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Updated: Jun 5, 2026

Modification and Functionalization of the Guanidine Group by Tailor-made Precursors
Published on: April 27, 2017
N,N'-Bis(2-iodo-benzyl-idene)ethane-1,2-diamine
1X-ray Crystallography Unit, School of Physics, Universiti Sains Malaysia, 11800 USM, Penang, Malaysia.
This study details a Schiff base compound, C(16)H(14)I(2)N(2), revealing its unique crystal structure. Key findings include intramolecular hydrogen bonds and short intermolecular iodine-nitrogen interactions forming 2D networks.
Area of Science:
- Crystal Engineering
- Supramolecular Chemistry
- Organic Synthesis
Background:
- Schiff base compounds are versatile organic molecules with diverse applications.
- Understanding crystal packing and intermolecular interactions is crucial for designing functional materials.
Purpose of the Study:
- To synthesize and characterize a novel Schiff base compound.
- To elucidate the crystal structure and intermolecular interactions of the synthesized compound.
- To investigate the formation of extended network structures.
Main Methods:
- Single-crystal X-ray diffraction analysis.
- Analysis of bond lengths, bond angles, and intermolecular interactions.
- Identification of hydrogen bonding and non-covalent interactions.
Main Results:
- The Schiff base compound C(16)H(14)I(2)N(2) was synthesized and its crystal structure determined.
- An intramolecular C-H⋯I hydrogen bond forms an S(5) ring motif.
- Short intermolecular I⋯N interactions (3.2096(15) Å) link molecules into 1D chains and 2D networks.
Conclusions:
- The crystal structure exhibits unique intramolecular and intermolecular interactions.
- The observed I⋯N interactions play a significant role in the self-assembly of molecules into extended networks.
- This study provides insights into the crystal engineering of Schiff base compounds.
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