Synthesis, Structural Characterization, and Catalytic Activity of IPrNi(styrene)2 in the Amination of Aryl Tosylates

被引:65
作者
Jose Iglesias, Maria [1 ]
Blandez, Juan F. [2 ]
Fructos, Manuel R. [1 ]
Prieto, Auxiliadora [3 ]
Alvarez, Eleuterio [4 ]
Belderrain, Tomas R. [1 ]
Carmen Nicasio, M. [2 ]
机构
[1] Univ Huelva, Lab Catalisis Homogenea, Dept Quim & Ciencias Mat, Unidad Asociada CSIC,Ctr Invest Quim Sostenible C, Huelva 21007, Spain
[2] Univ Seville, Dept Quim Inorgan, Seville 41071, Spain
[3] Univ Huelva, Dept Ingn Quim Quim Fis & Quim Organ, Huelva 21007, Spain
[4] Univ Seville, CSIC, Inst Invest Quim, Seville 41092, Spain
关键词
CROSS-COUPLING REACTIONS; N-HETEROCYCLIC CARBENES; C BOND FORMATION; ROOM-TEMPERATURE; BIARYL CONSTRUCTION; COMPLEXES; NHC; ACTIVATION; PALLADIUM; LIGANDS;
D O I
10.1021/om300566m
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A novel bis-styrene IPrNi0 derivative has been synthesized from the reaction of Ni(COD)(2) and free 1,3-bis(2,6-diisopropylphenyl)imidazolidene (IPr) ligand in the presence of styrene. The complex has been characterized by spectroscopic data as well as by X-ray crystallography. Its catalytic performance in the amination reaction of aryl tosylates is also reported. The catalytic reactions proceed in a very selective manner, affording moderate to high yields of cross-coupling products in short reaction times at 110 degrees C.
引用
收藏
页码:6312 / 6316
页数:5
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