Abstract
AbstractA nickel catalyst promoted the polymerization between various Grignard reagents with 2‐phenyl‐4,6‐bi(4‐fluorophenyl)‐1,3,5‐triazine. The reaction scope was thoroughly investigated and fully characterized. The Sp2‐C − F bond was successfully activated by the triazine group in Kumada coupling reactions. Also, di‐Grignard reagents showed higher activity than mono‐Grignard reagents. The reaction scope results reveal that a Grignard reagent with strong nucleophilicity and aryl fluoride with strong electrophilicity are necessary to lead to Kumada polycondensation of oligothiophenes with aryl fluoride. In this work, polymerization between di‐functionalized oligothiophene Grignard reagents with aryl fluoride was first conducted. The weight‐average molecular weight is high, up to 14.8 kDa. The π‐conjugated polymers obtained exhibit emission colours of blue, green and yellow with efficient photoluminescence. © 2016 Society of Chemical Industry
Sign-in/Register to access full text options 
Free) 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
