241-34-9

Upstream product

• 92-94-4 [1,1';4',1'']terphenyl 
• 113037-59-5 1,2,3,4,7,8,9,10-octahydro-dibenzo[d,d']benzo[1,2-b;4,5-b']dithiophene 
• 109508-95-4 6,12-dichloro-1,2,3,4,7,8,9,10-octahydro-dibenzo[d,d']benzo[1,2-b;4,5-b']dithiophene 
• 32090-20-3 2,2'-p-phenylenedimercapto-bis-cyclohexanone 
• 111527-06-1 2,2'-(2,5-dichloro-p-phenylenedimercapto)-bis-cyclohexanone 
• 3459-94-7 1,4-bis(phenylthio)benzene 
• 126218-83-5 1-bromo-2-(methylsulfinyl)benzene 
• 4612-26-4 1,4-Phenyldiboronic acid 
• 189095-25-8 1,4-difluoro-2,5-diiodobenzene 
• 244205-40-1 (2-bromophenyl)boronic acid 

Relevant academic research and scientific papers

Benzo[1,2-b:4,5-b′]bis[b]benzothiophene as solution processible organic semiconductor for field-effect transistors

Coplanar benzo[1,2-b:4,5-b′]bis[b]benzothiophenes (1a, 1b) for the application in organic field-effect transistors were synthesized by a simple two-step procedure involving triflic acid induced ring-closure reaction; such solution processed devices show a hole mobility of up to 0.01 cm2 V-1 s-1. The Royal Society of Chemistry.

Synthesis, properties, and structures of benzo[1,2-b:4,5-b′]bis[b] benzothiophene and benzo[1,2-b:4,5-b′]bis[b]benzoselenophene

(Chemical Equation Presented) Employing two consecutive cyclization reactions, benzo[1,2-b:4,5-b′]bis[b]benzochalcogenophenes, which are π-extended heteroarenes, were efficiently synthesized. Their electronic and crystal structures were elucidated on the

Facile Synthesis of Thienoacenes via Transition-Metal-Free Ladderization

Herein, we report a facile transition-metal-free approach to sulfur-containing heteroacenes from fluorinated oligophenylenes. Unlike most existing methods, the presented approach is not restricted to simple dibenzothiophene derivatives and thus appears to

Compound containing fused heterocycle structure, application of compound and organic electroluminescent device

The invention relates to the field of organic electroluminescent devices, and discloses a compound containing a fused heterocycle structure, an application of the compound and an organic electroluminescent device. The compound has the general formula structure shown in the formula (I); the compound has a high glass transition temperature, a high decomposition temperature and a high refractive index; and when the compound is applied to a covering layer on a device, the light extraction efficiency of the cathode can be improved, so that the luminous efficiency of the device is improved, and the service life of the device is prolonged.

Copper-Catalyzed Double S-Arylation of Potassium Thioacetate with Dibenziodolium Triflates: Facile Synthesis of Unsymmetrical Dibenzothiophenes

Much interest has been paid to cyclic diaryliodonium salts as bis(electrophile)s in transition-metal-catalyzed annulation reactions to produce polycyclic (hetero)aromatic hydrocarbons. Herein, we report that dibenziodolium triflates smoothly react with potassium thioacetate in the presence of CuCl2in THF or DMSO at 100–110 °C to afford the corresponding dibenzothiophenes in good-to-high yields. The coupling reaction tolerates reactive functional groups such as chloro and cyano and serves as a facile and reliable method for the synthesis of unsymmetrical dibenzothiophenes.

ORGANIC LIGHT COMPOUND AND ORGANIC LIGHT DEVICE USING THE SAME

PURPOSE: An organic light emitting device is provided to have improved luminance efficiency, low voltage operation, and excellent color. CONSTITUTION: An organic luminescent diode includes a first electrode, a second electrode, and at least one organic layer. The organic layer includes an organic light emitting compound represented by chemical formula F. In chemical formula F, X is O, S, Se, or N; B is zero if X is S, Se, or O; each of A1, A2, A3, and B is selected from H, D, F, C1-40 alkyl group, C5-40 aryl group, C5-40 heteroaryl group, C5-40 aryloxy group, C1-40 alkyloxy group, C5-40 arylamino group, C5-40 diarylamino, C6-40 arylalkyl group, C5-40 ketone group, C5-40 arylketon, C3-40 cycloalkyl group, and C3-40 heterocycloalkyl group.

Synthesis of dibenzothiophenes by pd-catalyzed dual C-H activation from diaryl sulfides

Palladium-catalyzed dual C-H functionalization of diaryl sulfides to form dibenzothiophenes (DBTs) by oxidative dehydrogenative cyclization is reported. This protocol afforded various DBTs in moderate to good yields with tolerance of a wide variety of substrates. Benzo[1,2-b:4,5-b]bis[b]benzothiophene was successfully synthesized by this method, which was used as an organic semiconductor for field-effect transistors.