148077-54-7

Upstream product

• 92-86-4 4-(4-bromophenyl)bromobenzene 
• 620-93-9 di-p-tolylamine 
• 105946-82-5 4-bromo-4'-iodobiphenyl 
• 106-38-7 para-bromotoluene 
• 106-49-0 p-toluidine 

Downstream Products

• 1311407-99-4 4’-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-N,N-di-p-tolyl-[1,1‘-biphenyl]-4-amine 
• 1311408-00-0 4-bromo-N,N-di-p-tolyl-[1,1':4',1-terphenyl]-4-amine 
• 1622206-15-8 N,N-bis[4'-(N',N'-di-4-tolylamino)biphenyl-4-yl]-3-(1-trimethylsiloxy-1,3,3,3-tetrameth yldisiloxan-1-yl)aniline 
• 108-88-3 toluene 
• 1259882-91-1 C₄₅H₃₅N₃ 
• 1259883-27-6 C₃₉H₃₀N₂S 
• 1259883-10-7 C₃₉H₃₀N₂O 
• 1088453-46-6 C₂₆H₂₄BNO₂ 

Relevant academic research and scientific papers

2,6-bis(diarylaminophenyl)benzene and derivatives thereof as hole-transport compounds in organic light-emitting devices

Compounds according to Formulas 1-33 may be useful in electronic devices such as light-emitting devices. For example, they may be used as hole-transport materials.

Organic light emitting host materials

Polyphenylene compounds such as compounds represented by Formulas 1-28 may be used in electronic devices such as organic light-emitting devices. For example, the compounds may be used as host material in an emissive layer.

Palladium-catalyzed formation of secondary and tertiary amines from aryl dihalides with air-stable ferrocenyl tri- and diphosphines: Synthesis and X-ray structure of efficient catalysts beyond [PdCl2(DPPF)]

Robust, air-stable tridentate and bidentate ferrocenylphosphines 1,2-bis(diphenylphosphino)-1′-(diisopropylphosphino)-4-tert- butylferrocene, L5, and 1,1′-bis(diisopropylphosphino)-3,3′- bis(tert-butyl)ferrocene, L9, combined with 1 mol% of [PdCl(η3- C3H5)]2 led to two new catalytic systems which allow the coupling of aniline derivatives with mono- and dihaloarenes to form functionalized diarylamines and triarylamines. The excellent selectivity of the reactions avoids the deleterious dehalogenation of the substrates and products. The X-ray structure characterization of the related complex [PdCl 2(L9)] is reported in which ligand L9 in its meso form is significantly distorted.

BENZOIMIDAZOLE DERIVATIVES FOR USE IN LIGHT - EMITTING DEVICES

Compounds including optionally substituted Ring Systems 1-4 may be used as hosts in light-emitting devices.

PHOTOTHERAPY METHODS AND DEVICES COMPRISING EMISSIVE ARYL-HETEROARYL COMPOUNDS

Disclosed herein are compounds represented by a formula: R1—Ar1—X—Ar2—Ar3-Het, wherein R1, Ar1, X, Ar2, Ar3, and Het are described herein. Compositions and light-emitting devices related thereto are also disclosed.

COMPOUNDS FOR USE IN LIGHT-EMITTING DEVICES

Compounds including optionally substituted Ring Systems 1-4 may be used as hosts in light-emitting devices.

EMISSIVE ARYL-HETEROARYL COMPOUNDS

Disclosed herein are compounds represented by Formula 1, wherein R1, Ar1, X, Ar2, Ar3, and Het are described herein. Compositions and light-emitting devices related thereto are also disclosed.

EMISSIVE ARYL-HETEROARYL COMPOUNDS

Disclosed herein are compounds represented by Formula 1, wherein R1, Ar1, X, Ar2, Ara, and Het are described herein. Compositions and light-emitting devices related thereto are also disclosed.

DYE COMPOUND AND DYE-SENSITIZED SOLAR CELL

A dye compound is described, which is expressed by formula (I): wherein A1, A2 and A3 each independently represent a substituted or unsubstituted 1,4-phenylene or 2,5-thiophene group, and B1 and B2 each independently represent a substituted or unsubstituted aryl group. The dye compound is suitably used as a dye sensitizer in a dye sensitized solar cell (DSSC).

Triaryl linked donor acceptor dyads for high-performance dye-sensitized solar cells

The effect of changing substituents of organic dyes for their performance on dye-sensitized solar cells (DSSCs) is examined. These dyes consist of an aromatic amine donor group, a cyanoacrylic acid acceptor group, and a triaryl spacer group, while they ar