化学
菲咯啉
电化学
氧化还原
超分子化学
晶体结构
氢键
金属
配体(生物化学)
分子
水溶液中的金属离子
热液循环
结晶学
无机化学
有机化学
电极
物理化学
化学工程
生物化学
工程类
受体
作者
Ri-Ming Zhong,Quan-Bin Xu,Geng-Yi Wang,Lingling Zheng,Jian‐Zhong Wu,Yong‐Cong Ou
标识
DOI:10.1080/00958972.2023.2176226
摘要
Two new isomorphic metal complexes, [M(phon)(H2O)4]·SO4·2H2O (M = Ni and Zn, 1-Ni and 1-Zn, respectively, phon = 1,10-phenanthroline-5,6-dione), were crystallized at room temperature. Single-crystal X-ray analyses reveal that a metal ion is coordinated with one phon ligand and four coordinated water molecules into a discrete coordination structure which expands into a 3D supramolecular structure via hydrogen bonding interactions. The thermal and electrochemical properties of the complexes are investigated. The results show that 1-Ni exhibits redox activity under alkaline conditions and has potential to act as a redox reaction mediator, while 1-Zn does not. The specific capacitance of 1-Ni0.5Zn0.5, obtained by mixing the two complexes under hydrothermal condition, is four times higher than that of 1-Ni.
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