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[Pi]-stacked polymers and molecules : theory, synthesis, and properties / / Tamaki Nakano, editor
| [Pi]-stacked polymers and molecules : theory, synthesis, and properties / / Tamaki Nakano, editor |
| Edizione | [1st ed. 2014.] |
| Pubbl/distr/stampa | Tokyo : , : Springer, , 2014 |
| Descrizione fisica | 1 online resource (xii, 270 pages) : illustrations (some color) |
| Disciplina | 547.7 |
| Collana | Gale eBooks |
| Soggetto topico | Conjugated polymers |
| ISBN | 4-431-54129-2 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Synthesis and Properties of π-Stacked Vinyl Polymers -- Reversible Polymerization Techniques Leading to π-Stacked Polymers -- Cyclophane-based π-Stacked Polymers -- π-Stacked Oligomers as Models for Semiconducting Conjugated Organic Materials -- π-Stacking on Density Functional Theory: A Review. |
| Record Nr. | UNINA-9910298638203321 |
| Tokyo : , : Springer, , 2014 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Conjugated polyelectrolytes [[electronic resource]] : fundamentals and applications / / edited by Bin Liu and Guillermo C. Bazan
| Conjugated polyelectrolytes [[electronic resource]] : fundamentals and applications / / edited by Bin Liu and Guillermo C. Bazan |
| Pubbl/distr/stampa | Weinheim an der Bergstrasse, Germany, : Wiley-VCH Verlag, c2013 |
| Descrizione fisica | 1 online resource (440 p.) |
| Disciplina | 541.372 |
| Altri autori (Persone) |
LiuBin
BazanGuillermo C |
| Soggetto topico |
Polyelectrolytes
Conjugated polymers |
| ISBN |
3-527-65572-7
3-527-65570-0 3-527-65573-5 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Conjugated Polyelectrolytes; Contents; Preface; List of Contributors; 1 Design and Synthesis of Conjugated Polyelectrolytes; 1.1 Introduction; 1.2 Poly(arylene)s; 1.2.1 Polythiophenes; 1.2.1.1 Anionic Polythiophenes; 1.2.1.2 Cationic Polythiophenes; 1.2.1.3 Zwitterionic Polythiophenes; 1.2.2 Poly(p-phenylene)s; 1.2.2.1 Anionic Poly(p-phenylene)s; 1.2.2.2 Cationic Poly(p-phenylene)s; 1.2.3 Poly(fluorene)s; 1.2.3.1 Cationic Poly(fluorene)s; 1.2.3.2 Anionic Poly(fluorene)s; 1.2.3.3 Zwitterionic Poly(fluorene)s; 1.3 Poly(arylene ethynylene)s; 1.3.1 Poly(phenylene ethynylene)s
1.3.1.1 Anionic Poly(phenylene ethynylene)s1.3.1.2 Cationic Poly(phenylene ethynylene)s; 1.3.2 Poly(fluorene ethynylene)s; 1.3.2.1 Cationic Poly(fluorene ethynylene)s; 1.3.2.2 Anionic Poly(fluorene ethynylene)s; 1.4 Poly(arylene vinylene)s; 1.4.1 Poly(phenylene vinylene)s; 1.4.1.1 Anionic Poly(phenylene vinylene)s; 1.4.1.2 Cationic Poly(phenylene vinylene)s; 1.4.2 Poly(fluorene vinylene)s; 1.4.2.1 Cationic Poly(fluorene vinylene)s; 1.4.2.2 Anionic Poly(fluorene vinylene)s; 1.5 Conclusion; References; 2 All-Conjugated Rod-Rod Diblock Copolymers Containing Conjugated Polyelectrolyte Blocks 2.1 Introduction2.2 All-Conjugated, Cationic Polyfluorene-b-Polythiophene Diblock Copolymers; 2.2.1 Synthesis; 2.2.2 Optical Properties; 2.2.3 Aggregation Behavior of Cationic PF-b-PT Diblock Copolymers; 2.2.4 Atomic Force Microscopy; 2.2.4.1 Confocal Microscopy; 2.2.4.2 Complexation with Anionic Surfactants; 2.2.4.3 Complexation with DNA; 2.2.4.4 Incorporation of PF2/6-b-P3TMAHT into Organic Electronic Devices; 2.3 All-Conjugated Cationic Polyfluorene-b-Polyfluorene Diblock Copolymers; 2.3.1 Synthesis; 2.3.2 Optical Properties; 2.3.3 Atomic Force Microscopy; 2.4 Conclusion; Acknowledgments References3 Ionically Functionalized Polyacetylenes; 3.1 Introduction; 3.2 Polymers from Ionically Functionalized Cyclooctatetraenes; 3.2.1 Synthesis and General Properties; 3.2.2 Electrochemistry; 3.2.2.1 Electrochemical Doping; 3.2.2.2 The Donnan Potential; 3.2.2.3 Internal Compensation; 3.2.3 Polyelectrolyte-Mediated and Self-Limiting Electrochemistry; 3.2.4 Junctions; 3.2.4.1 In situ Electrochemical Manipulation and the Tunable Diode; 3.2.4.2 Internally Compensated p-n Junctions; 3.2.4.3 Undoped Ionic Junctions; 3.3 Polymers from Ionically Functionalized Acetylenes 3.3.1 General Properties and Synthetic Approaches3.3.2 Polymer Chain Structure; 3.3.3 Poly(IA)s with Extended Conjugations; 3.4 Summary; Acknowledgment; References; 4 Aggregation Properties of Conjugated Polyelectrolytes; 4.1 Introduction; 4.2 Aggregation: from Disordered Clusters to Structured Vesicles; 4.3 Experimental Studies on Aggregation; 4.3.1 What Scattering Techniques Tell Us; 4.3.2 Microscopy Studies in Solution and Films; 4.3.3 Spectroscopic and Photophysical Studies; 4.3.4 Aggregation as Seen by Electrical Conductivity and NMR Spectroscopy; 4.3.5 Molecular Dynamics Simulations 4.4 Conjugated Polyelectrolyte Aggregation in Solution |
| Record Nr. | UNINA-9910133856703321 |
| Weinheim an der Bergstrasse, Germany, : Wiley-VCH Verlag, c2013 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Conjugated polyelectrolytes : fundamentals and applications / / edited by Bin Liu and Guillermo C. Bazan
| Conjugated polyelectrolytes : fundamentals and applications / / edited by Bin Liu and Guillermo C. Bazan |
| Edizione | [1st ed.] |
| Pubbl/distr/stampa | Weinheim an der Bergstrasse, Germany, : Wiley-VCH Verlag, c2013 |
| Descrizione fisica | 1 online resource (440 p.) |
| Disciplina | 541.372 |
| Altri autori (Persone) |
LiuBin
BazanGuillermo C |
| Soggetto topico |
Polyelectrolytes
Conjugated polymers |
| ISBN |
9783527655724
3527655727 9783527655700 3527655700 9783527655731 3527655735 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Conjugated Polyelectrolytes; Contents; Preface; List of Contributors; 1 Design and Synthesis of Conjugated Polyelectrolytes; 1.1 Introduction; 1.2 Poly(arylene)s; 1.2.1 Polythiophenes; 1.2.1.1 Anionic Polythiophenes; 1.2.1.2 Cationic Polythiophenes; 1.2.1.3 Zwitterionic Polythiophenes; 1.2.2 Poly(p-phenylene)s; 1.2.2.1 Anionic Poly(p-phenylene)s; 1.2.2.2 Cationic Poly(p-phenylene)s; 1.2.3 Poly(fluorene)s; 1.2.3.1 Cationic Poly(fluorene)s; 1.2.3.2 Anionic Poly(fluorene)s; 1.2.3.3 Zwitterionic Poly(fluorene)s; 1.3 Poly(arylene ethynylene)s; 1.3.1 Poly(phenylene ethynylene)s
1.3.1.1 Anionic Poly(phenylene ethynylene)s1.3.1.2 Cationic Poly(phenylene ethynylene)s; 1.3.2 Poly(fluorene ethynylene)s; 1.3.2.1 Cationic Poly(fluorene ethynylene)s; 1.3.2.2 Anionic Poly(fluorene ethynylene)s; 1.4 Poly(arylene vinylene)s; 1.4.1 Poly(phenylene vinylene)s; 1.4.1.1 Anionic Poly(phenylene vinylene)s; 1.4.1.2 Cationic Poly(phenylene vinylene)s; 1.4.2 Poly(fluorene vinylene)s; 1.4.2.1 Cationic Poly(fluorene vinylene)s; 1.4.2.2 Anionic Poly(fluorene vinylene)s; 1.5 Conclusion; References; 2 All-Conjugated Rod-Rod Diblock Copolymers Containing Conjugated Polyelectrolyte Blocks 2.1 Introduction2.2 All-Conjugated, Cationic Polyfluorene-b-Polythiophene Diblock Copolymers; 2.2.1 Synthesis; 2.2.2 Optical Properties; 2.2.3 Aggregation Behavior of Cationic PF-b-PT Diblock Copolymers; 2.2.4 Atomic Force Microscopy; 2.2.4.1 Confocal Microscopy; 2.2.4.2 Complexation with Anionic Surfactants; 2.2.4.3 Complexation with DNA; 2.2.4.4 Incorporation of PF2/6-b-P3TMAHT into Organic Electronic Devices; 2.3 All-Conjugated Cationic Polyfluorene-b-Polyfluorene Diblock Copolymers; 2.3.1 Synthesis; 2.3.2 Optical Properties; 2.3.3 Atomic Force Microscopy; 2.4 Conclusion; Acknowledgments References3 Ionically Functionalized Polyacetylenes; 3.1 Introduction; 3.2 Polymers from Ionically Functionalized Cyclooctatetraenes; 3.2.1 Synthesis and General Properties; 3.2.2 Electrochemistry; 3.2.2.1 Electrochemical Doping; 3.2.2.2 The Donnan Potential; 3.2.2.3 Internal Compensation; 3.2.3 Polyelectrolyte-Mediated and Self-Limiting Electrochemistry; 3.2.4 Junctions; 3.2.4.1 In situ Electrochemical Manipulation and the Tunable Diode; 3.2.4.2 Internally Compensated p-n Junctions; 3.2.4.3 Undoped Ionic Junctions; 3.3 Polymers from Ionically Functionalized Acetylenes 3.3.1 General Properties and Synthetic Approaches3.3.2 Polymer Chain Structure; 3.3.3 Poly(IA)s with Extended Conjugations; 3.4 Summary; Acknowledgment; References; 4 Aggregation Properties of Conjugated Polyelectrolytes; 4.1 Introduction; 4.2 Aggregation: from Disordered Clusters to Structured Vesicles; 4.3 Experimental Studies on Aggregation; 4.3.1 What Scattering Techniques Tell Us; 4.3.2 Microscopy Studies in Solution and Films; 4.3.3 Spectroscopic and Photophysical Studies; 4.3.4 Aggregation as Seen by Electrical Conductivity and NMR Spectroscopy; 4.3.5 Molecular Dynamics Simulations 4.4 Conjugated Polyelectrolyte Aggregation in Solution |
| Record Nr. | UNINA-9910827425303321 |
| Weinheim an der Bergstrasse, Germany, : Wiley-VCH Verlag, c2013 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Conjugated polymer synthesis : methods and reactions / / edited by Yoshiki Chujo
| Conjugated polymer synthesis : methods and reactions / / edited by Yoshiki Chujo |
| Edizione | [4th ed.] |
| Pubbl/distr/stampa | Weinheim : , : Wiley-VCH, , [2010] |
| Descrizione fisica | 1 online resource (331 p.) |
| Disciplina | 547.70457 |
| Altri autori (Persone) | ChujoY (Yoshiki) |
| Soggetto topico | Conjugated polymers |
| ISBN |
3-527-63266-2
3-527-63267-0 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Conjugated Polymer Synthesis: Methods and Reactions; Contents; Preface; List of Contributors; 1 Organometallic Polycondensation for Conjugated Polymers; 1.1 Basic Organometallic C-C Coupling; 1.2 Syntheses of π-Conjugated Polymers; 1.3 Optical Properties; 1.3.1 UV-Vis Data; 1.3.2 Photoluminescence; 1.3.3 Other Optical Properties; 1.4 Redox Behavior and Electrical Conductivity; 1.5 Linear Structure and Alignment on the Surface of Substrates; 1.6 Stacking in the Solid and Colloid; 1.7 Chemical Reactivity and Catalysis; 1.7.1 Metal Complexes and Modification of Nitrogen
1.8 Electronic and Optical Devices (ECD, Battery, EL, Diode, Transistor, Nonlinear Optical Device, etc.)1.8.1 Redox Functions; 1.8.2 Electronic and Optical Devices; 1.9 Conclusions; References; 2 Catalyst-Transfer Condensation Polymerization for Precision Synthesis of π-Conjugated Polymers; 2.1 Introduction; 2.2 Kumada-Tamao Coupling Polymerization with Ni Catalyst; 2.2.1 Polythiophene; 2.2.1.1 Discovery and Mechanism of Catalyst-Transfer Condensation Polymerization; 2.2.1.2 A Variety of Monomers; 2.2.1.3 Block Polythiophenes; 2.2.1.4 Block Copolymers of Polythiophene and Other Polymers 2.2.1.5 Graft Copolymers2.2.2 Polyphenylenes; 2.2.3 Polypyrroles; 2.2.4 Polyfluorenes and Polycarbazoles; 2.3 Suzuki-Miyaura Coupling Polymerization with Pd Catalyst; 2.3.1 Polyfluorenes; 2.3.2 Polyphenylenes; 2.4 Conclusion; References; 3 Regioregular and Regiosymmetric Polythiophenes; 3.1 Introduction; 3.2 Synthesis of Polythiophene and Regioirregular Polythiophenes; 3.3 Head-to-Tail Coupled Regioregular Poly(3-Alkylthiophene)s; 3.3.1 Design and Synthesis of rrP3ATs; 3.3.1.1 McCullough Method; 3.3.1.2 Rieke Method; 3.3.1.3 GRIM Method; 3.3.1.4 Palladium-Catalyzed Polymerization Methods 3.3.2 Mechanism of the Nickel-Catalyzed Polymerization3.4 Side Chain Functionalized HT Regioregular Polythiophenes; 3.4.1 Heteroatom-Containing Groups; 3.4.2 Aromatic-Containing Group; 3.4.3 Chiral Groups; 3.4.4 γ-Functionalized Groups; 3.5 End Group Functionalized HT Regioregular Polythiophenes; 3.5.1 Postpolymerization End Group Functionalization; 3.5.2 In Situ End Group Functionalization; 3.6 Block Copolymers Derived from HT Regioregular Polythiophenes; 3.6.1 All-Conjugated Block Copolymers; 3.6.2 Conjugated-Non-Conjugated Block Copolymers; 3.7 Universal Use of the GRIM Method 3.8 Regiosymmetric Polythiophenes3.9 Summary; References; 4 Functional Hyperbranched Polymers Constructed from Acetylenic An-Type Building Blocks; 4.1 Introduction; 4.2 Hyperbranched Polymers Constructed from Acetylenic An-Type Building Blocks; 4.2.1 Hyperbranched Poly(Alkylenephenylene)s (hb-PAPs); 4.2.1.1 Synthesis; 4.2.1.2 Structures; 4.2.1.3 Properties; 4.2.2 Hyperbranched Poly(Arylenephenylene)s (hb-PArPs); 4.2.2.1 Synthesis; 4.2.2.2 Structures; 4.2.2.3 Properties; 4.2.3 Hyperbranched Poly(Aroylphenylene)s (hb-PAkPs) and Poly(Aroxycarbonylphenylene)s (hb-PAePs); 4.2.3.1 Synthesis 4.2.3.2 Structures |
| Record Nr. | UNINA-9910139004803321 |
| Weinheim : , : Wiley-VCH, , [2010] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Conjugated polymer synthesis : methods and reactions / / edited by Yoshiki Chujo
| Conjugated polymer synthesis : methods and reactions / / edited by Yoshiki Chujo |
| Edizione | [4th ed.] |
| Pubbl/distr/stampa | Weinheim : , : Wiley-VCH, , [2010] |
| Descrizione fisica | 1 online resource (331 p.) |
| Disciplina | 547.70457 |
| Altri autori (Persone) | ChujoY (Yoshiki) |
| Soggetto topico | Conjugated polymers |
| ISBN |
3-527-63266-2
3-527-63267-0 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Conjugated Polymer Synthesis: Methods and Reactions; Contents; Preface; List of Contributors; 1 Organometallic Polycondensation for Conjugated Polymers; 1.1 Basic Organometallic C-C Coupling; 1.2 Syntheses of π-Conjugated Polymers; 1.3 Optical Properties; 1.3.1 UV-Vis Data; 1.3.2 Photoluminescence; 1.3.3 Other Optical Properties; 1.4 Redox Behavior and Electrical Conductivity; 1.5 Linear Structure and Alignment on the Surface of Substrates; 1.6 Stacking in the Solid and Colloid; 1.7 Chemical Reactivity and Catalysis; 1.7.1 Metal Complexes and Modification of Nitrogen
1.8 Electronic and Optical Devices (ECD, Battery, EL, Diode, Transistor, Nonlinear Optical Device, etc.)1.8.1 Redox Functions; 1.8.2 Electronic and Optical Devices; 1.9 Conclusions; References; 2 Catalyst-Transfer Condensation Polymerization for Precision Synthesis of π-Conjugated Polymers; 2.1 Introduction; 2.2 Kumada-Tamao Coupling Polymerization with Ni Catalyst; 2.2.1 Polythiophene; 2.2.1.1 Discovery and Mechanism of Catalyst-Transfer Condensation Polymerization; 2.2.1.2 A Variety of Monomers; 2.2.1.3 Block Polythiophenes; 2.2.1.4 Block Copolymers of Polythiophene and Other Polymers 2.2.1.5 Graft Copolymers2.2.2 Polyphenylenes; 2.2.3 Polypyrroles; 2.2.4 Polyfluorenes and Polycarbazoles; 2.3 Suzuki-Miyaura Coupling Polymerization with Pd Catalyst; 2.3.1 Polyfluorenes; 2.3.2 Polyphenylenes; 2.4 Conclusion; References; 3 Regioregular and Regiosymmetric Polythiophenes; 3.1 Introduction; 3.2 Synthesis of Polythiophene and Regioirregular Polythiophenes; 3.3 Head-to-Tail Coupled Regioregular Poly(3-Alkylthiophene)s; 3.3.1 Design and Synthesis of rrP3ATs; 3.3.1.1 McCullough Method; 3.3.1.2 Rieke Method; 3.3.1.3 GRIM Method; 3.3.1.4 Palladium-Catalyzed Polymerization Methods 3.3.2 Mechanism of the Nickel-Catalyzed Polymerization3.4 Side Chain Functionalized HT Regioregular Polythiophenes; 3.4.1 Heteroatom-Containing Groups; 3.4.2 Aromatic-Containing Group; 3.4.3 Chiral Groups; 3.4.4 γ-Functionalized Groups; 3.5 End Group Functionalized HT Regioregular Polythiophenes; 3.5.1 Postpolymerization End Group Functionalization; 3.5.2 In Situ End Group Functionalization; 3.6 Block Copolymers Derived from HT Regioregular Polythiophenes; 3.6.1 All-Conjugated Block Copolymers; 3.6.2 Conjugated-Non-Conjugated Block Copolymers; 3.7 Universal Use of the GRIM Method 3.8 Regiosymmetric Polythiophenes3.9 Summary; References; 4 Functional Hyperbranched Polymers Constructed from Acetylenic An-Type Building Blocks; 4.1 Introduction; 4.2 Hyperbranched Polymers Constructed from Acetylenic An-Type Building Blocks; 4.2.1 Hyperbranched Poly(Alkylenephenylene)s (hb-PAPs); 4.2.1.1 Synthesis; 4.2.1.2 Structures; 4.2.1.3 Properties; 4.2.2 Hyperbranched Poly(Arylenephenylene)s (hb-PArPs); 4.2.2.1 Synthesis; 4.2.2.2 Structures; 4.2.2.3 Properties; 4.2.3 Hyperbranched Poly(Aroylphenylene)s (hb-PAkPs) and Poly(Aroxycarbonylphenylene)s (hb-PAePs); 4.2.3.1 Synthesis 4.2.3.2 Structures |
| Record Nr. | UNINA-9910830240103321 |
| Weinheim : , : Wiley-VCH, , [2010] | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Conjugated Polymer Synthesis and Materials Applications
| Conjugated Polymer Synthesis and Materials Applications |
| Autore | Chujo Y (Yoshiki) |
| Edizione | [1st ed.] |
| Pubbl/distr/stampa | Newark : , : John Wiley & Sons, Incorporated, , 2026 |
| Descrizione fisica | 1 online resource (401 pages) |
| Disciplina | 547.84 |
| Soggetto topico |
Conjugated polymers
Materials science |
| ISBN |
3-527-84945-9
3-527-84944-0 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cover -- Half Title Page -- Title Page -- Copyright -- Contents -- About the Editor -- Preface -- 1. Transition Metal-catalyzed Polycondensation -- 1.1 Introduction -- 1.2 Ni-catalyzed Polycondensation -- 1.3 Pd-catalyzed Polycondensation -- 1.4 Pd-catalyzed Polycondensation via C-H Bond Functionalization -- 1.5 Cu- and Fe-catalyzed Polycondensation -- 1.6 Other Transition Metal-catalyzed Polymerization -- 1.7 Summary -- References -- 2. Living Conjugated Polymers -- 2.1 Introduction -- 2.2 Metal p -Binding in CTP -- 2.3 Catalysts for CTP -- 2.4 Kumada-Corriu Catalyst-transfer Polymerization -- 2.5 Catalyst-transfer Polymerization with Organolithium Reagents -- 2.6 Negishi Catalyst-transfer Polymerization -- 2.7 Suzuki-Miyaura Catalyst-transfer Polymerization -- 2.8 Stille Catalyst-transfer Polymerization (Stille CTP -- 2.9 Buchwald-Hartwig Amination and Direct Arylation Polymerization ( C-H Activation) -- 2.10 Chain-growth Polymerization of Aromatics Without Metal Catalysts -- 2.11 Conclusion -- Acknowledgment -- Abbreviations -- Polymers -- Metal Catalysts -- Ligands -- Miscellaneous Reagents and Terms -- References -- 3. Optically Active Through-space Conjugated Polymers Based on Planar Chiral [2.2]Paracyclophane -- 3.1 Introduction -- 3.2 Through-space Conjugation of [2.2]Paracyclophane-based Conjugated Polymers -- 3.3 Optically Active Through-space Conjugated Polymers Based on Planar Chiral [2.2]Paracyclophane -- 3.4 Optically Active Through-space Conjugated Cyclic Oligomers Based on Planar Chiral [2.2]Paracyclophane -- 3.5 Conclusion -- References -- 4. Development of Solid-state Luminescent Conjugated Polymers Containing Boron Element-blocks and Their Applications -- 4.1 Introduction -- 4.2 Boron Ketoiminates -- 4.2.1 Transformation of the Conventional Luminescent Complex to AIE-active One.
4.2.2 Modulation of the Direction of Color Changes in Mechanochromic Luminescence Behaviors by the Substituent Effect -- 4.2.3 Requirement of Heat-insensitive Mechanochromic Luminescent Materials -- 4.2.4 Development of Heat-insensitive Mechanochromic Luminescent Materials -- 4.2.5 Development of AIE-active Conjugated Polymers -- 4.2.6 Enhancement of Solid-state Luminescent Properties -- 4.2.7 Development of the Thermochromic and Mechanochromic Luminescent Polymers -- 4.2.8 Enhancement of Environmental Sensitivity -- 4.2.9 Mechanochromic Luminescent Sensor for Marking a Tiny Spot -- 4.3 Rational Design for AIE-active Molecules Based on Excitation-driven Complexes -- 4.3.1 Idea of Excitation-driven Complexes and Logical Design from Scratch -- 4.3.2 Design for Planar AIE-active Molecules -- 4.3.3 Development of Solid-state Luminescent Polymers -- 4.3.4 Stimuli-responsive Materials Based on Regioregular Conjugated Polymer -- 4.3.5 Injection of Stimuli-responsiveness into Conjugated Polymer by Element Replacement -- 4.4 AIE-active Materials Possessing NIR Luminescent Properties -- 4.4.1 Transformation to NIR-luminescent Materials by Aza-substitution at "the Isolated LUMO -- 4.4.2 NIR-AIE Molecules and Polymers and Their Applications -- 4.5 Conclusion -- References -- 5. Arsenic-containing Conjugated Polymers -- 5.1 Introduction -- 5.2 Arsenic in Organic Compounds -- 5.3 As-C Bond Formation -- 5.3.1 Conventional Methodologies -- 5.3.2 In Situ Generation of Organoarsenic Electrophile from Arsenic Homocycles -- 5.3.3 In Situ Generation of Organoarsenic Nucleophile from Arsenic Homocycles -- 5.3.4 Preparation and Utilization of Tribromoarsine -- 5.4 Arsenic-containing p -conjugated Systems -- 5.4.1 Arsole Derivatives -- 5.4.2 Other Arsenic-containing p -conjugated Systems -- 5.5 Poly(vinylene-arsine)s -- 5.5.1 Synthesis of Poly(vinylene-arsine)s. 5.5.2 Properties of Poly(vinylene-arsine)s -- 5.5.3 Poly(vinylene-phosphine)s and Poly(vinylene-stibine)s -- 5.5.4 Cross-linked Poly(vinylene-arsine)s -- 5.6 Arsole Polymers -- 5.7 p -Conjugated Polymers with Other Arsenic Units -- 5.8 Conclusion -- References -- 6. Carborane-containing Conjugated Polymers and Their Applications for Optoelectronic Materials -- 6.1 Introduction -- 6.2 Advanced Functional Materials -- 6.2.1 Hydrogen Storage -- 6.2.2 Enhancement of Thermal Stability of Composites -- 6.3 Electronic Properties of Carborane-containing Conjugated Polymers -- 6.3.1 Electrochemical Polymerization -- 6.3.2 Electric Devices -- 6.3.3 Applications for OPV -- 6.4 Luminescent Materials -- 6.4.1 Luminescent Materials and Devices -- 6.4.2 Aggregation-induced Emission -- 6.5 Photochemistry of o-carboranes -- 6.5.1 Demands for Solid-state Luminescent Materials -- 6.5.2 Experimental Proofs for Emission Annihilation Through the Bond Elongation at the Carbon-Carbon Bond in o-carborane -- 6.5.3 CT Emission of Aryl-modified o-carboranes -- 6.5.4 Angular Dependency of Electron Acceptor Properties of the o-carborane Unit -- 6.5.5 Twisted intramolecular Charge Transfer in the Crystalline State -- 6.6 Applications for Solid-state Luminescent Materials -- 6.6.1 Development of Highly Efficient Solid-state Luminescent Materials -- 6.6.2 High Emission Efficiency of Bis-o-carborane-modified Aromatic Systems -- 6.6.3 Solid-state Luminescence of Nido-carborane -- 6.6.4 Enhancement to Luminescent Efficiencies by Thermal Rearrangement from Ortho- to Meta-carborane -- 6.7 Stimuli-responsive Luminochromic Materials -- 6.7.1 Multi-stimuli-responsiveness of Bis-o-carborane-modified Anthracene -- 6.7.2 Real-time Thermochromic Luminescent Properties of Bis-o-carboranemodified Benzodithiophenes. 6.7.3 Constant Luminescent Properties During Phase Changes and Luminochromic Behaviors -- 6.7.4 Aggregation-caused Luminochromic Properties in the Polymer Film for Constructing Film-type Sensors -- 6.7.5 Thermochromic Luminescence by the Regulation of Rotation of o-carborane -- 6.8 Conclusion -- References -- 7. Low-bandgap Conjugated Polymers -- 7.1 Introduction -- 7.2 Design Principles of LBG-CPs -- 7.2.1 D-A Interaction for Bandgap Reduction -- 7.2.2 Stabilized Quinoidal Resonance for Bandgap Reduction -- 7.3 Synthesis of LBG-CPs -- 7.3.1 Stille Coupling for Constructing LBG-CPs -- 7.3.1.1 Synthesis of LBG-CPs Based on Thieno[3,4-b]Thiadiazole (TT) and Its Derivatives -- 7.3.1.2 Synthesis of LBG-CPs Based on Benzothiadiazole (BT) and Its Derivatives -- 7.3.1.3 Synthesis of LBG-CPs Based on Benzobisthiadiazole (BTT) and Its Derivatives -- 7.3.1.4 Synthesis of LBG-CPs Based on Diketopyrrolopyrrole (DPP) and Its Derivatives -- 7.3.1.5 Synthesis of LBG-CPs Based on Isoindigo (IID) and Its Derivatives -- 7.3.1.6 Synthesis of LBG-CPs Based on Benzofurandione (BFDO) and Its Derivatives -- 7.3.1.7 Synthesis of LBG-CPs Based on 4,4'-difluoro-4-bora-3a,4a-diazas- indacene (BODIPY) and Its Derivatives -- 7.3.2 Other Polymerization Methods for Constructing LBG-CPs -- 7.3.2.1 Suzuki Coupling -- 7.3.2.2 Aldol Condensation -- 7.4 Application of LBG-CPs -- 7.4.1 Application in OPDs -- 7.4.2 Application in OTEs -- 7.4.3 Application in Bioimaging and PTT -- 7.5 Conclusions and Perspective -- Acknowledgments -- References -- 8. Polymers with Three-dimensional Conjugated Molecules -- 8.1 Introduction -- 8.2 Corannulene-containing Polymer -- 8.3 Supramolecular Polymers Based on Bowl-shaped p -conjugated Molecules -- 8.4 Helicene-based Polymers -- 8.5 Conclusion and Outlook -- Acknowledgment -- References -- 9. Conjugated Polymers for Energy Storage Devices. 9.1 Introduction -- 9.2 Conjugated Polymers as Binder Materials in LIBs -- 9.2.1 Graphite Anodes -- 9.2.2 Si Anodes -- 9.3 Conjugated Polymers as Anodic Active Materials -- 9.3.1 Organic Anodes -- 9.3.2 Hard Carbons -- 9.4 Polymerizable Conjugated Molecules as Electrolyte Additives -- 9.5 p -Conjugated Polymers as Electrocatalysts -- 9.6 Conclusion -- 9.6.1 Binders -- 9.6.2 Active Materials -- 9.6.3 Electrolyte Additives -- 9.6.4 Catalysts in Li-O2 Batteries -- References -- 10. Conjugated Polymers and Their Applications in Organic Field Transistors, Organic Electrochemical Transistors, and Organic Thermoelectrics -- 10.1 Introduction -- 10.1.1 What Makes the CP Semiconducting -- 10.1.2 What Are the Charge Carriers -- 10.1.3 Formation of Charge Carriers -- 10.1.4 Band Structure -- 10.1.5 Ion Transport -- 10.1.6 Morphology and Multilevel Microstructures -- 10.2 Polymers for Organic Field Effect Transistors -- 10.2.1 Introduction -- 10.2.2 Example p-type Polymers -- 10.2.2.1 Thiophene-based Polymers -- 10.2.2.2 Indacenodithiophene-based Polymers -- 10.2.2.3 Isoindigo-based Polymers -- 10.2.2.4 Cyclopentadithiophene-based Polymers -- 10.2.3 Example n-type Polymers -- 10.2.4 Example Ambipolar Polymers -- 10.2.4.1 Isoindigo-based Polymers -- 10.2.5 Key Approaches to Improve OFET Performance -- 10.2.5.1 Backbone Modifications -- 10.2.5.2 Side Chain Modifications -- 10.2.5.3 Device Architecture -- 10.2.6 Application and Future Outlook -- 10.3 Organic Electrochemical Transistors -- 10.3.1 Design Principle -- 10.3.2 Example Polymers -- 10.3.2.1 P-type -- 10.3.3 N-type -- 10.3.3.1 Imide-based -- 10.3.3.2 Isoindigo -- 10.3.3.3 Diketopyrrolopyrrole -- 10.3.3.4 Ladder Type -- 10.3.3.5 Acceptor-Acceptor -- 10.3.4 Summary Tables of Reviewed p- and n-type Materials -- 10.3.4.1 P-type Materials -- 10.3.4.2 N-type Materials -- 10.4 Organic Thermoelectrics. 10.4.1 Introduction. |
| Record Nr. | UNINA-9911048000103321 |
Chujo Y (Yoshiki)
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| Newark : , : John Wiley & Sons, Incorporated, , 2026 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Conjugated polymers for biological and biomedical applications / / edited by Bin Liu
| Conjugated polymers for biological and biomedical applications / / edited by Bin Liu |
| Pubbl/distr/stampa | Weinheim, [Germany] : , : WILEY-VCH Verlag GmbH & Co. KGaA, , 2018 |
| Descrizione fisica | 1 online resource (411 pages) : illustrations |
| Disciplina | 547.70457 |
| Soggetto topico | Conjugated polymers |
| Soggetto genere / forma | Electronic books. |
| ISBN |
3-527-34275-3
3-527-34278-8 3-527-34274-5 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | ger |
| Record Nr. | UNINA-9910270890303321 |
| Weinheim, [Germany] : , : WILEY-VCH Verlag GmbH & Co. KGaA, , 2018 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Conjugated polymers for biological and biomedical applications / / edited by Bin Liu
| Conjugated polymers for biological and biomedical applications / / edited by Bin Liu |
| Pubbl/distr/stampa | Weinheim, [Germany] : , : WILEY-VCH Verlag GmbH & Co. KGaA, , 2018 |
| Descrizione fisica | 1 online resource (411 pages) : illustrations |
| Disciplina | 547.70457 |
| Soggetto topico | Conjugated polymers |
| ISBN |
3-527-34275-3
3-527-34278-8 3-527-34274-5 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | ger |
| Record Nr. | UNINA-9910830234103321 |
| Weinheim, [Germany] : , : WILEY-VCH Verlag GmbH & Co. KGaA, , 2018 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Doping in conjugated polymers [[electronic resource] /] / Pradip Kar
| Doping in conjugated polymers [[electronic resource] /] / Pradip Kar |
| Autore | Kar Pradip |
| Pubbl/distr/stampa | Hoboken, New Jersey, : John Wiley and Sons, Inc., 2013 |
| Descrizione fisica | 1 online resource (176 p.) |
| Disciplina | 660/.2977 |
| Collana | Polymer Science and Plastics Engineering |
| Soggetto topico |
Conjugated polymers
Conducting polymers Semiconductor doping |
| ISBN |
1-118-81661-7
1-118-81663-3 1-118-81676-5 |
| Classificazione | TEC009010 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cover; Title page; Copyright Page; Contents; Acknowledgement; Preface; 1 Introduction to Doping in Conjugated Polymer; 1.1 Introduction; 1.2 Molecular Orbital Structure of Conjugated Polymer; 1.3 Possibility of Electronic Conduction in Conjugated Polymer; 1.4 Necessity of Doping in Conjugated Polymer; 1.5 Concept of Doping in Conjugated Polymer; 1.5.1 Concept of Secondary Doping in Doped Conjugated Polymer; 1.5.2 Concept of Co-doping in Conjugated Polymer; 1.6 Doping as Probable Solution; 2 Classification of Dopants for the Conjugated Polymer; 2.1 Introduction
2.2 Classification of Dopant According to Electron Transfer2.2.1 p-Type Dopant; 2.2.2 n-Type Dopant; 2.3 Classification of Dopant According to Chemical Nature; 2.3.1 Inorganic Dopant; 2.3.2 Organic Dopant; 2.3.3 Polymeric Dopant; 2.4 Classification of Dopant According to Doping Mechanism; 2.4.1 Ionic Dopant or Redox Dopant; 2.4.2 Non-redox Dopant or Neutral Dopant; 2.4.3 Self-dopant; 2.4.4 Induced Dopant; 3 Doping Techniques for the Conjugated Polymer; 3.1 Introduction; 3.2 Electrochemical Doping; 3.2.1 Electrochemical Doping during Polymerization 3.2.2 Electrochemical Doping after Polymerization3.3 Chemical Doping; 3.3.1 Gaseous Doping; 3.3.2 Solution Doping; 3.4 In-situ doping; 3.5 Radiation-Induced Doping or Photo Doping; 3.6 Charge Injection Doping; 4 Role of Dopant on the Conduction of Conjugated Polymer; 4.1 Introduction; 4.2 Charge Defects within Doped Conjugated Polymer; 4.2.1 Soliton; 4.2.2 Polaron; 4.2.3 Bipolaron; 4.3 Charge Transport within the Doped Conjugated Polymer; 4.3.1 Electronic Parameter Responsible for Charge Transport; 4.3.2 Charge Transport Mechanism; 4.4 Migration of Dopant Counter Ions 4.4.1 Electrical Potential Difference and Redox-Potential Gradient4.4.2 Dopant Concentration Gradient or Doping Level; 5 Influence of Properties of Conjugated Polymer on Doping; 5.1 Introduction; 5.2 Conducting Property; 5.3 Spectroscopic Property; 5.3.1 UV-VIS Spectroscopy (Optical Property); 5.3.2 FTIR Spectroscopy; 5.3.3 NMR Spectroscopy; 5.3.4 Other Spectroscopy; 5.4 Electrochemical Property; 5.4.1 Cyclic Voltammetry; 5.4.2 Electrochemical Impedance Spectroscopy; 5.5 Thermal Property; 5.6 Structural Property; 5.6.1 Crystal Structure; 5.6.2 Morphological Structure 6 Some Special Classes of Dopants for Conjugated Polymer6.1 Introduction; 6.2 Iodine and Other Halogens; 6.2.1 Principle; 6.2.2 Doping Technique; 6.2.3 Property; 6.3 Halide Doping; 6.3.1 Principle; 6.3.2 Doping Technique; 6.3.3 Property; 6.4 Protonic Acid Doping; 6.4.1 Principle; 6.4.2 Doping Technique; 6.4.3 Property; 6.5 Covalent Doping; 7 Influence of Dopant on the Applications of Conjugated Polymer; 7.1 Introduction; 7.2 Sensors; 7.2.1 Chemical Sensors; 7.2.2 Biosensors; 7.3 Actuators; 7.4 Field Effect Transistor; 7.5 Rechargeable Batteries; 7.6 Electrochromic Devices 7.7 Optoelectronic Devices |
| Record Nr. | UNINA-9910141808603321 |
|
Kar Pradip
|
||
| Hoboken, New Jersey, : John Wiley and Sons, Inc., 2013 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Doping in conjugated polymers / / Pradip Kar
| Doping in conjugated polymers / / Pradip Kar |
| Autore | Kar Pradip |
| Edizione | [1st ed.] |
| Pubbl/distr/stampa | Hoboken, New Jersey, : John Wiley and Sons, Inc., 2013 |
| Descrizione fisica | 1 online resource (176 p.) |
| Disciplina | 660/.2977 |
| Collana | Polymer Science and Plastics Engineering |
| Soggetto topico |
Conjugated polymers
Conducting polymers Semiconductor doping |
| ISBN |
9781118816615
1118816617 9781118816639 1118816633 9781118816769 1118816765 |
| Classificazione | TEC009010 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cover; Title page; Copyright Page; Contents; Acknowledgement; Preface; 1 Introduction to Doping in Conjugated Polymer; 1.1 Introduction; 1.2 Molecular Orbital Structure of Conjugated Polymer; 1.3 Possibility of Electronic Conduction in Conjugated Polymer; 1.4 Necessity of Doping in Conjugated Polymer; 1.5 Concept of Doping in Conjugated Polymer; 1.5.1 Concept of Secondary Doping in Doped Conjugated Polymer; 1.5.2 Concept of Co-doping in Conjugated Polymer; 1.6 Doping as Probable Solution; 2 Classification of Dopants for the Conjugated Polymer; 2.1 Introduction
2.2 Classification of Dopant According to Electron Transfer2.2.1 p-Type Dopant; 2.2.2 n-Type Dopant; 2.3 Classification of Dopant According to Chemical Nature; 2.3.1 Inorganic Dopant; 2.3.2 Organic Dopant; 2.3.3 Polymeric Dopant; 2.4 Classification of Dopant According to Doping Mechanism; 2.4.1 Ionic Dopant or Redox Dopant; 2.4.2 Non-redox Dopant or Neutral Dopant; 2.4.3 Self-dopant; 2.4.4 Induced Dopant; 3 Doping Techniques for the Conjugated Polymer; 3.1 Introduction; 3.2 Electrochemical Doping; 3.2.1 Electrochemical Doping during Polymerization 3.2.2 Electrochemical Doping after Polymerization3.3 Chemical Doping; 3.3.1 Gaseous Doping; 3.3.2 Solution Doping; 3.4 In-situ doping; 3.5 Radiation-Induced Doping or Photo Doping; 3.6 Charge Injection Doping; 4 Role of Dopant on the Conduction of Conjugated Polymer; 4.1 Introduction; 4.2 Charge Defects within Doped Conjugated Polymer; 4.2.1 Soliton; 4.2.2 Polaron; 4.2.3 Bipolaron; 4.3 Charge Transport within the Doped Conjugated Polymer; 4.3.1 Electronic Parameter Responsible for Charge Transport; 4.3.2 Charge Transport Mechanism; 4.4 Migration of Dopant Counter Ions 4.4.1 Electrical Potential Difference and Redox-Potential Gradient4.4.2 Dopant Concentration Gradient or Doping Level; 5 Influence of Properties of Conjugated Polymer on Doping; 5.1 Introduction; 5.2 Conducting Property; 5.3 Spectroscopic Property; 5.3.1 UV-VIS Spectroscopy (Optical Property); 5.3.2 FTIR Spectroscopy; 5.3.3 NMR Spectroscopy; 5.3.4 Other Spectroscopy; 5.4 Electrochemical Property; 5.4.1 Cyclic Voltammetry; 5.4.2 Electrochemical Impedance Spectroscopy; 5.5 Thermal Property; 5.6 Structural Property; 5.6.1 Crystal Structure; 5.6.2 Morphological Structure 6 Some Special Classes of Dopants for Conjugated Polymer6.1 Introduction; 6.2 Iodine and Other Halogens; 6.2.1 Principle; 6.2.2 Doping Technique; 6.2.3 Property; 6.3 Halide Doping; 6.3.1 Principle; 6.3.2 Doping Technique; 6.3.3 Property; 6.4 Protonic Acid Doping; 6.4.1 Principle; 6.4.2 Doping Technique; 6.4.3 Property; 6.5 Covalent Doping; 7 Influence of Dopant on the Applications of Conjugated Polymer; 7.1 Introduction; 7.2 Sensors; 7.2.1 Chemical Sensors; 7.2.2 Biosensors; 7.3 Actuators; 7.4 Field Effect Transistor; 7.5 Rechargeable Batteries; 7.6 Electrochromic Devices 7.7 Optoelectronic Devices |
| Record Nr. | UNINA-9910829087903321 |
|
Kar Pradip
|
||
| Hoboken, New Jersey, : John Wiley and Sons, Inc., 2013 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
