Dibenzothiophene, 4-phenyl-6-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-

Description of Dibenzothiophene, 4-phenyl-6-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-

4-Phenyl-6-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]dibenzothiophene (CAS: 1858289-74-3) is a specialized boronic ester derivative of dibenzothiophene, serving as a key building block in organic synthesis. This compound enables the construction of extended π-conjugated systems for organic light-emitting diodes (OLEDs). It facilitates the development of high-efficiency host materials and phosphorescent emitters, enhancing device performance in displays and lighting applications.

Application of Dibenzothiophene, 4-phenyl-6-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-

4-Phenyl-6-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]dibenzothiophene is a specialized boronic ester intermediate pivotal in organic electronics, particularly for Suzuki-Miyaura cross-coupling reactions to construct extended π-conjugated frameworks in OLED devices. It enables the synthesis of high-performance host materials, phosphorescent emitters, and charge transport layers, enhancing luminous efficiency, color purity, and operational stability in displays and solid-state lighting. As a building block for dibenzothiophene-based heterocycles, it supports advancements in flexible electronics, sensors, and photovoltaic materials due to its thermal robustness and tunable electronic properties.

Storage of Dibenzothiophene, 4-phenyl-6-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-

It should be kept in a cool, dry, dark place at 2-8°C under an inert atmosphere (e.g., nitrogen) to prevent hydrolysis and oxidation. Use airtight, sealed containers. Avoid light, humidity, and temperature fluctuations.