voltage and efficiency, and to an organic light emitting device including the same. The phenanthroline-triazine compound is represented by formula 1 or 2. In the chemical formula 1 or 2, X1, X2, X3 and X4 are independently carbon or nitrogen.COPYRIGHT KIPO 2019

SPECIFICALLY SUBSTITUTED AZA-DIBENZOFURANS AND AZA-DIBENZOTHIOPHENES FOR ORGANIC ELECTRONIC DEVICES

Specifically substituted aza-dibenzofurans and aza-dibenzothiophenes of formula (I) and their use in electronic devices, especially electroluminescent devices. When used as charge transport material, charge blocker material and/or host material in electroluminescent devices, the specifically substituted aza-dibenzofurans and aza- dibenzothiophenes may provide improved efficiency, stability, manufacturability, or spectral characteristics of electroluminescent devices and reduced driving voltage of electroluminescent devices. In formula (I) Y is S or 0; one of X1-X8 is N; another X1-X8 is C-L(R9)-[X9X10X11]Ring; and the remaining X1-X8 are CR1-CR8 wherein R1-R8 are independently H, alkyl, alkenyl, aryl, etc.

TRIAZINE COMPOUND HAVING FLUORENE SKELETON GROUP

PROBLEM TO BE SOLVED: To provide a specific triazine compound that significantly improves the life properties and luminous efficiency of an organic electroluminescent element as compared to the well-known triazine compounds. SOLUTION: The present invention provides a triazine compound having a specific structure illustrated on the right side in the following formula, and an organic electroluminescent element containing the same as a component. SELECTED DRAWING: None COPYRIGHT: (C)2018,JPOandINPIT

The triazine compound, its manufacturing method, intermediate, and use thereof (by machine translation)

[Problem] excellent electron-injecting and electron transport characteristic with a low voltage elements and, high emitting efficiency, long driving element of a novel electron transport material. (1) A compound represented by the formula [a] triazine. {A

READILY SOLUBLE AZINE COMPOUND AND PRODUCTION METHOD THEREOF, AND ORGANIC ELECTROLUMINESCENT ELEMENT USING THE SAME

PROBLEM TO BE SOLVED: To provide a novel azine compound, and an organic electroluminescent element using the same excellent in drive voltage, luminous efficiency and durability. SOLUTION: The present invention provides an azine compound represented by general formula (3), and an organic electroluminescent element comprising the same as a component. (Ar3 is a nitrogen-containing aromatic group; R1 to R4 are each independently H, Cl, alkyl-substituted/unsubstituted C6-10 monocyclic, linked or fused aryl, or the like; and X1 is a leaving group.) SELECTED DRAWING: None COPYRIGHT: (C)2018,JPOandINPIT

BENZIMIDAZOLE FUSED HETEROARYLS

A compound of general formula (I): wherein A1, A2, A3, A4, B1, B2, B3, B4, C1, C2, C3, C4, X1 and X2 have the meanings as defined in the description provides electronic devices, preferably OLEDs, which ensure good efficiencies, good operative lifetimes and a high stability to thermal stress, and a low use and operating voltage of the OLEDs.

TRIAZINE COMPOUND AND ORGANIC ELECTROLUMINESCENT ELEMENT CONTAINING THE SAME

PROBLEM TO BE SOLVED: To provide a triazine compound that realizes better drive voltage and luminous efficacy of an organic electroluminescent element than conventional triazine compounds; and an organic electroluminescent element containing the compound. SOLUTION: The invention provides a triazine compound represented by general formula (1), and an organic electroluminescent element containing the same as a constituent. SELECTED DRAWING: None COPYRIGHT: (C)2018,JPOandINPIT

SPECIFICALLY SUBSTITUTED BENZOFURO- AND BENZOTHIENOQUINOLINES FOR ORGANIC LIGHT EMITTING DIODES

Specifically substituted benzofuro- and benzothienoquinolines and their use in electronic devices, especially electroluminescent devices. When used as charge transport material, charge blocker material and/or host material in electroluminescent devices, t

Phosphoryl substituted triazine derivatives and organic electroluminescent device including the same

The present invention relates to phosphoryl group bonded triazine derivatives represented by chemical formulas 1 and 2. In the chemical formulas 1 and 2, the definitions of the substituent groups are the same as defined in the specification. The triazine derivatives have excellent current density and durability in comparison to a conventional material. The organic electroluminescent device has reduced driving voltage, improved luminous efficiency, and extended lifespan.COPYRIGHT KIPO 2016