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一种用于合成聚(2,6-二甲基-1,4-亚苯基醚)的高效芳胺配体/氯化亚铜催化剂体系

A Highly Efficient Aromatic Amine Ligand/Copper(I) Chloride Catalyst System for the Synthesis of Poly(2,6-dimethyl-1,4-phenylene ether).

作者信息

Kim Kisoo, Shin Min Jae, Kim Yong Tae, Kim Joong-In, Kim Young Jun

机构信息

School of Chemical Engineering, Sungkyunkwan University, 2066 Seobu-ro, Jangan-gu, Suwon-si, Gyeonggi-do 16419, Korea.

Hyosung R&D Business Labs, 74 Simin-daero, Dongan-gu, Anyang-si 14080, Gyunggi-do, Korea.

出版信息

Polymers (Basel). 2018 Mar 22;10(4):350. doi: 10.3390/polym10040350.

DOI:10.3390/polym10040350
PMID:30966385
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6415001/
Abstract

Highly active catalyst systems for polymerizing 2,6-dimethylphenol were studied by using aromatic amine ligands and copper(I) chloride. The aromatic amine ligands employed were pyridine, 1-methylimidazole, 2-aminopyridine, 3-aminopyridine, and 4-aminopyridine. A mixture of chloroform and methanol (9:1, /) was used as a polymerization solvent. All experiments were performed with oxygen uptake measurement apparatus, while the reaction rate for each aromatic amine ligand-Cu catalyst system and the amount of by-product, 3,3',5,5'-Tetramethyl-4,4'diphenoquinone (DPQ), were measured to determine the efficiency of the catalyst systems. The 4-aminopyridine/Cu (I) catalyst system was found to be extremely efficient in poly(2,6-dimethyl-1,4-phenylene ether) (PPE) synthesis; it had the fastest reaction rate of 6.98 × 10 mol/L·s and the lowest DPQ production. The relatively high basicity of 4-aminopyridne and the less steric hindrance arising from a coordination of Cu and 4-aminopyridine in this catalyst are responsible for the fast polymerization rate. When 2-aminoprydine (an isomer of 4-aminopyridine) was used as a ligand, however, no polymerization occurred probably due to steric hindrance.

摘要

通过使用芳胺配体和氯化亚铜,研究了用于聚合2,6 - 二甲基苯酚的高活性催化剂体系。所使用的芳胺配体为吡啶、1 - 甲基咪唑、2 - 氨基吡啶、3 - 氨基吡啶和4 - 氨基吡啶。氯仿和甲醇的混合物(9:1,v/v)用作聚合溶剂。所有实验均使用吸氧测量装置进行,同时测量每个芳胺配体 - 铜催化剂体系的反应速率和副产物3,3',5,5'-四甲基 - 4,4'-二苯醌(DPQ)的量,以确定催化剂体系的效率。发现4 - 氨基吡啶/铜(I)催化剂体系在聚(2,6 - 二甲基 - 1,4 - 亚苯基醚)(PPE)合成中极其高效;它具有6.98×10⁻⁵mol/L·s的最快反应速率和最低的DPQ产量。4 - 氨基吡啶相对较高的碱性以及该催化剂中铜与4 - 氨基吡啶配位产生的空间位阻较小,是聚合速率快的原因。然而,当使用2 - 氨基吡啶(4 - 氨基吡啶的异构体)作为配体时,可能由于空间位阻而未发生聚合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6eb4/6415001/65dcd301960f/polymers-10-00350-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6eb4/6415001/986afb3d51ae/polymers-10-00350-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6eb4/6415001/6cdf68da926f/polymers-10-00350-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6eb4/6415001/c9c2b646fa58/polymers-10-00350-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6eb4/6415001/65dcd301960f/polymers-10-00350-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6eb4/6415001/986afb3d51ae/polymers-10-00350-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6eb4/6415001/6cdf68da926f/polymers-10-00350-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6eb4/6415001/c9c2b646fa58/polymers-10-00350-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6eb4/6415001/65dcd301960f/polymers-10-00350-g004.jpg

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本文引用的文献

1
Efficient oxidative coupling of 2,6-disubstituted phenol catalyzed by a dicopper(II) complex.双核铜(II)配合物催化 2,6-二取代苯酚的高效氧化偶联反应。
Dalton Trans. 2012 Jan 28;41(4):1158-64. doi: 10.1039/c1dt11065a. Epub 2011 Nov 24.
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Imidazole-based potential Bi- and tridentate nitrogen ligands: synthesis, characterization and application in asymmetric catalysis.基于咪唑的潜在双齿和三齿氮配体:合成、表征及其在不对称催化中的应用
Molecules. 2008 Sep 25;13(9):2326-39. doi: 10.3390/molecules13092326.