超分子化学
密度泛函理论
材料科学
纳米技术
超分子组装
功能(生物学)
超分子聚合物
设计要素和原则
分子动力学
产量(工程)
退化(生物学)
化学
分子
分子构象
作者
Ya‐Wen Zhang,Hai-Ning Zhang,Ming-Xia Wang,Xin Li,Ying-Feng Han
标识
DOI:10.1038/s41467-026-68348-w
摘要
Molecular information encoded within supramolecular frameworks offers a powerful paradigm for directing emergent function beyond the genetic code, but systematic investigations into alternative spatial configurations and their consequences remain scarce. Here we use metalla-[2]catenanes to probe sequence-function relationships in layered architectures. By combining two or three size-matched N-heterocyclic carbene ligands with Ag(I) nodes, we selectively construct heteroleptic metalla-[2]catenanes through both direct assembly and supramolecular fusion pathways. X-ray crystallographic analysis unambiguously confirms the targeted sequences, while semiempirical and density functional theory calculations reveal their thermodynamic preference over alternative isomers. Photothermal conversion studies further demonstrate that sequence-specific charge-transfer interactions yield distinct macroscopic responses. Collectively, these results identify heteroleptic metalla-[2]catenanes as a robust model for elucidating how spatial arrangement governs system-level behavior and for advancing molecular coding principles in functional supramolecular design.
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