Related Experiment Video
Updated: Aug 12, 2025

Line Shape Analysis of Dynamic NMR Spectra for Characterizing Coordination Sphere Rearrangements at a Chiral Rhenium Polyhydride Complex
Published on: July 27, 2022
Metallo-Supramolecular Hexagonal Wreath with Four Switchable States Based on a pH-Responsive Tridentate Ligand
Pingru Su1,2, Biaowen Wei1,2, Chenxing Guo1,2
1College of Chemistry and Environmental Engineering, Shenzhen University, Shenzhen 518060, Guangdong, China.
Researchers developed pH-responsive metallo-supramolecular hexagonal wreaths using a novel ligand. These structures reversibly switch between four states, enabling tunable physical properties for advanced materials.
Area of Science:
- Supramolecular Chemistry
- Coordination Chemistry
- Materials Science
Background:
- Biological systems exhibit reversible state switching in biomacromolecules like heme proteins.
- Artificial supramolecular systems struggle with reversible multi-state interconversion.
- Metallo-supramolecular chemistry aims to mimic biological complexity and functionality.
Purpose of the Study:
- To construct metallo-supramolecular systems capable of reversible interconversion among multiple states.
- To design and synthesize pH-responsive building blocks for self-assembly.
- To explore the tunable physical properties of these self-assembled constructs.
Main Methods:
- Coordination-driven self-assembly using a pH-responsive tridentate ligand (H2DAP).
- Incorporation of metal ions (Fe(II), Co(II), Ni(II)) into multitopic building blocks.
- Investigation of state interconversion triggered by pH and redox stimuli.
Main Results:
- Successfully constructed giant metallo-supramolecular hexagonal wreaths.
- Demonstrated reversible interconversion among four distinct states in a Co-linked wreath.
- Observed fine-tuning of physical properties, including backbone charge and metal ion valency.
- Facilitated layer-by-layer assembly of charge-switchable metallo-supramolecules on substrates.
Conclusions:
- Developed a novel pH-responsive ligand for creating complex metallo-supramolecular architectures.
- Achieved efficient, reversible multi-state switching in self-assembled wreaths.
- Highlighted the potential for charge-switchable supramolecular materials in advanced applications.
More Related Videos
12:30Synthesis of a Thiol Building Block for the Crystallization of a Semiconducting Gyroidal Metal-sulfur Framework
Published on: April 9, 2018
07:14Author Spotlight: Experimental Approaches for the Synthesis of Low-Valent Metal-Organic Frameworks from Multitopic Phosphine Linkers
Published on: May 12, 2023
Related Concept Videos
Metal-Ligand Bonds
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
Valence Bond Theory
Crystal Field Theory - Octahedral Complexes
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
Colors and Magnetism
When atoms or molecules absorb light at the proper frequency, their electrons are excited to higher-energy orbitals. For many main group atoms and molecules, the absorbed photons are in the ultraviolet range of the electromagnetic spectrum, which cannot be detected by the human eye. For coordination compounds, the energy difference between the d orbitals often allows photons in the visible range to be absorbed and emitted, which is seen as colors by the human...
Coordination Number and Geometry