| DOI | Trouver le DOI : https://doi.org/10.1023/A:1019074920329 |
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| Auteur | Rechercher : Ingold, K. U.1; Rechercher : Snelgrove, D.W.1; Rechercher : MacFaul, P.A.1; Rechercher : Oldroyd, R.D.; Rechercher : Thomas, J.M. |
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| Affiliation | - Conseil national de recherches Canada
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| Format | Texte, Article |
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| Résumé | The epoxidation of cyclohexene in acetonitrile under argon at room temperature on a titanium(IV)-containing MCM41 silica catalyst is faster and gives a greater final yield of cyclohexene oxide when the oxygen atom donor is 2-methyl-l-phenyl-2-propyl hydroperoxide (MPPH) than when it is tert-butyl hydroperoxide. This is shown to be due to stronger retardation of the oxidation by tert-butyl alcohol (TBA) than by the alcohol derived from MPPH. The difference in retardation between these two alcohols is attributed to the greater hydrophilicity of TBA. Acetonitrile is a better solvent for this reaction than isooctane, pyridine and a variety of alcohols. These solvent effects are attributed to the hydrophilic nature of the catalyst. |
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| Date de publication | 1997 |
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| Dans | |
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| Langue | anglais |
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| Publications évaluées par des pairs | Oui |
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| Numéro NPARC | 21276590 |
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| Exporter la notice | Exporter en format RIS |
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| Signaler une correction | Signaler une correction (s'ouvre dans un nouvel onglet) |
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| Identificateur de l’enregistrement | efbb797c-5cf7-47f6-b615-3201e76f045d |
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| Enregistrement créé | 2015-10-13 |
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| Enregistrement modifié | 2020-03-20 |
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