Aerobic intramolecular carbon-hydrogen bond oxidation promoted by Cu(I) complexes

被引:9
|
作者
Alvarez, Maria [1 ,2 ]
Molina, Francisco [1 ,2 ]
Fructos, Manuel R. [1 ,2 ]
Urbano, Juan [2 ]
Alvarez, Eleuterio [3 ]
Sodupe, Mariona [4 ]
Lledos, Agusti [4 ]
Perez, Pedro J. [1 ,2 ]
机构
[1] Univ Huelva, Lab Catalisis Homogenea, Unidad Asociada CSIC CIQSO Ctr Invest Quim Sosten, Huelva 21007, Spain
[2] Univ Huelva, Dept Quim, Huelva 21007, Spain
[3] Ctr Invest Isla Cartuja, Inst Invest Quim, Avda Americo Vespucio 49, Seville 41092, Spain
[4] Univ Autonoma Barcelona, Dept Quim, E-08193 Barcelona, Spain
关键词
C-H; COPPER; REACTIVITY; DIOXYGEN; MONOOXYGENASE; ACTIVATION; MODEL; BINUCLEAR; PROTEINS; METHYL;
D O I
10.1039/d0dt03198d
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The oxidation of C-H bonds by copper centres in enzymes with molecular oxygen takes place in nature under ambient conditions. Herein we report a similar transformation in which under ambient pressure and temperature (1 atm, 25 degrees C) the complex Tp(Ms)Cu(THF) (Tp(Ms) = hydrotris(3-mesityl-pyrazol-1-yl)borate) undergoes the intramolecular oxidation of an alkylic C-H bond with O-2, leading to the formation of a tri-nuclear compound where alkoxy and hydroxyl ligands are bonded to the copper centres, as inferred from X-ray studies. The presence of adventitious Cu(0) derived from the partial decomposition of initial Tp(Ms)Cu (THF) facilitates the formation of such a trinuclear compound. DFT studies support the reaction taking place through a Cu(III) alkoxy-hydroxyl copper intermediate.
引用
收藏
页码:14647 / 14655
页数:9
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