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Supramolecular Polymer Chemistry.

Presenting the work of pioneering experts in this exciting field of supramolecular polymer chemistry, this monograph covers an extensive range of applications, including drug delivery and catalysis. It focuses on new structures and phenomena of cyclodextrin-based supramolecular polymers and many oth...

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Detalles Bibliográficos
Clasificación:Libro Electrónico
Autor principal: Harada, Akira
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Hoboken : John Wiley & Sons, 2011.
Temas:
Acceso en línea:Texto completo

MARC

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245 1 0 |a Supramolecular Polymer Chemistry. 
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505 0 |a Supramolecular Polymer Chemistry; Contents; Preface; List of Contributors; Part One: Formation of Supramolecular Polymers; 1 Multiple Hydrogen-Bonded Supramolecular Polymers; 1.1 Introduction; 1.1.1 Historical Background; 1.1.2 Supramolecular Chemistry; 1.1.3 Supramolecular Polymerization Mechanisms; 1.2 General Concepts of Hydrogen-Bonding Motifs; 1.2.1 Arrays of Multiple Hydrogen Bonds; 1.2.2 Preorganization through Intramolecular Hydrogen Bonding; 1.2.3 Tautomeric Equilibria; 1.3 Hydrogen-Bonded Main-Chain Supramolecular Polymers; 1.3.1 The Establishment of Supramolecular Polymers. 
505 8 |a 1.3.2 Supramolecular Polymerizations1.3.3 Hydrophobic Compartmentalization; 1.4 From Supramolecular Polymers to Supramolecular Materials; 1.4.1 Thermoplastic Elastomers; 1.4.2 Phase Separation and Additional Lateral Interactions in Supramolecular Polymers in the Solid State; 1.4.3 Supramolecular Thermoplastic Elastomers Based on Additional Lateral Interactions and Phase Separation; 1.5 Future Perspectives; References; 2 Cyclodextrin-Based Supramolecular Polymers; 2.1 Introduction; 2.2 Supramolecular Polymers in the Solid State; 2.2.1 Crystal Structures of CD Aliphatic Tethers. 
505 8 |a 2.2.2 Crystal Structures of ß-CDs Aromatic Tethers2.3 Formation of Homo-Intramolecular and Intermolecular Complexes by CDs-Guest Conjugates; 2.3.1 Supramolecular Structures Formed by 6-Modified a-CDs; 2.3.2 Supramolecular Structures Formed by 6-Modified ß-CDs 39; 2.3.3 Supramolecular Structures Formed by 3-Modified a-CDs; 2.3.4 Hetero-Supramolecular Structures Formed by Modified CDs; 2.4 Formation of Intermolecular Complexes by CD and Guest Dimers; 2.5 Artificial Molecular Muscle Based on c2-Daisy Chain; 2.6 Conclusion and Outlook; References. 
505 8 |a 3 Supra-Macromolecular Chemistry: Toward Design of New Organic Materials from Supramolecular Standpoints3.1 Introduction; 3.2 Small Molecules, Macromolecules, and Supramolecules: Design of their Composite Materials; 3.2.1 Interactions between Small Molecules and Macromolecules; 3.2.2 Interactions between Small Molecules and Molecular Assemblies; 3.2.3 Interactions between Molecular Assemblies; 3.2.4 Interactions between Macromolecules; 3.2.5 Interactions between Macromolecular Assemblies; 3.2.6 Interactions between Macromolecules and Molecular Assemblies; 3.3 Conclusion and Outlook. 
504 |a References4 Polymerization with Ditopic Cavitand Monomers; 4.1 Introduction; 4.2 Cavitands; 4.3 Self-Assembly of Ditopic Cavitand Monomers; 4.3.1 Structural Monomer Classification of Supramolecular Polymerization; 4.3.2 Homoditopic Cavitands Self-Assembled via Solvophobic p-p Stacking Interactions; 4.3.3 Heteroditopic Cavitands Combining Solvophobic Interactions and Metal-Ligand Coordination; 4.3.4 Heteroditopic Cavitands Combining Solvophobic Interactions and Hydrogen Bonding; 4.3.5 Heteroditopic Cavitands Self-assembled via Host-Guest Interactions. 
505 8 |a 4.3.6 Homoditopic Cavitands Self-assembled via Host-Guest Interactions. 
520 |a Presenting the work of pioneering experts in this exciting field of supramolecular polymer chemistry, this monograph covers an extensive range of applications, including drug delivery and catalysis. It focuses on new structures and phenomena of cyclodextrin-based supramolecular polymers and many other compound classes. While providing a deeper insight in macromolecular recognition and the mechanisms of living systems, this book also introduces fascinating novel phenomena beyond natural systems. 
588 0 |a Print version record. 
546 |a English. 
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650 0 |a Polymers. 
650 0 |a Supramolecular chemistry. 
650 2 |a Polymers 
650 6 |a Polymères. 
650 6 |a Chimie supramoléculaire. 
650 7 |a polymers.  |2 aat 
650 7 |a Polymers  |2 fast 
650 7 |a Supramolecular chemistry  |2 fast 
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856 4 0 |u https://ebookcentral.uam.elogim.com/lib/uam-ebooks/detail.action?docID=827181  |z Texto completo 
880 0 |6 505-00/(S  |a Supramolecular Polymer Chemistry -- Contents -- Preface -- List of Contributors -- Part One: Formation of Supramolecular Polymers -- 1 Multiple Hydrogen-Bonded Supramolecular Polymers -- 1.1 Introduction -- 1.1.1 Historical Background -- 1.1.2 Supramolecular Chemistry -- 1.1.3 Supramolecular Polymerization Mechanisms -- 1.2 General Concepts of Hydrogen-Bonding Motifs -- 1.2.1 Arrays of Multiple Hydrogen Bonds -- 1.2.2 Preorganization through Intramolecular Hydrogen Bonding -- 1.2.3 Tautomeric Equilibria -- 1.3 Hydrogen-Bonded Main-Chain Supramolecular Polymers -- 1.3.1 The Establishment of Supramolecular Polymers -- 1.3.2 Supramolecular Polymerizations -- 1.3.3 Hydrophobic Compartmentalization -- 1.4 From Supramolecular Polymers to Supramolecular Materials -- 1.4.1 Thermoplastic Elastomers -- 1.4.2 Phase Separation and Additional Lateral Interactions in Supramolecular Polymers in the Solid State -- 1.4.3 Supramolecular Thermoplastic Elastomers Based on Additional Lateral Interactions and Phase Separation -- 1.5 Future Perspectives -- References -- 2 Cyclodextrin-Based Supramolecular Polymers -- 2.1 Introduction -- 2.2 Supramolecular Polymers in the Solid State -- 2.2.1 Crystal Structures of CD Aliphatic Tethers -- 2.2.2 Crystal Structures of β-CDs Aromatic Tethers -- 2.3 Formation of Homo-Intramolecular and Intermolecular Complexes by CDs-Guest Conjugates -- 2.3.1 Supramolecular Structures Formed by 6-Modified α-CDs -- 2.3.2 Supramolecular Structures Formed by 6-Modified β-CDs 39 -- 2.3.3 Supramolecular Structures Formed by 3-Modified α-CDs -- 2.3.4 Hetero-Supramolecular Structures Formed by Modified CDs -- 2.4 Formation of Intermolecular Complexes by CD and Guest Dimers -- 2.5 Artificial Molecular Muscle Based on c2-Daisy Chain -- 2.6 Conclusion and Outlook -- References. 
880 8 |6 505-00/(S  |a 3 Supra-Macromolecular Chemistry: Toward Design of New Organic Materials from Supramolecular Standpoints -- 3.1 Introduction -- 3.2 Small Molecules, Macromolecules, and Supramolecules: Design of their Composite Materials -- 3.2.1 Interactions between Small Molecules and Macromolecules -- 3.2.2 Interactions between Small Molecules and Molecular Assemblies -- 3.2.3 Interactions between Molecular Assemblies -- 3.2.4 Interactions between Macromolecules -- 3.2.5 Interactions between Macromolecular Assemblies -- 3.2.6 Interactions between Macromolecules and Molecular Assemblies -- 3.3 Conclusion and Outlook -- References -- 4 Polymerization with Ditopic Cavitand Monomers -- 4.1 Introduction -- 4.2 Cavitands -- 4.3 Self-Assembly of Ditopic Cavitand Monomers -- 4.3.1 Structural Monomer Classification of Supramolecular Polymerization -- 4.3.2 Homoditopic Cavitands Self-Assembled via Solvophobic π-π Stacking Interactions -- 4.3.3 Heteroditopic Cavitands Combining Solvophobic Interactions and Metal-Ligand Coordination -- 4.3.4 Heteroditopic Cavitands Combining Solvophobic Interactions and Hydrogen Bonding -- 4.3.5 Heteroditopic Cavitands Self-assembled via Host-Guest Interactions -- 4.3.6 Homoditopic Cavitands Self-assembled via Host-Guest Interactions -- 4.4 Conclusions and Outlook -- References -- Part Two: Supramolecular Polymers with Unique Structures -- 5 Polymers Containing Covalently Bonded and Supramolecularly Attached Cyclodextrins as Side Groups -- 5.1 Polymers with Covalently Bonded Cyclodextrins as Side Groups -- 5.1.1 Synthesis and Polymerization of Monofunctional Cyclodextrin Monomers -- 5.1.2 Polymer-Analogous Reaction with Monofunctional Cyclodextrin -- 5.1.3 Structure-Property Relationship of Polymers Containing Cyclodextrins as Side Group -- 5.2 Side Chain Polyrotaxanes and Polypseudorotaxanes -- 5.2.1 Side Chain Polyrotaxanes. 
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