1629-60-3Relevant articles and documents
New perspectives on polyoxometalate catalysts: Alcohol oxidation with Zn/Sb-polyoxotungstates
Ni, Lubin,Patzke, Greta R.,Patscheider, Joerg,Baldridge, Kim K.
, p. 13293 - 13298,6 (2012)
Catalytic belts are the crucial feature of Zn/Sb-polyoxometalates as efficient and selective catalysts for alcohol oxidation. Comprehensive theoretical, analytical, and catalytic studies identify the active role of the Sb atom in the polyoxometalate metal belt. This sheds new light on low-cost catalyst tuning strategies for crucial oxidative transformations.
Chromium-Catalyzed Production of Diols From Olefins
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Paragraph 0111, (2021/03/19)
Processes for converting an olefin reactant into a diol compound are disclosed, and these processes include the steps of contacting the olefin reactant and a supported chromium catalyst comprising chromium in a hexavalent oxidation state to reduce at least a portion of the supported chromium catalyst to form a reduced chromium catalyst, and hydrolyzing the reduced chromium catalyst to form a reaction product comprising the diol compound. While being contacted, the olefin reactant and the supported chromium catalyst can be irradiated with a light beam at a wavelength in the UV-visible spectrum. Optionally, these processes can further comprise a step of calcining at least a portion of the reduced chromium catalyst to regenerate the supported chromium catalyst.
A carboxylate-bridged Mn(II) compound with 6-methylanthranilate/bipy: oxidation of alcohols/alkenes and catalase-like activity
Kilic, Yalcin,Bolat, Serkan,Kani, Ibrahim
, p. 2293 - 2303 (2018/05/14)
A novel manganese compound, [Mn2(μ1,3-6-CH3-2-NH2C6H4COO)2(bipy)4](ClO4)2 (bipy?=?2,2′-bipyridine), was synthesized and used as a catalyst precursor in the oxidation of alkenes and primary alcohols to corresponding aldehydes, ketones, and acids. The six-coordinate compound has a binuclear structure in which two Mn(II) ions adopt a syn-anti μ1,3-bridging mode with two carboxylate groups and two chelated bipy ligands. The compound exhibits good activity in the oxidation of cyclohexene to 2-cyclohexene-1-one as the major product (93% conv. in 3?h, 79.3% selectivity) and of cinnamyl alcohol to cinnamaldehyde as the major product with 46% selectivity (100% conv. in 1.5?h) with tert-butyl hydroperoxide (TBHP) in acetonitrile at 70?°C. Furthermore, the catalase-like activity of the compound was studied in different solvents (acetonitrile, methanol, Tris-HCl buffer; TOF?=?29,910?h?1 in Tris-HCl buffer).
Fe3O4 magnetic nanoparticles (MNPs) as an efficient catalyst for selective oxidation of benzylic and allylic C-H bonds to carbonyl compounds with tert-butyl hydroperoxide
Zarghani, Monireh,Akhlaghinia, Batool
, p. 38592 - 38601 (2016/05/24)
Fe3O4 magnetic nanoparticles (MNPs) were prepared by a co-precipitation method with oleic acid as a surfactant and characterized by FT-IR, TEM, DLS, XRD, VSM techniques. XRD, DLS and TEM analysis of this catalyst clearly showed the formation of cubic structure Fe3O4 MNPs, with a mean size of 16 nm. Moreover, a magnetization measurement revealed that the Fe3O4 MNPs had superparamagnetic behaviour and the saturation magnetization of the catalyst was 54.6 emu g-1. The Fe3O4 MNPs in combination with tert-butyl hydroperoxide catalyzed the oxidation of various benzylic and allylic C-H bonds to the corresponding carbonyl compounds in excellent yields. These oxidation reactions were effectively and economically performed under mild conditions, and therefore the dual challenge of cost effectiveness and benign nature of the processes was met.
