0000000000873688

AUTHOR

Karl Kadish

showing 3 related works from this author

Cobalt Corroles with Bis‐Ammonia or Mono‐DMSO Axial Ligands. Electrochemical, Spectroscopic Characterizations and Ligand Binding Properties

2018

International audience; Four bis-ammonia ligated cobalt corroles and four mono-DMSO ligated cobalt corroles with different mesoaryl substituents on the macrocycle (A 2 Band A 3-corroles) were synthesized and investigated as to their electrochemical and spec-troscopic properties under different solution conditions. The complexation energies of the investigated cobalt corroles were theoretically calculated to illustrate the propensity of the cobalt center for pentacoordination or hexa-coordination with various axial ligands (DMSO, CO, py and NH 3). The structure of one hexacoordinate bis-NH 3 cobalt corrole complex was also determined by X-ray diffraction.

chemistry.chemical_classification010405 organic chemistrychemistry.chemical_element010402 general chemistryElectrochemistry01 natural sciences0104 chemical sciencesCoordination complexInorganic ChemistryAmmoniachemistry.chemical_compoundchemistry[CHIM.ANAL]Chemical Sciences/Analytical chemistryPolymer chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistryCobaltEuropean Journal of Inorganic Chemistry
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Insights into the crystal packing of phosphorylporphyrins based on the topology of their intermolecular interaction energies

2014

Four metal complexes of 5,15-bis(diethoxyphosphoryl)-10,20-diphenylporphyrin 1M (M = Cd(II), Ni(II), Pd(II), and Pt(II)) were synthesized and crystallographically characterized. The crystal organization patterns were analyzed using DFT (B97-D3/def2-SVP) calculations of the intermolecular interaction energies between complexes in the crystals. For the systematic analysis of crystal packing, the calculations were extended to previously reported compounds 1M (M = H2, Cu(II), and Zn(II)). Quantitative analysis of the interaction energies shows the essential role of weak intermolecular interactions, such as C-H⋯O, C-H⋯π and M⋯π, in the formation of basic structural motifs and their organization …

010405 organic chemistryIntermolecular forceGeneral Chemistry010402 general chemistryCondensed Matter Physics01 natural sciencesPorphyrin0104 chemical sciencesCrystalMetalchemistry.chemical_compoundCrystallographychemistryPolymorphism (materials science)Intermolecular interactionvisual_artvisual_art.visual_art_medium[CHIM]Chemical SciencesGeneral Materials ScienceComputingMilieux_MISCELLANEOUS
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Structural and Electrochemical Studies of Copper(I) Complexes with Diethoxyphosphoryl-1,10-phenanthrolines

2014

Two series of copper(I) complexes with diethoxyphosphoryl-substituted 1,10-phenanthroline ligands were synthesized and characterized in the solid state and in solution. The first comprised mixed-ligand CuI complexes with phenanthroline and triphenylphosphine. The second series includes bis-chelates with two phenanthroline ligands. According to the X-ray data for the six complexes, the ditopic phenanthroline ligands exhibit bidentate coordination to the copper(I) atom through two nitrogen atoms in both series. Solution equilibria involving different phenanthroline copper(I) species were studied by 1H and 31P NMR spectroscopy, electrochemistry, and spectroelectrochemistry. The solution specia…

Coordination sphereDenticityLigandPhenanthrolineInorganic chemistrySubstituentchemistry.chemical_elementCopperInorganic Chemistrychemistry.chemical_compoundchemistryPolymer chemistry[CHIM]Chemical SciencesSolvent effectsTriphenylphosphineComputingMilieux_MISCELLANEOUS
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