首页 | 本学科首页   官方微博 | 高级检索  
     检索      


Amination and Suzuki coupling reactions catalyzed by palladium complexes coordinated by cobalt-containing monodentate phosphine ligands with bis-trifluoromethyl substituents on bridged arylethynyl: Observation of some unusual metal-containing compounds
Authors:Po-Cheng Huang
Institution:Department of Chemistry, National Chung Hsing University, 250 Kuo-Kuang Road, Taichung 40227, Taiwan
Abstract:Two cobalt-containing bulky monodentate phosphines {(μ-PPh2CH2PPh2)Co2(CO)4](μ,η-(tBu)2PCtriple bond; length of mdashCAr]} (4cm: Ar = 3-CF3C6H4; 4cmm: Ar = 3,5-(CF3)2C6H3) were prepared from the reaction of Co2(CO)6(μ-PPh2CH2PPh2) (3) with each corresponding alkynes (tBu)2PCtriple bond; length of mdashCAr. Both compounds were converted to their oxidized forms {(μ-PPh2CH2PPh2)Co2(CO)4](μ,η-(tBu)2P(double bond; length as m-dashO)Ctriple bond; length of mdashCAr]} (4cmO: Ar = 3-CF3C6H3; 4cmmO: Ar = 3,5-(CF3)2C6H3) in the presence of oxide. Further reactions of 4cm and 4cmm with Pd(OAc)2 gave palladium complexes {(μ-PPh2CH2PPh2)Co2(CO)4](μ,η-(tBu)2PCtriple bond; length of mdashC(Ar)-κC1)]Pd(μ-OAc)} 5cm (Ar = 3-CF3C6H3) and 5cmm (Ar = 3,5-(CF3)2C6H2), respectively. By contrast, reactions of 4cm and 4cmm with Pd(COD)Cl2 gave products, {μ-P,P-PPh2CH2PPh2}Co2(CO)3(μ-CO){μ,η-(tBu)2PCtriple bond; length of mdashCAr}]-PdCl2] 8cm and 8cmm, respectively, with unique bonding modes. Several crystallines of (4cm)2Pd3(μ-Cl)(μ-CO)2)(μ-Cl)]2 (9) were obtained along with crystallines of 8cm during the crystallization process. The crystal structures of all three compounds, 4cmmO, 8cmm and 9 were determined by single-crystal X-ray diffraction methods. Fair to excellent efficiencies were observed for employing 4cmm/palladium salt as catalytic precursor in amination as well as in Suzuki coupling reactions.
Keywords:Suzuki-Miyaura cross-coupling reaction  Amination reaction  Phosphine ligand  Electron-withdrawing substituent  Palladium-cobalt bond  Palladium cluster
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号