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An Introduction to Redox Polymers for Energy-Storage Applications / / Ulrich S. Schubert, Andreas Winter, and George R. Newkome
An Introduction to Redox Polymers for Energy-Storage Applications / / Ulrich S. Schubert, Andreas Winter, and George R. Newkome
Autore Schubert U (Ulrich)
Pubbl/distr/stampa Weinheim, Germany : , : WILEY-VCH, , [2023]
Descrizione fisica 1 online resource (547 pages)
Disciplina 621.3126
Soggetto topico Energy storage
Polymers
ISBN 3-527-83928-3
3-527-84346-9
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Cover -- Title Page -- Copyright Page -- Contents -- List of Abbreviations -- Chapter 1 The Emergence of "Redox Polymers" in the Field of Energy-Storage Applications* -- 1.1 An Introduction to Battery Systems -- 1.2 Redox Polymers: A Short View on Their Long History -- 1.2.1 The First Era of Redox Polymers -- 1.2.2 The Second Era of Redox Polymers -- 1.2.3 The Third Era of Redox Polymers -- References -- Chapter 2 Polymer-Containing Batteries* -- Study Goals -- 2.1 Introduction -- 2.2 Working Principles -- 2.3 Characterization of Energy-Storage Devices -- 2.3.1 Performance Parameters -- 2.3.2 Charging/Discharging Characteristics -- 2.4 Battery Housing -- 2.5 Solid-State Batteries Incorporating Polymers, as Active Materials -- 2.5.1 Working Principle -- 2.5.2 Material Requirements -- 2.6 Capacitors Incorporating Polymers, as Active Materials -- 2.6.1 Historic Development and Working Principle -- 2.6.2 Material Requirements -- 2.7 Redox-Flow Batteries Incorporating Polymers as Active Materials -- 2.7.1 Working Principle -- 2.7.2 Materials Requirements -- 2.7.3 Aqueous pRFBs -- 2.7.4 Organic pRFBs -- 2.7.5 Suspension RFBs -- 2.8 Concluding Remarks -- References -- Chapter 3 Redox Polymers: Architectures, Synthesis, and Characterization* -- Study Goals -- 3.1 Introduction -- 3.2 Polymer Architecture vs. Battery Cell Performance -- 3.3 Polymer Architectures -- 3.3.1 Homopolymers -- 3.3.2 Copolymers -- 3.3.2.1 Alternating Copolymers -- 3.3.2.2 Statistical and Gradient Copolymers -- 3.3.2.3 Block Copolymers -- 3.3.3 Miscellaneous Polymer Architectures -- 3.4 Polymerization Methods -- 3.4.1 Step-Growth Polymerizations -- 3.4.2 Chain-Growth Polymerizations -- 3.4.2.1 Free-Radical Polymerization -- 3.4.2.2 Controlled Radical Polymerization -- 3.4.2.3 Anionic Polymerization -- 3.4.2.4 Cationic Polymerizations.
3.4.2.5 Ring-Opening Metathesis Polymerizations (ROMP) -- 3.4.3 Redox Polymerizations -- 3.5 TEMPO-Containing Redox Polymers: A Case Study on How the Backbone Structure Influences the Polymeric Properties -- 3.6 Characterization of Redox Polymers -- 3.6.1 Cyclic Voltammetry (CV) -- 3.6.2 Electrochemical Impedance Spectroscopy (EIS) -- 3.6.3 Electrochemical Methods Coupled to Other Analytical Techniques -- 3.7 Concluding Remarks -- References -- Chapter 4 Conjugated Polymers in the Context of Energy-Storage Applications -- Study Goals -- 4.1 Introduction -- 4.2 The Classic Conjugated Polymers at a Glance -- 4.2.1 Polyaniline (PAni) -- 4.2.2 Polypyrrole (PPy) -- 4.2.3 Polythiophene (PT) and PEDOT:PSS -- 4.2.4 Conjugated Polymers for Energy-Storage Applications: General Considerations -- 4.3 Conjugated Polymers, as Active Materials for Battery Systems -- 4.3.1 Polyacetylene -- 4.3.2 Polyaniline -- 4.3.3 Polypyrrole -- 4.3.4 Polythiophene, PEDOT, and Related Polymers -- 4.3.5 Beyond the "Big Three": Miscellaneous Conjugated Polymers -- 4.3.5.1 Poly(p-phenylene) -- 4.3.5.2 Polyindole -- 4.4 Concluding Remarks -- References -- Chapter 5 Redox-Active, Sulfur-Containing Polymers -- Study Goals -- 5.1 Introduction -- 5.2 Fundamentals of Sulfur-Containing Batteries -- 5.3 Composite Electrodes Incorporating Sulfur and Conductive Polymers -- 5.3.1 Polypyrrole, as the Matrix Polymer -- 5.3.2 Polyaniline, as the Matrix Polymer -- 5.3.3 Polythiophene, as the Matrix Polymer -- 5.3.4 Miscellaneous Matrix Polymers -- 5.4 Sulfur-Containing Polymers in Battery Applications -- 5.4.1 Polymers Containing Disulfide Moieties -- 5.4.2 Polymers Containing Oligosulfide or Polysulfide Moieties -- 5.4.3 Beyond Sulfides: Polymers Containing Other Redox-Active Organosulfur Moieties -- 5.5 Concluding Remarks -- References.
Chapter 6 Radical-Containing Polymers for Energy-Storage Applications* -- Study Goals -- 6.1 Introduction -- 6.2 Organic Radical Polymers -- 6.2.1 Free-Radical Moieties Used in ORPs -- 6.2.2 Influence of the Backbone Structure on the ORP Properties -- 6.2.3 Influence of the Polymer Architecture on the ORP Properties -- 6.3 TEMPO-Containing Polymers for Energy-Storage Applications -- 6.3.1 TEMPO-Containing Polymers in Solid-State Batteries -- 6.3.1.1 The Success Story of PTMA -- 6.3.1.2 Beyond PTMA: Polymers with Various Backbone Structures -- 6.3.2 TEMPO-Containing Polymers in Flow-Cell Applications -- 6.4 Beyond TEMPO: Other Nitroxyl Moieties in ORPs -- 6.5 Miscellaneous Free-Radical Moieties in ORPs -- 6.6 Concluding Remarks -- References -- Chapter 7 Polymers Equipped with Redox-Active Quinone Moieties* -- 7.1 Introduction -- 7.2 General Considerations Regarding Carbonyl Compounds, as Active Electrode Materials -- 7.3 Quinone-Containing Polymers for Energy-Storage Applications -- 7.3.1 Polymers with Quinone Moieties Within the Backbone -- 7.3.2 Polymers with Quinone Moieties, as Side Chains -- 7.4 Polyketone-Containing Polymers for Energy-Storage Applications -- 7.5 Polymers, Which Contain Miscellaneous Redox-Active Carbonyl Moieties -- 7.5.1 Side-Chain Polymers, Which Contain Redox-Active Carbonyl Moieties -- 7.5.2 Main-Chain Polymers, Which Contain Redox-Active Carbonyl Moieties -- 7.6 Concluding Remarks -- References -- Chapter 8 Polyimides and Related Polymers in Battery Applications* -- Study Goals -- 8.1 Introduction -- 8.2 Conventional PIs, as Active Materials -- 8.3 Non-conventional PIs, as Active Materials -- 8.3.1 Polyimides with Non-innocent Moieties Within the Spacer -- 8.3.2 Polyimides with Substituents on the Diimide Core -- 8.4 Conjugated Polymers Incorporating the Core of Diimide Moieties -- 8.5 Multidimensional Polyimides.
8.6 Miscellaneous Polymer Structures Incorporating Redox-Active Imide Moieties -- 8.7 Concluding Remarks -- References -- Chapter 9 Polymers Containing Redox-ActiveViologen-Type Moieties -- 9.1 Introduction -- 9.2 Viologen-Containing Polymers for Solid-State Batteries -- 9.3 Viologen-Containing Polymers for Supercapacitors -- 9.4 Viologen-Containing Polymers for Redox-Flow Batteries -- 9.4.1 Aqueous Redox-Flow Batteries -- 9.4.2 Nonaqueous Redox-Flow Batteries -- 9.5 Concluding Remarks -- References -- Chapter 10 Polymers: Containing Redox-Active N-Heterocyclic Moieties -- 10.1 Introduction -- 10.2 Polymers: Containing Triphenylamine Moieties -- 10.3 Polymers: Containing Redox-Active Carbazole Moieties -- 10.4 Polymers: Containing Redox-Active 5,10-Dihydrophenazine Moieties -- 10.5 Polymers: Containing Redox-Active Phenazine Moieties -- 10.6 Polymers: Containing Redox-Active Phenothiazine or Phenoxazine Moieties -- 10.7 Concluding Remarks -- References -- Chapter 11 Redox-Active Metallopolymers -- Study Goals -- 11.1 Introduction -- 11.2 Applications Related to Redox-Active Metallopolymers -- 11.3 Ferrocene-Containing Polymers for Energy-Storage Applications -- 11.4 Beyond Ferrocene: Other Types of Redox-Active Metallopolymers -- 11.5 Concluding Remarks -- References -- Chapter 12 Students' Section: Representative Exercises on Redox Polymers and Their Usage in Energy-Storage Applications -- 12.1 Introduction -- 12.2 Problems -- References -- Index -- EULA.
Record Nr. UNINA-9910686483703321
Schubert U (Ulrich)  
Weinheim, Germany : , : WILEY-VCH, , [2023]
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Modern terpyridine chemistry [[electronic resource] /] / Ulrich S. Schubert, Harald Hofmeier, George R. Newkome
Modern terpyridine chemistry [[electronic resource] /] / Ulrich S. Schubert, Harald Hofmeier, George R. Newkome
Autore Schubert U (Ulrich)
Pubbl/distr/stampa Weinheim, : Wiley-VCH, c2006
Descrizione fisica 1 online resource (239 p.)
Disciplina 151.79
658.51
Altri autori (Persone) HofmeierHarald
NewkomeGeorge R (George Richard)
Soggetto topico Pyridine
Chemistry
ISBN 1-280-72357-2
9786610723577
3-527-60848-6
3-527-60842-7
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Modern Terpyridine Chemistry; Preface; Contents; 1 Introduction; References; 2 Syntheses of Functionalized 2,2 ́:6 ́,2 ́ ́-Terpyridines; 2.1 Introduction; 2.2 Basic Synthetic Strategies; 2.2.1 Ring Assembly; 2.2.2 Cross-Coupling Procedures; 2.3 Synthesis of 2,2 ́:6 ́,2 ́ ́-Terpyridine Derivatives; 2.3.1 4 ́-Substituted-2,2 ́:6 ́,2 ́ ́-Terpyridinoxy Derivatives; 2.3.2 4 ́-Aryl-Substituted 2,2 ́:6 ́,2 ́ ́-Terpyridines; 2.3.3 Other 4 ́-Functionalized 2,2 ́:6 ́ ́2 ́-Terpyridines; 2.3.4 Unsymmetrically Terminally Substituted 2,2 ́:6 ́,2 ́ ́-Terpyridines; 2.3.5 Symmetrically Terminally Substituted 2,2 ́:6 ́,2 ́ ́-Terpyridines
2.3.6 Uniform All-Ring Substituted 2,2 ́:6 ́,2 ́ ́-Terpyridines2.3.7 Multifunctional 2,2 ́:6 ́,2 ́ ́-Terpyridines with Variable Substituents; 2.4 Summary and Outlook; References; 3 Chemistry and Properties of Terpyridine Metal Complexes; 3.1 Introduction; 3.2 Synthetic Strategies; 3.2.1 Metal Complexes; 3.2.1.1 Ruthenium Complexes; 3.2.1.2 Other Luminescent Metal Complexes; 3.3 Mononuclear Bisterpyridine Ruthenium Complexes; 3.4 Chiral Complexes; References; 4 Metallo-Supramolecular Terpyridine Architectures; 4.1 Introduction; 4.2 Dyads and Triads; 4.2.1 Switchable Dyads and Triads
4.3 Supramolecular Assemblies4.3.1 Grids and Racks; 4.3.2 Helicates; 4.3.3 Rotaxanes and Catenanes; 4.3.4 Other Assemblies; 4.4 Cycles; 4.5 Fullerene Terpyridine Complexes; 4.6 Complexes Containing Biochemical Groups; References; 5 New Functional Polymers Incorporating Terpyridine Metal Complexes; 5.1 Introduction; 5.2 Polymers with Terpyridine Units in the Side Chain; 5.2.1 Polymers with Terpyridine Units in the Polymer Backbone; 5.2.2 Polymers from Rigid Organic Building Blocks; 5.2.3 Polymers from Flexible Organic Building Blocks; 5.2.4 Polymers from Polymeric Building Blocks
5.2.5 Other Systems5.3 Biopolymers and Terpyridine Metal Complexes; References; 6 Functional 3-D Architectures Based on Terpyridine Complexes; 6.1 Introduction; 6.2 Dendrimers Containing Terpyridine Metal Complexes in the Dendrimer Core; 6.3 Dendrimers Containing Bisterpyridine Complexes as Non-Core Connectors; 6.4 Dendrimers Containing Bisterpyridine Complexes at the Surface; 6.5 Micelles Composed of Terpyridine-Complex-Containing Polymers; 6.6 Resins and Beads Modified with Terpyridine; References; 7 Surfaces Modified with Terpyridine Metal Complexes; 7.1 Introduction
7.2 Assemblies and Layers7.3 Surface Catalysts; 7.4 Photoactive Materials; References; Subject Index
Record Nr. UNINA-9910830866403321
Schubert U (Ulrich)  
Weinheim, : Wiley-VCH, c2006
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Modern terpyridine chemistry [[electronic resource] /] / Ulrich S. Schubert, Harald Hofmeier, George R. Newkome
Modern terpyridine chemistry [[electronic resource] /] / Ulrich S. Schubert, Harald Hofmeier, George R. Newkome
Autore Schubert U (Ulrich)
Pubbl/distr/stampa Weinheim, : Wiley-VCH, c2006
Descrizione fisica 1 online resource (239 p.)
Disciplina 151.79
658.51
Altri autori (Persone) HofmeierHarald
NewkomeGeorge R (George Richard)
Soggetto topico Pyridine
Chemistry
ISBN 1-280-72357-2
9786610723577
3-527-60848-6
3-527-60842-7
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Modern Terpyridine Chemistry; Preface; Contents; 1 Introduction; References; 2 Syntheses of Functionalized 2,2 ́:6 ́,2 ́ ́-Terpyridines; 2.1 Introduction; 2.2 Basic Synthetic Strategies; 2.2.1 Ring Assembly; 2.2.2 Cross-Coupling Procedures; 2.3 Synthesis of 2,2 ́:6 ́,2 ́ ́-Terpyridine Derivatives; 2.3.1 4 ́-Substituted-2,2 ́:6 ́,2 ́ ́-Terpyridinoxy Derivatives; 2.3.2 4 ́-Aryl-Substituted 2,2 ́:6 ́,2 ́ ́-Terpyridines; 2.3.3 Other 4 ́-Functionalized 2,2 ́:6 ́ ́2 ́-Terpyridines; 2.3.4 Unsymmetrically Terminally Substituted 2,2 ́:6 ́,2 ́ ́-Terpyridines; 2.3.5 Symmetrically Terminally Substituted 2,2 ́:6 ́,2 ́ ́-Terpyridines
2.3.6 Uniform All-Ring Substituted 2,2 ́:6 ́,2 ́ ́-Terpyridines2.3.7 Multifunctional 2,2 ́:6 ́,2 ́ ́-Terpyridines with Variable Substituents; 2.4 Summary and Outlook; References; 3 Chemistry and Properties of Terpyridine Metal Complexes; 3.1 Introduction; 3.2 Synthetic Strategies; 3.2.1 Metal Complexes; 3.2.1.1 Ruthenium Complexes; 3.2.1.2 Other Luminescent Metal Complexes; 3.3 Mononuclear Bisterpyridine Ruthenium Complexes; 3.4 Chiral Complexes; References; 4 Metallo-Supramolecular Terpyridine Architectures; 4.1 Introduction; 4.2 Dyads and Triads; 4.2.1 Switchable Dyads and Triads
4.3 Supramolecular Assemblies4.3.1 Grids and Racks; 4.3.2 Helicates; 4.3.3 Rotaxanes and Catenanes; 4.3.4 Other Assemblies; 4.4 Cycles; 4.5 Fullerene Terpyridine Complexes; 4.6 Complexes Containing Biochemical Groups; References; 5 New Functional Polymers Incorporating Terpyridine Metal Complexes; 5.1 Introduction; 5.2 Polymers with Terpyridine Units in the Side Chain; 5.2.1 Polymers with Terpyridine Units in the Polymer Backbone; 5.2.2 Polymers from Rigid Organic Building Blocks; 5.2.3 Polymers from Flexible Organic Building Blocks; 5.2.4 Polymers from Polymeric Building Blocks
5.2.5 Other Systems5.3 Biopolymers and Terpyridine Metal Complexes; References; 6 Functional 3-D Architectures Based on Terpyridine Complexes; 6.1 Introduction; 6.2 Dendrimers Containing Terpyridine Metal Complexes in the Dendrimer Core; 6.3 Dendrimers Containing Bisterpyridine Complexes as Non-Core Connectors; 6.4 Dendrimers Containing Bisterpyridine Complexes at the Surface; 6.5 Micelles Composed of Terpyridine-Complex-Containing Polymers; 6.6 Resins and Beads Modified with Terpyridine; References; 7 Surfaces Modified with Terpyridine Metal Complexes; 7.1 Introduction
7.2 Assemblies and Layers7.3 Surface Catalysts; 7.4 Photoactive Materials; References; Subject Index
Record Nr. UNINA-9910841254603321
Schubert U (Ulrich)  
Weinheim, : Wiley-VCH, c2006
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Ruthenium-containing polymers / / Ulrich S. Schubert, Andreas Winter, and George R. Newkome
Ruthenium-containing polymers / / Ulrich S. Schubert, Andreas Winter, and George R. Newkome
Autore Schubert U (Ulrich)
Pubbl/distr/stampa Cham, Switzerland : , : Springer, , [2021]
Descrizione fisica 1 online resource (475 pages)
Disciplina 547.7
Soggetto topico Ruthenium compounds
Polymers
ISBN 3-030-75598-3
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Intro -- Preface -- Contents -- Abbreviations -- 1 Introduction -- Abstract -- References -- 2 Polymers Incorporating Ru Complexes -- Abstract -- 2.1 General Considerations -- 2.2 Synthesis, Characterization, and Properties of Ru-Containing Polymers -- 2.2.1 Ruthenopolymers, Derived from the Functionalization of Preformed (Co)polymers -- 2.2.2 Ruthenopolymers, Derived from the Complexation at (Co)polymers -- 2.2.3 Main-Chain Ruthenopolymers, Classified as Metallo-Supramolecular Materials -- 2.2.3.1 Main-Chain Ruthenopolymers, Formed Via Coordinative Bonding -- 2.2.3.2 Main-Chain Ruthenopolymers, Formed via Ionic or Covalent Bonding -- 2.2.3.3 Main-Chain Ruthenopolymers, Formed via Arene-Π Complexation -- 2.2.4 Ruthenopolymers, Derived from RuII-Containing Initiators -- 2.2.5 Ruthenopolymers, Derived from the (Co)polymerization of RuII-Containing Monomers -- 2.2.5.1 Polymers Bearing RuII Centers in the Side Chains or Attached to the Backbone -- 2.2.5.2 Polymers Bearing RuII Centers Within the Backbone -- 2.3 Concluding Remarks -- References -- 3 Electropolymerization-An Item-Centered View on Ruthenopolymers -- Abstract -- 3.1 Introduction -- 3.2 Experimental Remarks -- 3.3 Reductive Electropolymerization of Vinyl-Containing Monomers -- 3.4 Oxidative Electropolymerization of Pyrrole-Containing Monomers -- 3.5 Oxidative Electropolymerization of Thiophene-Containing Monomers -- 3.6 Electropolymerization of Miscellaneous RuII-containing Monomers -- 3.7 Concluding Remarks -- References -- 4 Ruthenodendrimers -- Abstract -- 4.1 Introduction -- 4.2 Dendrimers, Containing RuII Complexes as the Branching Units -- 4.3 Dendrimers, Containing RuII Complexes as Building-Block Connectors -- 4.4 Dendrimers, Containing RuII Complexes as the Core -- 4.5 Dendrimers, Containing RuII Complexes at the Surface.
4.6 Supramolecular Assemblies, Derived from Dendrimers and RuII Complexes -- 4.7 Ru Species Immobilized Within Dendrimers -- 4.8 Concluding Remarks -- References -- 5 Polymers and Small-Molecule Ru Species -- Abstract -- 5.1 Introduction -- 5.2 Ru Complexes Embedded in Polymer Matrices: Catalytic Applications -- 5.3 Ru Complexes Embedded in Polymer Matrices: Biomedical Applications -- 5.4 Ru Complexes Embedded in Polymer Matrices: Opto-Electronic Applications -- 5.5 Polymer-Staining Using Ru Reagents -- 5.6 Concluding Remarks -- References -- 6 Metal-organic and Covalent Organic Frameworks Incorporating Ru Species -- Abstract -- 6.1 Introduction -- 6.2 Metal-organic-Frameworks with Embedded Ru Nanoparticles or RuII Complexes -- 6.3 Metal-organic-Frameworks Assembled from RuII Species -- 6.4 Covalent Organic-Frameworks Incorporating Ru Species -- 6.5 Concluding Remarks -- References -- 7 Polymer-Stabilized Ru Nanoparticles -- Abstract -- 7.1 Introduction -- 7.2 Synthesis of Ru Nanoparticles-General Considerations -- 7.3 Ru Nanoparticles, Stabilized by Polymers -- 7.4 Concluding Remarks -- References.
Record Nr. UNINA-9910485598803321
Schubert U (Ulrich)  
Cham, Switzerland : , : Springer, , [2021]
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Supramolecular polymers and assemblies : from synthesis to properties and applications / / Ulrich Schubert, George R. Newkome, Andreas Winter
Supramolecular polymers and assemblies : from synthesis to properties and applications / / Ulrich Schubert, George R. Newkome, Andreas Winter
Autore Schubert U (Ulrich)
Pubbl/distr/stampa Weinheim, Germany : , : Wiley-VCH, , [2021]
Descrizione fisica 1 online resource (546 pages)
Disciplina 541.226
Soggetto topico Supramolecular chemistry
Polymers
Soggetto genere / forma Electronic books.
ISBN 3-527-83240-8
3-527-83241-6
3-527-68532-4
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910555149503321
Schubert U (Ulrich)  
Weinheim, Germany : , : Wiley-VCH, , [2021]
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Supramolecular polymers and assemblies : from synthesis to properties and applications / / Ulrich Schubert, George R. Newkome, Andreas Winter
Supramolecular polymers and assemblies : from synthesis to properties and applications / / Ulrich Schubert, George R. Newkome, Andreas Winter
Autore Schubert U (Ulrich)
Pubbl/distr/stampa Weinheim, Germany : , : Wiley-VCH, , [2021]
Descrizione fisica 1 online resource (546 pages)
Disciplina 541.226
Soggetto topico Supramolecular chemistry
Polymers
ISBN 3-527-83240-8
3-527-83241-6
3-527-68532-4
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Record Nr. UNINA-9910830013503321
Schubert U (Ulrich)  
Weinheim, Germany : , : Wiley-VCH, , [2021]
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Terpyridine-based materials [[electronic resource] ] : for catalytic, optoelectronic and life science applications / / Ulrich S. Schubert, Andreas Winter, and George R. Newkome
Terpyridine-based materials [[electronic resource] ] : for catalytic, optoelectronic and life science applications / / Ulrich S. Schubert, Andreas Winter, and George R. Newkome
Autore Schubert U (Ulrich)
Pubbl/distr/stampa Weinheim, Germany, : Wiley-VCH, 2011
Descrizione fisica 1 online resource (544 p.)
Disciplina 547.593
Altri autori (Persone) WinterAndreas
NewkomeGeorge R (George Richard)
Soggetto topico Pyridine
ISBN 3-527-63963-2
1-283-37057-3
9786613370570
3-527-63962-4
3-527-63964-0
Classificazione 540
VK 7150
VK 7200
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Terpyridine-based Materials: For Catalytic, Optoelectronic and Life Science Applications; Contents; Preface; List of Abbreviations; 1: Introduction; 2: Synthesis, Properties, and Applications of Functionalized 2,2 ;-Terpyridines; 2.1: Introduction; 2.2: Basic Synthetic Strategies; 2.2.1: Ring-Assembly Methodologies; 2.2.2: Cross-Coupling Procedures; 2.3: Synthesis and Properties of 2,-Terpyridine Derivatives; 2.3.1: 4x2032;-Substituted 2, Terpyridinoxy Derivatives; 2.3.2: Miscellaneous 4;-Substituted 2,2032;-Terpyridine Derivatives
3.3.1: Synthesis of RuII and OsII Bis(terpyridine) Complexes 3.3.2: RuII Ions and Terpyridine Ligands - A Happy Marriage?; 3.3.2.1: Photophysical Properties; 3.3.2.2: Mononuclear RuII Bis(terpyridine) Complexes; 3.3.2.3: Oligonuclear Complexes Containing RuII/OsII Bis(terpyridine) Units; 3.3.2.4: Dendritic and Star-Shaped Systems Containing RuII Bis(terpyridine) Units; 3.4: Iridium(III) Complexes with Terpyridine Ligands; 3.5: Platinum(II) Mono(terpyridine) Complexes; 4: Metallo-Supramolecular Architectures Based on Terpyridine Complexes; 4.1: Introduction
4.2: Terpyridine-Containing Metallo-Macrocycles 4.3: The HETTAP Concept; 4.4: Racks and Grids; 4.5: Helicates; 4.6: Rotaxanes and Catenanes; 4.7: Miscellaneous Structures; 4.7.1: Cyclodextrin Derivatives; 4.7.2: Other Assemblies; 5: CO; -Conjugated Polymers Incorporating Terpyridine Metal Complexes; 5.1: Introduction; 5.2: Metallo-Supramolecular Polymerization; 5.3: Metallopolymers Based on CO; -Conjugated Bis(terpyridine)s; 5.3.1: Polymerization by Transition Metal Ion Coordination; 5.3.2: Self-Assembly of Metallopolymers; 5.3.3: Chiral Metallopolymers; 5.3.4: Non-Classical Metallopolymers
5.3.5: Polymerization Using the ''Complex First'' Method 5.4: Main-Chain Metallopolymers Based on Terpyridine-Functionalized CO; -Conjugated Polymers; 6: Functional Polymers Incorporating Terpyridine-Metal Complexes; 6.1: Introduction; 6.2: Polymers with Terpyridine Units in the Side-Chain; 6.2.1: Materials Based on Flexible Organic Polymers; 6.2.2: Materials Based on CO; -Conjugated Polymers; 6.3: Polymers with Terpyridines within the Polymer Backbone; 6.3.1: Polymers from Organic Small-Molecule Building Blocks; 6.3.2: Chain-Extended Polymers from Polymeric Building Blocks
6.3.3: Monotopic Macroligands by End-Group Functionalization
Record Nr. UNINA-9910139742503321
Schubert U (Ulrich)  
Weinheim, Germany, : Wiley-VCH, 2011
Materiale a stampa
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui
Terpyridine-based materials [[electronic resource] ] : for catalytic, optoelectronic and life science applications / / Ulrich S. Schubert, Andreas Winter, and George R. Newkome
Terpyridine-based materials [[electronic resource] ] : for catalytic, optoelectronic and life science applications / / Ulrich S. Schubert, Andreas Winter, and George R. Newkome
Autore Schubert U (Ulrich)
Pubbl/distr/stampa Weinheim, Germany, : Wiley-VCH, 2011
Descrizione fisica 1 online resource (544 p.)
Disciplina 547.593
Altri autori (Persone) WinterAndreas
NewkomeGeorge R (George Richard)
Soggetto topico Pyridine
ISBN 3-527-63963-2
1-283-37057-3
9786613370570
3-527-63962-4
3-527-63964-0
Classificazione 540
VK 7150
VK 7200
Formato Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione eng
Nota di contenuto Terpyridine-based Materials: For Catalytic, Optoelectronic and Life Science Applications; Contents; Preface; List of Abbreviations; 1: Introduction; 2: Synthesis, Properties, and Applications of Functionalized 2,2 ;-Terpyridines; 2.1: Introduction; 2.2: Basic Synthetic Strategies; 2.2.1: Ring-Assembly Methodologies; 2.2.2: Cross-Coupling Procedures; 2.3: Synthesis and Properties of 2,-Terpyridine Derivatives; 2.3.1: 4x2032;-Substituted 2, Terpyridinoxy Derivatives; 2.3.2: Miscellaneous 4;-Substituted 2,2032;-Terpyridine Derivatives
3.3.1: Synthesis of RuII and OsII Bis(terpyridine) Complexes 3.3.2: RuII Ions and Terpyridine Ligands - A Happy Marriage?; 3.3.2.1: Photophysical Properties; 3.3.2.2: Mononuclear RuII Bis(terpyridine) Complexes; 3.3.2.3: Oligonuclear Complexes Containing RuII/OsII Bis(terpyridine) Units; 3.3.2.4: Dendritic and Star-Shaped Systems Containing RuII Bis(terpyridine) Units; 3.4: Iridium(III) Complexes with Terpyridine Ligands; 3.5: Platinum(II) Mono(terpyridine) Complexes; 4: Metallo-Supramolecular Architectures Based on Terpyridine Complexes; 4.1: Introduction
4.2: Terpyridine-Containing Metallo-Macrocycles 4.3: The HETTAP Concept; 4.4: Racks and Grids; 4.5: Helicates; 4.6: Rotaxanes and Catenanes; 4.7: Miscellaneous Structures; 4.7.1: Cyclodextrin Derivatives; 4.7.2: Other Assemblies; 5: CO; -Conjugated Polymers Incorporating Terpyridine Metal Complexes; 5.1: Introduction; 5.2: Metallo-Supramolecular Polymerization; 5.3: Metallopolymers Based on CO; -Conjugated Bis(terpyridine)s; 5.3.1: Polymerization by Transition Metal Ion Coordination; 5.3.2: Self-Assembly of Metallopolymers; 5.3.3: Chiral Metallopolymers; 5.3.4: Non-Classical Metallopolymers
5.3.5: Polymerization Using the ''Complex First'' Method 5.4: Main-Chain Metallopolymers Based on Terpyridine-Functionalized CO; -Conjugated Polymers; 6: Functional Polymers Incorporating Terpyridine-Metal Complexes; 6.1: Introduction; 6.2: Polymers with Terpyridine Units in the Side-Chain; 6.2.1: Materials Based on Flexible Organic Polymers; 6.2.2: Materials Based on CO; -Conjugated Polymers; 6.3: Polymers with Terpyridines within the Polymer Backbone; 6.3.1: Polymers from Organic Small-Molecule Building Blocks; 6.3.2: Chain-Extended Polymers from Polymeric Building Blocks
6.3.3: Monotopic Macroligands by End-Group Functionalization
Record Nr. UNINA-9910822310903321
Schubert U (Ulrich)  
Weinheim, Germany, : Wiley-VCH, 2011
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