1028464-68-7Relevant articles and documents
Biomimetic alkene epoxidation and alkane hydroxylation with sodium periodate catalyzed by Mn(III)-salen supported on amberlite IRA-200
Mirkhani, Valiollah,Moghadam, Majid,Tangestaninejad, Shahram,Bahramian, Bahram
, p. 1303 - 1308 (2007)
The Mn(III)-salen, containing phosphonium groups at the 5,5′-positions of the salen ligand supported on Amberlite IRA-200 via electrostatic binding was used for the oxidation of alkenes and alkanes with sodium periodate at room temperature in the presence of imidazoles as axial ligands, and the effect of solvent, different axial ligands, and various oxygen donors was investigated. This heterogenized catalyst shows high catalytic activity in alkene epoxidation and alkane hydroxylation. It showed high selectivity in the epoxidation of stilbenes, α-pinene, and (R)-(+)-limonene, and exhibits a particular ability to epoxidize linear alkenes. The stability and reusability of this new heterogenized metallo-salen complex was also investigated. The catalyst was characterized by FTIR, UV-Vis, SEM, and thermal analysis.
Synthesis and characterization of supported heteropolymolybdate nanoparticles between silicate layers of Bentonite with enhanced catalytic activity for epoxidation of alkenes
Salavati, Hossein,Rasouli, Nahid
, p. 1853 - 1859 (2011)
A new heterogeneous catalyst (PVMo/Bentonite) consisting of vanadium substituted heteropolymolybdate with Keggin-type structure Na 5[PV2Mo10O40]·14H 2O (PVMo) supported between silicate layers of bentonite has been synthesized by impregnation method and characterized using X-ray diffraction, Fourier-transformed infrared spectroscopy, scanning electron microscopy, UV-vis diffuse reflectance spectroscopy, transmission electron microscopy and elemental analysis. X-ray diffraction and scanning electron microscopy analysis indicated that PVMo was finely dispersed into layers of bentonite as support. The PVMo/Bentonite used as an efficient heterogeneous catalyst for epoxidation of alkenes. Various cyclic and linear alkenes were oxidized into the corresponding epoxides in high yields and selectivity with 30% aqueous H2O 2. The catalyst was reused several times, without observable loss of activity and selectivity. The obtained results showed that the catalytic activity of the PVMo/Bentonite was higher than that of pure heteropolyanion (PVMo).
Sonocatalytic epoxidation of alkenes by vanadium-containing polyphosphomolybdate immobilized on multi-wall carbon nanotubes
Salavati, Hossein,Tangestaninejad, Shahram,Moghadam, Majid,Mirkhani, Valiollah,Mohammadpoor-Baltork, Iraj
, p. 453 - 459 (2010)
A Keggin type polyoxometalate (POM) has been immobilized in the unique network structure of multi-wall carbon nanotubes (CNTs). The vanadium-containing polyphosphomolybdate (PVMo) supported on CNTs, which was prepared by a one-step solid-state reaction, was characterized by FT-IR, XRD, SEM and elemental analyses. These uniform nanoparticles have an average size 20-30 nm. Furthermore, due to the chemical interaction between PVMo and carboxylic acid groups, PVMo nanoparticles were successfully immobilized on the CNTs. Moreover, the obtained composite was found as an efficient catalyst for oxidation of hydrocarbons under reflux and ultrasonic irradiation (US) conditions.
Development of rapid and selective epoxidation of α-pinene using single-step addition of H2O2in an organic solvent-free process
Eze, Valentine C.,Harvey, Adam P.,López Fernández, Ana María,Mukhtar Gunam Resul, Mohamad Faiz,Rehman, Abdul
, p. 33027 - 33035 (2021/12/07)
This study reports substantial improvement in the process for oxidising α-pinene, using environmentally friendly H2O2 at high atom economy (～93%) and selectivity to α-pinene oxide (100%). The epoxidation of α-pinene with H2O2 was catalysed by tungsten-based polyoxometalates without any solvent. The variables in the screening parameters were temperatures (30-70 °C), oxidant amount (100-200 mol%), acid concentrations (0.02-0.09 M) and solvent types (i.e., 1,2-dichloroethane, toluene, p-cymene and acetonitrile). Screening the process parameters revealed that almost 100% selective epoxidation of α-pinene to α-pinene oxide was possible with negligible side product formation within a short reaction time (～20 min), using process conditions of a 50 °C temperature in the absence of solvent and α-pinene/H2O2/catalyst molar ratio of 5?:?1?:?0.01. A kinetic investigation showed that the reaction was first-order for α-pinene and catalyst concentration, and a fractional order (～0.5) for H2O2 concentration. The activation energy (Ea) for the epoxidation of α-pinene was ～35 kJ mol-1. The advantages of the epoxidation reported here are that the reaction could be performed isothermally in an organic solvent-free environment to enhance the reaction rate, achieving nearly 100% selectivity to α-pinene oxide.
