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Functionalized conjugated polyelectrolytes : design and biomedical applications / / Shu Wang, Fengting Lv
| Functionalized conjugated polyelectrolytes : design and biomedical applications / / Shu Wang, Fengting Lv |
| Autore | Wang Shu |
| Edizione | [1st ed. 2013.] |
| Pubbl/distr/stampa | Heidelberg [Germany] : , : Springer, , 2013 |
| Descrizione fisica | 1 online resource (viii, 87 pages) : illustrations (some color) |
| Disciplina |
541.2254
547 547/.70457 |
| Collana | SpringerBriefs in Molecular Science |
| Soggetto topico |
Polyelectrolytes
Conjugated polymers |
| ISBN | 3-642-40540-1 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto | Introduction -- Diagnostic Applications of Functionalized Conjugated Polyelectrolytes -- Fluorescence Imaging Applications of Functionalized Conjugated Polyelectrolytes -- Biomacromolecule Delivery System Based on Functionalized Conjugated Polyelectrolytes -- Drug Screening Applications of Functionalized Conjugated Polyelectrolytes -- Therapeutic Applications of Functionalized Conjugated Polyelectrolytes -- Concluding Remarks. |
| Record Nr. | UNINA-9910437807903321 |
Wang Shu
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| Heidelberg [Germany] : , : Springer, , 2013 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Fundamentals of conjugated polymer blends, copolymers and composites : synthesis, properties and applications / / edited by Parveen Saini
| Fundamentals of conjugated polymer blends, copolymers and composites : synthesis, properties and applications / / edited by Parveen Saini |
| Pubbl/distr/stampa | Salem, Massachusetts : , : Scrivener Publishing, , 2015 |
| Descrizione fisica | 1 online resource (802 p.) |
| Disciplina | 547/.70457 |
| Soggetto topico |
Conjugated polymers
Copolymers |
| ISBN |
1-119-13710-1
1-119-13716-0 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cover; Title Page; Copyright Page; Contents; Foreword; Preface; Part 1: Multiphase Systems: Synthesis, Properties and Applications; 1 Conjugated Polymer-based Blends, Copolymers, and Composites: Synthesis, Properties, and Applications; 1.1 Introduction; 1.2 CPs/ICPs-Based Blends; 1.2.1 Classification of CPs/ICPs-Based Blends; 1.3 CPs/ICPs-Based Copolymers (CCPs); 1.3.1 Types of CPs/ICPs-Based Copolymers; 1.3.2 Sub-Classification of Linear or Graft BCPs; 1.4 CPs/ICPs-Based Composites/Nanocomposites/Hybrids; 1.4.1 Categorization of CPs/ICPs-Based NCs
1.5 Interpenetrating/Semi-Interpenetrating Polymer Network (IPN/SIPN)1.6 Synthesis of CPs/ICPs-Based BLNs, CCPs, and CMPs/NCs/HYBs; 1.6.1 Synthesis of Undoped CPs-Based BLNs; 1.6.2 Synthesis of Conjugated Polymers-Based Copolymers; 1.6.3 CPs/ICPs-Based CMPs/NCs; 1.7 Applications of CPs/ICPs-Based BLNs, CCPs, and CMPs/NCS/HYBs; 1.7.1 ICP-Based Systems; 1.7.2 CPs-Based Systems; 1.8 Conclusions; Acknowledgments; References; 2 Progress in Polyaniline Composites with Transition Metal Oxides; 2.1 Introduction; 2.2 PANI/Transition Metal Oxide Composites 2.2.1 PANI Composites with Oxides of the Copper Group of Transition Metals 2.2.2 PANI Composites with Oxides of the Zinc Group of Transition Metals; 2.2.3 PANI Composites with Oxides of the Scandium Group of Transition Metals; 2.2.4 PANI Composites with Oxides of the Titanium Group of Transition Metals; 2.2.5 PANI Composites with Oxides of the Vanadium Group of Transition Metals; 2.2.6 PANI Composites with Oxides of the Chromium Group of Transition Metals; 2.2.7 PANI Composites with Oxides of the Manganese Group of Transition Metals 2.2.8 PANI Composites with Oxides of Iron, Cobalt, and Nickel Groups of Transition Metals 2.3 Conclusions and Outlook; Abbreviations; References; 3 Conjugated-Polymer/Quantum-Confined Nanomaterials- Based Hybrids for Optoelectronic Applications; 3.1 Introduction; 3.2 Quantum-Confined Nanomaterials (QCNs); 3.2.1 Inorganic Quantum-Confined Nanomaterials (QCNs); 3.2.2 Organic Quantum-Confined Nanomaterials (QCNs); 3.3 Synthetic Approaches for Quantum-Confined Nanomaterials (QCNs); 3.3.1 Synthesis of Inorganic Quantum-Confined Nanomaterials 3.3.2 Synthesis of Organic Quantum-Confined Nanomaterials 3.3.3 Optical Properties; 3.4 Conjugated-Polymer/Quantum-Confined Nanomaterials (CP/QCN) Hybrids; 3.4.1 Methodologies for Making Conjugated-Polymer/ Inorganic QCN Hybrids; 3.4.2 Chemical Methods; 3.5 Optoelectronic Applications of Hybrids; 3.5.1 Hybrid Solar Cell; 3.5.2 Light-Emitting Diodes; 3.5.3 GQDs/Conjugated-Polymer-Based Counter Electrode for Dye-Sensitized Solar Cells; 3.6 Outlook and Perspective: Current Challenges and FutureScope/Prospects; Acknowledgments; References 4 Graphene/Conjugated Polymer Nanocomposites for Optoelectronic and Biological Applications |
| Record Nr. | UNINA-9910140460703321 |
| Salem, Massachusetts : , : Scrivener Publishing, , 2015 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Fundamentals of conjugated polymer blends, copolymers and composites : synthesis, properties and applications / / edited by Parveen Saini
| Fundamentals of conjugated polymer blends, copolymers and composites : synthesis, properties and applications / / edited by Parveen Saini |
| Pubbl/distr/stampa | Salem, Massachusetts : , : Scrivener Publishing, , 2015 |
| Descrizione fisica | 1 online resource (802 p.) |
| Disciplina | 547/.70457 |
| Soggetto topico |
Conjugated polymers
Copolymers |
| ISBN |
1-119-13710-1
1-119-13716-0 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cover; Title Page; Copyright Page; Contents; Foreword; Preface; Part 1: Multiphase Systems: Synthesis, Properties and Applications; 1 Conjugated Polymer-based Blends, Copolymers, and Composites: Synthesis, Properties, and Applications; 1.1 Introduction; 1.2 CPs/ICPs-Based Blends; 1.2.1 Classification of CPs/ICPs-Based Blends; 1.3 CPs/ICPs-Based Copolymers (CCPs); 1.3.1 Types of CPs/ICPs-Based Copolymers; 1.3.2 Sub-Classification of Linear or Graft BCPs; 1.4 CPs/ICPs-Based Composites/Nanocomposites/Hybrids; 1.4.1 Categorization of CPs/ICPs-Based NCs
1.5 Interpenetrating/Semi-Interpenetrating Polymer Network (IPN/SIPN)1.6 Synthesis of CPs/ICPs-Based BLNs, CCPs, and CMPs/NCs/HYBs; 1.6.1 Synthesis of Undoped CPs-Based BLNs; 1.6.2 Synthesis of Conjugated Polymers-Based Copolymers; 1.6.3 CPs/ICPs-Based CMPs/NCs; 1.7 Applications of CPs/ICPs-Based BLNs, CCPs, and CMPs/NCS/HYBs; 1.7.1 ICP-Based Systems; 1.7.2 CPs-Based Systems; 1.8 Conclusions; Acknowledgments; References; 2 Progress in Polyaniline Composites with Transition Metal Oxides; 2.1 Introduction; 2.2 PANI/Transition Metal Oxide Composites 2.2.1 PANI Composites with Oxides of the Copper Group of Transition Metals 2.2.2 PANI Composites with Oxides of the Zinc Group of Transition Metals; 2.2.3 PANI Composites with Oxides of the Scandium Group of Transition Metals; 2.2.4 PANI Composites with Oxides of the Titanium Group of Transition Metals; 2.2.5 PANI Composites with Oxides of the Vanadium Group of Transition Metals; 2.2.6 PANI Composites with Oxides of the Chromium Group of Transition Metals; 2.2.7 PANI Composites with Oxides of the Manganese Group of Transition Metals 2.2.8 PANI Composites with Oxides of Iron, Cobalt, and Nickel Groups of Transition Metals 2.3 Conclusions and Outlook; Abbreviations; References; 3 Conjugated-Polymer/Quantum-Confined Nanomaterials- Based Hybrids for Optoelectronic Applications; 3.1 Introduction; 3.2 Quantum-Confined Nanomaterials (QCNs); 3.2.1 Inorganic Quantum-Confined Nanomaterials (QCNs); 3.2.2 Organic Quantum-Confined Nanomaterials (QCNs); 3.3 Synthetic Approaches for Quantum-Confined Nanomaterials (QCNs); 3.3.1 Synthesis of Inorganic Quantum-Confined Nanomaterials 3.3.2 Synthesis of Organic Quantum-Confined Nanomaterials 3.3.3 Optical Properties; 3.4 Conjugated-Polymer/Quantum-Confined Nanomaterials (CP/QCN) Hybrids; 3.4.1 Methodologies for Making Conjugated-Polymer/ Inorganic QCN Hybrids; 3.4.2 Chemical Methods; 3.5 Optoelectronic Applications of Hybrids; 3.5.1 Hybrid Solar Cell; 3.5.2 Light-Emitting Diodes; 3.5.3 GQDs/Conjugated-Polymer-Based Counter Electrode for Dye-Sensitized Solar Cells; 3.6 Outlook and Perspective: Current Challenges and FutureScope/Prospects; Acknowledgments; References 4 Graphene/Conjugated Polymer Nanocomposites for Optoelectronic and Biological Applications |
| Record Nr. | UNISA-996210750703316 |
| Salem, Massachusetts : , : Scrivener Publishing, , 2015 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. di Salerno | ||
| ||
Fundamentals of conjugated polymer blends, copolymers and composites : synthesis, properties and applications / / edited by Parveen Saini
| Fundamentals of conjugated polymer blends, copolymers and composites : synthesis, properties and applications / / edited by Parveen Saini |
| Pubbl/distr/stampa | Salem, Massachusetts : , : Scrivener Publishing, , 2015 |
| Descrizione fisica | 1 online resource (802 p.) |
| Disciplina | 547/.70457 |
| Soggetto topico |
Conjugated polymers
Copolymers |
| ISBN |
1-119-13710-1
1-119-13716-0 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cover; Title Page; Copyright Page; Contents; Foreword; Preface; Part 1: Multiphase Systems: Synthesis, Properties and Applications; 1 Conjugated Polymer-based Blends, Copolymers, and Composites: Synthesis, Properties, and Applications; 1.1 Introduction; 1.2 CPs/ICPs-Based Blends; 1.2.1 Classification of CPs/ICPs-Based Blends; 1.3 CPs/ICPs-Based Copolymers (CCPs); 1.3.1 Types of CPs/ICPs-Based Copolymers; 1.3.2 Sub-Classification of Linear or Graft BCPs; 1.4 CPs/ICPs-Based Composites/Nanocomposites/Hybrids; 1.4.1 Categorization of CPs/ICPs-Based NCs
1.5 Interpenetrating/Semi-Interpenetrating Polymer Network (IPN/SIPN)1.6 Synthesis of CPs/ICPs-Based BLNs, CCPs, and CMPs/NCs/HYBs; 1.6.1 Synthesis of Undoped CPs-Based BLNs; 1.6.2 Synthesis of Conjugated Polymers-Based Copolymers; 1.6.3 CPs/ICPs-Based CMPs/NCs; 1.7 Applications of CPs/ICPs-Based BLNs, CCPs, and CMPs/NCS/HYBs; 1.7.1 ICP-Based Systems; 1.7.2 CPs-Based Systems; 1.8 Conclusions; Acknowledgments; References; 2 Progress in Polyaniline Composites with Transition Metal Oxides; 2.1 Introduction; 2.2 PANI/Transition Metal Oxide Composites 2.2.1 PANI Composites with Oxides of the Copper Group of Transition Metals 2.2.2 PANI Composites with Oxides of the Zinc Group of Transition Metals; 2.2.3 PANI Composites with Oxides of the Scandium Group of Transition Metals; 2.2.4 PANI Composites with Oxides of the Titanium Group of Transition Metals; 2.2.5 PANI Composites with Oxides of the Vanadium Group of Transition Metals; 2.2.6 PANI Composites with Oxides of the Chromium Group of Transition Metals; 2.2.7 PANI Composites with Oxides of the Manganese Group of Transition Metals 2.2.8 PANI Composites with Oxides of Iron, Cobalt, and Nickel Groups of Transition Metals 2.3 Conclusions and Outlook; Abbreviations; References; 3 Conjugated-Polymer/Quantum-Confined Nanomaterials- Based Hybrids for Optoelectronic Applications; 3.1 Introduction; 3.2 Quantum-Confined Nanomaterials (QCNs); 3.2.1 Inorganic Quantum-Confined Nanomaterials (QCNs); 3.2.2 Organic Quantum-Confined Nanomaterials (QCNs); 3.3 Synthetic Approaches for Quantum-Confined Nanomaterials (QCNs); 3.3.1 Synthesis of Inorganic Quantum-Confined Nanomaterials 3.3.2 Synthesis of Organic Quantum-Confined Nanomaterials 3.3.3 Optical Properties; 3.4 Conjugated-Polymer/Quantum-Confined Nanomaterials (CP/QCN) Hybrids; 3.4.1 Methodologies for Making Conjugated-Polymer/ Inorganic QCN Hybrids; 3.4.2 Chemical Methods; 3.5 Optoelectronic Applications of Hybrids; 3.5.1 Hybrid Solar Cell; 3.5.2 Light-Emitting Diodes; 3.5.3 GQDs/Conjugated-Polymer-Based Counter Electrode for Dye-Sensitized Solar Cells; 3.6 Outlook and Perspective: Current Challenges and FutureScope/Prospects; Acknowledgments; References 4 Graphene/Conjugated Polymer Nanocomposites for Optoelectronic and Biological Applications |
| Record Nr. | UNINA-9910809459203321 |
| Salem, Massachusetts : , : Scrivener Publishing, , 2015 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Self-doped conductiong polymers [[electronic resource] /] / Michael S. Freund and Bhavana A. Deore
| Self-doped conductiong polymers [[electronic resource] /] / Michael S. Freund and Bhavana A. Deore |
| Autore | Freund Michael S |
| Pubbl/distr/stampa | Chichester, England ; ; Hoboken, NJ, : Wiley, c2007 |
| Descrizione fisica | 1 online resource (340 p.) |
| Disciplina |
547.7
547.70457 547/.70457 |
| Altri autori (Persone) | DeoreBhavana |
| Soggetto topico |
Conducting polymers
Doped semiconductors Polymerization Electric apparatus and appliances - Materials |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-282-34575-3
9786612345753 0-470-06172-3 0-470-06173-1 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Self-Doped Conducting Polymers; Contents; About the Authors; Preface; 1 Introduction; 1.1 Conducting Polymers; 1.1.1 History of Conjugated Conducting Polymers; 1.1.2 Concept of Doping in Intrinsically Conducting Polymers; 1.1.3 Conduction Mechanism; 1.1.4 Synthesis; 1.1.5 Processability; 1.2 Self-Doped Conducting Polymers; 1.3 Types of Self-Doped Polymers; 1.4 Doping Mechanism in Self-Doped Polymers; 1.4.1 p-Type Doping; 1.4.2 n-Type Doping; 1.4.3 Auto Doping; 1.5 Effect of Substituents on Properties of Polymers; 1.5.1 Solubility; 1.5.2 DC Conductivity; 1.5.3 Molecular Weight
1.5.4 Redox Properties1.5.5 Electronic and Spectroscopic Properties; 1.5.6 Mechanical and Thermal Properties; 1.6 Applications of Self-Doped Polymers; 1.6.1 Molecular Level Processing; 1.6.2 Transistors; 1.6.3 Biosensors; 1.6.4 e-Beam Lithography; 1.6.5 Electrochromic Devices; 1.6.6 Ion Exchangers; 1.6.7 Rechargeable Batteries; 1.6.8 Dip-Pen Nanolithography; References; 2 Self-Doped Derivatives of Polyaniline; 2.1 Introduction; 2.2 Chemical Synthesis of Sulfonic Acid Derivatives; 2.2.1 Post-Polymerization Modification; 2.2.2 Polymerization of Monomers 2.3 Electrochemical Synthesis of Sulfonic Acid Derivatives2.3.1 Aqueous Media; 2.3.2 Non-Aqueous Media; 2.4 Enzymatic Synthesis of Sulfonic Acid Derivatives; 2.5 Properties of Sulfonic Acid Derivatives; 2.5.1 Solubility; 2.5.2 Conductivity; 2.5.3 pH Dependent Redox Behavior; 2.5.4 Electronic and Spectroscopic Properties; 2.5.5 Molecular Weight; 2.5.6 Thermal Stability; 2.5.7 Morphology; 2.6 Synthesis and Characterization of Carboxylic Acid Derivatives; 2.6.1 Chemical Synthesis; 2.6.2 Electrochemical Synthesis; 2.7 Synthesis and Characterization of Phosphonic Acid Derivatives 2.8 Self-Doped Polyaniline NanostructuresReferences; 3 Boronic Acid Substituted Self-Doped Polyaniline; 3.1 Introduction; 3.2 Synthesis; 3.2.1 Electrochemical Synthesis; 3.2.2 Chemical Synthesis; 3.3 Properties of Self-Doped PABA; 3.3.1 pH Dependent Redox Behavior; 3.3.2 Spectroscopy; 3.3.3 Molecular Weight; 3.4 Self-Crosslinked Self-Doped Polyaniline; 3.4.1 Introduction; 3.4.2 Synthesis and Characterization; 3.4.3 Mechanical Properties; 3.4.4 11B NMR; 3.4.5 Thermal Properties; 3.4.6 Temperature Dependent Conductivity; 3.5 Applications; 3.5.1 Saccharide Sensor; 3.5.2 Nucleotide Sensors 3.5.3 Amine Sensors3.5.4 Molecular Level Processing for Controlled Release of RNA; References; 4 Self-Doped Polythiophenes; 4.1 Sulfonic Acid Derivatives; 4.1.1 Electrochemical Polymerization; 4.1.2 Chemical Polymerization; 4.1.3 Post Polymerization Modification; 4.2 Carboxylic Acid Derivatives; 4.3 Phosphonic Acid Derivatives; References; 5 Miscellaneous Self-Doped Polymers; 5.1 Self-Doped Polypyrrole; 5.1.1 Electrochemical Polymerization; 5.1.2 Chemical Polymerization; 5.1.3 Polycondensation; 5.2 Carboxylic Acid Derivatives; 5.3 Self-Doped Poly(3,6-(carbaz-9-yl)propanesulfonate) 5.4 Self-Doped Poly(p-phenylene)s |
| Record Nr. | UNINA-9910143588803321 |
|
Freund Michael S
|
||
| Chichester, England ; ; Hoboken, NJ, : Wiley, c2007 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Self-doped conductiong polymers [[electronic resource] /] / Michael S. Freund and Bhavana A. Deore
| Self-doped conductiong polymers [[electronic resource] /] / Michael S. Freund and Bhavana A. Deore |
| Autore | Freund Michael S |
| Pubbl/distr/stampa | Chichester, England ; ; Hoboken, NJ, : Wiley, c2007 |
| Descrizione fisica | 1 online resource (340 p.) |
| Disciplina |
547.7
547.70457 547/.70457 |
| Altri autori (Persone) | DeoreBhavana |
| Soggetto topico |
Conducting polymers
Doped semiconductors Polymerization Electric apparatus and appliances - Materials |
| ISBN |
1-282-34575-3
9786612345753 0-470-06172-3 0-470-06173-1 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Self-Doped Conducting Polymers; Contents; About the Authors; Preface; 1 Introduction; 1.1 Conducting Polymers; 1.1.1 History of Conjugated Conducting Polymers; 1.1.2 Concept of Doping in Intrinsically Conducting Polymers; 1.1.3 Conduction Mechanism; 1.1.4 Synthesis; 1.1.5 Processability; 1.2 Self-Doped Conducting Polymers; 1.3 Types of Self-Doped Polymers; 1.4 Doping Mechanism in Self-Doped Polymers; 1.4.1 p-Type Doping; 1.4.2 n-Type Doping; 1.4.3 Auto Doping; 1.5 Effect of Substituents on Properties of Polymers; 1.5.1 Solubility; 1.5.2 DC Conductivity; 1.5.3 Molecular Weight
1.5.4 Redox Properties1.5.5 Electronic and Spectroscopic Properties; 1.5.6 Mechanical and Thermal Properties; 1.6 Applications of Self-Doped Polymers; 1.6.1 Molecular Level Processing; 1.6.2 Transistors; 1.6.3 Biosensors; 1.6.4 e-Beam Lithography; 1.6.5 Electrochromic Devices; 1.6.6 Ion Exchangers; 1.6.7 Rechargeable Batteries; 1.6.8 Dip-Pen Nanolithography; References; 2 Self-Doped Derivatives of Polyaniline; 2.1 Introduction; 2.2 Chemical Synthesis of Sulfonic Acid Derivatives; 2.2.1 Post-Polymerization Modification; 2.2.2 Polymerization of Monomers 2.3 Electrochemical Synthesis of Sulfonic Acid Derivatives2.3.1 Aqueous Media; 2.3.2 Non-Aqueous Media; 2.4 Enzymatic Synthesis of Sulfonic Acid Derivatives; 2.5 Properties of Sulfonic Acid Derivatives; 2.5.1 Solubility; 2.5.2 Conductivity; 2.5.3 pH Dependent Redox Behavior; 2.5.4 Electronic and Spectroscopic Properties; 2.5.5 Molecular Weight; 2.5.6 Thermal Stability; 2.5.7 Morphology; 2.6 Synthesis and Characterization of Carboxylic Acid Derivatives; 2.6.1 Chemical Synthesis; 2.6.2 Electrochemical Synthesis; 2.7 Synthesis and Characterization of Phosphonic Acid Derivatives 2.8 Self-Doped Polyaniline NanostructuresReferences; 3 Boronic Acid Substituted Self-Doped Polyaniline; 3.1 Introduction; 3.2 Synthesis; 3.2.1 Electrochemical Synthesis; 3.2.2 Chemical Synthesis; 3.3 Properties of Self-Doped PABA; 3.3.1 pH Dependent Redox Behavior; 3.3.2 Spectroscopy; 3.3.3 Molecular Weight; 3.4 Self-Crosslinked Self-Doped Polyaniline; 3.4.1 Introduction; 3.4.2 Synthesis and Characterization; 3.4.3 Mechanical Properties; 3.4.4 11B NMR; 3.4.5 Thermal Properties; 3.4.6 Temperature Dependent Conductivity; 3.5 Applications; 3.5.1 Saccharide Sensor; 3.5.2 Nucleotide Sensors 3.5.3 Amine Sensors3.5.4 Molecular Level Processing for Controlled Release of RNA; References; 4 Self-Doped Polythiophenes; 4.1 Sulfonic Acid Derivatives; 4.1.1 Electrochemical Polymerization; 4.1.2 Chemical Polymerization; 4.1.3 Post Polymerization Modification; 4.2 Carboxylic Acid Derivatives; 4.3 Phosphonic Acid Derivatives; References; 5 Miscellaneous Self-Doped Polymers; 5.1 Self-Doped Polypyrrole; 5.1.1 Electrochemical Polymerization; 5.1.2 Chemical Polymerization; 5.1.3 Polycondensation; 5.2 Carboxylic Acid Derivatives; 5.3 Self-Doped Poly(3,6-(carbaz-9-yl)propanesulfonate) 5.4 Self-Doped Poly(p-phenylene)s |
| Record Nr. | UNINA-9910830619903321 |
|
Freund Michael S
|
||
| Chichester, England ; ; Hoboken, NJ, : Wiley, c2007 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Self-doped conductiong polymers / / Michael S. Freund and Bhavana A. Deore
| Self-doped conductiong polymers / / Michael S. Freund and Bhavana A. Deore |
| Autore | Freund Michael S |
| Pubbl/distr/stampa | Chichester, England ; ; Hoboken, NJ, : Wiley, c2007 |
| Descrizione fisica | 1 online resource (340 p.) |
| Disciplina |
547.7
547.70457 547/.70457 |
| Altri autori (Persone) | DeoreBhavana |
| Soggetto topico |
Conducting polymers
Doped semiconductors Polymerization Electric apparatus and appliances - Materials |
| ISBN |
1-282-34575-3
9786612345753 0-470-06172-3 0-470-06173-1 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Self-Doped Conducting Polymers; Contents; About the Authors; Preface; 1 Introduction; 1.1 Conducting Polymers; 1.1.1 History of Conjugated Conducting Polymers; 1.1.2 Concept of Doping in Intrinsically Conducting Polymers; 1.1.3 Conduction Mechanism; 1.1.4 Synthesis; 1.1.5 Processability; 1.2 Self-Doped Conducting Polymers; 1.3 Types of Self-Doped Polymers; 1.4 Doping Mechanism in Self-Doped Polymers; 1.4.1 p-Type Doping; 1.4.2 n-Type Doping; 1.4.3 Auto Doping; 1.5 Effect of Substituents on Properties of Polymers; 1.5.1 Solubility; 1.5.2 DC Conductivity; 1.5.3 Molecular Weight
1.5.4 Redox Properties1.5.5 Electronic and Spectroscopic Properties; 1.5.6 Mechanical and Thermal Properties; 1.6 Applications of Self-Doped Polymers; 1.6.1 Molecular Level Processing; 1.6.2 Transistors; 1.6.3 Biosensors; 1.6.4 e-Beam Lithography; 1.6.5 Electrochromic Devices; 1.6.6 Ion Exchangers; 1.6.7 Rechargeable Batteries; 1.6.8 Dip-Pen Nanolithography; References; 2 Self-Doped Derivatives of Polyaniline; 2.1 Introduction; 2.2 Chemical Synthesis of Sulfonic Acid Derivatives; 2.2.1 Post-Polymerization Modification; 2.2.2 Polymerization of Monomers 2.3 Electrochemical Synthesis of Sulfonic Acid Derivatives2.3.1 Aqueous Media; 2.3.2 Non-Aqueous Media; 2.4 Enzymatic Synthesis of Sulfonic Acid Derivatives; 2.5 Properties of Sulfonic Acid Derivatives; 2.5.1 Solubility; 2.5.2 Conductivity; 2.5.3 pH Dependent Redox Behavior; 2.5.4 Electronic and Spectroscopic Properties; 2.5.5 Molecular Weight; 2.5.6 Thermal Stability; 2.5.7 Morphology; 2.6 Synthesis and Characterization of Carboxylic Acid Derivatives; 2.6.1 Chemical Synthesis; 2.6.2 Electrochemical Synthesis; 2.7 Synthesis and Characterization of Phosphonic Acid Derivatives 2.8 Self-Doped Polyaniline NanostructuresReferences; 3 Boronic Acid Substituted Self-Doped Polyaniline; 3.1 Introduction; 3.2 Synthesis; 3.2.1 Electrochemical Synthesis; 3.2.2 Chemical Synthesis; 3.3 Properties of Self-Doped PABA; 3.3.1 pH Dependent Redox Behavior; 3.3.2 Spectroscopy; 3.3.3 Molecular Weight; 3.4 Self-Crosslinked Self-Doped Polyaniline; 3.4.1 Introduction; 3.4.2 Synthesis and Characterization; 3.4.3 Mechanical Properties; 3.4.4 11B NMR; 3.4.5 Thermal Properties; 3.4.6 Temperature Dependent Conductivity; 3.5 Applications; 3.5.1 Saccharide Sensor; 3.5.2 Nucleotide Sensors 3.5.3 Amine Sensors3.5.4 Molecular Level Processing for Controlled Release of RNA; References; 4 Self-Doped Polythiophenes; 4.1 Sulfonic Acid Derivatives; 4.1.1 Electrochemical Polymerization; 4.1.2 Chemical Polymerization; 4.1.3 Post Polymerization Modification; 4.2 Carboxylic Acid Derivatives; 4.3 Phosphonic Acid Derivatives; References; 5 Miscellaneous Self-Doped Polymers; 5.1 Self-Doped Polypyrrole; 5.1.1 Electrochemical Polymerization; 5.1.2 Chemical Polymerization; 5.1.3 Polycondensation; 5.2 Carboxylic Acid Derivatives; 5.3 Self-Doped Poly(3,6-(carbaz-9-yl)propanesulfonate) 5.4 Self-Doped Poly(p-phenylene)s |
| Record Nr. | UNINA-9910877442103321 |
|
Freund Michael S
|
||
| Chichester, England ; ; Hoboken, NJ, : Wiley, c2007 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||