Halide substituted Schiff-bases: Different activities in methyltrioxorhenium(VII) catalyzed epoxidation via different substitution patterns

This report shows the influence of halide substituted Schiff-bases as ligands of methyltrioxorhenium (MTO) in epoxidation catalysis. Therefore, selected Schiff-bases were prepared by the reaction of hydroxy-benzaldehydes and aniline derivates. These differently substituted Schiff-bases were tested as MTO-ligands in cyclooctene- and 1-octene-epoxidation. Although no great disparities among the substitution patterns have been found, some conclusions can be drawn. Flourines are inferior to chlorines or bromines as substituents. Halides in ortho-position lead to higher activities than in para- or meta-position. The balance between electron donating and withdrawing influences at the Schiff-base plays a prominent role in their utility as ligand to MTO in epoxidation catalysis.

The MTO catalyzed cyclooctene- and 1-octene-epoxidation was examined in the presence of halide substituted Schiff-bases. The different substitution patterns can have a significant influence on the catalytic activity.Figure optionsDownload as PowerPoint slideHighlights
► MTO catalyzed cyclooctene- and 1-octene-epoxidation was examined.
► Halide substituted Schiff-bases were used as additives.
► The different substitution patterns can have an influence on the catalytic activity.
► Bromines and chlorines are superior to fluorines or nitro-groups.
►  Nitromethane is a better solvent than other common solvents like dichloromethane.