Two conjugated polymers HXS-1 and PDFCDTBT were prepared by direct C–H activation and Suzuki polycondensation and their chemical structures were characterized by 1H NMR spectroscopy.The molecular weight of conjugated...Two conjugated polymers HXS-1 and PDFCDTBT were prepared by direct C–H activation and Suzuki polycondensation and their chemical structures were characterized by 1H NMR spectroscopy.The molecular weight of conjugated polymer synthesized by direct C–H activation is lower than the corresponding polymers prepared by Suzuki polycondensation.Conjugated polymers synthesized by direct C–H activation have considerable solubility in common organic solvents and form amorphous film.The photovoltaic property of conjugated polymers synthesized by direct C–H activation is inferior to the corresponding polymers synthesized by Suzuki polycondensation.展开更多
基金supported by the National Basic Research Program of China(2011CB935702)the National Natural Science Foundation of China(51003006 and 21161160443)the Fundamental Research Funds for the Central Universities
文摘Two conjugated polymers HXS-1 and PDFCDTBT were prepared by direct C–H activation and Suzuki polycondensation and their chemical structures were characterized by 1H NMR spectroscopy.The molecular weight of conjugated polymer synthesized by direct C–H activation is lower than the corresponding polymers prepared by Suzuki polycondensation.Conjugated polymers synthesized by direct C–H activation have considerable solubility in common organic solvents and form amorphous film.The photovoltaic property of conjugated polymers synthesized by direct C–H activation is inferior to the corresponding polymers synthesized by Suzuki polycondensation.
