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Green solvent free epoxidation of olefins by a heterogenised hydrazone-dioxidotungsten(vi) coordination compound

A new mononuclear tungsten coordination compound, [WO(2)L(CH(3)OH)] (1), was synthesized by the reaction of WCl(6) and H(2)L (H(2)L = (E)-4-amino-N′-(5-bromo-2-hydroxybenzylidene)benzohydrazide) in methanol. Both the H(2)L and compound 1 were characterized by elemental analysis and UV-Vis, FT-IR and...

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Autores principales: Heydari, Neda, Bikas, Rahman, Shaterian, Maryam, Lis, Tadeusz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8981271/
https://www.ncbi.nlm.nih.gov/pubmed/35425511
http://dx.doi.org/10.1039/d1ra09217k
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author Heydari, Neda
Bikas, Rahman
Shaterian, Maryam
Lis, Tadeusz
author_facet Heydari, Neda
Bikas, Rahman
Shaterian, Maryam
Lis, Tadeusz
author_sort Heydari, Neda
collection PubMed
description A new mononuclear tungsten coordination compound, [WO(2)L(CH(3)OH)] (1), was synthesized by the reaction of WCl(6) and H(2)L (H(2)L = (E)-4-amino-N′-(5-bromo-2-hydroxybenzylidene)benzohydrazide) in methanol. Both the H(2)L and compound 1 were characterized by elemental analysis and UV-Vis, FT-IR and NMR spectroscopic methods. The molecular structure of compound 1 was also determined by single crystal X-ray analysis which confirmed the compound is a mononuclear coordination compound of cis-dioxidotungsten(vi) containing a free amine functionality on the ligand. Compound 1 was supported on propionyl chloride-functionalized silica gel by amidification reaction to obtain a heterogeneous catalyst. The obtained heterogeneous catalyst was characterized by FT-IR spectroscopy, thermal gravimetric analysis (TGA), diffuse-reflectance spectroscopy (DRS), X-ray diffraction analysis (XRD), energy-dispersive X-ray spectroscopy (EDX), X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM) and its catalytic activity was investigated in the epoxidation of olefins with hydrogen peroxide under solvent free conditions. The catalyst was successfully recovered several times and the recovered catalyst was also characterized by various methods including FT-IR, DRS, TGA, SEM and EDX analyses. The results indicated this heterogeneous catalytic system is an effective and selective catalyst for epoxidation of olefins and can be reused several times without significant change in its catalytic activity.
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spelling pubmed-89812712022-04-13 Green solvent free epoxidation of olefins by a heterogenised hydrazone-dioxidotungsten(vi) coordination compound Heydari, Neda Bikas, Rahman Shaterian, Maryam Lis, Tadeusz RSC Adv Chemistry A new mononuclear tungsten coordination compound, [WO(2)L(CH(3)OH)] (1), was synthesized by the reaction of WCl(6) and H(2)L (H(2)L = (E)-4-amino-N′-(5-bromo-2-hydroxybenzylidene)benzohydrazide) in methanol. Both the H(2)L and compound 1 were characterized by elemental analysis and UV-Vis, FT-IR and NMR spectroscopic methods. The molecular structure of compound 1 was also determined by single crystal X-ray analysis which confirmed the compound is a mononuclear coordination compound of cis-dioxidotungsten(vi) containing a free amine functionality on the ligand. Compound 1 was supported on propionyl chloride-functionalized silica gel by amidification reaction to obtain a heterogeneous catalyst. The obtained heterogeneous catalyst was characterized by FT-IR spectroscopy, thermal gravimetric analysis (TGA), diffuse-reflectance spectroscopy (DRS), X-ray diffraction analysis (XRD), energy-dispersive X-ray spectroscopy (EDX), X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM) and its catalytic activity was investigated in the epoxidation of olefins with hydrogen peroxide under solvent free conditions. The catalyst was successfully recovered several times and the recovered catalyst was also characterized by various methods including FT-IR, DRS, TGA, SEM and EDX analyses. The results indicated this heterogeneous catalytic system is an effective and selective catalyst for epoxidation of olefins and can be reused several times without significant change in its catalytic activity. The Royal Society of Chemistry 2022-02-09 /pmc/articles/PMC8981271/ /pubmed/35425511 http://dx.doi.org/10.1039/d1ra09217k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Heydari, Neda
Bikas, Rahman
Shaterian, Maryam
Lis, Tadeusz
Green solvent free epoxidation of olefins by a heterogenised hydrazone-dioxidotungsten(vi) coordination compound
title Green solvent free epoxidation of olefins by a heterogenised hydrazone-dioxidotungsten(vi) coordination compound
title_full Green solvent free epoxidation of olefins by a heterogenised hydrazone-dioxidotungsten(vi) coordination compound
title_fullStr Green solvent free epoxidation of olefins by a heterogenised hydrazone-dioxidotungsten(vi) coordination compound
title_full_unstemmed Green solvent free epoxidation of olefins by a heterogenised hydrazone-dioxidotungsten(vi) coordination compound
title_short Green solvent free epoxidation of olefins by a heterogenised hydrazone-dioxidotungsten(vi) coordination compound
title_sort green solvent free epoxidation of olefins by a heterogenised hydrazone-dioxidotungsten(vi) coordination compound
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8981271/
https://www.ncbi.nlm.nih.gov/pubmed/35425511
http://dx.doi.org/10.1039/d1ra09217k
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