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 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
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 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|