价(化学)
等结构
分子内力
离子
结晶学
化学
氧化态
配位复合体
协调数
密度泛函理论
配位聚合物
立体化学
金属
计算化学
晶体结构
有机化学
作者
Ning Li,Gang Wu,Shibo Xi,Fengxia Wei,Ming Lin,Jinjun Qiu,Jin‐Cheng Zheng,Jiabao Yi,Debbie Hwee Leng Seng,Coryl Jing Jun Lee,D. V. Maheswar Repaka,Xiaoming Liu,Zicong Marvin Wong,Qiang Zhu,Shuo‐Wang Yang,He‐Kuan Luo
标识
DOI:10.1002/smtd.202201166
摘要
Graphene-like 2D coordination polymers (GCPs) have been of central research interest in recent decades with significant impact in many fields. According to classical coordination chemistry, Cu(II) can adopt the dsp2 hybridization to form square planar coordination geometry, but not Cu(I); this is why so far, there has been few 2D layered structures synthesized from Cu(I) precursors. Herein a pair of isostructural GCPs synthesized by the coordination of benzenehexathiol (BHT) ligands with Cu(I) and Cu(II) ions, respectively, is reported. Spectroscopic characterizations indicate that Cu(I) and Cu(II) coexist with a near 1:1 ratio in both GCPs but remain indistinguishable with a fractional oxidation state of +1.5 on average, making these two GCPs a unique pair of Creutz-Taube mixed-valence 2D structures. Based on density functional theory calculations, an intramolecular pseudo-redox mechanism is further uncovered whereby the radicals on BHT ligands can oxidize Cu(I) or reduce Cu(II) ions upon coordination, thus producing isostructures with distinct electron configurations. For the first time, it is demonstrated that using Cu(I) or Cu(II), one can achieve 2D isostructures, indicating an unusual fact that a neutral periodic structure can host a different number of total electrons as ground states, which may open a new chapter for 2D materials.
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