2018
DOI: 10.1016/j.ica.2018.08.022
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Synthesis, structure, spectroscopic characterization and catalytic activity of chiral dioxidomolybdenum(VI) Schiff base complexes derived from R(−)-2-amino-1-propanol

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Cited by 13 publications
(8 citation statements)
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“…As we have previously reported, [ 21,22 ] the oxidation of styrene with catalytic amounts of molybdenum (VI) Schiff base complexes using aqueous 30% H 2 O 2 or TBHP as the terminal oxidants generally can result in five oxidation products, i.e. styrene oxide, benzaldehyde, benzoic acid, phenylacetaldehyde and 1‐phenylethane‐1,2‐diol.…”
Section: Resultsmentioning
confidence: 92%
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“…As we have previously reported, [ 21,22 ] the oxidation of styrene with catalytic amounts of molybdenum (VI) Schiff base complexes using aqueous 30% H 2 O 2 or TBHP as the terminal oxidants generally can result in five oxidation products, i.e. styrene oxide, benzaldehyde, benzoic acid, phenylacetaldehyde and 1‐phenylethane‐1,2‐diol.…”
Section: Resultsmentioning
confidence: 92%
“…For example in the cases of MoO 2 L 2 , MoO 2 L 3 and MoO 2 L 7 , the decrease in the reaction temperature was accompanied by longer reaction time but also a slight increase in enantioselectivity and without additional sulfone production (entries 3, 5, 10, 16, 18 and 23). In comparison with the other chiral but tridentate cis ‐dioxidomolybdenum (VI) Schiff base complexes, derived from amino alcohols, the conversions to thioanisole were similar, [ 21,22,33 ] but much higher amounts of catalysts (5 mol%) were needed to achieve them. Nevertheless, it seems that pathway for the formation of sulfoxide is very similar.…”
Section: Resultsmentioning
confidence: 98%
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“…The peaks in the range of 230–245 nm could be attributed to the ligand absorption peaks . The absorption band at 270–400 nm was attributed to charge transfer from ligand to Mo . After adding TBHP, the absorption peak of 270–400 nm decreased sharply.…”
Section: Resultsmentioning
confidence: 98%