Copper(I) complexes bases on a new indazol-4,7-dione ligand
Two new isomeric ligands, 1-(1-((2,6-diisopropylphenyl)imino)ethyl)-1H-benzo[f]indazole-4,9-dione (L-a) and 2-(1-((2,6-diisopropylphenyl)imino)ethyl)-2H-benzo[f]indazole-4,9-dione (L-b), were synthesized and fully characterized as well the derivative copper complexes; [Cu-I(L-b)(2)] (ClO4) (1) homoleptic and [Cu-I(L-b(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 Cu-II/Cu-I 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. (c) 2013 Elsevier Ltd. All rights reserved.
|Título según WOS:||Copper(I) complexes bases on a new indazol-4,7-dione ligand|
|Título según SCOPUS:||Copper(I) complexes bases on a new indazol-4,7-dione ligand|
|Título de la Revista:||POLYHEDRON|
|Editorial:||PERGAMON-ELSEVIER SCIENCE LTD|
|Fecha de publicación:||2013|
|Página de inicio:||66|