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钯介导的表面引发 Kumada 催化剂缩聚反应:一种制备取向共轭聚合物的简便方法。

Palladium-Mediated Surface-Initiated Kumada Catalyst Polycondensation: A Facile Route Towards Oriented Conjugated Polymers.

作者信息

Huddleston N Eric, Sontag S Kyle, Bilbrey Jenna A, Sheppard Gareth R, Locklin Jason

机构信息

Department of Chemistry and College of Engineering, University of Georgia, Riverbend Research South, 220 Riverbend Road, Athens, Georgia 30602, USA.

出版信息

Macromol Rapid Commun. 2012 Dec 21;33(24):2115-20. doi: 10.1002/marc.201200472. Epub 2012 Sep 12.

Abstract

Palladium-mediated surface-initiated Kumada catalyst transfer polycondensation is used to generate poly(3-methyl thiophene) films with controlled thickness up to 100 nm. The palladium initiator density is measured using cyclic voltammetry and a ferrocene-capping agent, where the surface density is found to be 55% (1.1 × 10(14) molecules per cm(2)). UV-Vis spectroscopy and AFM show increased aggregation in palladium-initiated films due to the higher grafting density of palladium initiators on the surface. The anisotropy of the P3MT films is determined using polarized UV-Vis spectroscopy, which indicates a degree of orientation perpendicular to the substrate. Evidence that palladium can maintain π-complexation even at elevated temperatures, is also shown through the exclusive intramolecular coupling of both a phenyl and thiophene-based magnesium bromide with different dihaloarenes.

摘要

钯介导的表面引发的熊田催化剂转移缩聚反应被用于制备厚度可控、高达100纳米的聚(3-甲基噻吩)薄膜。使用循环伏安法和二茂铁封端剂测量钯引发剂密度,发现表面密度为55%(每平方厘米1.1×10¹⁴个分子)。紫外-可见光谱和原子力显微镜显示,由于钯引发剂在表面的接枝密度较高,钯引发的薄膜中聚集增加。使用偏振紫外-可见光谱确定P3MT薄膜的各向异性,这表明存在垂直于基底的取向程度。通过苯基和噻吩基溴化镁与不同二卤代芳烃的专属分子内偶联,也证明了钯即使在高温下也能保持π络合。

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