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Updated: Jun 1, 2026

Thermochemical Studies of Ni(II) and Zn(II) Ternary Complexes Using Ion Mobility-Mass Spectrometry
Published on: June 8, 2022
Bis(triethano-lamine)nickel(II) sulfate.
This study details the crystal structure of a nickel(II) sulfate complex with triethanolamine (TEA) ligands. The research reveals a unique two-dimensional hydrogen-bonded network formed by sulfate anions and TEA coordination.
Area of Science:
- Coordination Chemistry
- Crystal Engineering
- Supramolecular Chemistry
Background:
- Nickel(II) complexes are of interest due to their diverse coordination geometries and applications.
- Triethanolamine (TEA) is a versatile ligand capable of coordinating through nitrogen and oxygen atoms.
- Understanding supramolecular assembly in metal-organic compounds is crucial for materials science.
Purpose of the Study:
- To elucidate the crystal structure of the [Ni(triethanolamine)2]SO4 complex.
- To investigate the coordination modes of triethanolamine ligands.
- To characterize the supramolecular architecture formed by hydrogen bonding.
Main Methods:
- Single-crystal X-ray diffraction analysis was performed.
- The coordination environment around the Ni(II) center was determined.
- Hydrogen bonding interactions and network formation were analyzed.
Main Results:
- The crystal structure revealed two triethanolamine ligands coordinated to a central Ni(II) ion.
- Each TEA ligand coordinated via its nitrogen atom and two oxygen atoms, with the third hydroxyl group oriented outwards.
- Sulfate anions formed a 2D supramolecular network through hydrogen bonds with both coordinated and free hydroxyl groups.
Conclusions:
- The study successfully characterized a novel nickel(II)-triethanolamine sulfate complex.
- The coordination behavior of TEA and the formation of a 2D hydrogen-bonded network were confirmed.
- This work contributes to the understanding of crystal engineering in coordination compounds.
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