Rh nanoparticles stabilized by PEG-substituted triphenyl-phosphine（PETPP,P[C6H4-p-（OCH2CH2）nOH]3） combining double stabilization effects demonstrated high activity and good recyclability in aqueous biphasic hydrog...Rh nanoparticles stabilized by PEG-substituted triphenyl-phosphine（PETPP,P[C6H4-p-（OCH2CH2）nOH]3） combining double stabilization effects demonstrated high activity and good recyclability in aqueous biphasic hydrogenation of benzene.The value of turnover frequency（TOF） was 3333 h^-1.Furthermore,the rhodium nanoparticle catalyst could be easily recycled for five times without loss in activity.展开更多
The complex [Rh（CO）（Pz）（TPPMS）]2, （TPPMS = m-sulfonatophenyl-diphenylphosphine, Pz = Pirazolate） was evaluated as a catalyst precursor in the hydroformylation of allylbenzenes （eugenol and estragol） and terp...The complex [Rh（CO）（Pz）（TPPMS）]2, （TPPMS = m-sulfonatophenyl-diphenylphosphine, Pz = Pirazolate） was evaluated as a catalyst precursor in the hydroformylation of allylbenzenes （eugenol and estragol） and terpenes （limonene and myrcene） and in the hydrogenation of α,β-unsaturated aldehydes （crotonaldehyde, cinnamaldehyde and citral） in a biphasic medium toluene/ionic liquid. Under the reaction conditions studied （P = 600 psi, T= 95 ℃, S/C = 300：1）, the rhodium system showed a high activity and selectivity towards the desired aldehydes. The catalytic phase could be recycled up to five times without any evident loss of activity or selectivity.展开更多
THE oxidative dehydrogenation of propane （ODP） to propene is one of the potentially important catalytic processes for the effective utilization of light alkanes. The VMgO catalysts which have better catalytic perfor...THE oxidative dehydrogenation of propane （ODP） to propene is one of the potentially important catalytic processes for the effective utilization of light alkanes. The VMgO catalysts which have better catalytic performances for the reaction have aroused much interest and argument.Kung et al. proposed that the active phase was magnesium orthovanadate （Mg<sub>3</sub>V<sub>2</sub>O<sub>8</sub>）, but Volta et al. suggested that magnesium pyrovanadate （α-Mg<sub>2</sub>V<sub>2</sub>O<sub>7</sub>） was the active phase; in this phase, V<sup>4+</sup> ions which are associated to the formation of oxygen vacancies could stably exist, and Mg<sub>3</sub>V<sub>2</sub>O<sub>8</sub> is responsible for the total oxidation due to nonexistence of V<sup>4+</sup> ions.展开更多
基金support from the National Natural Science Foundation of China(No.20573015)the Program for New Century Excellent Talents in University(No.NCET-07-0138)the Science and Technology Project in Universities from the Education Department of Liaoning Province(No.2008T233)
文摘Rh nanoparticles stabilized by PEG-substituted triphenyl-phosphine（PETPP,P[C6H4-p-（OCH2CH2）nOH]3） combining double stabilization effects demonstrated high activity and good recyclability in aqueous biphasic hydrogenation of benzene.The value of turnover frequency（TOF） was 3333 h^-1.Furthermore,the rhodium nanoparticle catalyst could be easily recycled for five times without loss in activity.
文摘The complex [Rh（CO）（Pz）（TPPMS）]2, （TPPMS = m-sulfonatophenyl-diphenylphosphine, Pz = Pirazolate） was evaluated as a catalyst precursor in the hydroformylation of allylbenzenes （eugenol and estragol） and terpenes （limonene and myrcene） and in the hydrogenation of α,β-unsaturated aldehydes （crotonaldehyde, cinnamaldehyde and citral） in a biphasic medium toluene/ionic liquid. Under the reaction conditions studied （P = 600 psi, T= 95 ℃, S/C = 300：1）, the rhodium system showed a high activity and selectivity towards the desired aldehydes. The catalytic phase could be recycled up to five times without any evident loss of activity or selectivity.
文摘THE oxidative dehydrogenation of propane （ODP） to propene is one of the potentially important catalytic processes for the effective utilization of light alkanes. The VMgO catalysts which have better catalytic performances for the reaction have aroused much interest and argument.Kung et al. proposed that the active phase was magnesium orthovanadate （Mg<sub>3</sub>V<sub>2</sub>O<sub>8</sub>）, but Volta et al. suggested that magnesium pyrovanadate （α-Mg<sub>2</sub>V<sub>2</sub>O<sub>7</sub>） was the active phase; in this phase, V<sup>4+</sup> ions which are associated to the formation of oxygen vacancies could stably exist, and Mg<sub>3</sub>V<sub>2</sub>O<sub>8</sub> is responsible for the total oxidation due to nonexistence of V<sup>4+</sup> ions.
