2014
DOI: 10.1007/s10934-014-9892-6
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Bidentate salen Cu(II) complex functionalized on mesoporous MCM-41 as novel nano catalyst for the oxidative coupling of thiols into disulfides using urea hydrogen peroxide (UHP)

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Cited by 48 publications
(26 citation statements)
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“…Initially, the MCM-41 mesoporous has been prepared using cetyltrimethylammoniumbromide (CTAB) as structure-directing agent and tetraethylorthosilicate (TEOS) as a source of silicon in NaOH solution according to the methods reported recently [5,11], and subsequently were functionalized with 3-aminopropyltriethoxysilane (APTES). The immobilized salen on MCM-41 was performed via condensation of isatin and supported-aminopropyl groups.…”
Section: Catalyst Preparationmentioning
confidence: 99%
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“…Initially, the MCM-41 mesoporous has been prepared using cetyltrimethylammoniumbromide (CTAB) as structure-directing agent and tetraethylorthosilicate (TEOS) as a source of silicon in NaOH solution according to the methods reported recently [5,11], and subsequently were functionalized with 3-aminopropyltriethoxysilane (APTES). The immobilized salen on MCM-41 was performed via condensation of isatin and supported-aminopropyl groups.…”
Section: Catalyst Preparationmentioning
confidence: 99%
“…Among the various nano materials, Inorganic nanoporous materials have recently been used in various fields, such as catalysis [5], adsorption [6], extraction [7], energy [8], drug delivery systems [9], and for their luminescent character [10], and especially in the isolation and recycling of expensive homogeneous catalysts [5]. Among them, mesoporous MCM-41 have been widely used as catalysts in many organic reactions because of some unique properties like as large specific surface area ([1000 m 2 /g), homogeneous hexagonal pore arrays with pore diameters between 1.5 and 10 nm, relatively hydrophobic nature, ease of functionalization, high thermal stability (900°C) and facile separation [11,12]. Its high thermal stability allows perform of organic reaction in high temperatures and also its very large pore size allows passage of large molecules such as organic ligands and metal complexes through the pores to reach to the surface of the channel [13].…”
Section: Introductionmentioning
confidence: 99%
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“…Furthermore, disulfides are relatively more stable to organic reactions such as oxidation, alkylation and acylation compared to the corresponding free thiols, also the thiol group can conveniently be protected as a disulfide [37]. For the conversion of thiols to disulfides many methods have been developed over the years to find efficient these organic transformations [38][39][40][41][42][43][44].…”
Section: Introductionmentioning
confidence: 99%