Hydrocarbon Oxidation by Alkylperoxo Complexes of Tervalent Iron and Cobalt PDF Download
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Author: Cattien Van Nguyen
Publisher:
ISBN:
Category : Transition metal compounds
Languages : en
Pages : 366
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Book Description
Author: Cattien Van Nguyen
Publisher:
ISBN:
Category : Transition metal compounds
Languages : en
Pages : 366
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Book Description
Author: Ferman Albert Chavez
Publisher:
ISBN:
Category : Cobalt compounds
Languages : en
Pages : 438
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Book Description
Author: Roy G. Neville
Publisher:
ISBN:
Category :
Languages : en
Pages : 202
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Book Description
Author: N. M. Emanuel'
Publisher: Elsevier
ISBN: 1483149250
Category : Science
Languages : en
Pages : 425
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Book Description
Approx.424 pages
Author: Yunzhou Chen
Publisher:
ISBN:
Category : Alkanes
Languages : en
Pages : 0
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Book Description
Direct use of dioxygen (O2) in functionalizing organic molecules is highly desirable. In nature, enzymes perform alkane oxidation efficiently at ambient conditions. The transition metals involved in the active sites of enzymes play vital roles in binding with O2 and transferring electrons and protons during metabolism. Many metal-oxygen species, such as hydro(alkyl) peroxo complexes, are invoked as reactive intermediates in these biological processes. Given the complexity of enzymes, studying the reactivity of these enzymes with simple synthetic coordination compounds is one of the strategies. This thesis is mainly concerned with the oxidation of alkanes and alkenes catalyzed by tailor-made cobalt(III) alkylperoxo complexes at ambient conditions. In the first part, we report the design and synthesis of the highly electrophilic cobalt(III) alkylperoxo complex, [CoIII(qpy)(OOtBu)(NCCH3)]2+ (2), supported by a planar tetradentate quaterpyridine ligand (qpy = 2,2′:6′,2′′:6′′,2′′′-quaterpyridine). This complex activates C(sp3)–H bonds of a variety of organic molecules at ambient conditions and yields a series of alkylperoxo complexes with the general formula [CoIII(qpy)(OOR)(NCCH3)]2+ [RH = Et2O (3), THF (4), tBuOMe (5), ethylbenzene (6), toluene (7), cyclopentene (8), and 3-hexyne (9)], which have been well characterized by various spectroscopic techniques including NMR, ESI-MS, UV-vis, FT-IR, and CHN elemental analysis. The structures of these complexes have also been characterized by X-ray crystallography. In the second part, the mechanism for the alkane oxidation catalyzed by [CoIII(qpy)(OOR)(NCCH3)]2+ was extensively studied at room temperature and one atmospheric pressure. NMR study reveals the reaction stoichiometry. ESI-MS study indicates exogeneous O2 is crucial with the support of 18O-labeled experiments. Kinetics study by UV-vis and a significant kinetic isotopic effect resulted for the oxidation of ethylbenzene by 2 suggest a rate-limiting hydrogen-atom abstraction from organic substrates (R′H) by [CoIII(qpy)OOR]2+ via the proximal oxygen atom of the peroxo group (i.e., [CoIII(qpy)OOR]2+ + R′H → [CoII(qpy)]2+ + R′• + ROOH). The resulting alkyl radical R′• bound with O2 to form alkyl peroxyl radical R′OO•, which was rapidly scavenged by the [CoII(qpy)]2+ to give another alkylperoxo complex [CoIII(qpy)OOR′]2+. The proposed mechanism in the peroxidation of organic molecules b y alkyl(hydro)peroxo complexes is unprecedented. In the third part, we examine the catalytic properties of [CoIII(qpy)(OOR)(NCCH3)]2+ in aerobic oxidation of various substrates. Using ethylbenzene, cumene, cyclopentene, and cyclohexene as the substrates, [CoIII(qpy)(OOR)(NCCH3)]2+ are found to be active and robust catalysts to produce the corresponding hydroperoxides, alcohols, and ketones catalytically. A turnover of >3000 is achieved in the oxidation of cyclohexene for 7 d. In the fourth part, the reactivities of [CoIII(qpy)OOR]2+ with alkenes were explored. Alkenes with weak C–H bonds (e.g., 1,4-cyclohexadiene and cycloalkenes) resulted in C–H functionalization. In case there are no weak C–Hs in the alkenes (e.g., styrene), [CoIII(qpy)OOR]2+ catalyzes the polymerization of styrenes in O2 to produce polyalkylperoxo species. The [CoIII(qpy)(OOCH(OOtBu)CH2Ph)(NCCH3)]2+ ( bisalkylperoxo 11), has complex, been isolated and characterized by ESI-MS, NMR, and X-ray crystallography. In summary, this work demonstrates the highly electrophilic character of Co(III) alkylperoxo complexes supported by the qpy ligand. Under ambient conditions, these complexes are suitable catalysts to perform aerobic peroxidation of a variety of alkanes and alkenes
Author: D. Nicholls
Publisher:
ISBN:
Category :
Languages : en
Pages : 1161
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Book Description
Author: J. A. McCleverty
Publisher: Newnes
ISBN: 0080913164
Category : Science
Languages : en
Pages : 11845
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Book Description
Comprehensive Coordination Chemistry II (CCC II) is the sequel to what has become a classic in the field, Comprehensive Coordination Chemistry, published in 1987. CCC II builds on the first and surveys new developments authoritatively in over 200 newly comissioned chapters, with an emphasis on current trends in biology, materials science and other areas of contemporary scientific interest.
Author: Roger Sheldon
Publisher: Elsevier
ISBN: 0323150047
Category : Science
Languages : en
Pages : 447
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Book Description
Metal-Catalyzed Oxidations of Organic Compounds: Mechanistic Principles and Synthetic focuses on the oxidative transformations of functional groups. This book explores oxidation as being extensively used in the laboratory synthesis of fine organic chemicals and in the manufacture of large-volume petrochemicals. Organized into two parts encompassing 13 chapters, this book starts with an overview of the mechanistic principles of oxidation–reduction in biochemical, organic, and inorganic systems. This text then proceeds with a discussion of the use of molecular oxygen, hydrogen peroxide, and alkyl hydroperoxides as primary oxidants. Other chapters explore stoichiometric oxidations with metal oxidants, which include permanganate and chromic acid. This book discusses as well the synthetic applications of catalytic oxidations as well as the technology of petrochemical oxidation. The final chapter deals with the autoxidations of sulfur, phosphorus, and nitrogen compounds. This book is intended for chemists involved in organic synthesis, catalysis, and organometallic chemistry, both in academic institutions and in industrial laboratories.
Author: Manas Sutradhar
Publisher: Royal Society of Chemistry
ISBN: 1839160896
Category : Science
Languages : en
Pages : 526
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Book Description
Vanadium is one of the more abundant elements in the Earth’s crust and exhibits a wide range of oxidation states in its compounds making it potentially a more sustainable and more economical choice as a catalyst than the noble metals. A wide variety of reactions have been found to be catalysed by homogeneous, supported and heterogeneous vanadium complexes and the number of applications is growing fast. Bringing together the research on the catalytic uses of this element into one essential resource, including theoretical perspectives on proposed mechanisms for vanadium catalysis and an overview of its relevance in biological processes, this book is a useful reference for industrial and academic chemists alike.
Author: Armando J. L. Pombeiro
Publisher: John Wiley & Sons
ISBN: 111937880X
Category : Science
Languages : en
Pages : 680
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Book Description
Presents state-of-the-art information concerning the syntheses of valuable functionalized organic compounds from alkanes, with a focus on simple, mild, and green catalytic processes Alkane Functionalization offers a comprehensive review of the state-of-the-art of catalytic functionalization of alkanes under mild and green conditions. Written by a team of leading experts on the topic, the book examines the latest research developments in the synthesis of valuable functionalized organic compounds from alkanes. The authors describe the various modes of interaction of alkanes with metal centres and examine theoxidative alkane functionalization upon C-O bond formation. They address the many types of mechanisms, discuss typical catalytic systems and highlight the strategies inspired by biological catalytic systems. The book also describes alkane functionalization upon C-heteroatom bond formation as well as oxidative and non-oxidative approaches. In addition, the book explores non-transition metal catalysts and metal-free catalytic systems and presents selected types of functionalization of sp3 C-H bonds pertaining to substrates other than alkanes. This important resource: Presents a guide to the most recent advances concerning the syntheses of valuable functionalized organic compounds from alkanes Contains information from leading experts on the topic Offers information on the catalytic functionalization of alkanes that allows for improved simplicity and sustainability compared to current multi-stage industrial processes Explores the challenges inherent with the application of alkanes as starting materials for syntheses of added value functionalized organic compounds Written for academic researchers and industrial scientists working in the fields of coordination chemistry, organometallic chemistry, catalysis, organic synthesis and green chemistry, Alkane Functionalization is an important resource for accessing the most up-to-date information available in the field of catalytic functionalization of alkanes.
