15754-53-7

Usage

Uses

Used in Plastics Industry:
Phosphine oxide, bis(4-bromophenyl)is used as a flame retardant additive in the plastics industry to reduce the flammability of plastic materials. Its incorporation into plastics helps to slow down the combustion process, thereby improving the fire safety of plastic products.
Used in Textile Industry:
In the textile industry, Phosphine oxide, bis(4-bromophenyl)is utilized as a flame retardant to enhance the fire resistance of fabrics and garments. By incorporating Phosphine oxide, bis(4-bromophenyl)- into textiles, the risk of fire accidents can be mitigated, providing an additional layer of safety for consumers.
Used in Electronic Industry:
Phosphine oxide, bis(4-bromophenyl)is also used in the electronic industry as a flame retardant for printed circuit boards (PCBs) and other electronic components. Its application helps to prevent the ignition of these components during operation, ensuring the safety and reliability of electronic devices.
Used in Construction Industry:
In the construction industry, Phosphine oxide, bis(4-bromophenyl)is employed as a flame retardant in various building materials, such as insulation, coatings, and adhesives. Its use contributes to the reduction of fire hazards in buildings, providing enhanced safety for occupants.

Upstream product

• 13792-89-7 bis(4-bromophenyl)N,N-diethylaminophosphoramidite 
• 106-37-6 1.4-dibromobenzene 
• 18620-02-5 (4-bromophenyl)magnesium bromide 
• 589-87-7 1,4-bromoiodobenzene 

Downstream Products

• 15754-56-0 Bis-(p-brom-phenyl)-thiolphosphinsaeure-phenylester 
• 190911-27-4 2-[bis-(4-bromo-phenyl)-phosphinoyl]-benzoic acid methyl ester 
• 109817-44-9 bis-(4-bromo-phenyl)-phosphinic acid 
• 190911-28-5 2-(bis-{4-[4-(tert-butyl-dimethyl-silanyloxy)-but-1-ynyl]-phenyl}-phosphinoyl)-benzoic acid methyl ester 
• 190911-29-6 2-(bis-{4-[4-(2-methoxy-ethoxymethoxy)-but-1-ynyl]-phenyl}-phosphinoyl)-benzoic acid methyl ester 
• 823220-69-5 2-(bis-{4-[4-(2-methoxy-ethoxymethoxy)-but-1-ynyl]-phenyl}-phosphanyl)-benzoic acid methyl ester 

Relevant academic research and scientific papers

Single molecular tuning of the charge balance in blue-emitting iridium dendrimers for efficient nondoped solution-processed phosphorescent OLEDs

The single molecular tuning of charge balance has been demonstrated here by integrating a p-type dendron, an n-type dendron and a blue emissive Ir core into one dendritic platform. Compared with the commonly used physical blending, not only can the charge

B(C6F5)3-catalyzed O-H insertion reactions of diazoalkanes with phosphinic acids

A highly efficient base-, metal-, and oxidant-free catalytic O-H insertion reaction of diazoalkanes and phosphinic acids in the presence of B(C6F5)3has been developed. This powerful methodology provides a green approach towards the synthesis of a broad spectrum of α-phosphoryloxy carbonyl compounds with good to excellent yields (up to 99% yield). The protocol features the advantages of operational simplicity, high atom economy, practicality, easy scalability and environmental friendliness.

Diamine monomer and preparation method thereof, polyimide and preparation method and application thereof

The invention discloses a diamine monomer and a preparation method thereof, and polyimide and a preparation method and application thereof. Based on a light-emitting structural unit, a novel thermallyactivated delayed fluorescence (TADF) polyimide polymer material is prepared by adopting a polymer room-temperature polycondensation synthesis method, and the polyimide has excellent solubility, highglass-transition temperature and high thermal stability. Furthermore, an organic light-emitting device with excellent device performance is prepared by taking the polymer as a light-emitting layer through a simple solution spin-coating mode. The methods provided by the invention have the main characteristics of extremely high step economy and atom economy, simple experimental method operation, low design difficulty, diverse combination modes and good reaction region selectivity.

Preparation of O-Protected Cyanohydrins by Aerobic Oxidation of α-Substituted Malononitriles in the Presence of Diarylphosphine Oxides

A mild, reagent-cyanide-free, and efficient synthesis of O-phosphinoyl-protected cyanohydrins from readily available α-substituted malononitriles was realized using diarylphosphine oxides in the presence of O2. Mechanistic studies indicated that in addition to the initial aerobic oxidation of the malononitrile derivative notable features of this process include the formation of a tetrahedral intermediate and a subsequent intramolecular rearrangement. The phosphinoyl-protecting group can be removed by alcoholysis or by reduction with DIBAL-H.