2006
DOI: 10.1016/j.apcata.2006.05.015
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Chromium-exchanged zeolite (CrE-ZSM-5) as catalyst for alcohol oxidation and benzylic oxidation with t-BuOOH

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Cited by 54 publications
(36 citation statements)
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“…In recent years, synthetic and natural zeolites have become increasingly important due to the wide range of their chemical and physical properties and have been studied for the liquid adsorption of dissolved pollutants in water and/or wastewater. A lot of studies have focused on the adsorption of methylene blue a cationic dye by synthesized and natural zeolites [23][24][25][26][27][28][29][30][31][32][33]. The results showed that the adsorption kinetics and isotherms could be well described by the pseudo-second-order model and the two-parameter model (i.e.…”
Section: Introductionmentioning
confidence: 96%
“…In recent years, synthetic and natural zeolites have become increasingly important due to the wide range of their chemical and physical properties and have been studied for the liquid adsorption of dissolved pollutants in water and/or wastewater. A lot of studies have focused on the adsorption of methylene blue a cationic dye by synthesized and natural zeolites [23][24][25][26][27][28][29][30][31][32][33]. The results showed that the adsorption kinetics and isotherms could be well described by the pseudo-second-order model and the two-parameter model (i.e.…”
Section: Introductionmentioning
confidence: 96%
“…Recently, several studies were reported on synthesis and characterization of chromiumcatalysts supported by mesoporous molecular sieves and zeolites. In them, cation exchange properties of the supports were found to play a fundamental role [4][5][6].…”
Section: Introductionmentioning
confidence: 98%
“…Among the many synthetic procedures devised for the preparation of aromatic ketones, esters and amides [32][33][34][35][36][37], including Friedel-Crafts acylation, esterification and amidation of benzoic acid derivatives [38][39][40][41][42][43][44][45][46], the oxidation of benzylic methylene compounds stands out as a simple approach that has attracted much attention in the last decades. Many reagents (KMnO 4 , iodine(V) species, t BuOOH, m-CPBA, H 2 O 2 , NHPI, inter alia) can oxidize the activated benzylic position of aromatic alkanes, benzyl ethers, and amines to provide the corresponding arylcarbonyl moiety (Scheme 1) by a process opposite to Clemmensen, Wolf-Kisnerr and related reduction reactions [47][48][49][50][51][52][53][54][55][56][57][58][59][60][61]. Although good yields and selectivities have been obtained in most cases, stoichiometric amounts of relatively harmful or unsafe oxidizing agents are required.…”
Section: Introductionmentioning
confidence: 99%