Coordination‐Driven Orthogonal Ligand Pairings through Dual Hydrogen‐Bonding/π‐π Interaction Complementarity

Multi-layered and orthogonal recognition is an excellent route to controlled molecular complexity. Here we report a series of heteroleptic complexes where two ligands pair together at a palladium(II) metal centre in complementary fashion and with orthogonality to others pairs. This complementarity is driven in part through hydrogen-bonding acceptor or donor sites proximal to the coordination domain (either DD:AA or AD:DA). These interactions alone are insufficient to control ligand pairing identity and/or orientation-secondary π-π interactions between electron-rich and electron-poor aromatic groups in the recognition domain combine with the hydrogen bonding to give high levels of complementarity. Importantly, the different heteroleptic complexes can be combined without significant scrambling or mismatching.

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Publication Details

Journal
Chemistry - A European Journal
Published
2025-09-10
DOI
https://doi.org/10.1002/chem.202502411
Citations
2
Primary Topic
Metal-Organic Frameworks: Synthesis and Applications
Type
article
Field-Weighted Citation Impact
1.07

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article

Coordination‐Driven Orthogonal Ligand Pairings through Dual Hydrogen‐Bonding/π‐π Interaction Complementarity

Rosemary J. Goodwin, Dan Preston, Nathan D. Lawson, Jordan N. Smith et al.
2 citations
Chemistry - A European Journal
Metal-Organic Frameworks: Synthesis and Applications
1.07
article

Coordination‐Driven Orthogonal Ligand Pairings through Dual Hydrogen‐Bonding/π‐π Interaction Complementarity

Rosemary J. Goodwin, Dan Preston, Nathan D. Lawson, Jordan N. Smith, Yolanda Yau
article en
2 citations

Abstract

Multi-layered and orthogonal recognition is an excellent route to controlled molecular complexity. Here we report a series of heteroleptic complexes where two ligands pair together at a palladium(II) metal centre in complementary fashion and with orthogonality to others pairs. This complementarity is driven in part through hydrogen-bonding acceptor or donor sites proximal to the coordination domain (either DD:AA or AD:DA). These interactions alone are insufficient to control ligand pairing identity and/or orientation-secondary π-π interactions between electron-rich and electron-poor aromatic groups in the recognition domain combine with the hydrogen bonding to give high levels of complementarity. Importantly, the different heteroleptic complexes can be combined without significant scrambling or mismatching.

Chemistry - A European JournalVol. 31(64)
Australian National University (AU)
National Computational Infrastructure, Australian Government, National Cancer Institute
Openalex Percentile: Top 21%
Metal-Organic Frameworks: Synthesis and Applications
1.07
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