Copper(I)-Arene Complexes with a Sterically Hindered Tris(pyrazolyl)borate Ligand

被引:2
|
作者
Alvarez, Maria [1 ,2 ]
Urbano, Juan [1 ,2 ]
Fructos, Manuel R. [1 ,2 ]
Alvarez, Eleuterio [3 ]
Perez, Pedro J. [1 ,2 ]
机构
[1] Univ Huelva, CIQSO Ctr Invest Quim Sostenible, Unidad Asociada CSIC, Lab Catalisis Homogenea, Campus El Carmen, Huelva 21007, Spain
[2] Univ Huelva, Dept Quim, Campus El Carmen, Huelva 21007, Spain
[3] Ctr Invest Isla Cartuja, Inst Invest Quim, Avda Americo Vespucio 49, Seville 41092, Spain
关键词
Copper; Arene ligands; Hindered tris(pyrazolyl)borate ligands; Aromatic interactions; Homogeneous catalysis; STRUCTURAL-CHARACTERIZATION; ETHYL DIAZOACETATE; COPPER; CHEMISTRY; CATALYSTS; FUNCTIONALIZATION; HOMOSCORPIONATE; REACTIVITY; OLEFINS; SILVER;
D O I
10.1002/ejic.201800176
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A series of arene copper(I) complexes bearing the hydrotris(3-mesitylpyrazolyl)borate ligand (Tp(Ms)) of general formula Tp(Ms)Cu(arene) (arene = toluene, 1; nitrobenzene, 2; chlorobenzene, 3; and iodobenzene, 4) has been structurally characterized. Complexes 1-3 show a (2)-arene coordination mode to the copper center, whereas the iodobenzene ligand in 4 is coordinated to Cu by the iodine atom. In the absence of excess arene, these compounds undergo arene loss and formation of the dinuclear complex [Tp(Ms)Cu](2) (5), which has also been structurally characterized. Given the number of catalytic systems described in which the Tp(x)Cu core plays the main role, the observation of these adducts assesses their presence in those catalytic systems, a feature not described to date.
引用
收藏
页码:2026 / 2030
页数:5
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