Abstract
A biphenyl-bridged bis-tris(urea) ligand L was rationally designed with a favorable angle to construct a hexagon-shaped A6L6 (A = anion) complex upon assembly with phosphate anions (PO43−) via anion-coordination-driven assembly (ACDA). Due to the moderate flexibility of L, another well-defined discrete architecture, a square-like A4L4 complex, has also been obtained from ligand L and PO43−. Interconversion between these two self-assemblies can be readily realized by solvent regulation. In addition, the two anionic architectures display different binding abilities for selected cationic guest molecules, enabling the uptake of a desired guest from a mixture of guests.
Original language | English |
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Pages (from-to) | 2043-2052 |
Number of pages | 10 |
Journal | CCS Chemistry |
Volume | 4 |
Issue number | 6 |
DOIs | |
Publication status | Published - Jun 2022 |
Externally published | Yes |
Keywords
- anion coordination
- host–guest chemistry
- self-assembly
- supramolecular transformation
- tris(urea)