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Organometallics for Green Catalysis de Pierre H. Dixneuf

Organometallics for Green Catalysis: Topics in Organometallic Chemistry, cartea 63

Editat de Pierre H. Dixneuf, Jean-François Soulé
en Limba Engleză Hardback – 6 mar 2019
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.

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Specificații

ISBN-13: 9783030109547
ISBN-10: 3030109542
Pagini: 240
Ilustrații: X, 301 p.
Dimensiuni: 155 x 235 mm
Greutate: 0.61 kg
Ediția:1st ed. 2019
Editura: Springer International Publishing
Colecția Springer
Seria Topics in Organometallic Chemistry

Locul publicării:Cham, Switzerland

Cuprins

Metal-Catalysed Hydrogenation of CO2 into Methanol.- Catalytic C-C Bond Formations from CO2 with Alkenes.- Recent advances on CO2 utilization as C1 building block in C-N and C-O bond formation.- “Alkene Metathesis for Transformation of Renewables”.- Metal-Catalyzed Aromatic C-O Bond Activation/Transformation.- Hydrogenation/Dehydrogenation of Unsaturated Bonds with Iron Pincer Catalysis.- Conversion of Alcohols to Carboxylates Using Water and Base with H2 Liberation.- Selective Transfer-hydrogenation of α,β-Unsaturated Carbonyl Compounds.- Functionalization of C(sp2)–H Bonds of Arenes and Heteroarenes Assisted by Photoredox-Catalysts for the C–C Bond Formation.- Green Cross-Coupling using Visible-light for C-O and C-N Bond Formation.

Notă biografică

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-edited6 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, academie des sciences IFP prize, Sacconi medal (Italy) in 2006 and Spanish-and Chinese Society of Chemistry award in 2014. He is currently an Emeritus Professor at the University of Rennes, France, where he was university vice-president for research (01-04) and founded the research “Institut de chimie de Rennes” in 2000. 

Jean-François Soulé received his MSc in molecular chemistry from the University Paul Sabatier, Toulouse (France). Then, he completed his PhD in 2007 working on the Petasis reaction applied on the synthesis of biological interest molecules under the supervision of the Prof. Jean-Marie Beau, at the Institut de Chimie des Substances Naturelles, Gif-sur- Yvette (France). In 2010, he joined the group of theProf. Shū Kobayashi at the University of Tokyo (Japan) as a postdoctoral fellow, where he worked on the development of heterogeneous nanoparticles to catalyze organic transformations, namely tandem oxidation using gold nanoparticles for the selective synthesis of amides or imines from simple alcohols and amines, then cross-coupling reactions using nickel nanoparticles.  In October 2013, he was appointed as "Chargé de Recherche" CNRS at the University of Rennes in the group of Dr. Henri Doucet. His main interest focuses on the development of sustainable chemistry, notably, transition-metals catalyzed C–H functionalizations.

Textul de pe ultima copertă

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.

Caracteristici

Provides an overview of the latest innovative organometallic catalysts including pincer and cyclometalated complex structures Discusses transformation of raw-materials into fine chemicals involving CO2 transformations and Hydrogen transfer reactions Presents recent advances in activation of C-O bonds and Functionalization of C–H bonds using light energy