dc.contributor.author | Hossain, Md. Kamal | |
dc.contributor.author | Plutenko, Maxym O. | |
dc.contributor.author | Schachner, Jörg A. | |
dc.contributor.author | Haukka, Matti | |
dc.contributor.author | Mösch-Zanetti, Nadia C. | |
dc.contributor.author | Fritsky, Igor O. | |
dc.contributor.author | Nordlander, Ebbe | |
dc.date.accessioned | 2021-04-12T06:32:48Z | |
dc.date.available | 2021-04-12T06:32:48Z | |
dc.date.issued | 2021 | |
dc.identifier.citation | Hossain, M. K., Plutenko, M. O., Schachner, J. A., Haukka, M., Mösch-Zanetti, N. C., Fritsky, I. O., & Nordlander, E. (2021). Dioxomolybdenum(VI) complexes of hydrazone phenolate ligands -syntheses and activities in catalytic oxidation reactions. <i>Journal of the Indian Chemical Society</i>, <i>98</i>(2), Article 100006. <a href="https://doi.org/10.1016/j.jics.2021.100006" target="_blank">https://doi.org/10.1016/j.jics.2021.100006</a> | |
dc.identifier.other | CONVID_51513345 | |
dc.identifier.uri | https://jyx.jyu.fi/handle/123456789/75013 | |
dc.description.abstract | The new cis-dioxomolybdenum(VI) complexes [MoO2(L2)(H2O)] (2) and [MoO2(L3) (H2O)] (3) containing the tridentate hydrazone-based ligands (H2L2 = N'-(3,5-di-tert-butyl-2-hydroxybenzylidene)-4-methylbenzohydrazide and H2L3 = N'-(2-hydroxybenzylidene)-2-(hydroxyimino)propanehydrazide) have been synthesised and characterized via IR, 1H and 13C NMR spectroscopy, mass spectrometry, and single crystal X-ray diffraction analysis. The catalytic activities of complexes 2 and 3, and the analogous known complex [MoO2(L1)(H2O)] (1) (H2L1 = N'-(2-hydroxybenzylidene)-4-methylbenzohydrazide) have been evaluated for various oxidation reactions, viz. oxygen atom transfer from dimethyl sulfoxide to triphenylphosphine, and sulfoxidation of methyl-p-tolylsulfide or epoxidation of different alkenes using tert-butyl hydroperoxide as terminal oxidant. The catalytic activities were found to be comparable for all three complexes, but complexes 1 and 3 showed better catalytic performances than complex 2, which contains a more sterically demanding ligand than the other two complexes. | en |
dc.format.mimetype | application/pdf | |
dc.language | eng | |
dc.language.iso | eng | |
dc.publisher | Elsevier B.V.; Indian Chemical Society | |
dc.relation.ispartofseries | Journal of the Indian Chemical Society | |
dc.rights | CC BY-NC-ND 4.0 | |
dc.subject.other | dioxomolybdenum(VI) complexes | |
dc.subject.other | hydrazone | |
dc.subject.other | schiff base | |
dc.subject.other | oxidation | |
dc.subject.other | epoxidation | |
dc.subject.other | sulfoxidation | |
dc.title | Dioxomolybdenum(VI) complexes of hydrazone phenolate ligands -syntheses and activities in catalytic oxidation reactions | |
dc.type | article | |
dc.identifier.urn | URN:NBN:fi:jyu-202104122325 | |
dc.contributor.laitos | Kemian laitos | fi |
dc.contributor.laitos | Department of Chemistry | en |
dc.contributor.oppiaine | Epäorgaaninen ja analyyttinen kemia | fi |
dc.contributor.oppiaine | Epäorgaaninen kemia | fi |
dc.contributor.oppiaine | Inorganic and Analytical Chemistry | en |
dc.contributor.oppiaine | Inorganic Chemistry | en |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | |
dc.type.coar | http://purl.org/coar/resource_type/c_2df8fbb1 | |
dc.description.reviewstatus | peerReviewed | |
dc.relation.issn | 0019-4522 | |
dc.relation.numberinseries | 2 | |
dc.relation.volume | 98 | |
dc.type.version | publishedVersion | |
dc.rights.copyright | © 2021 Indian Chemical Society | |
dc.rights.accesslevel | openAccess | fi |
dc.subject.yso | hapetus-pelkistysreaktio | |
dc.subject.yso | katalyytit | |
dc.subject.yso | kompleksiyhdisteet | |
dc.subject.yso | molybdeeni | |
dc.format.content | fulltext | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p28877 | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p15480 | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p30190 | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p11107 | |
dc.rights.url | https://creativecommons.org/licenses/by-nc-nd/4.0/ | |
dc.relation.doi | 10.1016/j.jics.2021.100006 | |
jyx.fundinginformation | This research has been carried out within the framework of COST Action CM1003 Biological oxidation reactions - mechanisms and design of new catalysts. M.K.H. thanks the European Commission for an Erasmus Mundus predoctoral fellowship. E.N and I.F. thank the Swedish Institute for a joint collaborative grant from the Visby program. | |
dc.type.okm | A1 | |