Room Temperature Stable Organocuprate Copper(III) Complex

被引:32
作者
Hannigan, Steven F. [1 ]
Lum, June S. [1 ]
Bacon, Jeffrey W. [1 ]
Moore, Curtis [2 ]
Golen, James A. [2 ]
Rheingold, Arnold L. [2 ]
Doerrer, Linda H. [1 ]
机构
[1] Boston Univ, Dept Chem, Boston, MA 02215 USA
[2] Univ Calif San Diego, Dept Chem & Biochem, La Jolla, CA 92093 USA
基金
美国国家科学基金会;
关键词
RAPID INJECTION NMR; C-H ACTIVATION; REDUCTIVE ELIMINATION; BOND FORMATION; LIGAND; CRYSTAL; 10-SI-5; FUNCTIONALIZATIONS; AZACALIXAROMATICS; SUSCEPTIBILITY;
D O I
10.1021/om4000538
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The paramagnetic trigonal-planar copper complexes {K(18C6)}[Cu-II(OC(CH3)(CF3)(2))(3)] (2) and K[Cu-II(OC(C6H5)(CF3)(2))(3)] (3) have been prepared and characterized, including X-ray crystallography, in 61% and 3% yields, respectively. The latter complex does not form preferentially, because CuBr2 and KOC(C6H5)(CF3)(2))(3) also form the diamagnetic complexes {K(18C6)}[K-2{Cu-I(OC(C6H5)(CF3)(2))(2)}(3)] (4) and {K(18C6)}[Cu-III(OC(C6H4)(CF3)(2))(2)] (5) These species were characterized by X-ray crystallography, UV-vis spectroscopy, H-1, C-13{H-1}, and F-19{H-1} NMR spectroscopy, and elemental analysis. The unique organocuprate Cu(III) species with {O2C2} coordination was formed by ortho metalation of two phenyl rings, resulting in trans-{O2C2} coordination of Cu(III), and is stable at room temperature in the solid state and in dark solutions of THF.
引用
收藏
页码:3429 / 3436
页数:8
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