2009
DOI: 10.1016/j.catcom.2008.12.059
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Tungstophosphoric acid (H3PW12O40) catalyzed oxidation of organic compounds with NaBrO3

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Cited by 29 publications
(10 citation statements)
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“…In (2)(3)(4)(5)(6)(7)(8)(9)(10)(11)(12) aqueous solution and different organic reagents. Soaking in the same volume of aqueous solution with pH range between 2-12 for 24 hours, as shown in Figure 3a, 3c, 3e, the PXRD peaks of the three compounds have no significant changes indicated that the three compounds were stable between the pH range of 2-12.…”
Section: Chemical Stability Studiesmentioning
confidence: 99%
See 1 more Smart Citation
“…In (2)(3)(4)(5)(6)(7)(8)(9)(10)(11)(12) aqueous solution and different organic reagents. Soaking in the same volume of aqueous solution with pH range between 2-12 for 24 hours, as shown in Figure 3a, 3c, 3e, the PXRD peaks of the three compounds have no significant changes indicated that the three compounds were stable between the pH range of 2-12.…”
Section: Chemical Stability Studiesmentioning
confidence: 99%
“…[4,5] With the enhancement of awareness of environment protection, scientist are working on small corrosion performance, low price, high performance catalyst. [6][7][8][9] Polyoxometalates (POMs), as a class of nanosized metaloxo clusters composed of group VI (Mo and W) and group V (V, Nb and Ta) elements in their highest oxidation state, have received increasing attention owing to their aesthetically appealing structures and wide applications such as in the fields of magnetism, [10][11][12] catalysis, [13][14][15][16][17][18][19][20] and proton conduction. [22][23][24] Due to their strong acidity and fast multielectron transformation activity, POMs can be employed as acid, redox and bifunctional (acid and redox) catalyst for organic reactions.…”
Section: Introductionmentioning
confidence: 99%
“…In a similar manner, alkyl benzenes are regioselectively oxidized at the a-position to afford the corresponding ketones. 11 The oxidation of alcohols and alkyl benzenes to carbonyl compounds can also be performed by treatment with NaBrO 3 in ionic liquids. 12 …”
Section: (B) Oxidation Of Alkyl Arenes and Alcohols To The Correspondmentioning
confidence: 99%
“…In a similar manner, alkyl benzenes are regioselectively oxidized at the a-position to afford the corresponding ketones. 11 The oxidation of alcohols and alkyl benzenes to carbonyl compounds can also be performed by treatment with NaBrO 3 in ionic liquids. 12 The oxidation of sulfides with NaBrO 3 in the presence of a catalytic amount of ceric ammonium nitrate (CAN) supported on silica lead to excellent yields of the corresponding sulfoxides with no overoxidation to sulfones.…”
Section: (B) Oxidation Of Alkyl Arenes and Alcohols To The Corresponding Carbonyl Compoundsmentioning
confidence: 99%
“…In this latter case, the recalcitrant sulfur compounds are oxidized to corresponding sulfoxides and sulfones, followed by distillation, liquid-liquid extraction, or solid-liquid adsorption removal procedures [47]. ODS is accomplished using t-butyl-hydroperoxide (TBHP) [48], superoxides [49], sodium bromate (NaBrO 3 ) [50] and hydrogen peroxide (H 2 O 2 ), along with mixtures of formic acid with H 2 O 2 [51][52][53][54] as primary oxidants. Hydrogen peroxide is the oxidant of choice for ODS, since it is a low cost, mild and environmentally benign reagent [55].…”
Section: Introductionmentioning
confidence: 99%