Aсtivity of binary vinadium compounds in reaction of epoxidation of 1-octene and decomposition of tert-butyl hydroperoxide
dc.citation.epage | 74 | |
dc.citation.issue | 1 | |
dc.citation.spage | 70 | |
dc.contributor.affiliation | Національний університет “Львівська політехніка” | |
dc.contributor.affiliation | Lviv Polytechnic National University | |
dc.contributor.author | Макота, О. І. | |
dc.contributor.author | Комаренська, З. М. | |
dc.contributor.author | Олійник, Л. П. | |
dc.contributor.author | Булгакова, Л. В. | |
dc.contributor.author | Кловак, Н. В. | |
dc.contributor.author | Makota, O. | |
dc.contributor.author | Komarenska, Z. | |
dc.contributor.author | Oliynyk, L. | |
dc.contributor.author | Bulgakova, L. | |
dc.contributor.author | Klovak, N. | |
dc.coverage.placename | Lviv | |
dc.coverage.placename | Lviv | |
dc.date.accessioned | 2021-01-28T11:23:55Z | |
dc.date.available | 2021-01-28T11:23:55Z | |
dc.date.created | 2020-02-24 | |
dc.date.issued | 2020-02-24 | |
dc.description.abstract | Досліджено вплив ванадійвмісних сполук як каталізаторів на реакцію епоксидування октену-1 гідропероксидом трет-бутилу та розкладу цього гідропероксиду. Показано, що каталітична активність сполук ванадію залежить від природи ліганда, що входить до складу каталізатора. Встановлено, що борид і карбід ванадію є найактивнішими каталізаторами гідропероксидного епоксидування, тоді як V2O5 найактивнішим каталізатором розкладу гідропероксиду трет-бутилу. Найвища селективність утворення 1,2-епоксиоктену спостерігається у разі використання як каталізатора VC. | |
dc.description.abstract | The influenceof vanadium-containing compounds as catalysts on the reaction of 1-octene epoxidation by tert-butyl hydroperoxide and the decomposition of this hydroperoxide was investigated. It is shown that the catalytic activity of vanadium compounds depends on catalyst ligand nature. It is established that vanadium boride and carbide are the most active catalysts for hydroperoxide epoxidation, while V2O5 is the most active catalyst of tert-butyl hydroxide decomposition. The highest selectivity of 1,2-epoxyoctene formation is observed when VC is used as a catalyst. | |
dc.format.extent | 70-74 | |
dc.format.pages | 5 | |
dc.identifier.citation | Aсtivity of binary vinadium compounds in reaction of epoxidation of 1-octene and decomposition of tert-butyl hydroperoxide / O. Makota, Z. Komarenska, L. Oliynyk, L. Bulgakova, N. Klovak // Chemistry, Technology and Application of Substances. — Lviv : Lviv Politechnic Publishing House, 2020. — Том 3. — № 1. — С. 70–74. | |
dc.identifier.citationen | Aсtivity of binary vinadium compounds in reaction of epoxidation of 1-octene and decomposition of tert-butyl hydroperoxide / O. Makota, Z. Komarenska, L. Oliynyk, L. Bulgakova, N. Klovak // Chemistry, Technology and Application of Substances. — Lviv : Lviv Politechnic Publishing House, 2020. — Vol 3. — No 1. — P. 70–74. | |
dc.identifier.doi | doi.org/10.23939/ctas2020.01.070 | |
dc.identifier.uri | https://ena.lpnu.ua/handle/ntb/56066 | |
dc.language.iso | en | |
dc.publisher | Lviv Politechnic Publishing House | |
dc.relation.ispartof | Chemistry, Technology and Application of Substances, 1 (3), 2020 | |
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dc.relation.references | 4. Xia, Q. H., Ge, H. Q., Ye, C. P., Liu, Z. M., Su K. X. (2005). Advancesin homogeneous and heterogeneous catalytic asymmetricepoxidation. Chemical Reviews, 105(5), 1603–1662. doi: 10.1021/cr0406458. Arends, I. W. C. E., Sheldon, R. A. (2001). Activities and stabilitiesof heterogeneous catalysts in selective liquid phase oxidations:recent developments. Applied Catalysis A, 212(1–2),175-187. doi: 10.1016/S0926-860X(00) 00855-3. | |
dc.relation.references | 5. Tietze, L. F., Eicher T., Diederichsen U., Speicher A. (2007). Reactions and Syntheses in the Organic Chemistry Laboratory. Wiley-VCH, Weinheim. ISBN: 978-3-527-33814-6. | |
dc.relation.references | 6. Mirzaee, M., Bahramian, B., Gholizadeh, Ja., Feizi, A., Gholami, R. (2016). Acetylacetonate complexes of vanadium and molybdenum supported on functionalized boehmite nano-particles for the catalytic epoxidation of alkenes.Chemical Engineering Journal, 308, 160–168. doi: 10.1016/j.cej.2016.09.055. | |
dc.relation.references | 7. Belaidi, N., Bedrane, S., Choukchou-Braham, A., Bachir, R. (2015). Novel vanadium-chromium-bentonite green catalysts for cyclohexene epoxidation. Applied Clay Science, 107, 14–24. doi: 10.1016/j.clay.2015.01.026. | |
dc.relation.references | 8. Arfaoui, Ji., KhalfallahBoudali, L., Ghorbel, A., (2010). Catalytic epoxidation of allylic alcohol (E)-2- Hexen-1-ol over vanadium supported on unsulfated and sulfated titanium pillared montmorillonite catalysts: Effect of sulfate groups and vanadium loading.Applied Clay Science, 48, 171–178. doi: 10.1016/j.clay.2009.12.005. | |
dc.relation.references | 9. Noji M., Kondo, H., Yazaki, C.,Yamaguchi, H., Ohkura, S., Takanami, T. (2019). An immobilized vanadiumbinaphthylbishydroxamic acid complex as a reusable catalyst for the asymmetric epoxidation of allylic alcohols. Tetrahedron Letters, 60(23), 1518–1521. doi: 10.1016/j.tetlet.2019.05.013. | |
dc.relation.references | 10. Yang, L., He, Ji., Zhang, Q., Wang, Y. (2010). Copper-catalyzed propylene epoxidation by oxygen: Significant promoting effect of vanadium on unsupported copper catalyst. Journal of Catalysis, 276(1), 76–84. doi: 10.1016/j.jcat.2010.09.002. | |
dc.relation.references | 11. Held A., Kowalska-Kuś Jo., Nowińska K., Góra-Marek, K. (2019). Potassium-modified silicasupported vanadium oxide catalysts applied for propene epoxidation. Journal of Catalysis, 347, 21–35. doi: 10.1016/j.jcat.2016.12.001. | |
dc.relation.references | 12. Milas N. A., Surgenor D. M. (1946). Studies in organic peroxides. VIII. t-Butyl hydroperoxide and di-tbutyl peroxide. Journal of the American Chemical Society, 68(2), 205–208. doi: 10.1021/ja01206a017. | |
dc.relation.referencesen | 1. Marco-Contelles, J., Molina, M. T., Anjum, S. (2004). Naturallyoccurring cyclohexane epoxides: Sources, biological activitiesand synthesis. Chemical Reviews, 104(6), 2857–2899. doi: 10.1021/cr980013j. | |
dc.relation.referencesen | 2. Diez, D., Beneitez, M. T., Marcos, I. S., Garrido, N. M., Basabe, P., Urones, J. G. (2002). Regio- and stereoselective ring openingof epoxides. Enantioselective synthesis of 2,3,4-trisubstitutedfive-membered heterocycles. Tetrahedron Asymmetry, 13(6), 639–646. doi: 10.1016/S0957-4166(02)00160–X | |
dc.relation.referencesen | 3. Yudin, A. K. (2006). Aziridines and Epoxides in Organic Synthesis. Wiley-VCH,Weinheim, Germany. doi: 10.1002/3527607862 | |
dc.relation.referencesen | 4. Xia, Q. H., Ge, H. Q., Ye, C. P., Liu, Z. M., Su K. X. (2005). Advancesin homogeneous and heterogeneous catalytic asymmetricepoxidation. Chemical Reviews, 105(5), 1603–1662. doi: 10.1021/cr0406458. Arends, I. W. C. E., Sheldon, R. A. (2001). Activities and stabilitiesof heterogeneous catalysts in selective liquid phase oxidations:recent developments. Applied Catalysis A, 212(1–2),175-187. doi: 10.1016/S0926-860X(00) 00855-3. | |
dc.relation.referencesen | 5. Tietze, L. F., Eicher T., Diederichsen U., Speicher A. (2007). Reactions and Syntheses in the Organic Chemistry Laboratory. Wiley-VCH, Weinheim. ISBN: 978-3-527-33814-6. | |
dc.relation.referencesen | 6. Mirzaee, M., Bahramian, B., Gholizadeh, Ja., Feizi, A., Gholami, R. (2016). Acetylacetonate complexes of vanadium and molybdenum supported on functionalized boehmite nano-particles for the catalytic epoxidation of alkenes.Chemical Engineering Journal, 308, 160–168. doi: 10.1016/j.cej.2016.09.055. | |
dc.relation.referencesen | 7. Belaidi, N., Bedrane, S., Choukchou-Braham, A., Bachir, R. (2015). Novel vanadium-chromium-bentonite green catalysts for cyclohexene epoxidation. Applied Clay Science, 107, 14–24. doi: 10.1016/j.clay.2015.01.026. | |
dc.relation.referencesen | 8. Arfaoui, Ji., KhalfallahBoudali, L., Ghorbel, A., (2010). Catalytic epoxidation of allylic alcohol (E)-2- Hexen-1-ol over vanadium supported on unsulfated and sulfated titanium pillared montmorillonite catalysts: Effect of sulfate groups and vanadium loading.Applied Clay Science, 48, 171–178. doi: 10.1016/j.clay.2009.12.005. | |
dc.relation.referencesen | 9. Noji M., Kondo, H., Yazaki, C.,Yamaguchi, H., Ohkura, S., Takanami, T. (2019). An immobilized vanadiumbinaphthylbishydroxamic acid complex as a reusable catalyst for the asymmetric epoxidation of allylic alcohols. Tetrahedron Letters, 60(23), 1518–1521. doi: 10.1016/j.tetlet.2019.05.013. | |
dc.relation.referencesen | 10. Yang, L., He, Ji., Zhang, Q., Wang, Y. (2010). Copper-catalyzed propylene epoxidation by oxygen: Significant promoting effect of vanadium on unsupported copper catalyst. Journal of Catalysis, 276(1), 76–84. doi: 10.1016/j.jcat.2010.09.002. | |
dc.relation.referencesen | 11. Held A., Kowalska-Kuś Jo., Nowińska K., Góra-Marek, K. (2019). Potassium-modified silicasupported vanadium oxide catalysts applied for propene epoxidation. Journal of Catalysis, 347, 21–35. doi: 10.1016/j.jcat.2016.12.001. | |
dc.relation.referencesen | 12. Milas N. A., Surgenor D. M. (1946). Studies in organic peroxides. VIII. t-Butyl hydroperoxide and di-tbutyl peroxide. Journal of the American Chemical Society, 68(2), 205–208. doi: 10.1021/ja01206a017. | |
dc.rights.holder | © Національний університет “Львівська політехніка”, 2020 | |
dc.subject | епоксидування | |
dc.subject | каталізатори | |
dc.subject | ванадійвмісні сполуки | |
dc.subject | октен-1 | |
dc.subject | гідропероксид трет-бутилу | |
dc.subject | epoxidation | |
dc.subject | catalysts | |
dc.subject | vanadium compounds | |
dc.subject | 1-octene | |
dc.subject | tert-butyl hydroperoxide | |
dc.title | Aсtivity of binary vinadium compounds in reaction of epoxidation of 1-octene and decomposition of tert-butyl hydroperoxide | |
dc.title.alternative | Активність бінарних сполук ванадію у реакції епоксидування октену-1 і розкладу гідропероксиду трет-бутилу | |
dc.type | Article |
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