4.6 Article

A 5-(2-Pyridyl)tetrazolate Complex of Molybdenum(VI), Its Structure, and Transformation to a Molybdenum Oxide-Based Hybrid Heterogeneous Catalyst for the Epoxidation of Olefins

期刊

CATALYSTS
卷 11, 期 11, 页码 -

出版社

MDPI
DOI: 10.3390/catal11111407

关键词

molybdenum; molybdenum oxide; organic-inorganic hybrid material; tetrazole; 5-(2-pyridyl)tetrazole; hydrogen bonds; epoxidation; bio-olefins

资金

  1. CICECOAveiro Institute of Materials [FCT (Fundacao para a Ciencia e a Tecnologia) [UIDB/50011/2020, UIDP/50011/2020]
  2. COMPETE 2020 Operational Thematic Program for Competitiveness and Internationalization [POCI-01-0145-FEDER-030075]
  3. FCT/MCTES
  4. European Union through the European Regional Development Fund under the Portugal 2020 Partnership Agreement
  5. FCT [2021.06403.BD, 2021.04756.BD, CEECIND/00553/2017]
  6. Fundação para a Ciência e a Tecnologia [2021.06403.BD, 2021.04756.BD] Funding Source: FCT

向作者/读者索取更多资源

The study focused on developing organomolybdenum heterogeneous catalysts for efficient epoxidation of olefins, where material 2 demonstrated excellent catalytic performance and recyclability.
There is a considerable practical interest in discovering new ways to obtain organomolybdenum heterogeneous catalysts for olefin epoxidation that are easier to recover and reuse and display enhanced productivity. In this study, the complex salt (H(2)pytz)[MoO2Cl2(pytz)] (1) (Hpytz = 5-(2-pyridyl)tetrazole) has been prepared, structurally characterized, and employed as a precursor for the hydrolysis-based synthesis of a microcrystalline molybdenum oxide/organic hybrid material formulated as [MoO3(Hpytz)] (2). In addition to single-crystal X-ray diffraction (for 1), compounds 1 and 2 were characterized by FT-IR and Raman spectroscopies, solid-state C-13{H-1} cross-polarization (CP) magic-angle spinning (MAS) NMR, and scanning electron microscopy (SEM). Compounds 1 and 2 were evaluated as olefin epoxidation catalysts using the model reaction of cis-cyclooctene (Cy8) with tert-butyl hydroperoxide (TBHP), at 70 & DEG;C, which gave 100% epoxide selectivity up to 100% conversion. While 1 behaved as a homogeneous catalyst, hybrid 2 behaved as a heterogeneous catalyst and could be recovered for recycling without showing structural degradation or loss of catalytic performance over consecutive reaction cycles. The substrate scope was broadened to monoterpene DL-limonene (Lim) and biobased unsaturated fatty acid methyl esters, methyl oleate (MeOle), and methyl linoleate (MeLin), which gave predominantly epoxide products.

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