1021849-53-5

Upstream product

• 1263039-56-0 5,8-bis(hexylthiophen-2-yl)-2,3-bis(4-(octyloxy)phenyl)quinoxaline 
• 35763-07-6 1,2-bis[4-(octyloxy)phenyl]ethane-1,2-dione 
• 96693-05-9 1-bromo-4-octyloxybenzene 
• 69272-50-0 1,2-diamine-3,6-dibromobenzene 
• 111-83-1 1-bromo-octane 
• 106-41-2 4-bromo-phenol 
• 15155-41-6 4,7-dibromobenzo[c][1,2,5]thiadiazole 
• 773094-62-5 5,8-dibromo-2,3-bis[4-(octyloxy)phenyl]quinoxaline 
• 273-13-2 benzo[1,2,5]thiadiazole 

Downstream Products

• 1358763-34-4 2,3-bis(4-octyloxyphenyl)-5,8-bis(4'-hexyl-2,2'-bithiophene-5-ly)quinoxaline 
• 1358763-36-6 2,3-bis(4-octyloxyphenyl)-5,8-bis(5'-bromo-4'-hexyl-2,2'-bithiophene-5-ly)quinoxaline 

Relevant academic research and scientific papers

Synthesis and photovoltaic properties of a low-band-gap copolymer of dithieno[3,2- b:2′,3′-d]thiophene and dithienylquinoxaline

The synthesis and photovoltaic properties of new thiophene-bridged dithienothiophene (DTT)-containing D-π-A conjugated low-band-gap and solution-processable polymers was reported. The low-band-gap copolymer of Dithieno[3,2-b:2',3'-d]thiophene and Dithieny

Synthesis and characterization of quinoxaline-based thiophene copolymers as photoactive layers in organic photovoltaic cells

A series of new quinoxaline-based thiophene copolymers (PQx2T, PQx4T, and PQx6T) was synthesized via Yamamoto and Stille coupling reactions. The M ws of PQx2T, PQx4T, and PQx6T were found to be 20,000, 12,000, and 29,000, with polydispersity in

Synthesis and photovoltaic properties of quinoxaline-based alternating copolymers for high-efficiency bulk-heterojunction polymer solar cells

A series of quinoxaline-based copolymers, namely, poly[N-9″- heptadecanyl-2,7-carbazole-alt-5,5-(5′,8′-di-2-thienylquinoxaline)] (P1), poly[N-9″-heptadecanyl-2,7-carbazole-alt-5,5-(5′,8′-di- 2-thienyl-2,3-bis(4-octyloxyl)phenyl)quinoxaline] (P2), and poly