Affiliation:
1. Department of Chemistry Faculty of Science Suez University 43533 Suez Egypt
2. Institut für Anorganische Chemie und Strukturchemie Heinrich-Heine Universität Düsseldorf Düsseldorf Germany
3. Department of Chemistry College of Science Jouf University Sakaka Saudi Arabia
4. Department of Chemistry Faculty of Science Port Said University 42526 Port Said Egypt
5. Department of Chemistry College of Science University of Jeddah Jeddah Saudi Arabia
Abstract
AbstractA new chelating task‐specific ionic liquid (TSIL), lutidinium‐based salicylaldoxime (LSOH), and its square pyramidal vanadyl(II) complex (VO(LSO)2) have been successfully synthesized and structurally characterized using elemental (CHN), spectral, and thermal analyses. The catalytic activity of the lutidinium‐salicylaldoxime complex (VO(LSO)2) in the alkene epoxidation reactions was studied under various reaction conditions, such as solvent effect, alkene/oxidant molar ratio, pH, reaction temperature, reaction time, and the catalyst dose. The results demonstrated that the CHCl3 solvent, 1 : 3 of the cyclohexene/H2O2 ratio, pH 8, temperature of 340 K, and catalyst dose of 0.012 mmol are assigned as the optimum conditions for achieving maximum catalytic activity for VO(LSO)2. Moreover, the VO(LSO)2 complex has the potential for application in the effective and selective epoxidation of alkenes. Notably, under optimal VO(LSO)2 conditions, cyclic alkenes convert more efficiently to their corresponding epoxides than linear alkenes.
Subject
Molecular Biology,Molecular Medicine,General Chemistry,Biochemistry,General Medicine,Bioengineering
Cited by
1 articles.
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