Incorporation of Different End Groups in Conjugated Polymers Using Functional Nickel Initiators

被引:112
作者
Smeets, Alfons [1 ]
Van den Bergh, Karlien [1 ]
De Winter, Julien [2 ]
Gerbaux, Pascal [2 ]
Verbiest, Thierry [1 ]
Koeckelberghs, Guy [1 ]
机构
[1] Katholieke Univ Leuven, Lab Mol Elect & Photon, B-3001 Heverlee, Belgium
[2] Univ Mons, Mass Spectrometry Ctr, Organ Chem Lab, B-7000 Mons, Belgium
关键词
CATALYST-TRANSFER POLYCONDENSATION; CHAIN-GROWTH POLYMERIZATION; TRANSFER CONDENSATION POLYMERIZATION; CONTROLLED MOLECULAR-WEIGHT; DIBLOCK; POLYTHIOPHENE; COPOLYMERS; POLY(3-ALKOXYTHIOPHENE)S; POLY(3-ALKYLTHIOPHENES); POLY(P-PHENYLENE);
D O I
10.1021/ma901888h
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The synthesis of functionalized Ni catalysts and their use for the synthesis of conjugated polymers end-capped with these functional groups has been reported. These polymers significantly owe their potential to the fact that their polymerization can proceed via a chain growth mechanism. The purity and stability of the externally prepared initiator are of crucial importance, since traces of any Ni2+salt result in polymer chains that are not initiated by the initiator and therefore lack the functional group. The decomposition appears to proceed quite rapidly, which complicates the isolation of this complex. This concept should therefore be applicable to a wide variety of conjugated monomers which can be polymerized using a Kumada catalyst- transfer mechanism. The living nature of the polymerization can be exploited to terminate the polymer chain with two different end groups.
引用
收藏
页码:7638 / 7641
页数:4
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