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Anodic Chlorination of Selenophene-Containing Polymers: Reaction Efficiency and Selective Reaction of Single Segment in Rod-Rod Diblockcopolymer

机译:含硒的聚合物的阳极氯化聚合物:杆杆二嵌块二嵌段单段的反应效率和单段的选择性反应

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摘要

The post-polymerization modification of selenophene-containing (co) polymers is presented based on the electrochemical polymer reaction (ECPR). Selenophene-or thiophene-containing (co) polymers, which are known to be promising materials in optoelectronic devices, were synthesized through Kumada catalyst transfer polymerization to give their homopolymers and block-or statistical copolymers with various side chains. Each of the series of polymers was subjected to post-modification through the ECPR, and the reaction efficiencies were systematically compared. Selenophene-containing polymers were successfully modified with better ECPR reaction efficiencies than their thiophene analogues. Moreover, the dramatic inhibiting effect of a branched side chain on the ECPR was observed and rationalized, which was very unexpected. Based on the basic tendency observed here, we have finally demonstrated the selective modification of a single segment of a rod-rod block copolymer for the first time.
机译:基于电化学聚合物反应(ECPR),提出了含硒丙烯烯(CO)聚合物的聚合性改性。 通过Kumada催化剂转移聚合合成含硒丙烯烯或含噻吩的聚合物(CO)聚合物,其已知是光电器件中的有前途的材料,得到它们的均聚物和具有各种侧链的均聚物和嵌段或统计共聚物。 通过ECPR进行各种聚合物的每种聚合物进行后修饰,并系统地进行反应效率。 以优于其噻吩类似物的ECPR反应效率成功修饰含硒的聚合物。 此外,观察到分枝侧链对ECPR对ECPR的显着抑制作用,合理化,这非常出乎意料。 基于此处观察到的基本趋势,我们最终证明了第一次选择性修饰杆杆嵌段共聚物的单个区段。

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