质子化
氮气
兴奋剂
石墨烯
离子
电化学
催化作用
材料科学
无机化学
光化学
化学
化学物理
纳米技术
物理化学
电极
有机化学
光电子学
作者
Feifan Wang,Yuxiang Wang,Qiong Wu,Ling Chai,Xuan‐Wen Chen,Yuan‐Zhi Tan
标识
DOI:10.1002/anie.202315302
摘要
Abstract Nitrogen‐doped cavities are pervasive in graphenic materials, and represent key sites for catalytic and electrochemical activity. However, their structures are generally heterogeneous. In this study, we present the synthesis of a well‐defined molecular cutout of graphene featuring N‐doped cavity. The graphitization of a macrocyclic pyridinic precursor was achieved through photochemical cyclodehydrochlorination. In comparison to its counterpart with pyridinic nitrogen at the edges, the pyridinic nitrogen atoms in this nanographene cavity exhibit significantly reduced basicity and selective binding to Ag + ion. Analysis of the protonation and coordination equilibria revealed that the tri‐N‐doped cavity binds three protons, but only one Ag + ion. These distinct protonation and coordination behaviors clearly illustrate the space confinement effect imparted by the cavities.
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