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A mild and efficient method for the cobalt-catalyzed hydroxyperfluoroalkylation of alkenes has been developed. This method demonstrated broad substrate scope, good yields, and mild conditions with the tolerance of mono-, di-, and trisubstituted alkenes including both styrenes and non-activated aliphatic olefins. This strategy offered a valuable solution for rapid and efficient construction of β-perfluoro-alkyl alcohols using widely available and inexpensive perfluoroalkyl bromides- and atmospheric oxygen. [ABSTRACT FROM AUTHOR]

[Display omitted] The photoreduction of the green-house gas CO 2 into carbon monoxide (CO) is a growing process due to the use of CO for the production of methanol in the Fischer-Tropsch process and the synthesis of many of the bulk chemicals. Here, we have synthesized phosphorous doped graphitic carbon nitride (P-g-C 3 N 4) sensitized by the cobalt phthalocyanine complex for the molecular reduction of CO 2 into CO under visible-light irradiation—the doping of phosphorous improved the stability as well as the harvesting of the visible region. The CoPc@P-g-C 3 N 4 hybrid photocatalyst exhibited the highest efficiency for the photoreduction of CO 2 with a high yield of 295 μmol-g−1 for CO under the experimental conditions. Also, hydrogen with low concentration was identified as a by-product under the experimental conditions. The photocatalyst had stability for six consecutive runs with negligible loss of the activity and no leaching of the cobalt content at the end of the sixth run of the photoreduction experiment. The stability of the photocatalysts is an advantage, which made it a suitable candidate for the current reaction system. [ABSTRACT FROM AUTHOR]