Advances in Organometallic Chemistry and Catalysis

Name: Advances in Organometallic Chemistry and Catalysis | The Silver / Gold Jubilee International Conference on Organometallic Chemistry Celebratory Book
Brand: Wiley
Price: 169.99 EUR
Availability: OnlineOnly

The Silver / Gold Jubilee International Conference on Organometallic Chemistry Celebratory Book

Armando J. L. Pombeiro(Herausgeber*in)

Wiley (Verlag)

Erschienen am 9. Oktober 2013

736 Seiten

E-Book

ePUB mit Adobe-DRM

Systemvoraussetzungen

E-Book

PDF mit Adobe-DRM

Systemvoraussetzungen

978-1-118-74280-8 (ISBN)

169,99 €inkl. 7% MwSt.

Systemvoraussetzungen

für ePUB mit Adobe-DRM und PDF mit Adobe-DRM

(Hinweis: Die Auswahl des von Ihnen gewünschten Dateiformats und des Kopierschutzes erfolgt erst im System des E-Book Anbieters)

E-Book Einzellizenz

Als Download verfügbar

Beschreibung

Weitere Details

Weitere Ausgaben

Person

Inhalt

Cover
Title Page
Contents
Preface
Contributors
Part I Activation and Functionalization of Carbon Single Bonds and of Small Molecules
Chapter 2 Toward Functionalization of Alkanes Under Environmentally Benign Conditions
2.1 Introduction
2.2 Peroxidative Oxidations of Alkanes to Alcohols and Ketones, Catalyzed by Transition Metal Complexes
2.3 Metal-Free Alkane Hydrocarboxylation and Related Carboxylation
2.4 Final Remarks
Acknowledgments
References
Chapter 3 Self-assembled Multicopper Complexes and Coordination Polymers for Oxidation and Hydrocarboxylation of Alkanes
3.1 Introduction
3.2 Self-Assembly Synthesis in Aqueous Medium
3.3 Aminoalcoholate Multicopper Complexes and Coordination Polymers
3.4 Application in Alkane Oxidation
3.5 Application in Alkane Hydrocarboxylation
3.6 Concluding Remarks
Abbreviations
Acknowledgments
References
Chapter 4 Activation of C-O and C-F Bonds by Pincer-iridium Complexes
4.1 Introduction
4.2 Cleavage and Oxidative Addition Of C-O Bonds
4.3 Cleavage and Oxidative Addition of C-F Bonds
4.4 Summary
Acknowledgments
References
Chapter 5 Functionalization of sp2 and sp3 Carbon Centers Catalysed by Polyoxometalates and Metalloporphyrins
5.1 Introduction
5.2 Functionalization of sp3 Carbon Centers under Homogeneous Conditions
5.3 Functionalization of sp2 Carbon Centers under Homogeneous Conditions
5.4 Functionalization of sp2 AND sp3 Carbon Centers under Heterogeneous Conditions
5.5 Final Remarks
Acknowledgments
References
Chapter 6 Quasi-borinium Cation Based on Cobalt Bis(dicarbollide): Its Lewis Acidity and C-H and C-X Bond Activation
6.1 Introduction
6.2 Quasi-Borinium Cations: Formation and Reactivity
6.3 C-H Activation of Arenes
6.4 C-X Activation of Halogen Alkanes
6.5 Lewis Acidity of Quasi-Borinium Cation
References
Chapter 7 Transition-metal-promoted Functionalization of Carboranes
7.1 Introduction
7.2 [2+2+2] Cycloaddition of Ni-Carboryne with Alkynes
7.3 Coupling Reaction of Ni-Carboryne with Alkenes
7.4 [2+2+2] Cycloaddition of Ni-Carboryne with Activated Alkenes and Alkynes
7.5 Ni-Catalyzed [2+2+2] Cycloaddition of Carboryne with Alkynes
7.6 Pd/Ni-Cocatalyzed [2+2+2] Cycloaddition of 1,3-Dehydro-o-Carborane with Alkynes
7.7 Reaction of Zirconocene-Carboryne with Polar Unsaturated Molecules
7.8 Reaction of Zirconocene-Carboryne with Pyridines
7.9 Reaction of Zirconocene-Carboryne with Alkynes and Alkenes
7.10 Zr/Ni Co-Mediated [2+2+2] Cycloaddition of Carboryne with Two Different Alkynes
7.11 Zr/Ni Co-Mediated [2+2+2] Cycloaddition of Carboryne with Unactivated Alkenes and Alkynes
7.12 Conclusions and Perspectives
Acknowledgment
References
Chapter 8 Weak Interactions and M-H Bond Activation
8.1 Introduction
8.2 Metal Hydrides in Hydrogen Bonding
8.3 Hydrogen Bonding and Proton Transfer
8.4 Activation of H2 in the Metal Coordination Sphere
8.5 Conclusions
Acknowledgment
References
Chapter 1 Organometallic Complexes as Catalysts in Oxidation of C-H Compounds
1.1 Introduction
1.2 Oxygenation Reactions with Oxidants other than Peroxides
1.3 Oxygenation of C-H Bonds with Peroxides
1.4 Conclusions and Outlook
Acknowledgment
References
Part II Organometallic Synthesis and Catalysis
Chapter 9 Complexes with Protic N-Heterocyclic Carbene (NR,NH-NHC) Ligands
9.1 Introduction
9.2 Complexes with NR,NH- And NH,NH-NHCS from Cyclic Ligand Precursors
9.3 Complexes with NR,NH- And NH,NH-NHCs by Template-Controlled Cyclization Reactions
9.4 Complexes with NR,NH-NHCs by Oxidative Addition of Azoles
9.5 Conclusion
Acknowledgment
References
Chapter 10 Cyclopentadienyl-functionalized N-Heterocyclic Carbene Complexes of Iron and Nickel: Catalysts for Reductions
10.1 Introduction
10.2 Preparation of Cyclopentadienyl-Functionalized N-Heterocyclic Carbene Ligands
10.3 Cyclopentadienyl-Functionalized N-Heterocyclic Carbene Complexes of Iron and Nickel
10.4 Half-Sandwich Iron and Nickel NHC Complexes as Catalysts for Reductions
References
Chapter 11 Palladium-(acyclic diaminocarbene) Species as Alternative to Palladium-(nitrogen heterocyclic carbenes) in Cross-coupling Catalysis
11.1 Introduction
11.2 Synthetic Approaches to Palladium Complexes Bearing ADC Ligands
11.3 Catalytic Applications of Palladium-(ADC)s
11.4 Final Remarks
Acknowledgments
References
Chapter 12 Synthesis of Metallocenes Via Metathesis in Metal Coordination Spheres
12.1 Introduction
12.2 Polymers Bearing Metallocene Moieties by Ring-Opening Metathesis Polymerization or Acyclic Diene Metathesis Polymerization
12.3 Synthesis of Metallocenes by Ring-Closing Metathesis
12.4 Synthesis of Metallocenes by Cross-Metathesis
12.5 Conclusions and Outlook
References
Chapter 13 Metal-mediated [2+3] Dipolar Cycloaddition to Substrates with CN Triple Bond: Recent Advances
13.1 Introduction
13.2 Metal-Mediated [2 + 3] DIpolar Cycloaddition to Nitriles and Isocyanides: Synthetic Studies
13.3 Metal-Mediated [2 + 3] Cycloaddition to Nitriles and Isocyanides: Theoretical Studies
13.4 Final Remarks
Acknowledgments
References
Chapter 14 Coordination Chemistry of Oxazoline/Thiazoline-based P,N Ligands
14.1 Definition of Polyfunctional Ligands
14.2 P,N-Chelating Ligands Based on Oxazoline/Thiazoline System
Summary
Acknowledgments
References
Chapter 15 ``Click'' Copper Catalyzed Azide-alkyne Cycloaddition (CuAAC) in Aqueous Medium
15.1 Introduction
15.2 CuAAC: Organic Solvents Versus Aqueous Media
15.3 Final Remarks
Acknowledgments
References
Chapter 16 Organogold Catalysis: Homogeneous Gold-catalyzed Transformations for a Golden Jubilee
16.1 Introduction
16.2 Electrophilic Gold Species: Principle and Main Modes of Reactivity
16.3 Gold Catalysts
16.4 Gold-Catalyzed Activation of Multiple Carbon-Carbon Bonds: Functionalization by Addition of Oxygen, Nitrogen, Sulfur, or Carbon Nucleophiles
16.5 Intermolecular Trapping of Reactive Organogold Intermediates
16.6 Oxene and Nitrene Precursors as Nucleophiles
16.7 Coupling Reactions
16.8 Generation of Structural Complexity
16.9 Asymmetric Catalysis
16.10 Gold Catalysis and Total Synthesis
16.11 Conclusion
References
Chapter 17 Vanadium(IV) Complexes Derived from Aromatic o-Hydroxyaldehydes and Tyrosine Derivatives: Catalytic Evaluation in Sulfoxidations
17.1 Introduction
17.2 Results and Discussion
17.3 Conclusions
Acknowledgments
References
Chapter 18 Microwave-assisted Catalytic Oxidation of Alcohols to Carbonyl Compounds
8.1 Introduction
18.2 Homogeneous Catalysis
18.3 Heterogeneous Catalysis
18.4 Conclusions
References
Chapter 19 Oxidation of Glycerol with Hydrogen Peroxide Catalyzed by Metal Complexes
19.1 Introduction
19.2 Glycerol Oxidation with H2O2 Catalyzed by the Os3(CO)12/Pyridine Combination
19.3 Oxidation of Glycerol with H2O2 Catalyzed by Soluble Complex [LMn(O)3MnL](PF6)2 and its Heterogenized form [LMn(O)3MnL]2[SiW12O40]
19.4 Oxidation of Glycerol with TBHP or H2O2 Catalyzed by Water-Soluble Tetracopper(II) Triethanolaminate Copper Comple
19.5 Conclusions
Acknowledgments
References
Chapter 20 Involvement of an Acetato Ligand in the Reductive Elimination Step of the Rhodium-catalyzed Methanol Carbonylation
20.1 Introduction
20.2 NMR and Infrared High Pressure Studies and DFT Calculations
20.3 Conclusion
References
Chapter 21 Half-sandwich Rhodium(III), Iridium(III), and Ruthenium(II) Complexes with Ancillary Pyrazole-based Ligands
21.1 Introduction
21.2 Half-Sandwich Ru(II) Derivatives
21.3 Half-Sandwich Rh(III) and Ir(III) Derivatives
21.4 Half-Sandwich Derivatives with Acylpyrazolone Ligands
21.5 Conclusions and Perspectives
References
Chapter 22 Carbon-scorpionate Complexes in Oxidation Catalysis
22.1 Introduction
22.2 Peroxidative Oxygenations of Alkanes
22.3 Oxidation of Alkanes by Molecular Oxygen
22.4 Carboxylation of Light Alkanes
22.5 Baeyer-Villiger Oxidation of Ketones
22.6 Final Remarks
Acknowledgments
References
Chapter 23 Toward Chemoselective Bioconjugative Desulfitative Catalysis
23.1 Introduction
23.2 Thioorganic-Boronic Acid Desulfitative Cross-Coupling
23.3 Cu-Catalyzed Desulfitative Coupling
23.4 Conclusion: Approaching Aqueous Desulfitative Reaction Conditions for Biological Applications
References
Chapter 24 Sulfoxide Redox Chemistry with Molybdenum Catalysts
24.1 Introduction
24.2 Results and Discussion
24.3 Conclusions
24.4 Computational Details
Acknowledgment
References
Chapter 25 A New Family of Zirconium Complexes Anchored by Dianionic Cyclam-based Ligands: Syntheses, Structures, and Catalytic Applications
25.1 Introduction
25.2 Syntheses and Molecular Structures
25.3 Thermaly Induced Orthometallation and Intramolecular Hydroamination of Aminoalkenes
25.4 ROP of Lactide and Cyclam Functionalization
25.5 Concluding Remarks
Aknowledgment
References
Chapter 26 Metal-organo Multicatalysis: An Emerging Concept
26.1 Introduction
26.2 Cooperative Catalysis
26.3 Amines as Catalysts
26.4 N-Heterocyclic Carbenes as Organocatalysts
26.5 Brønsted Acids as Organocatalysts
26.6 Relay and Sequential Catalysis
26.7 N-Heterocyclic Carbenes as Organocatalysts
26.8 Brønsted Acids as Organocatalysts
26.9 Conclusion
References
Part III Organometallic Polymerization Catalysis
Chapter 27 Coordinative Chain Transfer Polymerisations and Copolymerisations by Means of Rare Earths Organometallic Catalysts for the Synthesis of Tailor-made Polymers
27.1 Introduction
27.2 Basic Concepts
27.3 Catalytic Systems and Their Applications in Coordinative Chain Transfer Polymerization
27.4 Catalytic Systems and their Applications in Coordinative Chain Transfer Copolymerization (CCTCOP)
27.5 Discussion
27.6 Conclusion-Perspectives
References
Chapter 28 Charge-neutral and Cationic Complexes of Large Alkaline Earths for Ring-opening Polymerization and Fine Chemicals Catalysis
28.1 Synthesis of Charge-Neutral Heteroleptic Ring-Opening Polymerization Catalysts Based on Large Alkaline Earths
28.2 Synthesis of Well-Defined, Solvent-Free Cationic Complexes of the Large Alkaline Earths
28.3 Immortal Ring-Opening Polymerizations of Cyclic Esters Catalyzed by Single-Site Alkaline Earth Catalysts
28.4 Intermolecular Hydroamination of Activated Alkenes Catalyzed by Charge-Neutral Heteroleptic Complexes of Large Alkaline Earths
28.5 Intermolecular Hydrophosphination of Styrene Catalyzed by Charge-Neutral Heteroleptic Complexes of Large Alkaline Earths
28.6 Hydrophosphonylation of Aldehydes and Nonactivated Ketones by Charge-Neutral Homoleptic and Heteroleptic Complexes of Large Alkaline Earths
Acknowledgments
References
Part IV Organometallic Polymers and Materials
Chapter 29 Organometallic Polymers
29.1 Introduction
29.2 Metal-Backbone Organometallic Polymers
29.3 Metallic-Side Organometallic Polymers
29.4 Summary And Conclusions
Acknowledgements
References
Chapter 30 From Serendipity to Porosity: Synthesis and Reactivity of Coordination Polymers Based on Copper Trinuclear Triangular Motifs
30.1 Introduction
30.2 Coordination Polymers
30.3 Trinuclear Triangular CuII Moieties to Build CPs
30.4 Cu(pz)2-Based Coordination Polymers. A Case of "Porosity Without Pores"
30.5 Concluding Remarks
Acknowledgments
Dedication
References
Chapter 31 Organometallic Nanoparticles
31.1 Introduction
31.2 Ruthenium
31.3 Ligand-Stabilized Ruthenium Nanoparticles
31.4 Iron
31.5 Cobalt
31.6 Conclusion
Acknowledgments
References
Chapter 32 Organometallic Compounds in the Synthesis of New Materials: Old Ligands, New Tricks
32.1 Introduction
32.2 Functionalized Alcohols as Ligands
32.3 Organometallics in the Synthesis of Heterometallic Complexes
32.4 Conclusions
Acknowledgments
References
Chapter 33 The Role of Organometallic Complexes in the Synthesis of Shaped Carbon Materials
33.1 Introduction
33.2 General Comments
33.3 The Shapes Taken by Carbon
33.4 The Catalyst-Carbon Interaction
33.5 Mechanism of Carbon Growth from a Metal Particle
33.6 Organometallic Catalysts and Carbon Synthesis
33.7 Conclusion
Acknowledgments
References
Chapter 34 Metal Catalysis in Fullerene Chemistry
34.1 Introduction to Fullerenes
34.2 General Remarks on the Chemical Reactivity of Fullerenes
34.3 Metal-Mediated Reactions in Fullerene Chemistry
34.4 Asymmetric Catalysis in Fullerene Chemistry
34.5 Conclusions
References
Chapter 35 Organometallic Complexes of Sumanene
35.1 Introduction
35.2 Organolithium Complexes of Sumanene
35.3 ?6-Coordination Complexes of Sumanene
35.4 Concluding Remarks and Future Prospects
Acknowledgements
References
Chapter 36 Advances in Luminescent Tetracoordinate Organoboron Compounds
36.1 Introduction
36.2 Luminescent Tetracoordinate Organoboron Compounds
36.3 Applications
36.4 Conclusions
Acknowledgment
References
Chapter 37 Mechanochemistry: A Tool in the Synthesis of Catalysts, Metallodrugs, and Metallopharmaceuticals
37.1 Introduction
37.2 Mechanochemistry in Supramolecular Synthesis
37.3 Mechanochemistry in Organic and Coordination Synthesis
37.4 Mechanochemistry in Metallopharmaceuticals and Metallodrugs
37.5 Mechanochemistry in Catalysis and Catalysts
37.6 Conclusions
References
Part V Organometallic Chemistry and Sustainable Energy
Chapter 38 Organometallic Complexes for Dye-sensitized Solar Cells (DSSC)
38.1 Introduction
38.2 Ruthenium Complexes for DSSC
38.3 Non-Ruthenium Metal Complexes for DSSC
38.4 Structure of Metal Complex Sensitizers
38.5 Performance Evaluation of Dye-Sensitized Solar Cells
38.6 Research Development on Metal Complexes for Dye-Sensitized Solar Cells
38.7 The Interaction and the Binding Mode of Dyes on TiO2 Surface
38.8 Metal Complexes as Redox Mediators for DSSC
38.9 Conclusion
References
Chapter 39 Synthetic Photosynthesis for the Conversion of Large Volumes of Carbon Dioxide into Energy-Rich Molecules: Saving Fossil Fuels by Recycling Carbon
39.1 Introduction
39.2 The Past
39.3 The Present
39.4 The Future: Synthetic Photosynthesis
39.5 Concluding Remarks
References
Chapter 40 Ionic Liquids for Hydrogen Storage: Opportunities for Organometallic Chemistry
40.1 Introduction
40.2 Ionic Liquids
40.3 Hydrogen Storage Materials: Hydrogen-Rich Molecules
40.4 Hydrogen Storage Systems Involving Ionic Liquids
40.5 Conclusion and Outlook
References
Part VI Bioorganometallic Chemistry
Chapter 41 Metal Carbonyls for CO-based Therapies: Challenges and Successes
41.1 Introduction
41.2 CO in Biology and in Therapy-Origin, Targets, and Therapeutic Potential
41.3 Therapeutic Delivery of CO
41.4 Final Remarks and Perspectives
References
Chapter 42 The Ferrocifen Family as Potent and Selective Antitumor Compounds: Mechanisms of Action
42.1 Introduction
42.2 Context and Background
42.3 Ferrocene and Medicinal Chemistry
42.4 Synthesis and Behavior of Ferrocifen Derivatives
42.5 Synthesis and Behavior of Ferrocenophane Derivatives
42.6 Ferrocenophane Transposition Products and Pinacols
42.7 Formulation: Research into Nanocapsules Best Suited for in Vivo Testing of Ferrocifens
42.8 Conclusion
Acknowledgements
References
Chapter 43 On the Track to Cancer Therapy: Paving New Ways With Ruthenium Organometallics
43.1 Introduction
43.2 Our Strategy in Bioorganometallic Chemistry
43.3 Biological Activity
43.4 Distribution in the Blood
43.5 Intracellular Distribution
43.6 Mechanisms of Action
43.7 Final Remarks
Acknowledgments
References
Chapter 44 Organometallic Chemistry of Rhenium and Technetium Fueled by Biomedical Applications
44.1 Introduction
44.2 Basic Concepts on Nuclear Medicine and Radiopharmaceuticals
44.3 Re(I) and Tc(I) Tricarbonyl Precursors
44.4 Organometallic Building Blocks for the Design of Radiopharmaceuticals
44.5 Perfusion Agents
44.6 Target-Specific Complexes
44.7 Concluding Remarks
References
Chapter 45 Metal-based Indolobenzazepines and Indoloquinolines: From Moderate cdk Inhibitors to Potential Antitumor Drugs
45.1 Introduction
45.2 Indolobenzazepines as Moderate cdk Inhibitors
45.3 Toward Metal-Based Indolobenzazepines as Potential Anticancer Drugs
45.4 Indolo[3,2-c]Quinolines and Their Metal Complexes
45.5 Outlook
Acknowledgments
References
Chapter 46 Metal-based Chelates and Nanosystems as MRI Contrast Agents
46.1 Introduction
46.2 Magnetic Resonance Imaging
46.3 Contrast Enhancement
46.4 Contrast Agents
46.5 T1 Contrast Agents
46.6 T2 Contrast Agents
46.7 Classification of Contrast Agents
46.8 Nanocarriers
References
Part VII Organometallic Electrochemistry
Chapter 47 Electrochemistry and Supramolecular Interactions of ``Ferrocifen'' Anticancer Drugs with Cyclodextrins and Lipid Bilayers: An Electrochemical Overview
47.1 Introduction
47.2 Deciphering the Activation Sequence of Ferrocifens
47.3 Supramolecular Interactions of Ferrocifens with Cyclodextrins and Lipid Bilayers
47.4 Conclusion
Acknowledgments
References
Chapter 48 Electrochemistry of Fischer Aminocarbene Complexes: Effects of Structure on Redox Properties, Electron Distribution, and Reaction Mechanisms
48.1 Introduction
48.2 Value of Electrochemistry
48.3 Fundamental Electrochemical Behavior of Aminocarbene Complexes
48.4 Basic Group of Aminocarbenes
48.5 Hetaryl Chromium(0) Aminocarbenes
48.6 Mechanistic Investigations
48.7 Comparison of Aminocarbene and Alkoxycarbene Complexes
48.8 Summary
References
Chapter 49 Electron Transfer-induced Coordination Changes in Organometallic Complexes with Non-innocent Hemilabile Ligands
49.1 Introduction
49.2 Discussion of Results
49.3 Concluding Remarks
Acknowledgments
References
Chapter 50 Redox Potential-Structure Relationships and Parameterization in Characterization and Identification of Organometallic Compounds
50.1 Introduction
50.2 Parameterization of Ligands and Metal Centers
50.3 Final Comments
Acknowledgments
Abbreviations
References
Chapter 51 Endohedral Metallofullerenes Today: More and More Versatile Ships in Multiform Bottles-Electrochemistry of X-Ray Characterized Monometallofullerenes
51.1 Introduction
51.2 C60-Monometal Endohedral Metallofullerenes
51.3 C72-Monometal Endohedral Metallofullerenes
51.4 C74-Monometal Endohedral Metallofullerenes
51.5 C80-Monometal Endohedral Metallofullerenes
51.6 C82-Monometal Endohedral Metallofullerenes
51.7 C84-Monometal Endohedral Metallofullerenes
51.8 C90-Monometal Endohedral Metallofullerenes
51.9 C92-Monometal Endohedral Metallofullerenes
51.10 C94-Monometal Endohedral Metallofullerenes
51.11 Conclusion
Aknowledgment
References
Postscript: A Short History of the ICOMC Conferences
Index
bins

Systemvoraussetzungen

Dateiformat: ePUB
Kopierschutz: Adobe-DRM (Digital Rights Management)

Systemvoraussetzungen:

Computer (Windows; MacOS X; Linux): Installieren Sie bereits vor dem Download die kostenlose Software Adobe Digital Editions (siehe E-Book Hilfe).
Tablet/Smartphone (Android; iOS): Installieren Sie bereits vor dem Download die kostenlose App Adobe Digital Editions oder die App PocketBook (siehe E-Book Hilfe).
E-Book-Reader: Bookeen, Kobo, Pocketbook, Sony, Tolino u.v.a.m. (nicht Kindle)

Das Dateiformat ePUB ist sehr gut für Romane und Sachbücher geeignet – also für „fließenden” Text ohne komplexes Layout. Bei E-Readern oder Smartphones passt sich der Zeilen- und Seitenumbruch automatisch den kleinen Displays an.
Mit Adobe-DRM wird hier ein „harter” Kopierschutz verwendet. Wenn die notwendigen Voraussetzungen nicht vorliegen, können Sie das E-Book leider nicht öffnen. Daher müssen Sie bereits vor dem Download Ihre Lese-Hardware vorbereiten.

Bitte beachten Sie: Wir empfehlen Ihnen unbedingt nach Installation der Lese-Software diese mit Ihrer persönlichen Adobe-ID zu autorisieren!

Weitere Informationen finden Sie in unserer E-Book Hilfe.

Dateiformat: PDF
Kopierschutz: Adobe-DRM (Digital Rights Management)

Systemvoraussetzungen:

Computer (Windows; MacOS X; Linux): Installieren Sie bereits vor dem Download die kostenlose Software Adobe Digital Editions (siehe E-Book Hilfe).
Tablet/Smartphone (Android; iOS): Installieren Sie bereits vor dem Download die kostenlose App Adobe Digital Editions oder die App PocketBook (siehe E-Book Hilfe).
E-Book-Reader: Bookeen, Kobo, Pocketbook, Sony, Tolino u.v.a.m. (nicht Kindle)

Das Dateiformat PDF zeigt auf jeder Hardware eine Buchseite stets identisch an. Daher ist eine PDF auch für ein komplexes Layout geeignet, wie es bei Lehr- und Fachbüchern verwendet wird (Bilder, Tabellen, Spalten, Fußnoten). Bei kleinen Displays von E-Readern oder Smartphones sind PDF leider eher nervig, weil zu viel Scrollen notwendig ist.
Mit Adobe-DRM wird hier ein „harter” Kopierschutz verwendet. Wenn die notwendigen Voraussetzungen nicht vorliegen, können Sie das E-Book leider nicht öffnen. Daher müssen Sie bereits vor dem Download Ihre Lese-Hardware vorbereiten.

Bitte beachten Sie: Wir empfehlen Ihnen unbedingt nach Installation der Lese-Software diese mit Ihrer persönlichen Adobe-ID zu autorisieren!

Weitere Informationen finden Sie in unserer E-Book Hilfe.

Als PDF speichern Als Link merken