具有 N,N-二叉醛基咪唑烷-2-亚胺/胍辅助配体的强效钴催化剂用于异戊二烯聚合反应

IF 6.5 1区 化学 Q2 CHEMISTRY, PHYSICAL Journal of Catalysis Pub Date : 2024-05-31 DOI:10.1016/j.jcat.2024.115581
Mingyuan Li , Moris S. Eisen , Zhengguo Cai
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引用次数: 0

摘要

我们设计并成功合成了一系列新的定义明确的钴配合物(Co1-Co7),这些配合物带有 N,N-二价螯合醛亚胺咪唑烷-2-亚胺/胍辅助配体。通过单晶 X 射线衍射分析,对所有目标金属配合物进行了结构表征。结果表明,Co 原子采用了扭曲的四面体配位几何形状,形成了独特的六元螯合环,与传统的基于 N^N 的 α-二亚胺和 β-二亚胺 Co 配合物在结构上有所区别。这些 Co 配合物与极少量的 Et2AlCl(低至 50 等份)结合,在异戊二烯的配位聚合中表现出很高的活性(6 小时内产率高达 99%)和良好的热稳定性(高达 80 °C),可得到分子量 Mn(25.9-138.4 kg/mol)和顺式-1,4 含量(64.7-73.3%)可调的顺式-1,4/3,4-聚异戊二烯。这些 Co 催化剂上的不同取代基对催化行为、链微结构和聚合物性能也有影响。本研究是首个用于异戊二烯聚合的咪唑烷-亚胺/胍类似物配位钴络合物的实例。
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Robust cobalt catalysts with N,N-bidentate aldimine imidazolidine-2-imine/guanidine ancillary ligand for isoprene polymerization

A new family of well-defined cobalt complexes (Co1Co7) bearing N,N-bidentate chelate aldimine imidazolidine-2-imine/guanidine ancillary ligands were designed and successfully synthesized. All of the target metal complexes were structurally characterized by single-crystal X-ray diffraction analysis. It revealed that the Co atom adopted distorted tetrahedral coordination geometry and formed a unique six-membered chelate ring which exhibited structural distinctions with traditional N^N-based α-diimine and β-diimine Co complexes. In combination with a very low amount of Et2AlCl (as low as 50 equiv.), these Co complexes exhibited high activity (up to 99 % yield within 6 hrs) and good thermal stability (up to 80 °C) in the coordination polymerizations of isoprene to afford cis-1,4/3,4-polyisoprenes with adjustable molecular weights Mn (25.9–138.4 kg/mol) and cis-1,4 contents (64.7–73.3 %). The different substituents on these Co catalysts also exerted influence on catalytic behaviors, chain microstructures, and polymer properties. This study represents the first example of imidazolidine-imine/guanidine analog ligated Cobalt complexes for the polymerization of isoprene.

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来源期刊
Journal of Catalysis
Journal of Catalysis 工程技术-工程:化工
CiteScore
12.30
自引率
5.50%
发文量
447
审稿时长
31 days
期刊介绍: The Journal of Catalysis publishes scholarly articles on both heterogeneous and homogeneous catalysis, covering a wide range of chemical transformations. These include various types of catalysis, such as those mediated by photons, plasmons, and electrons. The focus of the studies is to understand the relationship between catalytic function and the underlying chemical properties of surfaces and metal complexes. The articles in the journal offer innovative concepts and explore the synthesis and kinetics of inorganic solids and homogeneous complexes. Furthermore, they discuss spectroscopic techniques for characterizing catalysts, investigate the interaction of probes and reacting species with catalysts, and employ theoretical methods. The research presented in the journal should have direct relevance to the field of catalytic processes, addressing either fundamental aspects or applications of catalysis.
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