化学
共价键
卟啉
吡啶
共价有机骨架
聚合
冷凝
吩嗪
原位
组合化学
化学工程
密度泛函理论
光化学
高分子化学
有机化学
聚合物
计算化学
热力学
物理
工程类
作者
Elham Tavakoli,Arvin Kakekhani,Shayan Kaviani,Peng Tan,Mahdi Mohammadi Ghaleni,Mohsen Asle Zaeem,Andrew M. Rappe,Siamak Nejati
摘要
Synthesis and processing of two- or three-dimensional covalent organic frameworks (COFs) have been limited by solvent intractability and sluggish condensation kinetics. Here, we report on the electrochemical deposition of poly(5,10,15,20-tetrakis(4-aminophenyl)porphyrin)-covalent organic frameworks (POR-COFs) via formation of phenazine linkages. By adjusting the synthetic parameters, we demonstrate the rapid and bottom-up synthesis of COF dendrites. Both experiment and density functional theory underline the prominent role of pyridine, not only as a polymerization promoter but as a stabilizing sublattice, cocrystallizing with the framework. The crucial role of pyridine in dictating the structural properties of such a cocrystal (Py-POR-COF) is discussed. Also, a structure-to-function relationship for this class of materials, governing their electrocatalytic activity for the oxygen reduction reaction in alkaline media, is reported.
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