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A Multi-Stimuli Transformational Network of Benzil-Based Pd(II) Assemblies.

Zhiwei Zeng1,2, A Priscila Gia1,3, Alexander S Mikherdov1

  • 1Department of Chemistry and Chemical Biology, TU Dortmund University, Dortmund, Germany.

Angewandte Chemie (International Ed. in English)
|July 9, 2026
PubMed
Summary

Researchers developed a new ligand (LA) for palladium(II) coordination assemblies, enabling control over structure and transformations. This ligand

Keywords:
chemical networkscoordination cagespost‐assembly modificationself‐assemblysupramolecular chemistry

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Published on: February 7, 2017

Area of Science:

  • Coordination chemistry
  • Supramolecular chemistry
  • Materials science

Background:

  • Precise control over supramolecular topology and nuclearity in coordination-driven self-assemblies is challenging.
  • Ligand design is crucial for directing self-assembly outcomes.

Purpose of the Study:

  • To introduce a flexible ligand (LA) capable of adopting multiple conformations.
  • To explore the formation of diverse palladium(II) assemblies with varying topologies and nuclearities.
  • To investigate stimuli-responsive transformations of these assemblies.

Main Methods:

  • Synthesis of ligand LA based on a benzil backbone.
  • Coordination of LA with Pd(II) to form homoleptic and heteroleptic assemblies.
  • Characterization of resulting supramolecular structures.
  • Post-assembly modification via ligand condensation.

Main Results:

  • Formation of mononuclear (PdLA2) and cage (Pd2LA4) homoleptic assemblies.
  • Synthesis of heteroleptic assemblies (cis-Pd2LA2LC2, Pd3LA2LD4) with secondary ligands.
  • Demonstration of interconversion and guest-induced transformations between architectures.
  • Post-assembly conversion to a rigid quinoxaline-based complex (PdLB2).

Conclusions:

  • Ligand conformation and assembly environment dictate structural outcomes and reactivity.
  • Demonstrated a stimuli-responsive system for dynamic control over supramolecular structures.
  • Highlighted the potential for mimicking natural systems' control over reactivity via confinement and allosteric effects.