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Updated: May 27, 2026

Preparation of a Corannulene-functionalized Hexahelicene by Copper(I)-catalyzed Alkyne-azide Cycloaddition of Nonplanar Polyaromatic Units
Published on: September 18, 2016
catena-Poly[[aqua-bromidocopper(II)]-μ(3)-(picolinato N-oxide)]
Xin-Yu Wang1, Xiao-Qing Zhang, Wen-Shi Wu
1College of Materials Science and Engineering, Huaqiao University, Xiamen, Fujian 361021, People's Republic of China.
This study details the layered structure of a copper-bromine complex, [CuBr(C(6)H(4)NO(3))(H(2)O)](n). The structure is stabilized by hydrogen bonds and π-π interactions between pyridine rings.
Area of Science:
- Coordination Chemistry
- Crystal Engineering
- Materials Science
Background:
- Understanding the supramolecular assembly of metal complexes is crucial for designing novel materials.
- Layered structures in coordination compounds can lead to unique physical and chemical properties.
Purpose of the Study:
- To elucidate the crystal structure and supramolecular architecture of the title copper complex.
- To identify the key non-covalent interactions responsible for stabilizing the observed layered structure.
Main Methods:
- Single-crystal X-ray diffraction was used to determine the molecular and crystal structure.
- Analysis of intermolecular interactions, including hydrogen bonding and π-π stacking, was performed.
Main Results:
- The copper complex, [CuBr(C(6)H(4)NO(3))(H(2)O)](n), forms a one-dimensional coordination polymer with a layered structure.
- Intermolecular O-H⋯O and O-H⋯Br(-) hydrogen bonds, van der Waals forces, and π-π interactions between pyridine rings (centroid-centroid distance = 3.747(4) Å) stabilize the layers.
Conclusions:
- The title complex exhibits a robust layered supramolecular architecture.
- The interplay of hydrogen bonding and π-π stacking dictates the crystal packing and stability of this coordination polymer.
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