Copper(I) complexes bases on a new indazol-4,7-dione ligand
The synthesis of two new isomeric ligands, 1-(1-((2,6-diisopropylphenyl)imino)ethyl)-1H-benzo[f]indazole-4,9-dione (La) and 2-(1-((2,6-diisopropylphenyl)imino)ethyl)-2H-benzo[f]indazole-4,9-dione (Lb), and of their [Cu(I)(Lb)2] (ClO4) (1) homoleptic and [Cu(I)(Lb(PPh3)2] (ClO4) (2) heteroleptic copp...
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Published in: | Polyhedron Vol. 62; pp. 66 - 74 |
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Abstract | The synthesis of two new isomeric ligands, 1-(1-((2,6-diisopropylphenyl)imino)ethyl)-1H-benzo[f]indazole-4,9-dione (La) and 2-(1-((2,6-diisopropylphenyl)imino)ethyl)-2H-benzo[f]indazole-4,9-dione (Lb), and of their [Cu(I)(Lb)2] (ClO4) (1) homoleptic and [Cu(I)(Lb(PPh3)2] (ClO4) (2) heteroleptic copper(I) complex derivatives is reported. The chemical stability, and the spectroscopic and electrochemical properties of the complexes are discussed.
Two new isomeric ligands, 1-(1-((2,6-diisopropylphenyl)imino)ethyl)-1H-benzo[f]indazole-4,9-dione (La) and 2-(1-((2,6-diisopropylphenyl)imino)ethyl)-2H-benzo[f]indazole-4,9-dione (Lb), were synthesized and fully characterized as well the derivative copper complexes; [CuI(Lb)2] (ClO4) (1) homoleptic and [CuI(Lb(PPh3)2] (ClO4) (2) heteroleptic copper(I) complexes.
The X-ray diffraction shows an irregular tetrahedral coordination around of metal in both monometallic complexes with little differences in Cu–N distances and N–Cu–N bite angles than involved the indazole ligand between two complexes.
The proton spectra show a different variation in chemical shift relative to free ligand, which was discussed by steric and magnetic current effects of another coordinated ligand. The differences in the energy of metal-to ligand-charge-transfer (MLCT) and in redox potentials to CuII/CuI process in both complexes show the notorious influence of the phosphine which by back-donating effect, modified the energy of HOMO orbital centered in Cu atom. The coordinative and redox stability in solution was established for several days in non-coordinating solvent. However in acetonitrile the ligand substitution is very fast. |
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AbstractList | The synthesis of two new isomeric ligands, 1-(1-((2,6-diisopropylphenyl)imino)ethyl)-1H-benzo[f]indazole-4,9-dione (La) and 2-(1-((2,6-diisopropylphenyl)imino)ethyl)-2H-benzo[f]indazole-4,9-dione (Lb), and of their [Cu(I)(Lb)2] (ClO4) (1) homoleptic and [Cu(I)(Lb(PPh3)2] (ClO4) (2) heteroleptic copper(I) complex derivatives is reported. The chemical stability, and the spectroscopic and electrochemical properties of the complexes are discussed.
Two new isomeric ligands, 1-(1-((2,6-diisopropylphenyl)imino)ethyl)-1H-benzo[f]indazole-4,9-dione (La) and 2-(1-((2,6-diisopropylphenyl)imino)ethyl)-2H-benzo[f]indazole-4,9-dione (Lb), were synthesized and fully characterized as well the derivative copper complexes; [CuI(Lb)2] (ClO4) (1) homoleptic and [CuI(Lb(PPh3)2] (ClO4) (2) heteroleptic copper(I) complexes.
The X-ray diffraction shows an irregular tetrahedral coordination around of metal in both monometallic complexes with little differences in Cu–N distances and N–Cu–N bite angles than involved the indazole ligand between two complexes.
The proton spectra show a different variation in chemical shift relative to free ligand, which was discussed by steric and magnetic current effects of another coordinated ligand. The differences in the energy of metal-to ligand-charge-transfer (MLCT) and in redox potentials to CuII/CuI process in both complexes show the notorious influence of the phosphine which by back-donating effect, modified the energy of HOMO orbital centered in Cu atom. The coordinative and redox stability in solution was established for several days in non-coordinating solvent. However in acetonitrile the ligand substitution is very fast. |
Author | Escobar, Manuel A. Fröhlich, Roland Rojas, René S. Tapia, Ricardo A. Jara, Danilo H. Guerrero, Juan Lemus, Luis |
Author_xml | – sequence: 1 givenname: Manuel A. surname: Escobar fullname: Escobar, Manuel A. organization: Departamento de Química Inorgánica, Facultad de Química, Pontificia Universidad Católica de Chile, Casilla 306, Santiago-22, Chile – sequence: 2 givenname: Danilo H. surname: Jara fullname: Jara, Danilo H. organization: Facultad de Química y Biología, Universidad de Santiago de Chile, Av. Libertador Bernardo O’Higgins 3363, Estación Central, Casilla 40, Correo 33, Santiago, Chile – sequence: 3 givenname: Ricardo A. surname: Tapia fullname: Tapia, Ricardo A. organization: Departamento de Química Inorgánica, Facultad de Química, Pontificia Universidad Católica de Chile, Casilla 306, Santiago-22, Chile – sequence: 4 givenname: Luis surname: Lemus fullname: Lemus, Luis organization: Facultad de Química y Biología, Universidad de Santiago de Chile, Av. Libertador Bernardo O’Higgins 3363, Estación Central, Casilla 40, Correo 33, Santiago, Chile – sequence: 5 givenname: Roland surname: Fröhlich fullname: Fröhlich, Roland organization: Organisch-Chemisches Institut, Universität Münster, Corrensstrasse 40, 48149 Münster, Germany – sequence: 6 givenname: Juan surname: Guerrero fullname: Guerrero, Juan email: juan.guerrero@usach.cl organization: Facultad de Química y Biología, Universidad de Santiago de Chile, Av. Libertador Bernardo O’Higgins 3363, Estación Central, Casilla 40, Correo 33, Santiago, Chile – sequence: 7 givenname: René S. surname: Rojas fullname: Rojas, René S. email: rrojasg@uc.cl organization: Departamento de Química Inorgánica, Facultad de Química, Pontificia Universidad Católica de Chile, Casilla 306, Santiago-22, Chile |
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Keywords | Homoleptic copper(I) Heteroleptic copper(I) Copper(I) complex Indazol-4,7 dione |
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SubjectTerms | Copper(I) complex Heteroleptic copper(I) Homoleptic copper(I) Indazol-4,7 dione |
Title | Copper(I) complexes bases on a new indazol-4,7-dione ligand |
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