05326nam 2200649Ia 450 991013762640332120230801232029.01-283-64409-63-527-65015-63-527-65014-83-527-65012-1(CKB)3190000000022664(EBL)1033025(OCoLC)813397929(SSID)ssj0000667323(PQKBManifestationID)11389509(PQKBTitleCode)TC0000667323(PQKBWorkID)10684082(PQKB)11693950(MiAaPQ)EBC1033025(Au-PeEL)EBL1033025(CaPaEBR)ebr10606049(CaONFJC)MIL395659(EXLCZ)99319000000002266420120112d2012 uy 0engur|n|---|||||txtccrSupramolecular chemistry of fullerenes and carbon nanotubes[electronic resource] /edited by Nazario Martin and Jean-Francois NierengartenWeinheim Wiley-VCHc20121 online resource (421 p.)Description based upon print version of record.3-527-32789-4 Includes bibliographical references and index.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 Structures2.3 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 Nanorings3.5 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; References5 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 Bonding6.2.5 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]Fullerene8.3.1 Ionic InteractionCollating our current knowledge and the latest developments for enabling breakthrough discoveries, this book focuses on the synthesis and applications of materials that are based on supramolecular assemblies of carbon nanostructures, with an emphasis on fullerenes and nanotubes. In so doing, it provides readers with an overview of the different types of supramolecular architectures, accentuating the outstanding geometrical, electronic and photophysical properties of the building blocks and the resulting structures. It makes use of basic concepts and real-life applications -- from simple syntheFullerenesNanotubesFullerenes.Nanotubes.546.681Martin Nazario885456Nierengarten Jean-Francois885457MiAaPQMiAaPQMiAaPQBOOK9910137626403321Supramolecular chemistry of fullerenes and carbon nanotubes1977232UNINA