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Updated: Jun 5, 2026

Modification and Functionalization of the Guanidine Group by Tailor-made Precursors
Published on: April 27, 2017
μ-1,2-Di-4-pyridylethane-κN:N'-bis-[bis-(N,N-diisopropyl-dithio-carbamato-κS,S')zinc(II)]
Vanessa Avila1, Edward R T Tiekink
1Department of Chemistry, The University of Texas at San Antonio, One UTSA Circle, San Antonio, Texas 78249-0698, USA.
This study details a dinuclear zinc compound with a unique trigonal-bipyramidal geometry. Crystal structure analysis reveals intermolecular hydrogen bonds, offering insights into coordination chemistry.
Area of Science:
- Inorganic Chemistry
- Coordination Chemistry
- Crystallography
Background:
- Dinuclear metal complexes are crucial in catalysis and materials science.
- Understanding zinc coordination geometries is vital for designing novel functional materials.
- Dithiocarbamate ligands offer versatile coordination modes in metal complexes.
Purpose of the Study:
- To synthesize and characterize a novel dinuclear zinc compound.
- To elucidate the coordination geometry and crystal structure of the title compound.
- To investigate intermolecular interactions within the crystal lattice.
Main Methods:
- Single-crystal X-ray diffraction was employed to determine the molecular and crystal structure.
- Elemental analysis confirmed the compound's composition.
- Spectroscopic methods were used for preliminary characterization.
Main Results:
- The title compound, [Zn(2)(C(7)H(14)NS(2))(4)(C(12)H(12)N(2))], was successfully synthesized.
- Each zinc atom exhibits a distorted trigonal-bipyramidal coordination geometry with a ZnNS(4) environment.
- The crystal structure is stabilized by intermolecular C-H⋯S hydrogen bonds.
Conclusions:
- The study provides a detailed structural characterization of a novel dinuclear zinc complex.
- The observed coordination geometry and intermolecular interactions offer fundamental insights into zinc coordination chemistry.
- This work contributes to the understanding of supramolecular assembly in metal-organic compounds.
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