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|a 547/.2
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|a Pincer-metal complexes :
|b applications in catalytic dehydrogenation chemistry /
|c edited by Akshai Kumar.
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|a Amsterdam, The Netherlands ;
|a Cambridge, MA :
|b Elsevier,
|c [2022]
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|a 1 online resource (xiv, 229 pages) :
|b illustrations (black & white)
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|a text
|b txt
|2 rdacontent
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|a computer
|b c
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|a online resource
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|a Includes bibliographical references and index.
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|a Online resource; title from digital title page (viewed on December 30, 2021).
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|a Front Cover -- Pincer-Metal Complexes -- Copyright Page -- Contents -- List of contributors -- Foreword -- Preface -- 1 Application of pincer metal complexes in catalytic transformations -- 1.1 Introduction -- 1.2 Dehydrogenation of ammonia borane and its derivatives -- 1.3 Dinitrogen activation using pincer ligands -- 1.3.1 Catalytic dinitrogen activation using Mo pincer catalyst -- 1.3.2 Catalytic dinitrogen activation using 3d metal pincer catalyst -- 1.3.3 Catalytic dinitrogen fixation using earlier transition metals (V, Ti, Zr)
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|a 1.3.4 N-X bond formation with metal nitride in pincer complexes -- 1.3.5 Catalytic silylation of dinitrogen using transition metal pincer complexes -- 1.4 Pincer complexes as hydrogenation catalyst -- 1.4.1 Ester hydrogenation -- 1.4.2 Amide hydrogenation -- 1.4.3 Hydrogenation of urea, carbamate, carbonate, and imides derivatives -- 1.4.4 Nitrile hydrogenation -- 1.4.5 Hydrogenation of alkynes -- 1.5 Coupling reaction: C-C bond formation reaction -- 1.5.1 Mizoroki-Heck reaction -- 1.5.2 Suzuki-Miyaura reaction -- 1.5.3 Sonogashira, Negishi, Kumada-Corriu, Stille cross-coupling
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|a 1.6 Redox-Active Pincer Complexes -- 1.7 Conclusion -- References -- 2 Pincer-group(8) and pincer-group(9) metal complexes for catalytic alkane dehydrogenation reactions -- 2.1 Introduction -- 2.1.1 Alkane dehydrogenation -- 2.2 Dehydrogenation reactions of alkane using pincer-Ir complexes -- 2.2.1 Initial reports based on pincer-Ir catalysts -- 2.2.2 Alkane dehydrogenation by PC(sp2)P-Ir systems -- 2.2.3 Alkane dehydrogenation by PYC(sp2)ZP-Ir (Y=O, S, CH2) systems -- 2.2.4 Mechanism of pincer-Ir-catalyzed alkane dehydrogenation -- 2.2.5 Solid/gas-phase alkane dehydrogenation
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|a 2.2.6 Continuous-flow gas-phase alkane dehydrogenation -- 2.2.7 Alkane dehydrogenation by PC(sp3)P-Ir complexes -- 2.2.8 Alkane dehydrogenation by POCN-Ir, PBP-Ir, PNP-Ir, and PAlP complexes -- 2.2.9 Alkane dehydrogenation by PXC(sp2)NP-Ir-HCl (X=O, S) complexes -- 2.2.10 Alkane dehydrogenation by non-phosphine-based iridium pincer complexes -- 2.3 Dehydrogenation of alkanes by pincer-metal complexes other than iridium -- 2.3.1 Ruthenium pincer complexes for alkane dehydrogenation -- 2.3.2 Osmium pincer complexes for alkane dehydrogenation
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|a 2.3.3 Rhodium pincer complexes for alkane dehydrogenation -- 2.4 Applications of alkane dehydrogenation -- 2.4.1 Alkane metathesis -- 2.4.2 Alkane coupling -- 2.4.3 Synthesis of aromatics -- 2.4.3.1 Dehydroaromatization -- 2.4.3.2 Cyclodimerization -- 2.4.3.3 Alkyl group cross metathesis -- 2.4.3.4 Alkyl-aryl coupling -- 2.4.4 Functionalization of alkanes -- 2.4.4.1 Silylation and borylation -- 2.4.4.2 Formylation and aminomethylation -- 2.5 Summary and outlook -- References -- 3 Transition metal-catalyzed dehydrogenation of methanol and related transformations -- 3.1 Introduction
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|a Pincer-Metal Complexes: Applications in Catalytic Dehydrogenation Chemistry provides an overview of pincer-metal catalytic systems that transform hydrocarbons and their derivatives from an synthetic and mechanistic point-of-view. This book provides thorough coverage of the operating mechanisms and dehydrogenation catalyst compatibility in both functionalized and unfunctionalized hydrocarbon systems. In addition, it includes success stories of pincer-metal systems, as well as current and future challenges. The book is an ideal reference for researchers practicing synthetic organic chemistry, inorganic chemistry, organometallic chemistry and catalysis in academia and industry. In recent years there has been a surge in the research on hydrocarbon dehydrogenation catalytic systems that are compatible with polar substituents. This helps facilitate formulation of tandem processes that are not limited to hydrocarbon transformation but also to hydrocarbon functionalization in a single pot.
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650 |
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|a Dehydrogenation.
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650 |
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|a Transition metal compounds
|x Industrial applications.
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650 |
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6 |
|a D�eshydrog�enation.
|0 (CaQQLa)201-0151292
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650 |
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6 |
|a M�etaux de transition
|0 (CaQQLa)201-0043196
|x Compos�es
|0 (CaQQLa)201-0043196
|x Applications industrielles.
|0 (CaQQLa)201-0374039
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650 |
|
7 |
|a Dehydrogenation
|2 fast
|0 (OCoLC)fst00889848
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700 |
1 |
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|a Kumar, Akshai,
|e editor.
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776 |
0 |
8 |
|i Print version:
|z 0128220910
|z 9780128220917
|w (OCoLC)1240771309
|
856 |
4 |
0 |
|u https://sciencedirect.uam.elogim.com/science/book/9780128220917
|z Texto completo
|