1304773-87-2

Upstream product

• 1293389-28-2 5,6‐difluoro‐2,1,3‐benzothiadiazole 
• 1304773-88-3 5,6-difluoro-4,7-di(thiophen-2-yl)benzo[c][1, 2, 5]thiadiazole 
• 1304773-86-1 2,3-difluoro-1,4-di(2-thienyl)-5,6-dinitro-benzene 
• 1283598-32-2 1,4-dibromo-2,3-difluoro-5,6-dinitrobenzene 
• 156682-52-9 1,4-dibromo-2,3-difluoro-benzene 

Downstream Products

• 1596358-45-0 5,8-bis(5-bromothiophen-2-yl)-6,7-difluoro-2,3-diphenylquinoxaline 
• 1596358-51-8 6,7-difluoro-2,3-diphenyl-5,8-di(thiophene-2-yl)quinoxaline 

Relevant academic research and scientific papers

Enhanced open-circuit voltages of trifluoromethylated quinoxaline-based polymer solar cells

Three quinoxaline-based conjugated polymers with donor-π-acceptor configurations have been synthesized by Stille coupling reaction. The electron-donating 2,3-dioctylthienyl- substituted benzodithiophene (BDT) unit was linked to the electron-accepting 2,3-

Triazole derivative containing boron-nitrogen group, polymer and preparation methods and applications of triazole derivative and polymer

The invention belongs to the technical field of organic photoelectricity, and discloses a triazole derivative containing a boron-nitrogen group, a polymer and preparation methods and applications of the triazole derivative and the polymer. The chemical st

Step-by-step improvement in photovoltaic properties of fluorinated quinoxaline-based low-band-gap polymers

A series of fluorinated quinoxaline-based polymers with typical donor-π-acceptor configurations has been synthesized by Stille coupling reaction. The electron-donating dialkoxy-substituted benzodithiophene (BDT) is connected to the electron-withdrawing 2,

FLUORINATED MONOMERS, OLIGOMERS AND POLYMERS FOR USE IN ORGANIC ELECTRONIC DEVICES

Compounds of Formula (I): (formula (I)) where: X1 and X2 are the same or different and each is independently Cl, Br, I, a substituted or unsubstituted aryl group or a substituted or unsubstituted heteroaryl group; and, Y is O, S, Se,