Synthesis of Conjugated Polymers Containing Octafluorobiphenylene Unit via Pd-Catalyzed Cross-Dehydrogenative-Coupling Reaction

被引:47
作者
Aoki, Hideaki [1 ]
Saito, Hitoshi [1 ]
Shimoyama, Yuto [1 ]
Kuwabara, Junpei [1 ]
Yasuda, Takeshi [2 ]
Kanbara, Takaki [1 ]
机构
[1] Univ Tsukuba, Grad Sch Pure & Appl Sci, Tsukuba Res Ctr Energy Mat Sci TREMS, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058573, Japan
[2] Natl Inst Mat Sci, Res Ctr Funct Mat, 1-2-1 Sengen, Tsukuba, Ibaraki 3050047, Japan
关键词
C-H ARYLATION; DIRECT (HETERO)ARYLATION POLYMERIZATION; HIGH-PERFORMANCE; SIDE REACTIONS; COPOLYMERS; FACILE; ACCESS; POLYFLUOROARENES; THIOPHENES;
D O I
10.1021/acsmacrolett.7b00887
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Polycondensation via Pd-catalyzed cross-dehydrogenative-coupling reaction of 2,2',3,3',5,5',6,6'-octafluorobiphenyl with thiophene analogues was studied. The synthetic protocol, in which employment of prefunctionalized starting monomers was fully avoided, allowed straightforward access to an alternating pi-conjugated polymer. The addition of K2CO3 to the catalytic system promotes the cross-coupling reaction and suppresses the undesired homocoupling reaction, producing the corresponding donor acceptor type pi-conjugated polymers with minor homocoupling defects. The reaction also proceeded using O-2 as the terminal oxidant, resulting in lower loading of the Ag oxidant. The obtained polymer was evaluated as an emitting material for an organic light-emitting diode.
引用
收藏
页码:90 / 94
页数:5
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