| Title | Direct observation of Cu-I/Cu-III redox steps relevant to Ullmann-type coupling reactions |
| Publication Type | Journal Article |
| Year of Publication | 2010 |
| Authors | Casitas, A, King, AE, Parella, T, Costas, M, Stahl, SS, Ribas, X |
| Journal | Chemical Science |
| Volume | 1 |
| Pagination | 326-330 |
| Date Published | Sep |
| Accession Number | ISI:000281374100006 |
| Keywords | activation, Aryl halides, bond, catalyzed amination, Complexes, copper(iii) intermediate, formation, ligands, nitrogen, substitution, triarylamines |
| Abstract | A series of aryl-copper(III)-halide complexes have been synthesized and characterized by NMR and UV-visible spectroscopy, cyclic voltammetry and X-ray crystallography. These complexes closely resemble elusive intermediates often invoked in catalytic reactions, such as Ullmann-Goldberg cross-coupling reactions, and their preparation has enabled direct observation and preliminary characterization of aryl halide reductive elimination from Cu-III and oxidative addition to Cu-I centers. In situ spectroscopic studies (H-1 NMR, UV-visible) of a Cu-catalyzed C-N coupling reaction provides definitive evidence for the involvement of an aryl-copper(III)-halide intermediate in the catalytic mechanism. These results provide the first direct observation of the Cu-I/Cu-III redox steps relevant to Ullmann-type coupling reactions. |