Cyrene (dihydrolevoglucosenone) and its derivative Cygnet 0.0, recognized as eco-friendly alternatives to polar aprotic solvents, were utilized in atom transfer radical polymerization (ATRP) of a wide range of both hydrophobic and hydrophilic (meth)acrylates. The detailed kinetics study and electrochemical experiments of the catalytic complex in these solvents reveal the opportunities and limitations of their use in controlled radical polymerization.
View Article and Find Full Text PDFCoffee, the most popular beverage in the 21st century society, was tested as a reaction environment for activators regenerated by electron transfer atom transfer radical polymerization (ARGET ATRP) without an additional reducing agent. Two blends were selected: pure Arabica beans and a proportional blend of Arabica and Robusta beans. The use of the solution received from the mixture with Robusta obtained a high molecular weight polymer product in a short time while maintaining a controlled structure of the synthesized product.
View Article and Find Full Text PDFThe oxygenation of cyclohexane and toluene by O and HO catalyzed by VO(acac) and Co(acac) was studied at 40-100 °C and 1-10 atm. Upon such conditions, the process can be remarkably (30× times) enhanced by the minute (6-15 mM) additives of oxalic acid (H) or -hydroxyphthalimide (NHPI). The revealed effect of H on HO-piloted oxidation is closely associated with the nature of the catalyst cation and boosted by VO(acac).
View Article and Find Full Text PDFCyclohexane oxidation by HO to cyclohexanol, cyclohexanone, and cyclohexylhydroperoxide under mild (40 °C, 1 atm) conditions is significantly enhanced in the system composed of VO(acac) (starting catalyst) and small additives of oxalic acid (process promoter). In corroboration of this, several times higher yield of the desired products was obtained compared to that obtained in the acid-free process. The revealed advantage was addressed to elevate the electrical conductance (or , decreasing the resistance, 1/) of the reaction medium.
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