二苯并呋喃衍生的 Pd-NHCs:二氯烯单体铃木-宫拉缩聚反应的高效前催化剂

IF 4.1 2区 化学 Q2 POLYMER SCIENCE
Yuman Guo, Hao Wu, Meng-Jiao Zhang and Feng-Shou Liu
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引用次数: 0

摘要

钯催化的铃木-米亚乌拉缩聚反应(SMPs)已成为合成共轭聚合物(CPs)的有力方法。尽管已有大量报道利用二溴芳烃和二碘芳烃衍生物作为单体,但由于条件苛刻且效率较低,有关使用非活性二氯烯的研究较少。本研究旨在克服这些挑战并开发出坚固耐用的钯前催化剂,设计并合成了一系列二苯并芘衍生的 N-杂环碳化钯(Pd-NHC)。研究发现,这些 Pd-IPrDBB 的 "大而灵活 "性质以及 "可丢弃 "配体有助于提高 Pd(0) 物种和聚合过程的稳定性。此外,还对缩聚条件(如碱、溶剂和温度的选择)进行了优化。这项研究提出了一种高产率、高分子量共轭聚合物的高效合成方案,展示了广泛的单体范围,其性能优于传统的钯基膦催化体系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Dibenzobarrelene-derived Pd-NHCs: efficient precatalysts for the Suzuki–Miyaura polycondensations of dichloroarene monomers†

Dibenzobarrelene-derived Pd-NHCs: efficient precatalysts for the Suzuki–Miyaura polycondensations of dichloroarene monomers†

Pd-catalyzed Suzuki–Miyaura polycondensations (SMPs) have emerged as a powerful method for synthesizing conjugated polymers (CPs). While numerous reports have utilized dibromoarene and diiodoarene derivatives as monomers, there has been less research on the use of the deactive dichloroarenes due to harsh conditions and low efficiency. In this study, aiming to overcome these challenges and develop robust palladium precatalysts, a series of dibenzobarrelene-derived palladium N-heterocyclic carbenes (Pd-NHCs) were designed and synthesized. It was observed that the “large-but-flexible” nature of these Pd-IPrDBB complexes as well as the “throw-away” ligands facilitated the stability of Pd(0) species and the polymerization process. Additionally, optimization of polycondensation conditions such as choice of base, solvent, and temperature was conducted. This work presents an efficient protocol for synthesizing conjugated polymers with high yields and high molecular weights, demonstrating a broad monomer scope and outperforming conventional palladium phosphine-based catalytic systems.

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来源期刊
Polymer Chemistry
Polymer Chemistry POLYMER SCIENCE-
CiteScore
8.60
自引率
8.70%
发文量
535
审稿时长
1.7 months
期刊介绍: Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.
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