2004
DOI: 10.1016/j.apcata.2004.09.001
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Styrene oxidation with H2O2 over Ti-containing molecular sieves with MFI, BEA and MCM-41 topologies

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Cited by 189 publications
(100 citation statements)
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“…Selective oxidation is an active field of research due to the complex chemical processes. The styrene oxidation at side chain is of academic and commercial interests for the synthesis of two important products of styrene oxide and of phenylacetaldehyde [28]. While phenylacetaldehyde could be further polymerized to produce oligomeric aldehyde using costly Wilkinson's catalyst (RhCl(PPh 3 ) 3 ) or other dirhodium complexes catalysts [29], which is interesting in the organic chemical industry.…”
Section: Resultsmentioning
confidence: 99%
“…Selective oxidation is an active field of research due to the complex chemical processes. The styrene oxidation at side chain is of academic and commercial interests for the synthesis of two important products of styrene oxide and of phenylacetaldehyde [28]. While phenylacetaldehyde could be further polymerized to produce oligomeric aldehyde using costly Wilkinson's catalyst (RhCl(PPh 3 ) 3 ) or other dirhodium complexes catalysts [29], which is interesting in the organic chemical industry.…”
Section: Resultsmentioning
confidence: 99%
“…These reaction products are common and have also been identified earlier by other workers. [19][20][21] Scheme 5.…”
Section: Oxidation Of Styrenementioning
confidence: 99%
“…Benzaldehyde formation may also be facilitated by direct oxidative cleavage of the styrene side chain double bond by a radical mechanism. [19] Formation of other products such as benzoic acid from benzaldehyde is rather slow in all reactions. Similarly the formation of phenylacetaldehyde, a product formed by isomerisation of styrene oxide, is less in all cases.…”
Section: Oxidation Of Styrenementioning
confidence: 99%
“…However, despite some successes in the functionalization of bulky active sites, the overall stability and limitations in scope for a wider integration of transition metals, restricted their industrial applicability. For example, tetrahedral Ti(IV) ions were incorporated into the framework of Ti-MCM-41 (mesopore aperture 30 Å), but the resulting material did not evoke the same catalytic potential of its microporous analogue, TS-1 [33,34]. This shortcoming inspired a generation to try to combine the advantages of design in a microporous systems, with the improved diffusion offered by ordered mesoporous networks, to create novel hierarchically porous (HP) catalysts (figure 1) [35][36][37][38][39][40].…”
Section: Introduction and Design Strategymentioning
confidence: 99%