2023
DOI: 10.1016/j.cattod.2023.114273
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Molybdenum(VI) complexes with ligands derived from 5-(2-pyridyl)-2H-tetrazole as catalysts for the epoxidation of olefins

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Cited by 6 publications
(4 citation statements)
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“…Recently, the Lindqvist-type POM [ t Bu-Hptz] 2 [Mo 6 O 19 ] ( t Bu-Hptz = 2- tert -butyl-5-(2-pyridyl)tetrazole) was studied as epoxidation catalysts using readily available and relatively eco-friendly hydroperoxide oxidants (hydrogen peroxide and tert -butyl hydroperoxide). 87 This POM acted as a homogeneous catalyst and could be recycled by employing an IL solvent. It was found that the type of anion of the IL could affect the catalytic performance.…”
Section: The Catalytic Application Of Il–mocsmentioning
confidence: 99%
“…Recently, the Lindqvist-type POM [ t Bu-Hptz] 2 [Mo 6 O 19 ] ( t Bu-Hptz = 2- tert -butyl-5-(2-pyridyl)tetrazole) was studied as epoxidation catalysts using readily available and relatively eco-friendly hydroperoxide oxidants (hydrogen peroxide and tert -butyl hydroperoxide). 87 This POM acted as a homogeneous catalyst and could be recycled by employing an IL solvent. It was found that the type of anion of the IL could affect the catalytic performance.…”
Section: The Catalytic Application Of Il–mocsmentioning
confidence: 99%
“…The introduction of alkyl substituent groups in the anilinium cation did not seem to improve the catalytic performance, which may be partly due to differences in catalyst solubility and/or acid-base properties of the anilinium derivatives [31]. The 0-D pyridinium-tetrazole-based polyoxometallates (Hptz) 4 [SiMo 12 O 40 ]•nH 2 O and (tBu-ptz) 2 [Mo 6 O 19 ] performed differently under somewhat comparable reaction conditions, with the latter being less active (88% Ole conversion at 6 h) than the former (97% Ole conversion at 3 h) (entries 8 and 9) [32,33]. Both compounds were less active than 3-5.…”
Section: Biobased Olefin Epoxidationmentioning
confidence: 99%
“…Under somewhat similar reaction conditions to those used for 1-6, the catalyst (Hptz)4[SiMo12O40]•nH2O (ptz = 5-(2-pyridyl)tetrazole) led to 60%/28% LinOx selectivity, 31%/33% LinDiOx selectivity and 9%/40% LinFur selectivity at 87%/100% Lin conversion (6 h/24 h) [32]. On the other hand, only epoxides were formed for a related ionic compound with a substituted ptz organic fragment (tBu-Hptz)2[Mo6O19], which led to 83% LinOx and 17% LinDiOx selectivity at 85% Lin conversion, 24 h/70 °C [33]. For this catalyst, the selectivity towards epoxides remained high at 90 °C (63% and 37% of LinOx and LinDiOx selectivity, respectively, at 100% Lin conversion, 2 h), and no LinFur products were formed [33].…”
Section: Biobased Olefin Epoxidationmentioning
confidence: 99%
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