http://repository.iitr.ac.in/handle/123456789/25138
DC Field | Value | Language |
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dc.contributor.author | Maurya, Mannar Ram | - |
dc.contributor.author | Jangra N. | - |
dc.contributor.author | Avecilla F. | - |
dc.contributor.author | Correia I. | - |
dc.date.accessioned | 2022-04-22T05:54:14Z | - |
dc.date.available | 2022-04-22T05:54:14Z | - |
dc.date.issued | 2019 | - |
dc.identifier.citation | European Journal of Inorganic Chemistry, 2019(2): 314-329 | - |
dc.identifier.issn | 14341948 | - |
dc.identifier.uri | https://doi.org/10.1002/ejic.201801243 | - |
dc.identifier.uri | http://repository.iitr.ac.in/handle/123456789/25138 | - |
dc.description.abstract | Four ONO donor ligands are isolated from the condensation of 4,6-diacetyl resorcinol with isonicotinoyl hydrazide (H2dar-inh, I), nicotinoyl hydrazide (H2dar-nah, II), benzoyl hydrazide (H2dar-bhz, III), and 2-furoyl hydrazide (H2dar-fah, IV) on refluxing in MeOH. The reaction of in situ generated aqueous K[H2VVO4] with ligands I–IV at neutral pH gives complexes [K(H2O)2][VO2(dar-inh)] (1), [K(H2O)2][VO2(dar-nah)] (2), [K(H2O)2][VO2(dar-bhz)] (3), and [K(H2O)2][VO2(dar-fah)] (4), respectively. The reaction of [VIVO(acac)2] (acac = acetylacetonato) with these ligands (I–IV) under aerobic conditions in methanol yields oxidomethoxidovanadium(V) complexes [VO(OMe)(MeOH)(dar-inh)] (5), [VO(OMe)(MeOH)(dar-nah)] (6), [VO(OMe)(MeOH)(dar-bhz)] (7), and [VO(OMe)(MeOH)(dar-fah)] (8). All the isolated complexes are characterized by elemental, thermal, electrochemical, and spectroscopic techniques [FTIR, UV/Vis, NMR (1H, 13C and 51V NMR)], and single-crystal X-ray diffraction analysis (for 1, 6, 7, and 8). X-ray analysis confirms the coordination of the ligands through Ophenolate, Nazomethine, and Oenolate to the metal center. In the molecular structure of [K(H2O)(EtOH)][VVO2(dar-inh)] (abbreviated as 1a where one molecule of water is replaced by EtOH), water molecules act as bridges between two K+ ions and the complex shows a dimeric structure due to the presence of electrostatic interactions between V=O oxygen atoms with K+ ions. These complexes are active catalysts for the oxidative bromination of thymol in the presence of KBr, HClO4, and H2O2 and give 2-bromothymol, 4-bromothymol, and 2,4-dibromothymol as major products. Complexes 1–4 were also tested as catalysts for the epoxidation of various alkenes (namely styrene, cyclohexene, cis-cyclooctene, 1-hexene, 1-octene, cyclohexenone, and trans-stilbene) with H2O2 in the presence of NaHCO3 as promoter, giving the corresponding epoxides selectively. © 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim | - |
dc.language.iso | en_US | - |
dc.publisher | Wiley-VCH Verlag | - |
dc.relation.ispartof | European Journal of Inorganic Chemistry | - |
dc.subject | Epoxidation of alkenes | - |
dc.subject | Haloperoxidase models | - |
dc.subject | Homogeneous catalysis | - |
dc.subject | Oxidative bromination | - |
dc.subject | Structure elucidation | - |
dc.subject | Vanadium | - |
dc.title | 4,6-Diacetyl Resorcinol Based Vanadium(V) Complexes: Reactivity and Catalytic Applications | - |
dc.type | Article | - |
dc.scopusid | 7005255411 | - |
dc.scopusid | 57200598949 | - |
dc.scopusid | 6602180279 | - |
dc.scopusid | 7003557498 | - |
dc.affiliation | Maurya, M.R., Department of Chemistry, Indian Institute of Technology Roorkee, Roorkee, 247667, India | - |
dc.affiliation | Jangra, N., Department of Chemistry, Indian Institute of Technology Roorkee, Roorkee, 247667, India | - |
dc.affiliation | Avecilla, F., Grupo Xenomar, Centro de Investigacións Científicas Avanzadas (CICA), Facultade de Ciencias, Universidade da Coruña, Campus de A Coruña, Coruña, 15071A, Spain | - |
dc.affiliation | Correia, I., Centro de Química Estrutural, Instituto Superior Técnico, Universidade Lisboa, Lisboa, 1049-001, Portugal | - |
dc.description.funding | - | |
dc.description.correspondingauthor | Maurya, M.R.; Department of Chemistry, India; email: rkmanfcy@iitr.ac.in | - |
Appears in Collections: | Journal Publications [CY] |
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