Protein binding regulates complex configuration: comparative analysis of three dynamically racemic europium(iii)
Huishan Li1, Dominic J Black2, Robert Pal2
1Department of Chemistry, Hong Kong Baptist University Kowloon Tong Hong Kong SAR China davidparker@hkbu.edu.hk.
RSC Advances
|May 20, 2026
Summary
Europium complexes show poor water solubility due to aggregation. Hydrogencarbonate addition improves solubility and forms stable adducts, with different serum albumins selectively binding specific enantiomers.
Area of Science:
- Coordination Chemistry
- Supramolecular Chemistry
- Luminescence Spectroscopy
Background:
- Dynamically racemic lanthanide complexes, specifically Eu(iii) with heptadentate triazacyclononane ligands, present challenges in aqueous media.
- Understanding their aggregation behavior and solubility is crucial for potential applications in solution.
Purpose of the Study:
- To investigate the binding behavior and aqueous solution properties of three dynamically racemic Eu(iii) complexes.
- To explore strategies for enhancing water solubility and understand interactions with biomolecules like serum albumin.
Main Methods:
- Luminescence spectroscopy was employed to study the europium complexes.
- Circularly polarized luminescence (CPL) spectroscopy was used to differentiate enantiomers and analyze binding events.
Main Results:
- Low water solubility was attributed to intermolecular carboxylate ligation leading to oligomerization.
- Hydrogencarbonate addition enhanced solubility by forming a stable, reversible 1:1 ternary adduct.
- Selective binding of Λ or Δ enantiomers by human serum albumin and bovine serum albumin, respectively, was observed via CPL.
Conclusions:
- The solubility and aggregation of these Eu(iii) complexes are directly influenced by solution conditions and ligand interactions.
- Hydrogencarbonate acts as an effective solubilizing agent, forming well-defined adducts.
- Serum albumins exhibit enantioselective recognition of the europium complexes, highlighting potential for chiral sensing applications.
Related Concept Videos
Complexation Equilibria: The Chelate Effect
In complexation reactions, metal atoms or cations interact with ligands to form donor-acceptor adducts called metal complexes. Ligands that bind through one donor site are monodentate, ligands with two donor sites are bidentate, and those with more than two donor sites are polydentate ligands. For example, ethylene diamine is a bidentate ligand that binds through two nitrogen donor atoms, forming a five-membered ring. EDTA is a polydentate ligand that binds through four oxygen and two nitrogen...
The Equilibrium Binding Constant and Binding Strength
The equilibrium binding constant (Kb) quantifies the strength of a protein-ligand interaction. Kb can be calculated as follows when the reaction is at equilibrium:
The Equilibrium Binding Constant and Binding Strength
The equilibrium binding constant (Kb) quantifies the strength of a protein-ligand interaction. Kb can be calculated as follows when the reaction is at equilibrium:
EDTA: Chemistry and Properties
Polydentate ligands are most widely used in complexometric titrations because they form more stable complexes with the metal ions than mono- or bidentate ligands due to the chelate effect. Examples of polydentate ligands are ethylenediaminetetraacetic acid (EDTA), crown ethers, and cryptands. The most important feature of optimal polydentate ligands is the ability to form 1:1 complexes in a single-step process. Amino carboxylic acid derivatives are frequently used as complexing agents. EDTA is...
Complexometric Titration: Ligands
Different monodentate and polydentate ligands are used as complexing agents in complexometric titration reactions. The formation of complexes by mono- and bidentate ligands involves two or more intermediate steps, limiting their use as complexing agents. In comparison, polydentate ligands can form complexes with metal ions in a single-step process, facilitating sharper end points. This means polydentate ligands, such as amino carboxylic acid derivatives, are most commonly employed in...
Complexation Equilibria: Factors Influencing Stability of Complexes
In complexation reactions, metal cations are the electron pair acceptors, and the ligands are the electron pair donors. The stability of the metal complexes depends primarily on the complexing ability of the central metal ion and the nature of the ligands. Generally, the complexing ability of the metal ion depends on the size and charge of the ion. As the metal ion size increases, the stability of the metal complexes decreases, provided that the valency of the metal ion and the ligands remain...

