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Updated: Apr 19, 2026

Construction and Systematical Symmetric Studies of a Series of Supramolecular Clusters with Binary or Ternary Ammonium Triphenylacetates
Published on: February 15, 2016
Crystal structure of (NH4)2[Fe(II) 5(HPO3)6], a new open-framework phosphite
Teresa Berrocal1, Jose Luis Mesa1, Edurne Larrea2
1Dpto. de Química Inorgánica, Facultad de Ciencia y Tecnología, Universidad del País Vasco, UPV/EHU, 48080 Leioa, Spain.
A novel open framework material, di-ammonium hexa-phosphito-penta-ferrate(II), was synthesized. Its crystal structure features iron-oxygen octahedra forming channels for ammonium cations, confirmed by IR spectroscopy.
Area of Science:
- Inorganic Chemistry
- Crystal Engineering
- Materials Science
Background:
- Synthesis of novel inorganic compounds is crucial for developing new materials.
- Open framework structures offer potential for various applications due to their porosity.
Purpose of the Study:
- To synthesize and characterize a new di-ammonium hexa-phosphito-penta-ferrate(II) compound.
- To elucidate the crystal structure and properties of the synthesized material.
Main Methods:
- Hydrothermal synthesis under mild conditions and autogenous pressure.
- Single crystal X-ray diffraction for structure determination.
- Infrared (IR) spectroscopy for vibrational analysis.
Main Results:
- Successful synthesis of twinned crystals of di-ammonium hexa-phosphito-penta-ferrate(II), (NH4)2[Fe5(HPO3)6].
- The crystal structure reveals an open framework of [Fe(II)5(HPO3)6](2-) with NH4+ counter-cations.
- The framework consists of (001) sheets of [FeO6] octahedra linked by phosphite anions, forming channels (radius ~3.1 Å) accommodating disordered NH4+.
- IR spectrum confirmed the presence of phosphite and ammonium functional groups.
Conclusions:
- Di-ammonium hexa-phosphito-penta-ferrate(II) represents a new open framework inorganic material.
- The unique structure with channels suggests potential for ion exchange or host-guest chemistry.
- The synthesis and characterization provide a foundation for further investigation of related compounds.
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