Abstract

All-conjugated graft copolymers containing poly(3-hexylthiophene) (P3HT) side chains and both of p-type and n-type backbones that are connected with all π-conjugated linkages were synthesized via a two-step method involving the Stille coupling reaction and Kumada catalyst-transfer polycondensation (KCTP). A series of naphthalene diimide copolymers with different compositions of 3-(4′-chloro-3′-tolyl)thiophene (CTT) units (PNDICTT) were designed as n-type backbones, while the poly(3-(4′-chloro-3′-tolyl)thiophene-alt-thiophene) (PCTT) was designed as a p-type backbone which were converted into n-type or p-type macroinitiators, and P3HT side chains were then in situ grafted from the macroinitiators via an externally initiated KCTP at room temperature. By using this newly developed two-step method for the synthesis of all-conjugated graft copolymers, the number of P3HT side chains in the graft copolymers can be simply controlled by varying the composition of the CTT units in PNDICTT. Meanwhile, the chain leng...

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