Synthesis and X-ray crystal structure of the copper(I) dicarboxylic acid complex [Cu(η1-bdoaH)(PPh3)3] (bdoaH2 = benzene-1,2- dioxyacetic acid)
Autor: | Michael Devereux, James F. Cronin, Malachy McCann, Maire A. Convery, Valerie Quillet, Christine J. Cardin |
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Rok vydání: | 1994 |
Předmět: |
chemistry.chemical_classification
Ligand Inorganic chemistry chemistry.chemical_element Crystal structure Copper Inorganic Chemistry chemistry.chemical_compound Crystallography Dicarboxylic acid chemistry Materials Chemistry Molecule Carboxylate Physical and Theoretical Chemistry Triphenylphosphine Acetonitrile |
Zdroj: | Polyhedron. 13:2359-2366 |
ISSN: | 0277-5387 |
DOI: | 10.1016/s0277-5387(00)88148-6 |
Popis: | The copper(II) complex [Cu(bdoa)(H2O)2] (bdoaH2 = benzene-1,2-dioxyacetic acid) reacts with triphenylphosphine (1:4 mol ratio) to give the colourless copper(I) complex [Cu(η1-bdoaH)(PPh3)3] (1) in good yield. The X-ray crystal structure of the complex shows the copper atom at the centre of a distorted tetrahedron, and is ligated by the phosphorus atoms of the three triphenylphosphines and one carboxylate oxygen atom of the bdoaH− ligand. Significant intermolecular hydrogen-bonding exists between the pendant carboxylate OH function of one molecule and the uncoordinated “ketonic” oxygen of a neighbouring molecule. Complex 1 is non-conducting in chloroform but ionizes readily in acetonitrile. The cyclic voltammogram of an acetonitrile solution of 1 shows a single irreversible anodic peak for the oxidation of the PPh3 ligands and the copper(I) centre, and a single irreversible cathodic peak for the reduction of the bdoaH− ion. IR and mass spectral data for 1 are given. |
Databáze: | OpenAIRE |
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