1263559-47-2

Upstream product

• 16433-88-8 2,7-dibromo-9H-fluorene 
• 53463-68-6 1-bromo-10-decanol 
• 111-25-1 1-bromo-hexane 
• 106-41-2 4-bromo-phenol 
• 1263559-39-2 [10-(4-bromo-phenyl)-decyloxy]-tert-butyl-dimethyl-silane 
• 1092781-56-0 10-(4-bromophenoxy)-decan-1-ol 
• 928853-19-4 2-bromo-5-[7-(5-bromo-2-thienyl)-9,9-dihexyl-9H-fluoren-2-yl]thiophene 

Downstream Products

• 1263559-53-0 10-(4-(5-(9,9-dihexyl-7-(5'-(pyridin-4-yl)-2,2'-bithiophen-5-yl)-9H-fluoren-2-yl)thiophen-2-yl)phenoxy)decan-1-ol 
• 1263559-56-3 10-(4-(5-(9,9-dihexyl-7-(5'-(pyridin-4-yl)-2,2'-bithiophen-5-yl)-9H-fluoren-2-yl)thiophen-2-yl)phenoxy)decyl methacrylate 
• 1263559-50-7 4-(5'-(7-(5-(4-(10-(tert-butyldimethylsilyloxy)decyloxy)phenyl)thiophen-2-yl)-9,9-dihexyl-9H-fluoren-2-yl)-2,2'-bithiophen-5-yl)pyridine 

Relevant academic research and scientific papers

Synthesis and application of H-Bonded cross-linking polymers containing a conjugated pyridyl H-Acceptor side-chain polymer and various carbazole-based H-Donor dyes bearing symmetrical cyanoacrylic acids for organic solar cells

A series of novel hydrogen-bonded (H-bonded) cross-linking polymers were generated by complexing various proton-donor (H-donor) solar cell dyes containing 3,6- and 2,7-functionalized electron-donating carbazole cores bearing symmetrical thiophene linkers