850264-92-5

Usage

Uses

Used in Organic Electronics and Optoelectronics:
3,3'-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,1'-biphenyl is used as a key component in organic electronics and optoelectronic devices for its high thermal stability and efficient energy transfer, which are crucial for the performance and longevity of these devices.
Used in Organic Light-Emitting Diodes (OLEDs):
In the application industry of OLEDs, 3,3'-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,1'-biphenyl is used as a fluorescent dopant. It serves as a host material to enhance device performance by improving the efficiency of energy transfer and contributing to the blue-light emission, which is essential for the color balance in display technologies.
Used in Next-Generation Display and Lighting Technologies:
3,3'-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,1'-biphenyl is utilized in the development of next-generation display and lighting technologies due to its outstanding thermal and photophysical properties. These properties make BMBP a promising candidate for creating more efficient, durable, and environmentally friendly lighting solutions.

Upstream product

• 591-18-4 1-Bromo-3-iodobenzene 
• 16400-51-4 3,3'-dibromobiphenyl 
• 73183-34-3 bis(pinacol)diborane 
• 89598-96-9 (3-bromophenyl)boronic acid 

Downstream Products

• 1408283-79-3 C₂₄H₁₆Br₂ 

Relevant academic research and scientific papers

Fluorescence Enhancement of Aromatic Macrocycles by Lowering Excited Singlet State Energies

A series of cyclo-meta-phenylene congeners with a variation of interphenylene bridges was synthesized by adopting concise synthetic routes to investigate the structure-fluorescence relationships of macrocycles. With fundamental UV-vis absorption and fluor

Fluorescent molecular spring that visualizes the extension and contraction motions of a double-stranded helicate bearing terminal pyrene units triggered by release and binding of alkali metal ions

A novel double-stranded spiroborate helicate bearing terminal pyrene residues exhibited reversible fluorescence color changes (green and blue colors) due to the unique unidirectional springlike motions of the helicate triggered by catch and release of alk

Oxidative homocoupling reaction of aryltrimethylsilanes by Pd/o-chloranil catalysis

A practical oxidative homocoupling reaction of aryltri-methylsilanes has been achieved by Pd/o-chloranil catalytic system. The reaction shows the good functional group tolerability toward bromo, fluoro, ester, and methoxy groups to give a series of biaryls bearing electron-withdrawing and -donating groups. The boronate group is also retained on biaryls without any ArB bond cleavage, which is highly advantageous for orthogonal coupling.

NOVEL COMPOUND, MATERIAL FOR ORGANIC ELECTROLUMINESCENCE DEVICE, AND ORGANIC ELECTROLUMINESCENCE DEVICE

A specific material for organic electroluminescence device having m-phenylene skeleton in its molecule realizes a highly heat-resistant and long lifetime organic electroluminescence device capable of driving at low voltage with high efficiency.