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多组分[PdABCD]笼的非统计组装

Non-statistical assembly of multicomponent [PdABCD] cages.

作者信息

Wu Kai, Benchimol Elie, Baksi Ananya, Clever Guido H

机构信息

Department of Chemistry and Chemical Biology, TU Dortmund University, Dortmund, Germany.

MOE Key Laboratory of Bioinorganic and Synthetic Chemistry, LIFM, IGCME, School of Chemistry, Sun Yat-Sen University, Guangzhou, China.

出版信息

Nat Chem. 2024 Apr;16(4):584-591. doi: 10.1038/s41557-023-01415-7. Epub 2024 Jan 19.

Abstract

Self-assembled hosts, inspired by biological receptors and catalysts, show application potential in sustainable synthesis, energy conversion and medicine. Implementing multiple functionalities in the form of distinguishable building blocks, however, is difficult without risking narcissistic self-sorting or a statistical mess. Here we report a systematic series of integratively self-assembled heteroleptic cages in which two square-planar Pd cations are bridged by four different bis-pyridyl ligands, A, B, C and D, via synergistic effects to exclusively form a single isomer-the lantern-shaped cage [PdABCD]. This self-sorting goal-forming just one out of 55 possible structures-is reached under full thermodynamic control and can be realized progressively (by combining progenitors, such as [PdAC] with [PdBD]), directly from ligands and Pd cations or by mixing all four corresponding homoleptic cages. The rational design of complex multicomponent assemblies that enables the modular incorporation of diverse chemical moieties will advance their applicability in functional nanosystems.

摘要

受生物受体和催化剂启发的自组装主体在可持续合成、能量转换和医学领域展现出应用潜力。然而,以可区分的构建块形式实现多种功能而不冒出自排序或统计混乱的风险是困难的。在此,我们报告了一系列系统的整合自组装杂配笼,其中两个平面正方形钯阳离子通过四种不同的双吡啶配体A、B、C和D通过协同效应桥连,专门形成单一异构体——灯笼形笼[PdABCD]。这种自分类目标——从55种可能结构中仅形成一种——是在完全热力学控制下实现的,并且可以逐步实现(通过将前体,如[PdAC]与[PdBD]组合),直接从配体和钯阳离子开始,或者通过混合所有四个相应的同配笼。能够模块化引入不同化学部分的复杂多组分组装体的合理设计将推动其在功能纳米系统中的适用性。

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