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首页> 外文期刊>Macromolecules >Synthesis of Poly(3-hexylthiophene), Poly(3-hexylselenophene), and Poly(3-hexylselenophene-alt-3-hexylthiophene) by Direct C-H Arylation Polymerization via N-Heterocyclic Carbene Palladium Catalysts
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Synthesis of Poly(3-hexylthiophene), Poly(3-hexylselenophene), and Poly(3-hexylselenophene-alt-3-hexylthiophene) by Direct C-H Arylation Polymerization via N-Heterocyclic Carbene Palladium Catalysts

机译:N-杂环碳钯催化剂通过直接C-H芳基化聚合反应合成聚(3-己基噻吩),聚(3-己基硒吩-)和聚(3-己基硒基-alt-3-己基噻吩)

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摘要

Direct C-H arylation polymerization of 2-bromo-3-1-hexylselenophene and 2-bromo-3-hexylthiophene catalyzed by N-heterocyclic carbene (NHC) palladium-based and Pd(OAc)(2)-based, systems has been carried out and investigated. Under the optimized conditions, high molecular weight poly(3-hexylthiohphene) (P3HT), (M-n=26.9K g/mol) with high head-to-tail regioregularity (94%) can he obtained by using [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene]chloro[3-phenylallyl]-palladium(II) (Pd-IPr) 8 the catalyst. Pd-IPr exhibits a wide range of working temperatures froth 70 to 140 degrees C and good catalytic reproducibility as a result of its high thermal stability. It was found that the presence of additional phosphine ligand, such as tris(o-methoxyphenyl)phosphine,, can increase the polymerization efficiency in the Pd(OAc)2 system. This improvement is linked to the stability enhancement for the active species during the course of catalysis. For the first time, poly(3-hexylselenophene) (P3HS) was also obtained by direct-arylation polymerization in this research. The modest molecular weight is attributed to the poor solubility P3HS in the used solvents. Density-functional-theory (DFT) calculations were performed to investigate the postulated reaction mechanisms for our catalytic systems. The,experimental observations can thus be elucidated by the help of computation: Most significantly, a main-chain alternating and side-chain regioregular (RR = 94%) poly(3-hexylselenophene-alt-3-hexylthiophene) (Alt-P3HST) with high molecular weight (20.0K g/mol) was successfully synthesized via the Pd-IPr-catalyzed direct-arylation polymerization of a well-designed 2-bromo-8-hexyl-5-(3-hexylseleophen-2-yl)thiophene monomer. The molecular properties of the Alt-P3HST were characterized to compare with those of P3HT and P3HS. This research demonstrates in-depth investigation on the NHC-based palladium catalysts for the synthesis of Conjugated polymers via direct C-H bond polymerization.
机译:N-杂环卡宾(NHC)钯基和Pd(OAc)(2)基催化的2-溴-3-1-己基硒吩和2-溴-3-己基噻吩的直接CH芳基化反应体系并进行调查。在最佳条件下,使用[1,3-bis]可制得具有高头尾区域规整度(94%)的高分子量聚(3-己基噻吩)(P3HT)(Mn = 26.9K g / mol)。 (2,6-二异丙基苯基)咪唑-2-亚烷基]氯[3-苯基烯丙基]-钯(II)(Pd-IPr)8。由于其高的热稳定性,Pd-IPr的工作温度范围从70到140摄氏度不等,并且具有良好的催化重现性。发现存在额外的膦配体,例如三(邻甲氧基苯基)膦,可以提高Pd(OAc)2体系中的聚合效率。这种改进与催化过程中活性物质稳定性的提高有关。在本研究中,还首次通过直接芳基化聚合获得了聚(3-己基硒吩)(P3HS)。适中的分子量归因于在所用溶剂中不良的P3HS溶解度。进行密度泛函理论(DFT)计算以研究我们催化系统的假定反应机理。因此,可以通过计算来阐明实验观察结果:最显着的是,主链交替和侧链区域规则(RR = 94%)聚(3-己基硒吩-alt-3-己基噻吩)(Alt-P3HST)通过精心设计的2-bromo-8-hexyl-5-(3-hexylseleophen-2-yl)噻吩的Pd-IPr催化直接芳基化聚合反应成功合成了高分子量(20.0K g / mol)的高分子量聚合物单体。表征了Alt-P3HST的分子特性,使其与P3HT和P3HS的分子特性相比。这项研究表明,对通过直接C-H键聚合合成共轭聚合物的NHC基钯催化剂进行了深入研究。

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