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Carbon dioxide thermodynamic properties handbook [[electronic resource] ] : covering temperatures from -20° to 250°C and pressures up to 1000 bar / / Sara Anwar and John J. Carroll
Carbon dioxide thermodynamic properties handbook [[electronic resource] ] : covering temperatures from -20° to 250°C and pressures up to 1000 bar / / Sara Anwar and John J. Carroll
Autore Anwar Sara
Pubbl/distr/stampa Hoboken, New Jersey, : John Wiley & Sons
Descrizione fisica 1 online resource (590 p.)
Disciplina 546.6812
546/.6812
Altri autori (Persone) CarrollJohn J. <1958->
Soggetto topico Carbon dioxide - Thermal properties
Carbon compounds
Soggetto genere / forma Electronic books.
ISBN 1-118-09950-8
1-283-37447-1
9786613374479
1-118-06568-9
1-61344-188-6
1-118-06569-7
Classificazione TEC031030
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Carbon Dioxide Thermodynamic Properties Handbook Covering Temperatures from -20° to 250°C and Pressures up to 1000 bar; Contents; Acknowledgement; Preface; Introduction; 1 Density (kg/m3) of Saturated Carbon Dioxide; 2 Enthalpy (J/mol) of Saturated Carbon Dioxide; 3 Entropy (J/mol ·Κ) of Saturated Carbon Dioxide; 4 Heat Capacity, Cp, (J/mol · K) of Saturated Carbon Dioxide; 5 Density (kg/m3) of Carbon Dioxide as a Function of Temperature and Pressure; 6 Enthalpy (J/mol) of Carbon Dioxide as a Function of Temperature and Pressure
7 Entropy (J/mol ·Κ) of Carbon Dioxide as a Function of Temperature and Pressure8 Heat Capacity, Cp, (J/mol · K) of Carbon Dioxide as a Function of Temperature and Pressure
Record Nr. UNINA-9910133451103321
Anwar Sara  
Hoboken, New Jersey, : John Wiley & Sons
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Carbon dioxide thermodynamic properties handbook [[electronic resource] ] : covering temperatures from -20° to 250°C and pressures up to 1000 bar / / Sara Anwar and John J. Carroll
Carbon dioxide thermodynamic properties handbook [[electronic resource] ] : covering temperatures from -20° to 250°C and pressures up to 1000 bar / / Sara Anwar and John J. Carroll
Autore Anwar Sara
Pubbl/distr/stampa Hoboken, New Jersey, : John Wiley & Sons
Descrizione fisica 1 online resource (590 p.)
Disciplina 546.6812
546/.6812
Altri autori (Persone) CarrollJohn J. <1958->
Soggetto topico Carbon dioxide - Thermal properties
Carbon compounds
ISBN 1-118-09950-8
1-283-37447-1
9786613374479
1-118-06568-9
1-61344-188-6
1-118-06569-7
Classificazione TEC031030
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Carbon Dioxide Thermodynamic Properties Handbook Covering Temperatures from -20° to 250°C and Pressures up to 1000 bar; Contents; Acknowledgement; Preface; Introduction; 1 Density (kg/m3) of Saturated Carbon Dioxide; 2 Enthalpy (J/mol) of Saturated Carbon Dioxide; 3 Entropy (J/mol ·Κ) of Saturated Carbon Dioxide; 4 Heat Capacity, Cp, (J/mol · K) of Saturated Carbon Dioxide; 5 Density (kg/m3) of Carbon Dioxide as a Function of Temperature and Pressure; 6 Enthalpy (J/mol) of Carbon Dioxide as a Function of Temperature and Pressure
7 Entropy (J/mol ·Κ) of Carbon Dioxide as a Function of Temperature and Pressure8 Heat Capacity, Cp, (J/mol · K) of Carbon Dioxide as a Function of Temperature and Pressure
Record Nr. UNINA-9910830047103321
Anwar Sara  
Hoboken, New Jersey, : John Wiley & Sons
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Carbon dioxide thermodynamic properties handbook : covering temperatures from -20° to 250°C and pressures up to 1000 bar / / Sara Anwar and John J. Carroll
Carbon dioxide thermodynamic properties handbook : covering temperatures from -20° to 250°C and pressures up to 1000 bar / / Sara Anwar and John J. Carroll
Autore Anwar Sara
Pubbl/distr/stampa Hoboken, New Jersey, : John Wiley & Sons
Descrizione fisica 1 online resource (590 p.)
Disciplina 546.6812
546/.6812
Altri autori (Persone) CarrollJohn J. <1958->
Soggetto topico Carbon dioxide - Thermal properties
Carbon compounds
ISBN 1-118-09950-8
1-283-37447-1
9786613374479
1-118-06568-9
1-61344-188-6
1-118-06569-7
Classificazione TEC031030
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Carbon Dioxide Thermodynamic Properties Handbook Covering Temperatures from -20° to 250°C and Pressures up to 1000 bar; Contents; Acknowledgement; Preface; Introduction; 1 Density (kg/m3) of Saturated Carbon Dioxide; 2 Enthalpy (J/mol) of Saturated Carbon Dioxide; 3 Entropy (J/mol ·Κ) of Saturated Carbon Dioxide; 4 Heat Capacity, Cp, (J/mol · K) of Saturated Carbon Dioxide; 5 Density (kg/m3) of Carbon Dioxide as a Function of Temperature and Pressure; 6 Enthalpy (J/mol) of Carbon Dioxide as a Function of Temperature and Pressure
7 Entropy (J/mol ·Κ) of Carbon Dioxide as a Function of Temperature and Pressure8 Heat Capacity, Cp, (J/mol · K) of Carbon Dioxide as a Function of Temperature and Pressure
Record Nr. UNINA-9911018888903321
Anwar Sara  
Hoboken, New Jersey, : John Wiley & Sons
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Carbon-Based Nanomaterials for Green Applications
Carbon-Based Nanomaterials for Green Applications
Autore Kumar Upendra
Edizione [1st ed.]
Pubbl/distr/stampa Newark : , : John Wiley & Sons, Incorporated, , 2025
Descrizione fisica 1 online resource (642 pages)
Disciplina 620.193
Altri autori (Persone) SonkarPiyush Kumar
TripathiSuman Lata
Soggetto topico Carbon compounds
Nanostructured materials
ISBN 9781394243426
1394243421
9781394243402
1394243405
9781394243419
1394243413
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Cover -- Series Page -- Title Page -- Copyright Page -- Dedication -- Contents -- About the Editors -- List of Contributors -- Preface -- Acknowledgments -- Chapter 1 Green Energy: An Introduction, Present, and Future Prospective -- 1.1 Introduction -- 1.2 Present Status of Green Energy -- 1.3 Global Renewable Energy Capacity -- 1.4 Leading Green Energy Technologies -- 1.5 Challenges in Green Energy Adoption -- 1.6 Prospects of Green Energy -- 1.7 Sustainable Practices in Green Energy -- 1.8 Case Studies of Successful Green Energy Projects -- 1.9 Policy and Regulatory Framework for Green Energy -- 1.10 Opportunities and Challenges in the Evolution to a Green Energy Future -- 1.10.1 Opportunities -- 1.10.2 Challenges -- 1.11 Conclusion -- References -- Chapter 2 Properties of Carbon-Based Nanomaterials and Techniques for Characterization -- 2.1 Introduction -- 2.1.1 Carbon Nanotubes -- 2.1.2 Graphene -- 2.1.3 Graphene Oxide -- 2.1.4 Fullerenes -- 2.2 Significance in Green Energy -- 2.2.1 Energy Storage -- 2.2.2 Solar Energy -- 2.2.3 Catalysis and Fuel Cells -- 2.2.4 Thermal Management -- 2.2.5 Environmental Remediation -- 2.3 Techniques for Characterization of Properties of Carbon Nanomaterials -- 2.3.1 Electrical Conductivity -- 2.3.2 Thermal Conductivity -- 2.3.3 Mechanical Strength -- 2.3.4 Surface Area Characterization -- 2.3.5 Scanning Electron Microscopy -- 2.3.6 Energy Dispersive X-ray Spectroscopy -- 2.3.7 Transmission Electron Microscopy -- 2.3.8 Electron Energy Loss Spectroscopy -- 2.3.9 Atomic Force Microscopy -- 2.3.10 Raman Spectroscopy -- 2.3.11 Photoluminescence -- 2.3.12 Time-Resolved Photoluminescence -- 2.3.13 Thermal Gravimetric Analysis and Differential Scanning Calorimetry -- 2.3.14 Fourier Transform Infrared Spectroscopy -- 2.3.15 UV-Vis-NIR Spectroscopy -- 2.3.16 X-ray Photoelectron Spectroscopy.
2.3.17 Small Angle X-ray Scattering -- 2.3.18 X-ray Diffraction Analysis -- 2.3.19 Scanning Electrochemical Microscopy -- 2.3.20 Electrochemical Impedance Spectroscopy -- 2.4 Conclusion -- References -- Chapter 3 Green Energy: Present and Future Prospectives -- 3.1 Introduction -- 3.1.1 Systematic Review Survey Reports -- 3.2 Sustainable Energy Resources -- 3.2.1 Wind Energy -- 3.2.1.1 Applications of Wind Turbine Systems -- 3.2.1.2 Advantages of Wind Energy -- 3.2.1.3 Disadvantages of Wind Energy -- 3.2.1.4 Future Prospectives and Challenges -- 3.2.2 Solar Energy -- 3.2.2.1 Applications of Solar Energy -- 3.2.2.2 Advantages of Solar Energy -- 3.2.2.3 Disadvantages of Solar Energy -- 3.2.2.4 Future Prospectives and Challenges -- 3.2.3 Biomass -- 3.2.3.1 Applications of Biomass -- 3.2.3.2 Benefits and Disadvantages of Biomass -- 3.2.3.3 Future Prospectives and Challenges -- 3.2.4 Geothermal Energy -- 3.2.4.1 Applications and Future Prospectives -- 3.2.5 Hydropower -- 3.2.6 Tidal and Wave Energy -- 3.2.6.1 Tidal Power -- 3.2.6.2 Wave Power -- 3.2.6.3 Benefits of Tidal and Wave Energy Systems -- 3.2.6.4 Challenges of Tidal and Wave Energy Systems -- 3.3 Non-Sustainable Energy Resources -- 3.3.1 Fossil Fuels -- 3.3.2 Atomic Energy -- 3.4 Existing Green Energy Models -- 3.5 Conclusions -- References -- Chapter 4 Carbon-Based 2D Materials: Synthesis, Characterization, and Their Green Energy Applications -- 4.1 Introduction -- 4.2 Synthesis of Graphene and Its Derivatives -- 4.2.1 Graphene-Based 2D Materials -- 4.2.2 Graphene -- 4.2.3 Graphene Oxide -- 4.2.4 Reduced Graphene Oxide -- 4.2.5 Graphitic Carbon Nitride -- 4.2.5.1 g-CN-ThinFilm -- 4.2.5.2 Graphitic Carbon Nitride (g-CN)-PowderForm -- 4.2.5.3 Thin Film of g-CN -- 4.3 Properties of g-CN -- 4.3.1 Morphologvical Properties -- 4.3.2 Band Gap -- 4.3.3 Other Properties -- 4.4 Applications of g-CN.
4.4.1 g-CN Role in Organic Solar Cells -- 4.4.2 g-CN Role in Perovskite Solar Cells -- 4.4.3 g-CN Role in Dye-Sensitized Solar Cells -- 4.4.4 g-CN Role as a Photocatalyst -- 4.4.5 g-CN-Sensing Applications -- 4.4.6 g-CN Environmental Applications -- 4.5 Conclusion -- References -- Chapter 5 Exploring the Potential of Graphene in Sustainable Energy Solutions -- 5.1 Introduction -- 5.2 Usage of Graphene in Various Sectors -- 5.3 Implicit Operations of Graphene in the Renewable Energy Sector -- 5.3.1 Battery Technology -- 5.3.2 Touchscreen -- 5.3.3 Integrated Circuits -- 5.3.4 Flexible Memory -- 5.3.5 Solar Power Generation -- 5.3.6 Photovoltaic Cells -- 5.3.7 Solar Cells -- 5.3.8 Lithium-Ion Batteries -- 5.3.9 Supercapacitors -- 5.3.10 Graphene Transistors -- 5.3.11 Graphene Semiconductors -- 5.3.12 Graphene Sensors -- 5.4 Catalysis -- 5.5 Renewable Energies -- 5.6 Nanotechnology -- 5.7 Conclusion -- Chapter 6 Fullerene for Green Hydrogen Energy Application -- 6.1 Introduction -- 6.2 Green Hydrogen Energy -- 6.3 Fullerene as a Hydrogen Storage Material -- 6.4 Size Effect of Fullerene and Hydrogen Storage Efficiency -- 6.5 Functionalized Fullerene, Chemical Structure, and Its Hydrogen Storage Performance -- 6.5.1 Boron -- 6.5.2 Phosphorene or Black Phosphorus -- 6.5.3 Hexagonal Boron Nitride -- 6.5.4 Silicene -- 6.5.5 Carbon Nanotubes -- 6.5.6 Graphene -- 6.5.7 Ferrocene -- 6.5.8 MoS2 -- 6.5.9 Organometallic Framework -- 6.6 Charged Fullerene as Hydrogen Storage System -- 6.7 Hydrogen Storage in Hydro- or Hydrogenated Fullerene -- 6.8 Conclusions and Future Outlook -- Acknowledgments -- References -- Chapter 7 Graphyne-Based Carbon Nanomaterials for Green Energy Applications -- 7.1 Introduction -- 7.1.1 Structural Aspects of Graphyne -- 7.2 Graphyne-Based Carbon Nanomaterials for Green Energy Applications.
7.2.1 Mechanisms Involved in Growth, Doping, Energy Storage, and Conversion Involving Graphyne -- 7.3 Fuel Cells -- 7.3.1 Oxygen Reduction Reaction (ORR) Catalyst for Hydrogen Fuel Cells or Metal-Air Batteries (MABs) -- 7.3.2 Lithium-Ion and Lithium-Metal Batteries -- 7.3.3 Supercapacitors -- 7.3.4 Wind Energy -- 7.4 Solar Energy -- 7.5 Wastewater Treatment -- 7.6 Perspectives and Conclusion -- Acknowledgments -- References -- Chapter 8 Mesoporous Carbon for Green Energy Applications -- 8.1 Introduction -- 8.2 Recent Advances in Synthetic Techniques -- 8.2.1 Hard Template Technique -- 8.2.1.1 Carbon Precursors -- 8.2.2 Soft Template Technique -- 8.3 Applications of Mesoporous Carbon -- 8.3.1 Applications in Lithium Batteries -- 8.3.2 Applications in Supercapacitors -- 8.3.3 Applications in Fuel Cells -- 8.4 Further Directions, Opportunities, and Challenges -- 8.5 Conclusions -- References -- Chapter 9 Green Synthesis of Carbon Dots and Its Application in Hydrogen Generation Through Water Splitting -- 9.1 Introduction -- 9.2 Carbon Dots -- 9.3 Processes Used for Synthesis of CDs -- 9.3.1 Bottom-Up Synthesis Processes -- 9.3.1.1 Solvothermal/Hydrothermal Method -- 9.3.1.2 Sol-GelMethod -- 9.3.1.3 Microwave Irradiation -- 9.3.1.4 Carbonization Route -- 9.3.2 Top-Down Synthesis Processes -- 9.3.2.1 Laser Ablation -- 9.3.2.2 Arc Discharge -- 9.3.2.3 Chemical and Electrochemical Oxidation Methods -- 9.3.2.4 Ultrasonic Treatment -- 9.4 Green Synthesis of Carbon Dots -- 9.4.1 Biomass-Based Green Synthesis of CDs -- 9.4.1.1 Plant Waste-BasedGreen Synthesis of Carbon Dots -- 9.4.1.2 Animal Waste-BasedGreen Synthesis of CDs -- 9.5 Application of CDs in Water Splitting -- 9.5.1 Hydrogen Generation via Water Splitting (Photoreduction) -- 9.5.2 Photocatalytic Degradation of Organic Pollutants.
9.6 Factors Affecting Characteristics of Nanomaterials of Carbon in Photocatalytic H2 Production -- 9.6.1 Doping -- 9.6.2 Defects -- 9.6.3 Dimensions -- 9.7 Conclusion -- References -- Chapter 10 Carbon-Based Nanomaterials in Energy Storage Devices: Solar Cells -- 10.1 Introduction -- 10.2 Carbon Nanotubes -- 10.2.1 Synthesis Techniques Concerning Carbon Nanotubes -- 10.2.2 Carbon Nanotube Applications in Solar Cell Technology -- 10.2.2.1 Transparent Conductive Electrodes -- 10.2.2.2 Charge Transport Materials -- 10.2.2.3 Enhanced Electron Transport -- 10.2.2.4 Improved Charge Collection -- 10.2.2.5 Transparency and Flexibility -- 10.2.2.6 Lightweight and Flexible Design -- 10.2.2.7 Tunable Aspects of Optics -- 10.2.2.8 Durability and Longevity -- 10.2.2.9 Compatibility with Other Materials -- 10.2.2.10 Scalability -- 10.2.3 Recent Advancements and Challenges -- 10.2.3.1 Recent Advancements -- 10.2.3.2 Challenges -- 10.3 Graphene -- 10.3.1 Synthesis Techniques -- 10.3.2 Utilizing Graphene in Solar Cell Applications -- 10.3.2.1 Transparent Conductive Electrodes -- 10.3.2.2 Charge Transport Layers -- 10.3.2.3 Light-HarvestingEnhancements -- 10.3.3 Recent Advancements and Challenges -- 10.3.3.1 Recent Advancements -- 10.3.3.2 Challenges -- 10.4 Carbon Dots -- 10.4.1 Synthesis Techniques -- 10.4.2 Applications of Solar Cell Carbon Dots -- 10.4.2.1 Light Harvesting and Sensitization -- 10.4.2.2 Charge Separation and Transport of Electrons -- 10.4.2.3 Energy Storage and Electrochemical Applications -- 10.4.3 Recent Advancements and Challenges -- 10.4.3.1 Recent Advancements -- 10.4.3.2 Challenges -- 10.5 The Future of Carbon-Based Nanomaterials in Solar Cell Technology -- 10.5.1 Enhanced Light Harvesting and Absorption -- 10.5.2 Improved Charge Transport and Collection -- 10.5.3 Enhanced Stability and Durability.
10.5.4 Scalable Synthesis and Manufacturing.
Record Nr. UNINA-9911018907203321
Kumar Upendra  
Newark : , : John Wiley & Sons, Incorporated, , 2025
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Carbon-based solids and materials [[electronic resource] /] / Pierre Delhaes
Carbon-based solids and materials [[electronic resource] /] / Pierre Delhaes
Autore Delhaes Pierre
Pubbl/distr/stampa London, : ISTE
Descrizione fisica 1 online resource (658 p.)
Disciplina 620.1/93
620.193
Collana ISTE
Soggetto topico Carbon composites
Carbon compounds
Soggetto genere / forma Electronic books.
ISBN 1-118-55761-1
1-118-60088-6
1-118-60089-4
1-299-18749-8
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto pt. 1. Carbon phases, precursors and parent compounds -- pt. 2. Physical properties of solid carbons -- pt. 3. Carbon materials and uses.
Record Nr. UNINA-9910138852603321
Delhaes Pierre  
London, : ISTE
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Carbon-based solids and materials [[electronic resource] /] / Pierre Delhaes
Carbon-based solids and materials [[electronic resource] /] / Pierre Delhaes
Autore Delhaes Pierre
Pubbl/distr/stampa London, : ISTE
Descrizione fisica 1 online resource (658 p.)
Disciplina 620.1/93
620.193
Collana ISTE
Soggetto topico Carbon composites
Carbon compounds
ISBN 1-118-55761-1
1-118-60088-6
1-118-60089-4
1-299-18749-8
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto pt. 1. Carbon phases, precursors and parent compounds -- pt. 2. Physical properties of solid carbons -- pt. 3. Carbon materials and uses.
Record Nr. UNINA-9910830086603321
Delhaes Pierre  
London, : ISTE
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Carbon-based solids and materials / / Pierre Delhaes
Carbon-based solids and materials / / Pierre Delhaes
Autore Delhaes Pierre
Pubbl/distr/stampa London, : ISTE
Descrizione fisica 1 online resource (658 p.)
Disciplina 620.1/93
Collana ISTE
Soggetto topico Carbon composites
Carbon compounds
ISBN 9781118557617
1118557611
9781118600887
1118600886
9781118600894
1118600894
9781299187498
1299187498
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto pt. 1. Carbon phases, precursors and parent compounds -- pt. 2. Physical properties of solid carbons -- pt. 3. Carbon materials and uses.
Record Nr. UNINA-9911019346803321
Delhaes Pierre  
London, : ISTE
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Carbon-rich compounds [[electronic resource] ] : from molecules to materials / / edited by Michael M. Haley and Rik R. Tykwinski
Carbon-rich compounds [[electronic resource] ] : from molecules to materials / / edited by Michael M. Haley and Rik R. Tykwinski
Pubbl/distr/stampa Weinheim, : Wiley-VCH
Descrizione fisica 1 online resource (665 p.)
Disciplina 547
Altri autori (Persone) HaleyMichael
TykwinskiR. R (Rik R.)
Soggetto topico Carbon compounds
Chemistry, Organic
Soggetto genere / forma Electronic books.
ISBN 1-280-85431-6
9786610854318
3-527-60799-4
3-527-60724-2
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Carbon-Rich Compounds; Foreword; Contents; Preface; List of Contributors; 1 Pioneers of Carbon-rich Compounds; 1.1 Introduction; 1.2 19th Century Achievements; 1.3 1900-1928: Dawn of the Twentieth Century; 1.4 1929-1949: Rise of the Polycyclic Aromatic Hydrocarbon; 1.5 1950-1969; 1.5.1 The Annulenes, Dehydrobenzoannulenes, and Phenylacetylene Scaffolding; 1.5.2 Fused Polycyclic and peri-Condensed Benzenoid Systems; 1.5.3 The Helicenes, Radialenes, Fulvalenes, and Circulenes; 1.6 1970-Present: The Way Ahead; References; 2 Electronic Conduction in Photoactive Metallo-wires; 2.1 Introduction
2.2 Attenuation along Molecular Bridges2.3 Information Transfer; 2.3.1 Intramolecular Triplet Energy Transfer; 2.3.2 Short Covalent Bridges; 2.3.3 Supramolecular Systems; 2.3.4 Prolonging the Excited State Lifetime; 2.3.5 Long-range Triplet Energy Transfer; 2.4 Molecular-scale Switches; 2.5 Perspectives; 2.6 Experimental: Selected Procedures; 2.6.1 General Procedure for the Preparation of the Mononuclear [RuL(n)]; 2.6.2 General Procedure for the Preparation of the Hetero-Dinuclear Complexes 81(1) and 81(5); 2.6.3 Synthesis at the Complex; Acknowledgements; Abbreviations; References
3 All-benzenoid Polycyclic Aromatic Hydrocarbons: Synthesis, Self-assembly and Applications in Organic Electronics3.1 A Brief Introduction to Polycyclic Aromatic Hydrocarbons; 3.2 All-benzenoid PAHs - Synthesis, Structural Characterizations and Electronic Properties; 3.2.1 Hexa-peri-hexabenzocoronene - An Old Story with New Discoveries; 3.2.2 All-benzenoid Graphitic PAHs Larger than HBCs; 3.2.3 PAHs with Varying Peripheries; 3.2.4 ''Superbenzene'' Chemistry and Others; 3.3 Self-assembly and Application of Columnar Liquid Crystals based on PBAHs
3.3.1 Columnar Superstructures in the Bulk State3.3.2 Alignment on Substrates and Device Applications of Columnar Liquid Crystals; 3.3.3 Controlled Self-assembly in Solution; 3.3.4 Two-dimensional Crystals at the Solid/Liquid Interface; 3.4 Conclusion; 3.5 Experimental: Selected Procedures; 3.5.1 Synthesis of hexa-peri-hexabenzocoronene 10 by Cu(II)-mediated oxidative cyclodehydrogenation - a general procedure to prepare unsubstituted graphitic molecules [35]
3.5.2 Synthesis of hexakis(4-dodecylphenyl)-peri-hexabenzocoronene (HBC-PhC12) - a general synthetic method towards six-fold alkyl- and alkylphenyl-substituted HBCs [38]3.5.3 Functionalization of insoluble HBC building blocks 30-32 by Sonogashira coupling reactions [48]. Synthesis of hexakis(1-dodecynylphenyl)-peri-hexabenzocoronene (34a) as a representative example; 3.5.4 Synthesis of C96-C12 precursor 1,3,5-tris[3 ́,4 ́-di(4 ́ ́-dodecylphenyl)-2 ́,5 ́-diphenylphenyl]benzene (44a) by Diels-Alder cycloaddition reaction - a representative procedure for the synthesis of branched oligophenylenes [50]
3.5.5 Hydrogenation of hexakis-dodecyl-peri-hexabenzocoronenes 74 [66]
Record Nr. UNINA-9910144321703321
Weinheim, : Wiley-VCH
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Carbon-rich compounds [[electronic resource] ] : from molecules to materials / / edited by Michael M. Haley and Rik R. Tykwinski
Carbon-rich compounds [[electronic resource] ] : from molecules to materials / / edited by Michael M. Haley and Rik R. Tykwinski
Pubbl/distr/stampa Weinheim, : Wiley-VCH
Descrizione fisica 1 online resource (665 p.)
Disciplina 547
Altri autori (Persone) HaleyMichael
TykwinskiR. R (Rik R.)
Soggetto topico Carbon compounds
Chemistry, Organic
ISBN 1-280-85431-6
9786610854318
3-527-60799-4
3-527-60724-2
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Carbon-Rich Compounds; Foreword; Contents; Preface; List of Contributors; 1 Pioneers of Carbon-rich Compounds; 1.1 Introduction; 1.2 19th Century Achievements; 1.3 1900-1928: Dawn of the Twentieth Century; 1.4 1929-1949: Rise of the Polycyclic Aromatic Hydrocarbon; 1.5 1950-1969; 1.5.1 The Annulenes, Dehydrobenzoannulenes, and Phenylacetylene Scaffolding; 1.5.2 Fused Polycyclic and peri-Condensed Benzenoid Systems; 1.5.3 The Helicenes, Radialenes, Fulvalenes, and Circulenes; 1.6 1970-Present: The Way Ahead; References; 2 Electronic Conduction in Photoactive Metallo-wires; 2.1 Introduction
2.2 Attenuation along Molecular Bridges2.3 Information Transfer; 2.3.1 Intramolecular Triplet Energy Transfer; 2.3.2 Short Covalent Bridges; 2.3.3 Supramolecular Systems; 2.3.4 Prolonging the Excited State Lifetime; 2.3.5 Long-range Triplet Energy Transfer; 2.4 Molecular-scale Switches; 2.5 Perspectives; 2.6 Experimental: Selected Procedures; 2.6.1 General Procedure for the Preparation of the Mononuclear [RuL(n)]; 2.6.2 General Procedure for the Preparation of the Hetero-Dinuclear Complexes 81(1) and 81(5); 2.6.3 Synthesis at the Complex; Acknowledgements; Abbreviations; References
3 All-benzenoid Polycyclic Aromatic Hydrocarbons: Synthesis, Self-assembly and Applications in Organic Electronics3.1 A Brief Introduction to Polycyclic Aromatic Hydrocarbons; 3.2 All-benzenoid PAHs - Synthesis, Structural Characterizations and Electronic Properties; 3.2.1 Hexa-peri-hexabenzocoronene - An Old Story with New Discoveries; 3.2.2 All-benzenoid Graphitic PAHs Larger than HBCs; 3.2.3 PAHs with Varying Peripheries; 3.2.4 ''Superbenzene'' Chemistry and Others; 3.3 Self-assembly and Application of Columnar Liquid Crystals based on PBAHs
3.3.1 Columnar Superstructures in the Bulk State3.3.2 Alignment on Substrates and Device Applications of Columnar Liquid Crystals; 3.3.3 Controlled Self-assembly in Solution; 3.3.4 Two-dimensional Crystals at the Solid/Liquid Interface; 3.4 Conclusion; 3.5 Experimental: Selected Procedures; 3.5.1 Synthesis of hexa-peri-hexabenzocoronene 10 by Cu(II)-mediated oxidative cyclodehydrogenation - a general procedure to prepare unsubstituted graphitic molecules [35]
3.5.2 Synthesis of hexakis(4-dodecylphenyl)-peri-hexabenzocoronene (HBC-PhC12) - a general synthetic method towards six-fold alkyl- and alkylphenyl-substituted HBCs [38]3.5.3 Functionalization of insoluble HBC building blocks 30-32 by Sonogashira coupling reactions [48]. Synthesis of hexakis(1-dodecynylphenyl)-peri-hexabenzocoronene (34a) as a representative example; 3.5.4 Synthesis of C96-C12 precursor 1,3,5-tris[3 ́,4 ́-di(4 ́ ́-dodecylphenyl)-2 ́,5 ́-diphenylphenyl]benzene (44a) by Diels-Alder cycloaddition reaction - a representative procedure for the synthesis of branched oligophenylenes [50]
3.5.5 Hydrogenation of hexakis-dodecyl-peri-hexabenzocoronenes 74 [66]
Record Nr. UNINA-9910830795503321
Weinheim, : Wiley-VCH
Materiale a stampa
Lo trovi qui: Univ. Federico II
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Carbon-rich compounds : from molecules to materials / / edited by Michael M. Haley and Rik R. Tykwinski
Carbon-rich compounds : from molecules to materials / / edited by Michael M. Haley and Rik R. Tykwinski
Pubbl/distr/stampa Weinheim, : Wiley-VCH
Descrizione fisica 1 online resource (665 p.)
Disciplina 547
Altri autori (Persone) HaleyMichael
TykwinskiR. R (Rik R.)
Soggetto topico Carbon compounds
Chemistry, Organic
ISBN 9786610854318
9781280854316
1280854316
9783527607990
3527607994
9783527607242
3527607242
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Carbon-Rich Compounds; Foreword; Contents; Preface; List of Contributors; 1 Pioneers of Carbon-rich Compounds; 1.1 Introduction; 1.2 19th Century Achievements; 1.3 1900-1928: Dawn of the Twentieth Century; 1.4 1929-1949: Rise of the Polycyclic Aromatic Hydrocarbon; 1.5 1950-1969; 1.5.1 The Annulenes, Dehydrobenzoannulenes, and Phenylacetylene Scaffolding; 1.5.2 Fused Polycyclic and peri-Condensed Benzenoid Systems; 1.5.3 The Helicenes, Radialenes, Fulvalenes, and Circulenes; 1.6 1970-Present: The Way Ahead; References; 2 Electronic Conduction in Photoactive Metallo-wires; 2.1 Introduction
2.2 Attenuation along Molecular Bridges2.3 Information Transfer; 2.3.1 Intramolecular Triplet Energy Transfer; 2.3.2 Short Covalent Bridges; 2.3.3 Supramolecular Systems; 2.3.4 Prolonging the Excited State Lifetime; 2.3.5 Long-range Triplet Energy Transfer; 2.4 Molecular-scale Switches; 2.5 Perspectives; 2.6 Experimental: Selected Procedures; 2.6.1 General Procedure for the Preparation of the Mononuclear [RuL(n)]; 2.6.2 General Procedure for the Preparation of the Hetero-Dinuclear Complexes 81(1) and 81(5); 2.6.3 Synthesis at the Complex; Acknowledgements; Abbreviations; References
3 All-benzenoid Polycyclic Aromatic Hydrocarbons: Synthesis, Self-assembly and Applications in Organic Electronics3.1 A Brief Introduction to Polycyclic Aromatic Hydrocarbons; 3.2 All-benzenoid PAHs - Synthesis, Structural Characterizations and Electronic Properties; 3.2.1 Hexa-peri-hexabenzocoronene - An Old Story with New Discoveries; 3.2.2 All-benzenoid Graphitic PAHs Larger than HBCs; 3.2.3 PAHs with Varying Peripheries; 3.2.4 ''Superbenzene'' Chemistry and Others; 3.3 Self-assembly and Application of Columnar Liquid Crystals based on PBAHs
3.3.1 Columnar Superstructures in the Bulk State3.3.2 Alignment on Substrates and Device Applications of Columnar Liquid Crystals; 3.3.3 Controlled Self-assembly in Solution; 3.3.4 Two-dimensional Crystals at the Solid/Liquid Interface; 3.4 Conclusion; 3.5 Experimental: Selected Procedures; 3.5.1 Synthesis of hexa-peri-hexabenzocoronene 10 by Cu(II)-mediated oxidative cyclodehydrogenation - a general procedure to prepare unsubstituted graphitic molecules [35]
3.5.2 Synthesis of hexakis(4-dodecylphenyl)-peri-hexabenzocoronene (HBC-PhC12) - a general synthetic method towards six-fold alkyl- and alkylphenyl-substituted HBCs [38]3.5.3 Functionalization of insoluble HBC building blocks 30-32 by Sonogashira coupling reactions [48]. Synthesis of hexakis(1-dodecynylphenyl)-peri-hexabenzocoronene (34a) as a representative example; 3.5.4 Synthesis of C96-C12 precursor 1,3,5-tris[3 ́,4 ́-di(4 ́ ́-dodecylphenyl)-2 ́,5 ́-diphenylphenyl]benzene (44a) by Diels-Alder cycloaddition reaction - a representative procedure for the synthesis of branched oligophenylenes [50]
3.5.5 Hydrogenation of hexakis-dodecyl-peri-hexabenzocoronenes 74 [66]
Record Nr. UNINA-9911019945603321
Weinheim, : Wiley-VCH
Materiale a stampa
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