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Usage

Uses

Used in Organic Chemistry:
1,3,5-Tris[(4-phenylboronic acid)]benzene is used as a building block for the synthesis of various pharmaceuticals and materials. Its boronic acid groups are known to participate in important chemical reactions, such as Suzuki-Miyaura cross-coupling reactions, which are crucial for the formation of carbon-carbon bonds.
Used in Optoelectronics:
TPBB has been studied for its potential applications in optoelectronics due to its unique structure and properties. Its ability to form carbon-carbon bonds and its reactivity with boronic acid groups make it a promising candidate for the development of new optoelectronic materials.
Used in Materials Science:
In materials science, 1,3,5-Tris[(4-phenylboronic acid)]benzene is used for its potential to contribute to the development of new materials with unique properties. 1,3,5-Tris[(4-phenylboronic acid)]benzene's reactivity and structure allow for the creation of novel materials with applications in various industries.

Upstream product

• 7511-49-1 1,3,5-tris(4-bromophenyl)benzene 
• 1017967-97-3 2,2',2''-([1,1':3',1''-terphenyl]-4,4'',5'-triyl)tris(4,4,5,5-tetramethyl-1,3,2-dioxaborolane) 

Downstream Products

• 1438391-89-9 C₈₁H₈₇B₃F₆N₆O₆ 
• 1438391-90-2 C₉₉H₉₉B₃F₆N₆O₆ 

Relevant academic research and scientific papers

7-Azaindolyl- and indolyl-functionalized starburst molecules with a 1,3,5-triazine or a benzene core - Syntheses and luminescence

The syntheses of several new 7-azaindolyl-, indolyl-, and 3-methylindolyl-functionalized starburst molecules that contain either a 1,3,5-triazine, a benzene, a 2,4,6-triphenyl-2,4,6-triazine, a 1,3,5-triphenylbenzene, a 2,4,6-tris(biphenyl)-1,3,5-triazine, or a 1,3,5-tris(biphenyl)benzene core have been achieved. The synthetic methods used for these new compounds involve mostly Ullmann condensation and Suzuki coupling reactions. The thermal properties of the new molecules have been found to be highly dependent on the molecular weight and the central core. Glass transition temperatures greater than 150 °C were observed for the large starburst molecules based on the 2,4,6-tris(biphenyl)-1,3,5-triazine or the 1,3,5-tris(biphenyl)benzene core. The new starburst molecules are luminescent in the violet-blue region in solution and in the solid state. The emission energy and the quantum efficiency were found to be highly dependent on the central core and the functional group. In general, the triazine-based molecules were found to have a smaller HOMO-LUMO energy gap than the benzene-based analogues. The triphenyltriazine- or triphenylbenzene-based molecules were found to display a higher emission quantum efficiency than the large tris(biphenyl)triazine- or tris(biphenyl)benzene-based molecules.

Inflating face-capped Pd6L8 coordination cages

Tritopic metalloligands were used to form two Pd6L8-type coordination cages. With molecular weights of more than 15 kDa and Pd?Pd distances of up to 4.2 nm, these complexes are among the largest palladium cages described to date.