1759-64-4Relevant articles and documents
Siegel et al.
, p. 2802,2803, 2806 (1966)
Ionic-liquid-like copolymer stabilized nanocatalysts in ionic liquids: II. Rhodium-catalyzed hydrogenation of arenes
Zhao, Chen,Wang, Han-zhi,Yan, Ning,Xiao, Chao-xian,Mu, Xin-dong,Dyson, Paul J.,Kou, Yuan
, p. 33 - 40 (2008/09/18)
Rhodium nanoparticles stabilized by the ionic-liquid-like copolymer poly[(N-vinyl-2-pyrrolidone)-co-(1-vinyl-3-butylimidazolium chloride)] were used to catalyze the hydrogenation of benzene and other arenes in ILs. The nanoparticle catalysts can endure forcing conditions (75 °C, 40 bar H2), resulting in high reaction rates and high conversions compared with other nanoparticles that operate in ILs. The hydrogenation of benzene attained record total turnovers of 20,000, and the products were easily separated without being contaminated by the catalysts. Other substrates, including alkyl-substituted arenes, phenol, 4-n-propylphenol, 4-methoxylphenol, and phenyl-methanol, were studied and in most cases were found to afford partially hydrogenated products in addition to cyclohexanes. In-depth investigations on reaction optimization, including characterization of copolymers, transmission electron microscopy, and an infrared spectroscopic study of nanocatalysts, were also undertaken.
Catalytic hydrohydrazination of a wide range of alkenes with a simple Mn complex
Waser, Jerome,Carreira, Erick M.
, p. 4099 - 4102 (2007/10/03)
Enhanced activity, lower catalyst loading, shorter reaction times, and expanded substrate scope are the advantages of [Mn(dpm)3] over Co catalysts in the hydrohydrazination reaction of alkenes (see scheme). Thus, sterically hindered alkenes, including tetrasubstituted alkenes, can now also readily undergo this reaction.