Diverse copper(III) trifluoromethyl complexes with mono-, bi- and tridentate ligands and their versatile reactivity

作者：Zhang, Song-Lin^*; Xiao, Chang; Wan, Hai-Xing

来源：Dalton Transactions, 2018, 47(14): 4779-4784.

DOI：10.1039/c8dt00291f

• FLUOROFORM-DERIVED CUCF3
• OXIDATIVE TRIFLUOROMETHYLATION
• BORONIC ACIDS
• CATALYZED TRIFLUOROMETHYLATION
• REDUCTIVE ELIMINATION
• ARYLBORONIC ACIDS
• ALKYNES
• FLUORINE
• REAGENT
• PERFLUOROALKYLATION

Cu(iii) trifluoromethyl complexes are proposed as essential intermediates for many copper-promoted trifluoromethylation reactions, but remain elusive and scarcely explored. We report herein the isolation and spectroscopic and X-ray crystallographic characterization of diverse Cu-III-CF3 complexes (6-10) with varied coordinating motifs (mono-, bi- or tridentate) and formal charges (neutral or monoanionic) for the ligand L (L is pyridine, 2,4,6-trimethylpyridine, quinol-8-yloxide or 2,6-bis(2-pyridyl)pyridine). Square planar complexes 6, 7 and 9 show rapid dynamic behavior in solution possibly due to the weak Cu-CF3 bonds that can quickly dissociate and recombine with the CF3 radical. In contrast, 10, with octahedral geometry, is more rigid. Reactivity studies show that except for ion-pair complex 8, they are highly reactive for the trifluoromethylation of arylboronic acids and the C-H bond of terminal alkynes. Furthermore, syn-fluoro- and -oxy-trifluoromethylation across the triple bond of alkynes can be achieved using 6 and CsF or NaOPh. These results greatly expand the scope of isolated and well-characterized Cu(iii)-CF3 complexes, and establish their versatile reactivity that may be widely involved in copper-mediated trifluoromethylation reactions, thus substantiating the essential yet undeveloped aspects of trifluoromethylation chemistry.

• 出版日期2018-4-14
• 单位江南大学