110155-13-0

Usage

Chemical compound

2,2′-dibromotriphenylamine is a chemical compound consisting of carbon, hydrogen, and bromine atoms.

Common use

It is commonly used as a light stabilizer in plastics and polymers.

Substitution

It is a substituted triphenylamine compound, meaning that two bromine atoms are attached to the central amine group.

Protective function

2,2′-dibromotriphenylamine is added to various materials to protect them from the damaging effects of UV radiation, which can cause degradation and discoloration.

Mechanism of action

The compound works by absorbing and dissipating the energy from UV light, preventing it from causing harmful reactions in the material.

Strong UV absorption

2,2′-dibromotriphenylamine has strong UV absorption capabilities, making it an effective additive for extending the longevity of plastics and polymers.

High thermal stability

The compound exhibits high thermal stability, which contributes to its effectiveness in various applications.

Upstream product

• 583-55-1 1-Bromo-2-iodobenzene 
• 62-53-3 aniline 
• 591-50-4 iodobenzene 
• 67242-17-5 2,2’-dibromodiphenylamine 

Downstream Products

• 5472-23-1 10-phenylacridin-9(10H)-one 

Relevant academic research and scientific papers

Planarized: B, N -phenylated dibenzoazaborine with a carbazole substructure: Electronic impact of the structural constraint

A B,N-diphenyl-5,10-dihydro-dibenzo-1,4-azaborine, in which both phenyl groups on the boron and nitrogen atoms are planarized to generate a carbazole substructure, was synthesized. The structral constraint around the boron and nitrogen atoms alters the π-conjugation mode and thus the photophysical and electrochemical properties. Specifically, this structurally constrained dibenzoazaborine showed an intense blue emission with a narrow full width at half maximum. One of its derivatives exhibited near infrared absorption in the one-electron-oxidized state.

Planarized B,N-diarylated dibenzoazaborine compounds for deep blue fluorescence

A series of planarized B,N-diarylated dibenzoazaborine compounds (5a–5e) in which various functional groups are introduced into the B-Ph and N-Ph moieties of nonsubstituted dibenzoazaborine compound (I) were prepared. All compounds exhibit strong low-energy absorptions at ca. 410–426 nm with a gradual red-shift depending on the electron-accepting property of the four substituents (4-R?=?4-Ph tBu group into the N-Ph ring further shifts slightly the absorption band toward a lower-energy region (5e). Importantly, all compounds undergo gradual red-shifts in the emission leading to deep blue fluorescence for CN-substituted 5d and 5e. Furthermore, the emissions have narrow full width at half maximum values of ca. 30 nm, high photoluminescence quantum yields (ΦPL ≈ 100%), and small Stokes shifts (11–16 nm). The electrochemical and theoretical studies further support the bandgap control and photophysical properties of compounds.

A 6H - naphtho [2, 1, 8, 7 - klmn] stronger cooperation derivatives and use thereof

The invention relates to compounds disclosed as Formula (1), wherein n is 1 or 2; Ar1 and Ar2 are respectively aryl group or heteroaryl group; R1-R5 are five substituent groups on Ar2 in different positions, are identical or different, and are respectively independently selected from H atom, C1-C20 aliphatic straight-chain or branched-chain hydrocarbyl groups and aromatic groups; A is N atom or CH; and L is a single bond C4-C10 aromatic ring or aromatic heterocyclic ring. The invention also relates to application of the compounds in organic electroluminescent devices especially as an electron transport material and/or light-emitting body material of an OLED (organic light-emitting diode).

FOUR-COORDINATE BORON COMPOUNDS

A compound having a four-coordinate boron atom to which is connected a first C3-C25 substituent, a second C3-C25 substituent and a bridging substituent comprising from eight to forty non-hydrogen atoms and havin