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Preparation of a Corannulene-functionalized Hexahelicene by Copper(I)-catalyzed Alkyne-azide Cycloaddition of Nonplanar Polyaromatic Units
Published on: September 18, 2016
N-Cyclo-hexyl-cyclo-hexa-naminium chloride
Acta Crystallographica. Section E, Structure Reports Online
|April 28, 2011
Summary
This study details the crystal structure of a cyclohexylammonium chloride salt. The research highlights the chair conformations of cyclohexyl rings and intermolecular hydrogen bonding in the crystal lattice.
Area of Science:
- Crystallography
- Chemical Physics
- Materials Science
Background:
- Cyclohexylammonium salts are important in various chemical applications.
- Understanding their crystal structures provides insights into molecular interactions and material properties.
Purpose of the Study:
- To elucidate the crystal structure of cyclohexylammonium chloride.
- To analyze the conformational preferences of the cyclohexyl rings and the N-H bond orientation.
- To investigate intermolecular interactions within the crystal lattice.
Main Methods:
- Single-crystal X-ray diffraction was employed to determine the crystal structure.
- Analysis of bond angles, bond lengths, and hydrogen bonding patterns was performed.
Main Results:
- The cyclohexyl rings adopt chair conformations with the amino group in an equatorial position.
- A large C-N-C bond angle of 117.99(14)° was observed due to bulky cyclohexyl groups.
- Intermolecular N-H⋯Cl hydrogen bonds form infinite zigzag chains along the c axis.
- The crystal was identified as a racemic twin with a twin fraction of 0.28(18).
Conclusions:
- The crystal structure of cyclohexylammonium chloride is characterized by specific conformational arrangements and hydrogen bonding.
- The observed structural features are attributed to steric effects of the cyclohexyl rings and intermolecular forces.
- The study provides a detailed structural characterization relevant to supramolecular chemistry and solid-state science.
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