Add time:09/03/2019         Source:sciencedirect.com

New oxime-derived palladacycles were prepared, spectral characterized, and immobilized on silica gel. Homogeneous catalysis indicates that pyridine coordinated oxime-derived palladacycles 1 and 2 were very effective in the methanolysis of fenitrothion, but suffered from the formation of the inactive dimmer at higher concentration. Immobilization of oxime-derived chloro-coordinated mononuclear and chloro-bridged dinuclear palladacycles afforded the high efficient and recoverable heterogeneous catalysts Si–Pd1 and Si–Pd2, both solid catalysts proved to be reusable in 10 runs and fascinated the degradation of a series of phosphorothionate pesticides up to 4.9 × 108 folds at sspH 8.8 and 25 °C.

We also recommend Trading Suppliers and Manufacturers of (2-NITROPHENYL)ACETONE OXIME (cas 15582-89-5). Pls Click Website Link as below: cas 15582-89-5 suppliers