Carbon nanotubes and related structures [[electronic resource] ] : synthesis, characterization, functionalization, and applications / / edited by Dirk M. Guldi and Nazario Martin |
Pubbl/distr/stampa | Weinheim, : Wiley-VCH Verlag GmbH & Co., 2010 |
Descrizione fisica | 1 online resource (563 p.) |
Disciplina | 546.681 |
Altri autori (Persone) |
GuldiD. M (Dirk M.)
MartinNazario |
Soggetto topico |
Carbon
Nanostructured materials |
ISBN |
3-527-62993-9
1-282-49159-8 9786612491597 3-527-62994-7 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Carbon Nanotubes and Related Structures: Synthesis, Characterization, Functionalization, and Applications; Contents; Preface; List of Contributors; 1 Carbon Nanotubes and Related Structures: Production and Formation; 2 Theory of Electronic and Optical Properties of DNA-SWNT Hybrids; 3 Electrochemistry; 4 Photophysics; 5 Noncovalent Functionalization of Carbon Nanotubes; 6 Covalent Functionalization of Carbon Nanotubes; 7 Carbon-Based Nanomaterial Applications in Biomedicine; 8 Ground and Excited State Charge Transfer and its Implications
9 Photovoltaic Devices Based on Carbon Nanotubes and Related Structures10 Layer-by-Layer Assembly of Multifunctional Carbon Nanotube Thin Films; 11 Carbon Nanotubes for Catalytic Applications; 12 Carbon Nanotubes as Containers; 13 Carbon Nanohorn; 14 Self-Organization of Nanographenes; 15 Endohedrals; 16 Carbon Nanostructures: Calculations of Their Energetics, Thermodynamics, and Stability; Index |
Record Nr. | UNINA-9910139472003321 |
Weinheim, : Wiley-VCH Verlag GmbH & Co., 2010 | ||
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Lo trovi qui: Univ. Federico II | ||
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Carbon nanotubes and related structures [[electronic resource] ] : synthesis, characterization, functionalization, and applications / / edited by Dirk M. Guldi and Nazario Martin |
Pubbl/distr/stampa | Weinheim, : Wiley-VCH Verlag GmbH & Co., 2010 |
Descrizione fisica | 1 online resource (563 p.) |
Disciplina | 546.681 |
Altri autori (Persone) |
GuldiD. M (Dirk M.)
MartinNazario |
Soggetto topico |
Carbon
Nanostructured materials |
ISBN |
3-527-62993-9
1-282-49159-8 9786612491597 3-527-62994-7 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Carbon Nanotubes and Related Structures: Synthesis, Characterization, Functionalization, and Applications; Contents; Preface; List of Contributors; 1 Carbon Nanotubes and Related Structures: Production and Formation; 2 Theory of Electronic and Optical Properties of DNA-SWNT Hybrids; 3 Electrochemistry; 4 Photophysics; 5 Noncovalent Functionalization of Carbon Nanotubes; 6 Covalent Functionalization of Carbon Nanotubes; 7 Carbon-Based Nanomaterial Applications in Biomedicine; 8 Ground and Excited State Charge Transfer and its Implications
9 Photovoltaic Devices Based on Carbon Nanotubes and Related Structures10 Layer-by-Layer Assembly of Multifunctional Carbon Nanotube Thin Films; 11 Carbon Nanotubes for Catalytic Applications; 12 Carbon Nanotubes as Containers; 13 Carbon Nanohorn; 14 Self-Organization of Nanographenes; 15 Endohedrals; 16 Carbon Nanostructures: Calculations of Their Energetics, Thermodynamics, and Stability; Index |
Record Nr. | UNINA-9910830585503321 |
Weinheim, : Wiley-VCH Verlag GmbH & Co., 2010 | ||
![]() | ||
Lo trovi qui: Univ. Federico II | ||
|
Carbon nanotubes and related structures : synthesis, characterization, functionalization, and applications / / edited by Dirk M. Guldi and Nazario Martin |
Pubbl/distr/stampa | Weinheim, : Wiley-VCH Verlag GmbH & Co., 2010 |
Descrizione fisica | 1 online resource (563 p.) |
Disciplina | 546.681 |
Altri autori (Persone) |
GuldiD. M (Dirk M.)
MartinNazario |
Soggetto topico |
Carbon
Nanostructured materials |
ISBN |
3-527-62993-9
1-282-49159-8 9786612491597 3-527-62994-7 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Carbon Nanotubes and Related Structures: Synthesis, Characterization, Functionalization, and Applications; Contents; Preface; List of Contributors; 1 Carbon Nanotubes and Related Structures: Production and Formation; 2 Theory of Electronic and Optical Properties of DNA-SWNT Hybrids; 3 Electrochemistry; 4 Photophysics; 5 Noncovalent Functionalization of Carbon Nanotubes; 6 Covalent Functionalization of Carbon Nanotubes; 7 Carbon-Based Nanomaterial Applications in Biomedicine; 8 Ground and Excited State Charge Transfer and its Implications
9 Photovoltaic Devices Based on Carbon Nanotubes and Related Structures10 Layer-by-Layer Assembly of Multifunctional Carbon Nanotube Thin Films; 11 Carbon Nanotubes for Catalytic Applications; 12 Carbon Nanotubes as Containers; 13 Carbon Nanohorn; 14 Self-Organization of Nanographenes; 15 Endohedrals; 16 Carbon Nanostructures: Calculations of Their Energetics, Thermodynamics, and Stability; Index |
Record Nr. | UNINA-9910841100403321 |
Weinheim, : Wiley-VCH Verlag GmbH & Co., 2010 | ||
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Lo trovi qui: Univ. Federico II | ||
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Fullerene polymers [[electronic resource] ] : synthesis, properties and applications / / edited by Nazario Martin, Francesco Giacalone |
Pubbl/distr/stampa | Weinheim, : Wiley-VCH, 2009 |
Descrizione fisica | 1 online resource (331 p.) |
Disciplina |
546.681
620.193 |
Altri autori (Persone) |
MartinNazario
GiacaloneFrancesco |
Soggetto topico |
Fullerene polymers
Fullerene polymers - Synthesis Fullerene polymers - Industrial applications |
Soggetto genere / forma | Electronic books. |
ISBN |
1-282-27853-3
9786612278532 3-527-62874-6 3-527-62875-4 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Fullerene Polymers; Foreword; Contents; Preface; Contributors; 1: Fullerene-Containing Polymers: An Overview; 1.1 Polyfullerenes: A Brief History; 1.2 Classification of Polyfullerenes; 1.2.1 All-C60 Polymers; 1.2.2 Organometallic Polymers; 1.2.3 Crosslinked Polymers; 1.2.4 End-Capped Polymers; 1.2.5 C60-Dendrimers; 1.2.6 Star-Shaped Polymers; 1.2.7 Main-Chain Polymers; 1.2.8 Side-Chain Polymers; 1.2.8.1 Double-Cable Polymers; 1.2.9 Supramolecular Polymers; 1.3 Outlook and Perspective; References; 2: Main-Chain and Side-Chain C60-Polymers; 2.1 Introduction; 2.2 Main-Chain Polymers
2.3 Side-Chain Polymers2.3.1 Polystyrene-C60 Polymers; 2.3.2 Polyacrylate-and Methacrylate-C60 Polymers and Copolymers; 2.3.3 Polycarbonate-C60 Polymers; 2.3.4 Aminofishing Side-Chain Polymers; 2.3.5 Polyvinylcarbazoles; 2.3.6 Polyphosphazenes and Polysiloxanes; 2.3.7 Side-Chain C60-Polysaccarides; 2.3.8 Polyether-C60 Polymers; 2.3.9 Side-Chain Polymers Prepared by Organometallic Catalysis; 2.4 Conclusions and Further Perspectives; References; 3: Acrylate and Methacrylate C60-End-Capped Polymers; 3.1 Introduction; 3.2 Synthesis of C60-End-Capped Polymers 3.2.1 General Synthetic Approaches for C60-Containing Polymers3.2.2 Well-Defined C60 End-Capped Polymers by Controlled Radical Polymerization; 3.3 Aggregation of C60-End-Capped Polymers in Solution; 3.3.1 Self-Assembly of C60-End-Capped Polymers in Organic Solvents; 3.3.2 Aggregation of C60-End-Capped Polymers in Aqueous Solution; 3.3.2.1 pH-Responsive C60-Containing Polymers; 3.3.2.2 Temperature-Responsive C60-Containing Polymers; 3.3.2.3 C60-Containing Polyampholytes; 3.3.2.4 Supramolecular Fractal Patterning; 3.3.2.5 Surfactant Induced Nano-Structures; 3.4 Summary; References 4: Semi-Interpenetrating Polymer Networks Involving C60-Polymers4.1 Introduction; 4.2 Synthesis and Properties of Double-C60-End-Capped Polymers; 4.3 Mechanical Properties of Pseudo-SIPNs; 4.3.1 FPEOF/PMMA Pseudo-SIPNs; 4.3.2 FPEOF/Poly(L-Lactic Acid)Pseudo-SIPNs; 4.3.3 FPBMAF/PVC Pseudo-SIPNs; 4.4 Optical Transmission Characteristics of Pseudo-SIPNs; 4.5 Conclusions; References; 5: Star-Shaped Polymers with a Fullerene Core; 5.1 Introduction; 5.2 Grafting of Linear Polymer Chains onto C60; 5.2.1 Grafting via Radicals; 5.2.1.1 Radical Copolymerization of Fullerenes with Vinyl Monomers 5.2.1.2 Addition of Macro-radicals Obtained by"Controlled" Radical Polymerization5.2.1.3 Addition of Macro-radicals Obtained by Cleavage of Macro-initiators; 5.2.2 Grafting via Nucleophilic Addition; 5.2.2.1 Grafting of Neutral Nucleophiles; 5.2.2.2 Grafting of Charged Nucleophiles; 5.2.3 Other Grafting Reactions; 5.3 Polymerization of a Monomer Using Charged or Functionalized Fullerenes as Initiators; 5.3.1 Controlled Radical Polymerization Using a C60(X)n as Initiator 5.3.2 Anionic Polymerization Initiated by Fullerides C60x-(M+)x or "Living" Polymer Stars with a Fullerene Core (Polymer)x C60x-(M+)x ( x 6 |
Record Nr. | UNINA-9910139932903321 |
Weinheim, : Wiley-VCH, 2009 | ||
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Lo trovi qui: Univ. Federico II | ||
|
Fullerene polymers [[electronic resource] ] : synthesis, properties and applications / / edited by Nazario Martin, Francesco Giacalone |
Pubbl/distr/stampa | Weinheim, : Wiley-VCH, 2009 |
Descrizione fisica | 1 online resource (331 p.) |
Disciplina |
546.681
620.193 |
Altri autori (Persone) |
MartinNazario
GiacaloneFrancesco |
Soggetto topico |
Fullerene polymers
Fullerene polymers - Synthesis Fullerene polymers - Industrial applications |
ISBN |
1-282-27853-3
9786612278532 3-527-62874-6 3-527-62875-4 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Fullerene Polymers; Foreword; Contents; Preface; Contributors; 1: Fullerene-Containing Polymers: An Overview; 1.1 Polyfullerenes: A Brief History; 1.2 Classification of Polyfullerenes; 1.2.1 All-C60 Polymers; 1.2.2 Organometallic Polymers; 1.2.3 Crosslinked Polymers; 1.2.4 End-Capped Polymers; 1.2.5 C60-Dendrimers; 1.2.6 Star-Shaped Polymers; 1.2.7 Main-Chain Polymers; 1.2.8 Side-Chain Polymers; 1.2.8.1 Double-Cable Polymers; 1.2.9 Supramolecular Polymers; 1.3 Outlook and Perspective; References; 2: Main-Chain and Side-Chain C60-Polymers; 2.1 Introduction; 2.2 Main-Chain Polymers
2.3 Side-Chain Polymers2.3.1 Polystyrene-C60 Polymers; 2.3.2 Polyacrylate-and Methacrylate-C60 Polymers and Copolymers; 2.3.3 Polycarbonate-C60 Polymers; 2.3.4 Aminofishing Side-Chain Polymers; 2.3.5 Polyvinylcarbazoles; 2.3.6 Polyphosphazenes and Polysiloxanes; 2.3.7 Side-Chain C60-Polysaccarides; 2.3.8 Polyether-C60 Polymers; 2.3.9 Side-Chain Polymers Prepared by Organometallic Catalysis; 2.4 Conclusions and Further Perspectives; References; 3: Acrylate and Methacrylate C60-End-Capped Polymers; 3.1 Introduction; 3.2 Synthesis of C60-End-Capped Polymers 3.2.1 General Synthetic Approaches for C60-Containing Polymers3.2.2 Well-Defined C60 End-Capped Polymers by Controlled Radical Polymerization; 3.3 Aggregation of C60-End-Capped Polymers in Solution; 3.3.1 Self-Assembly of C60-End-Capped Polymers in Organic Solvents; 3.3.2 Aggregation of C60-End-Capped Polymers in Aqueous Solution; 3.3.2.1 pH-Responsive C60-Containing Polymers; 3.3.2.2 Temperature-Responsive C60-Containing Polymers; 3.3.2.3 C60-Containing Polyampholytes; 3.3.2.4 Supramolecular Fractal Patterning; 3.3.2.5 Surfactant Induced Nano-Structures; 3.4 Summary; References 4: Semi-Interpenetrating Polymer Networks Involving C60-Polymers4.1 Introduction; 4.2 Synthesis and Properties of Double-C60-End-Capped Polymers; 4.3 Mechanical Properties of Pseudo-SIPNs; 4.3.1 FPEOF/PMMA Pseudo-SIPNs; 4.3.2 FPEOF/Poly(L-Lactic Acid)Pseudo-SIPNs; 4.3.3 FPBMAF/PVC Pseudo-SIPNs; 4.4 Optical Transmission Characteristics of Pseudo-SIPNs; 4.5 Conclusions; References; 5: Star-Shaped Polymers with a Fullerene Core; 5.1 Introduction; 5.2 Grafting of Linear Polymer Chains onto C60; 5.2.1 Grafting via Radicals; 5.2.1.1 Radical Copolymerization of Fullerenes with Vinyl Monomers 5.2.1.2 Addition of Macro-radicals Obtained by"Controlled" Radical Polymerization5.2.1.3 Addition of Macro-radicals Obtained by Cleavage of Macro-initiators; 5.2.2 Grafting via Nucleophilic Addition; 5.2.2.1 Grafting of Neutral Nucleophiles; 5.2.2.2 Grafting of Charged Nucleophiles; 5.2.3 Other Grafting Reactions; 5.3 Polymerization of a Monomer Using Charged or Functionalized Fullerenes as Initiators; 5.3.1 Controlled Radical Polymerization Using a C60(X)n as Initiator 5.3.2 Anionic Polymerization Initiated by Fullerides C60x-(M+)x or "Living" Polymer Stars with a Fullerene Core (Polymer)x C60x-(M+)x ( x 6 |
Record Nr. | UNINA-9910830438103321 |
Weinheim, : Wiley-VCH, 2009 | ||
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Lo trovi qui: Univ. Federico II | ||
|
Fullerene polymers : synthesis, properties and applications / / edited by Nazario Martin, Francesco Giacalone |
Pubbl/distr/stampa | Weinheim, : Wiley-VCH, 2009 |
Descrizione fisica | 1 online resource (331 p.) |
Disciplina |
546.681
620.193 |
Altri autori (Persone) |
MartinNazario
GiacaloneFrancesco |
Soggetto topico |
Fullerene polymers
Fullerene polymers - Synthesis Fullerene polymers - Industrial applications |
ISBN |
1-282-27853-3
9786612278532 3-527-62874-6 3-527-62875-4 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Fullerene Polymers; Foreword; Contents; Preface; Contributors; 1: Fullerene-Containing Polymers: An Overview; 1.1 Polyfullerenes: A Brief History; 1.2 Classification of Polyfullerenes; 1.2.1 All-C60 Polymers; 1.2.2 Organometallic Polymers; 1.2.3 Crosslinked Polymers; 1.2.4 End-Capped Polymers; 1.2.5 C60-Dendrimers; 1.2.6 Star-Shaped Polymers; 1.2.7 Main-Chain Polymers; 1.2.8 Side-Chain Polymers; 1.2.8.1 Double-Cable Polymers; 1.2.9 Supramolecular Polymers; 1.3 Outlook and Perspective; References; 2: Main-Chain and Side-Chain C60-Polymers; 2.1 Introduction; 2.2 Main-Chain Polymers
2.3 Side-Chain Polymers2.3.1 Polystyrene-C60 Polymers; 2.3.2 Polyacrylate-and Methacrylate-C60 Polymers and Copolymers; 2.3.3 Polycarbonate-C60 Polymers; 2.3.4 Aminofishing Side-Chain Polymers; 2.3.5 Polyvinylcarbazoles; 2.3.6 Polyphosphazenes and Polysiloxanes; 2.3.7 Side-Chain C60-Polysaccarides; 2.3.8 Polyether-C60 Polymers; 2.3.9 Side-Chain Polymers Prepared by Organometallic Catalysis; 2.4 Conclusions and Further Perspectives; References; 3: Acrylate and Methacrylate C60-End-Capped Polymers; 3.1 Introduction; 3.2 Synthesis of C60-End-Capped Polymers 3.2.1 General Synthetic Approaches for C60-Containing Polymers3.2.2 Well-Defined C60 End-Capped Polymers by Controlled Radical Polymerization; 3.3 Aggregation of C60-End-Capped Polymers in Solution; 3.3.1 Self-Assembly of C60-End-Capped Polymers in Organic Solvents; 3.3.2 Aggregation of C60-End-Capped Polymers in Aqueous Solution; 3.3.2.1 pH-Responsive C60-Containing Polymers; 3.3.2.2 Temperature-Responsive C60-Containing Polymers; 3.3.2.3 C60-Containing Polyampholytes; 3.3.2.4 Supramolecular Fractal Patterning; 3.3.2.5 Surfactant Induced Nano-Structures; 3.4 Summary; References 4: Semi-Interpenetrating Polymer Networks Involving C60-Polymers4.1 Introduction; 4.2 Synthesis and Properties of Double-C60-End-Capped Polymers; 4.3 Mechanical Properties of Pseudo-SIPNs; 4.3.1 FPEOF/PMMA Pseudo-SIPNs; 4.3.2 FPEOF/Poly(L-Lactic Acid)Pseudo-SIPNs; 4.3.3 FPBMAF/PVC Pseudo-SIPNs; 4.4 Optical Transmission Characteristics of Pseudo-SIPNs; 4.5 Conclusions; References; 5: Star-Shaped Polymers with a Fullerene Core; 5.1 Introduction; 5.2 Grafting of Linear Polymer Chains onto C60; 5.2.1 Grafting via Radicals; 5.2.1.1 Radical Copolymerization of Fullerenes with Vinyl Monomers 5.2.1.2 Addition of Macro-radicals Obtained by"Controlled" Radical Polymerization5.2.1.3 Addition of Macro-radicals Obtained by Cleavage of Macro-initiators; 5.2.2 Grafting via Nucleophilic Addition; 5.2.2.1 Grafting of Neutral Nucleophiles; 5.2.2.2 Grafting of Charged Nucleophiles; 5.2.3 Other Grafting Reactions; 5.3 Polymerization of a Monomer Using Charged or Functionalized Fullerenes as Initiators; 5.3.1 Controlled Radical Polymerization Using a C60(X)n as Initiator 5.3.2 Anionic Polymerization Initiated by Fullerides C60x-(M+)x or "Living" Polymer Stars with a Fullerene Core (Polymer)x C60x-(M+)x ( x 6 |
Record Nr. | UNINA-9910840860803321 |
Weinheim, : Wiley-VCH, 2009 | ||
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Lo trovi qui: Univ. Federico II | ||
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Supramolecular chemistry of fullerenes and carbon nanotubes [[electronic resource] /] / edited by Nazario Martin and Jean-Francois Nierengarten |
Pubbl/distr/stampa | Weinheim, : Wiley-VCH, c2012 |
Descrizione fisica | 1 online resource (421 p.) |
Disciplina | 546.681 |
Altri autori (Persone) |
MartinNazario
NierengartenJean-Francois |
Soggetto topico |
Fullerenes
Nanotubes |
ISBN |
1-283-64409-6
3-527-65015-6 3-527-65014-8 3-527-65012-1 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Supramolecular Chemistry of Fullerenes and Carbon Nanotubes; Contents; Preface; List of Contributors; 1 Carbon Nanostructures: Covalent and Macromolecular Chemistry; 1.1 Introduction; 1.2 Fullerene-Containing Polymers; 1.3 Carbon Nanotubes; 1.3.1 Defect Functionalization; 1.3.2 Sidewall Functionalization; 1.4 Graphenes; 1.4.1 Covalent Functionalization; 1.4.2 Noncovalent Functionalization; 1.5 Summary and Conclusions; References; 2 Hydrogen-Bonded Fullerene Assemblies; 2.1 Introduction; 2.2 Hydrogen-Bonded Fullerene-Based Supramolecular Structures
2.3 Hydrogen-Bonded Fullerene-Based Donor-Acceptor Structures2.4 Applications; References; 3 Receptors for Pristine Fullerenes Based on Concave-Convex π-π Interactions; 3.1 Introduction; 3.2 Fullerene Receptors Based on Traditional Hosts; 3.2.1 Simple Traditional Hosts; 3.2.2 Modified Traditional Host Molecules; 3.2.3 Receptors Bearing a Dimeric Structure of Traditional Host Molecules; 3.3 Hydrocarbon Receptors; 3.4 Receptors Bearing a Curved Conjugated System; 3.4.1 Receptors Based on Bowl-Shaped Conjugated Systems; 3.4.2 Receptors Bearing a Cylindrical Cavity; 3.4.3 Carbon Nanorings 3.5 ConclusionsReferences; 4 Cooperative Effects in the Self-Assembly of Fullerene Donor Ensembles; 4.1 Introduction; 4.2 Allosteric Cooperativity; 4.2.1 General Principle; 4.2.2 Allosteric Cooperativity in Supramolecular Fullerene Donor Ensembles; 4.3 Chelate Cooperativity; 4.3.1 General Principle; 4.3.2 Binding of a Divalent Ligand AA to a Divalent Receptor BB; 4.3.3 Binding of a Divalent Asymmetric Ligand AC to a Complementary Receptor BD; 4.4 Conclusions; 4.5 Experimental Details; 4.5.1 General; 4.5.2 UV-Visible Titrations; 4.5.3 Luminescence Titrations; References 5 Fullerene-Containing Rotaxanes and Catenanes5.1 Introduction; 5.1.1 Synthetic Strategies; 5.1.1.1 Rotaxanes; 5.1.1.2 Catenanes; 5.1.2 Bistable Rotaxanes and Catenanes; 5.2 Fullerene Rotaxanes and Catenanes; 5.2.1 Metal Coordination; 5.2.2 π Stacking Interactions; 5.2.3 Hydrogen Bonds; 5.3 Conclusions; References; 6 Biomimetic Motifs Toward the Construction of Artificial Reaction Centers; 6.1 Introduction; 6.2 Supramolecular Architectures for Solar Energy Conversion; 6.2.1 General Considerations; 6.2.2 Coulomb Interactions; 6.2.3 π-π Stacking; 6.2.4 Hydrogen Bonding 6.2.5 Metal-Ligand Coordination6.3 Outlook; References; 7 Supramolecular Chemistry of Fullerene-Containing Micelles and Gels; 7.1 Introduction; 7.2 Solubilization of Pristine C60 in Surfactant Assemblies; 7.2.1 Solubilizaiton in Micelles; 7.2.2 Solubilization in Vesicles; 7.3 Self-Assemblies of Amphiphilic C60 Derivatives; 7.4 Gels of Fullerenes; 7.5 Conclusions and Outlook; References; 8 Fullerene-Containing Supramolecular Polymers and Dendrimers; 8.1 Introduction; 8.2 Fabrication of [60]Fullerene Polymeric Array; 8.3 Supramolecular Polymerization of Functionalized [60]Fullerene 8.3.1 Ionic Interaction |
Record Nr. | UNINA-9910137626403321 |
Weinheim, : Wiley-VCH, c2012 | ||
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Lo trovi qui: Univ. Federico II | ||
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Supramolecular chemistry of fullerenes and carbon nanotubes / / edited by Nazario Martin and Jean-Francois Nierengarten |
Edizione | [1st ed.] |
Pubbl/distr/stampa | Weinheim, : Wiley-VCH, c2012 |
Descrizione fisica | 1 online resource (421 p.) |
Disciplina | 546.681 |
Altri autori (Persone) |
MartinNazario
NierengartenJean-Francois |
Soggetto topico |
Fullerenes
Nanotubes |
ISBN |
1-283-64409-6
3-527-65015-6 3-527-65014-8 3-527-65012-1 |
Formato | Materiale a stampa ![]() |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Supramolecular Chemistry of Fullerenes and Carbon Nanotubes; Contents; Preface; List of Contributors; 1 Carbon Nanostructures: Covalent and Macromolecular Chemistry; 1.1 Introduction; 1.2 Fullerene-Containing Polymers; 1.3 Carbon Nanotubes; 1.3.1 Defect Functionalization; 1.3.2 Sidewall Functionalization; 1.4 Graphenes; 1.4.1 Covalent Functionalization; 1.4.2 Noncovalent Functionalization; 1.5 Summary and Conclusions; References; 2 Hydrogen-Bonded Fullerene Assemblies; 2.1 Introduction; 2.2 Hydrogen-Bonded Fullerene-Based Supramolecular Structures
2.3 Hydrogen-Bonded Fullerene-Based Donor-Acceptor Structures2.4 Applications; References; 3 Receptors for Pristine Fullerenes Based on Concave-Convex π-π Interactions; 3.1 Introduction; 3.2 Fullerene Receptors Based on Traditional Hosts; 3.2.1 Simple Traditional Hosts; 3.2.2 Modified Traditional Host Molecules; 3.2.3 Receptors Bearing a Dimeric Structure of Traditional Host Molecules; 3.3 Hydrocarbon Receptors; 3.4 Receptors Bearing a Curved Conjugated System; 3.4.1 Receptors Based on Bowl-Shaped Conjugated Systems; 3.4.2 Receptors Bearing a Cylindrical Cavity; 3.4.3 Carbon Nanorings 3.5 ConclusionsReferences; 4 Cooperative Effects in the Self-Assembly of Fullerene Donor Ensembles; 4.1 Introduction; 4.2 Allosteric Cooperativity; 4.2.1 General Principle; 4.2.2 Allosteric Cooperativity in Supramolecular Fullerene Donor Ensembles; 4.3 Chelate Cooperativity; 4.3.1 General Principle; 4.3.2 Binding of a Divalent Ligand AA to a Divalent Receptor BB; 4.3.3 Binding of a Divalent Asymmetric Ligand AC to a Complementary Receptor BD; 4.4 Conclusions; 4.5 Experimental Details; 4.5.1 General; 4.5.2 UV-Visible Titrations; 4.5.3 Luminescence Titrations; References 5 Fullerene-Containing Rotaxanes and Catenanes5.1 Introduction; 5.1.1 Synthetic Strategies; 5.1.1.1 Rotaxanes; 5.1.1.2 Catenanes; 5.1.2 Bistable Rotaxanes and Catenanes; 5.2 Fullerene Rotaxanes and Catenanes; 5.2.1 Metal Coordination; 5.2.2 π Stacking Interactions; 5.2.3 Hydrogen Bonds; 5.3 Conclusions; References; 6 Biomimetic Motifs Toward the Construction of Artificial Reaction Centers; 6.1 Introduction; 6.2 Supramolecular Architectures for Solar Energy Conversion; 6.2.1 General Considerations; 6.2.2 Coulomb Interactions; 6.2.3 π-π Stacking; 6.2.4 Hydrogen Bonding 6.2.5 Metal-Ligand Coordination6.3 Outlook; References; 7 Supramolecular Chemistry of Fullerene-Containing Micelles and Gels; 7.1 Introduction; 7.2 Solubilization of Pristine C60 in Surfactant Assemblies; 7.2.1 Solubilizaiton in Micelles; 7.2.2 Solubilization in Vesicles; 7.3 Self-Assemblies of Amphiphilic C60 Derivatives; 7.4 Gels of Fullerenes; 7.5 Conclusions and Outlook; References; 8 Fullerene-Containing Supramolecular Polymers and Dendrimers; 8.1 Introduction; 8.2 Fabrication of [60]Fullerene Polymeric Array; 8.3 Supramolecular Polymerization of Functionalized [60]Fullerene 8.3.1 Ionic Interaction |
Record Nr. | UNINA-9910809734503321 |
Weinheim, : Wiley-VCH, c2012 | ||
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Lo trovi qui: Univ. Federico II | ||
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