共轭体系
堆积
共价键
共价有机骨架
材料科学
电化学
纳米材料
动态共价化学
金属有机骨架
纳米技术
纳米颗粒
组合化学
化学工程
化学
聚合物
分子
电极
超分子化学
有机化学
物理化学
吸附
工程类
复合材料
作者
Phuong H. Le,Andong Liu,Leo B. Zasada,Jackson Geary,Ashlyn A. Kamin,Devin S. Rollins,Hao Nguyen,Audrey M. Hill,Yayuan Liu,Dianne J. Xiao
标识
DOI:10.1002/anie.202421822
摘要
Here we report a series of nitrogen‐rich conjugated macrocycles that mimic the structure and function of semiconducting 2D metal–organic and covalent organic frameworks while providing greater solution processability and surface tunability. Using a new tetraaminotriphenylene building block that is compatible with both coordination chemistry and dynamic covalent chemistry reactions, we have synthesized two distinct macrocyclic cores containing Ni–N and phenazine‐based linkages, respectively. The fully conjugated macrocycle cores support strong interlayer stacking and accessible nanochannels. For the metal–organic macrocycles, good out‐of‐plane charge transport is preserved, with pressed pellet conductivities of 10–3 S/cm for the nickel variants. Finally, using electrochemically mediated CO2 capture as an example, we illustrate how colloidal phenazine‐based organic macrocycles improve electrical contact and active site electrochemical accessibility relative to bulk covalent organic framework powders. Together, these results highlight how simple macrocycles can enable new synthetic directions as well as new applications by combining the properties of crystalline porous frameworks, the processability of nanomaterials, and the precision of molecular synthesis.
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