Abstract
The search for efficient, active and universal catalyst systems for transition-metal catalyzed cross-coupling reactions, continues to be of interest to researchers world-wide. Herein, we report two new Pd(II) complexes, effortlessly prepared from N,N-dialkylamino-phosphines for Suzuki-Miyaura cross-coupling reactions. These sufficiently hindered (% VBur=30.0–31.5 %) and electron rich (vCO=1947.41–1946.29 cm−1) aminophosphines formed active catalysts for Suzuki-Miyaura coupling of aryl bromides and chlorides.
Original language | English |
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Pages (from-to) | 2578-2582 |
Number of pages | 5 |
Journal | European Journal of Inorganic Chemistry |
Volume | 2021 |
Issue number | 26 |
DOIs | |
Publication status | Published - 15 Jul 2021 |
Keywords
- Aminophosphines
- Biaryl
- Cross-coupling
- Ligand parameters
- Suzuki-Miyaura
ASJC Scopus subject areas
- Inorganic Chemistry