Backbone‐Bridging Promotes Diversity in Heteroleptic Cages
The combination of shape‐complementary bis‐monodentate ligands LA and LB with PdII cations yields heteroleptic cages cis‐[Pd2LA2LB2] by self‐sorting. Herein, we report how such assemblies can be diversified by introduction of covalent backbone bridges between two LA units. Together with solvent and...
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Published in: | Angewandte Chemie International Edition Vol. 60; no. 12; pp. 6403 - 6407 |
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Main Authors: | , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Germany
Wiley Subscription Services, Inc
15-03-2021
John Wiley and Sons Inc |
Edition: | International ed. in English |
Subjects: | |
Online Access: | Get full text |
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Summary: | The combination of shape‐complementary bis‐monodentate ligands LA and LB with PdII cations yields heteroleptic cages cis‐[Pd2LA2LB2] by self‐sorting. Herein, we report how such assemblies can be diversified by introduction of covalent backbone bridges between two LA units. Together with solvent and guest effects, the flexibility of these linkers can modulate nuclearity, topology, and number of cavities in a family of four structurally diverse assemblies. Ligand LA1, with flexible linker, reacts in CH3CN with its LB counterpart to a tetranuclear dimer D1. In DMSO, however, a trinuclear pseudo‐tetrahedron T1 is formed. The product of LA2, with rigid linker, looks similar to D1, but with a rotated ligand arrangement. In presence of an anionic guest, this dimer D2 transforms and a hexanuclear prismatic barrel P2 crystallizes. We demonstrate how controlling a ligand's coordination mode can trigger structural differentiation and increase complexity in metallo‐supramolecular assembly.
Rich structural variety in shape‐complementary metallo‐supramolecular assemblies is achieved by bridging ligands via their backbones. A series of unprecedented heteroleptic assemblies ranging from dimeric cages over a prismatic structure to a pseudo‐tetrahedron were obtained. The influence of linker flexibility, solvent and presence of guest molecules was studied. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1433-7851 1521-3773 |
DOI: | 10.1002/anie.202012425 |