分子机器
共轭体系
红外光谱学
化学
吡啶
转化(遗传学)
纳米尺度
配体(生物化学)
溶剂
结晶学
拓扑(电路)
材料科学
纳米技术
聚合物
有机化学
数学
受体
组合数学
基因
生物化学
作者
Li‐Long Dang,Tingting Zhang,Tian Chen,Ying Zhao,Xiang Gao,Francisco Aznárez,Lu‐Fang Ma,Guo‐Xin Jin
标识
DOI:10.1002/anie.202301516
摘要
Intricately interwoven topologies are continually being synthesized and are ultimately equally versatile and significant at the nanoscale level; however, reports concerning ravel structures, which are highly entwined new topological species, are extremely rare and fraught with tremendous synthesis challenges. To solve the synthesis problem, a tetrapodontic pyridine ligand L1 with two types of olefinic bond units and two Cp*M-based building blocks (E1, M=Rh; E2, M=Ir) featuring large conjugated planes was prepared to perform the self-assembly. Two unprecedented [5+10] icosanuclear molecular 4-ravels containing four crossings were obtained by parallel-displaced π⋅⋅⋅π interactions in a single-step strategy. Remarkably, reversible structural transformations between the 4-ravel and the corresponding metallocage could be realized by concentration changes and solvent- and guest-induced effects. X-ray crystallographic data and NMR spectroscopy provide full confirmation of these phenomena.
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