Springer Organometallics for Green Catalysis: 63 (Topics in Organometallic Chemistry, 63)

Product Description This volume presents the latest developments in the use of organometallic catalysis for the formation of bulk chemicals and the production of energy, via green processes including efficient utilization of waste feedstocks from industry. The chemistry of carbon dioxide relating to its hydrogenation into methanol –an eco-friendly energy storage strategy– and its uses as C1 synthon for the formation of important building-blocks for fine chemicals industry are covered. Catalytic hydrogenations of various functional groups and hydrogen transfer reactions including the use of first row metal catalysts are presented as well as the conversion of alcohols to carboxylates via hydrogen transfer with a zero-waste strategy using water. Transformation of renewable or bio-based raw materials is surveyed through alkene metathesis and C–O bond activations and functionalizations. A green aspect for selective formation of C-C, C-O and C-N bonds involves direct regioselective C–H bond activations and functionalizations. These transformations can now be promoted under mild reaction conditions due to the use photoredox catalyts. C–H bond oxidation using visible light leads mainly to the formation of C–O and C–N bonds, whereas cross-coupled C–C bonds can be formed through the radical additions on (hetero) arenes using photoredox assisted mechanism. From the Back Cover This volume presents the latest developments in the use of organometallic catalysis for the formation of bulk chemicals and the production of energy, via green processes including efficient utilization of waste feedstocks from industry. The chemistry of carbon dioxide relating to its hydrogenation into methanol –an eco-friendly energy storage strategy– and its uses as C1 synthon for the formation of important building-blocks for fine chemicals industry are covered. Catalytic hydrogenations of various functional groups and hydrogen transfer reactions including the use of first row metal catalysts are presented as well as the conversion of alcohols to carboxylates via hydrogen transfer with a zero-waste strategy using water. Transformation of renewable or bio-based raw materials is surveyed through alkene metathesis and C–O bond activations and functionalizations. A green aspect for selective formation of C-C, C-O and C-N bonds involves direct regioselective C–H bond activations and functionalizations. These transformations can now be promoted under mild reaction conditions due to the use photoredox catalyts. C–H bond oxidation using visible light leads mainly to the formation of C–O and C–N bonds, whereas cross-coupled C–C bonds can be formed through the radical additions on (hetero) arenes using photoredox assisted mechanism. About the Author Pierre H. Dixneuf obtained his doctorate of Science in Rennes (France) with Prof René Dabard, on ferrocene chemistry, and carried out postdoctoral work as a CNRS researcher on the first steps of N-Heterocyclic Carbene metal complexes with Michael F. Lappert at the University of Brighton, UK. He became a professor at the University of Rennes in 1978. His research interests include both organometallic chemistry toward carbon rich complexes and innovative catalytic processes promoted by ruthenium catalysts. He developed first selective transformations of alkynes and incorporation of CO2, such as vinylcarbamates and carbonates, ruthenium-vinylidenes and –allenylidenes in catalysis, catalytic synthesis of heterocycles, alkene metathesis catalysts from allenylidenes and transformation of plant oils. He is contributing to  C–H bond activation/functionalization using ruthenium(II) catalysts especially operating in water. He has co-authored more than 450 publications, co-edited 6 books and his work has been acknowledged with several prizes including: A. v Humboldt prize for Research 1990, Le Bel SFC award and Grignard-Wittig Prize (GDCh) 2000, Institut universitaire de France membership since 2000, academ