1193104-83-4

Usage

Chemical Properties

White solid

InChI:InChI=1S/C27H23BO2/c1-18-7-11-20(12-8-18)27(21-13-9-19(2)10-14-21)25-6-4-3-5-23(25)24-16-15-22(28(29)30)17-26(24)27/h3-17,29-30H,1-2H3

Upstream product

• 474918-33-7 2-bromo-9,9-di-p-tolyl-9H-fluorene 
• 121-43-7 Trimethyl borate 
• 7732-18-5 water 

Downstream Products

• 1193104-90-3 C₃₉H₃₃BrO₄ 
• 1260234-78-3 9-(3,5-dimethyl-4-(octyloxy)phenyl)-3,6-bis[9,9-di(p-tolyl-fluorene-2-yl)]-9H-carbazole 
• 1260234-79-4 2-(3-methyl-4-[9,9-di(p-tolyl-fluorene-2-yl)]phenyl)-5-(2-methyl-4-[9,9-di(p-tolyl-fluorene-2-yl)]phenyl)-1,3,4-ozadiazole 
• 1260234-80-7 9,10-bis[9,9-di(p-tolyl-fluorene-2-yl)]anthracene 
• 1383449-49-7 3,7-bis(9,9-(di-p-tolyl)-2-fluorenyl)-dibenzothiophene-S,S-dioxide 

Relevant academic research and scientific papers

New condensed aryl compounds and organic light-emitting diode including the same

PURPOSE: A fused aryl compound is provided to improve low driving voltage and luminous efficiency by having excellent luminous performance while having stability. CONSTITUTION: A fused aryl compound is indicated in chemical formula 1. An organic electroluminescent device comprises an anode, a cathode, and a fused aryl compound inserted between the anode and the cathode. The fused aryl compound is comprised in an electroluminescent layer between the anode and the cathode. One or more layers selected from a hole injection layer, a hole transport layer, an electron block layer, a hole block layer, an electron transport layer, and an electron injection layer\ are additionally comprised in between the anode and the cathode.

Synthesis and electronic properties of isotruxene-derived star-shaped ladder-type oligophenylenes: Bandgap tuning with two-dimensional conjugation

The synthesis of star-shaped ladder-type oligophenylenes Sn (n = 4, 7, 10, 13, and 16), where n is the number of π-conjugated phenylene rings, is reported. The two-dimensional conjugation interactions in Sn result in a lower bandgap for S16 than the curre