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A phosphorylation of alkenyl and aryl C-O bonds at room temperature via photoredox/nickel dual catalysis is reported. By starting from easily available and inexpensive sulfonates, a variety of important alkenyl phosphonates and aryl phosphine oxides are generated in moderate to excellent yields. This method features mild reaction conditions, high selectivity, good functional group tolerance, wide substrate scope, and easy scalability. [ABSTRACT FROM AUTHOR]

The rare earth conversion film has attracted more and more attention in recent years because of its good corrosion resistance and non - toxicity. The concept and film forming mechanism of rare earth conversion film were briefly introduced, and the application of rare earth in corrosion prevention for ferrous metals as well as the nonferrous metals of aluminum, magnesium, zinc and their alloys was summarized. This study found that the corrosion resistance of composite rare earth conversion film was better than that of the single rare earth conversion film. Moreover, it also explained the reason why cerium conversion film had better corrosion resistance than other rare earth conversion films. Finally, it pointed out that the composite rare earth conversion film, rare earth composite alloy coating and densification of rare earth conversion film would be the development direction.

Herein, we report a highly regio- and enantioselective copper-catalyzed reductive hydroxymethy-lation of styrenes and 1,3-dienes with 1 atm of CO2. Diverse important chiral homobenzylic alcohols were readily prepared from styrenes. Moreover, a variety of 1,3-dienes also were converted to chiral homoallylic alcohols with high yields and excellent regio-, enantio-, and Z/E-selectivities. The utility of this transformation was demonstrated by a broad range of styrenes and 1,3-dienes, facile product modification, and synthesis of bioactive compounds (R)-(-)-curcumene and (S)-(+)-ibuprofen. Mechanistic studies demonstrated the carboxylation of phenylethylcopper complexes with CO2 as one key step. [ABSTRACT FROM AUTHOR]