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![[(DPEPhos)(bcp)Cu]PF6: A General and Broadly Applicable Copper-Based Photoredox Catalyst](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F59739.jpg&w=3840&q=50)
[(DPEPhos)(bcp)Cu]PF6: A General and Broadly Applicable Copper-Based Photoredox Catalyst
Published on: May 21, 2019
trans-Dichloridotetrakis(3,5-dimethylpyridine)copper(II)
Daniel P Martone1, Andrew W Maverick, Frank R Fronczek
1Department of Chemistry, Louisiana State University, Baton Rouge, LA 70803-1804, USA.
This study details the crystal structure of a copper(II) chloride complex with 3,5-lutidine ligands. The compound exhibits high crystallographic symmetry, similar to its nickel and cobalt counterparts.
Area of Science:
- Inorganic chemistry
- Crystallography
- Coordination chemistry
Background:
- The structural characterization of metal halide complexes provides insight into coordination geometries and bonding.
- Investigating isomorphous compounds aids in understanding trends in crystal packing and symmetry.
Purpose of the Study:
- To determine the precise crystal structure of the title compound, [CuCl2(C7H9N)4].
- To compare the crystallographic properties of the copper complex with its known nickel and cobalt analogues.
Main Methods:
- Single-crystal X-ray diffraction analysis was employed to elucidate the molecular and crystal structure.
- The crystal structure was solved and refined in the P4/nnc space group.
Main Results:
- The title compound, [CuCl2(C7H9N)4], crystallizes in the P4/nnc space group with D(4) symmetry.
- The copper and chlorine atoms are situated on a fourfold axis, while the 3,5-lutidine ligands occupy twofold axes.
- Key bond distances were determined: Cu-Cl at 2.7649 (7) Å and Cu-N at 2.0510 (12) Å.
- The space group for the cobalt analogue was revised to P4/nnc, confirming isomorphism.
Conclusions:
- The copper(II) chloride complex with 3,5-lutidine demonstrates high symmetry, consistent with isomorphous Ni and Co analogues.
- The structural data provides valuable information for understanding the coordination environment and packing in this series of metal complexes.
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