Porphyrin-containing conjugated poly- mers with fluorene or carbazole as spacer groups were prepared by Sonogashira cross-coupling reac- tions. The polymers were of high molecular weight and the flexible alkyl chains ...Porphyrin-containing conjugated poly- mers with fluorene or carbazole as spacer groups were prepared by Sonogashira cross-coupling reac- tions. The polymers were of high molecular weight and the flexible alkyl chains on fluorene or carbazole units made the conjugated polymers soluble in common organic solvents, such as THF and methyl- ene chloride. The polymers could form high quality durable films from solution casting. Their optical and photocurrent responsive properties were investigated. It was found that the photocurrent response was di- rectly proportional to the content of porphyrin. The incorporation of carbazole units into the polymer chains also gave positive contribution to the photo- current generation in some extent.展开更多
基金This work was supported by the National Natural Science Foundation of China (Grant Nos. 20225415, 20423003 and 20374053)the Major State Basic Research Development Program (Grant No. 2002CB613401).
文摘Porphyrin-containing conjugated poly- mers with fluorene or carbazole as spacer groups were prepared by Sonogashira cross-coupling reac- tions. The polymers were of high molecular weight and the flexible alkyl chains on fluorene or carbazole units made the conjugated polymers soluble in common organic solvents, such as THF and methyl- ene chloride. The polymers could form high quality durable films from solution casting. Their optical and photocurrent responsive properties were investigated. It was found that the photocurrent response was di- rectly proportional to the content of porphyrin. The incorporation of carbazole units into the polymer chains also gave positive contribution to the photo- current generation in some extent.