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Functionalization of graphene / / edited by Vasilios Georgakilas
| Functionalization of graphene / / edited by Vasilios Georgakilas |
| Pubbl/distr/stampa | Weinheim an der Bergstrasse, Germany : , : Wiley-VCH, , 2014 |
| Descrizione fisica | 1 online resource (426 p.) |
| Disciplina | 546.681 |
| Soggetto topico |
Graphene
Graphene - Industrial applications |
| ISBN |
3-527-67277-X
3-527-67279-6 3-527-67278-8 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | ger |
| Nota di contenuto |
Functionalization of Graphene; Contents; Preface; List of Contributors; Chapter 1 An Introduction to Graphene; 1.1 Brief History of Graphite; 1.2 Graphene and Graphene Oxide; 1.2.1 Preparation of Graphene from Graphene Oxide; 1.2.2 Isolation of Pristine Graphene Monolayers; 1.2.3 Large Scale Production of GO by Langmuir-Blodgett Methods; 1.2.4 Other Methods of Graphene Production; 1.3 Characterization of Graphene; 1.3.1 Microscopic Observation; 1.3.2 Raman Spectroscopy; 1.3.3 Thermogravimetric Analysis; 1.3.4 Optical Properties of Graphene; 1.3.5 X-Ray Diffraction Pattern; References
Chapter 2 Covalent Attachment of Organic Functional Groups on Pristine Graphene2.1 Introduction; 2.2 Cycloaddition Reactions; 2.2.1 1,3-Dipolar Cycloaddition of Azomethine Ylide; 2.2.1.1 Through a Substituted Aldehyde Pathway; 2.2.1.2 Through Substituted α Amino Acid Pathway; 2.2.2 Cycloaddition by Zwitterionic Intermediate; 2.2.3 Diels-Alder Cycloaddition; 2.2.4 Nitrene Addition; 2.2.5 Carbene Addition; 2.2.6 Aryne Addition; 2.3 Addition of Free Radicals; 2.3.1 Diazonium Salt Reaction; 2.3.2 Other Radical Additions; 2.4 Nucleophilic Addition; 2.5 Electrophilic Addition on Graphene 2.6 Organometallic Chemistry of Graphene2.7 Post Functionalization Reactions; 2.8 Conclusion; References; Chapter 3 Addition of Organic Groups through Reactions with Oxygen Species of Graphene Oxide; 3.1 Introduction; 3.1.1 Graphene/Polymer Nanocomposites; 3.2 The Role of Carboxylic Acids of GO; 3.2.1 Organic Functionalization through Amide Bond Formation; 3.2.1.1 Lipophilic Derivatives; 3.2.1.2 Hydrophilic - Biocompatible Derivatives; 3.2.1.3 Addition of Chromophores; 3.2.1.4 Polymer Graphene Composite; 3.2.2 Esterification of GO 3.2.3 Functionalization of GO through Heterocyclic Ring Formation3.3 The Role of Hydroxyl Groups of GO; 3.4 Miscellaneous Additions; 3.4.1 Reaction of Carboxylic Acid and Hydroxyl Groups with Isocyanate Derivatives; 3.4.2 Reaction of Epoxides with Carboxylic Acids or Hydroxyl Groups; 3.4.3 Interaction of Ammonia with Carboxylic Acids and Epoxides of GO; 3.4.4 Enrichment of GO in Carboxylic Acids; 3.4.5 Addition of Gallium-Phthalocyanine (Ga-Pc) to GO through Ga-O Covalent Bond; 3.5 The Role of Epoxide Groups of GO; 3.5.1 Nucleophilic Addition of Amine to Epoxides 3.5.2 Addition of Chromophores3.5.3 Addition of Polymers; 3.6 Post Functionalization of GO; 3.6.1 Post Functionalization of Organically Modified GO via Click Chemistry; 3.6.2 Counter Anion Exchange; 3.7 Conclusions; References; Chapter 4 Chemical Functionalization of Graphene for Biomedical Applications; 4.1 Introduction; 4.2 Covalent Functionalization of Graphene Nanomaterials; 4.2.1 Synthesis of GO and rGO; 4.2.1.1 Synthesis of Graphene Oxide; 4.2.1.2 Reduction of Graphene Oxide; 4.2.2 Functionalization of Graphene Oxide with Polymers; 4.2.2.1 PEGylated-GO Conjugates 4.2.2.2 Covalent Linkage of Biopolymers |
| Record Nr. | UNINA-9910132214103321 |
| Weinheim an der Bergstrasse, Germany : , : Wiley-VCH, , 2014 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Functionalization of graphene / / edited by Vasilios Georgakilas
| Functionalization of graphene / / edited by Vasilios Georgakilas |
| Pubbl/distr/stampa | Weinheim an der Bergstrasse, Germany : , : Wiley-VCH, , 2014 |
| Descrizione fisica | 1 online resource (426 p.) |
| Disciplina | 546.681 |
| Soggetto topico |
Graphene
Graphene - Industrial applications |
| ISBN |
3-527-67277-X
3-527-67279-6 3-527-67278-8 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | ger |
| Nota di contenuto |
Functionalization of Graphene; Contents; Preface; List of Contributors; Chapter 1 An Introduction to Graphene; 1.1 Brief History of Graphite; 1.2 Graphene and Graphene Oxide; 1.2.1 Preparation of Graphene from Graphene Oxide; 1.2.2 Isolation of Pristine Graphene Monolayers; 1.2.3 Large Scale Production of GO by Langmuir-Blodgett Methods; 1.2.4 Other Methods of Graphene Production; 1.3 Characterization of Graphene; 1.3.1 Microscopic Observation; 1.3.2 Raman Spectroscopy; 1.3.3 Thermogravimetric Analysis; 1.3.4 Optical Properties of Graphene; 1.3.5 X-Ray Diffraction Pattern; References
Chapter 2 Covalent Attachment of Organic Functional Groups on Pristine Graphene2.1 Introduction; 2.2 Cycloaddition Reactions; 2.2.1 1,3-Dipolar Cycloaddition of Azomethine Ylide; 2.2.1.1 Through a Substituted Aldehyde Pathway; 2.2.1.2 Through Substituted α Amino Acid Pathway; 2.2.2 Cycloaddition by Zwitterionic Intermediate; 2.2.3 Diels-Alder Cycloaddition; 2.2.4 Nitrene Addition; 2.2.5 Carbene Addition; 2.2.6 Aryne Addition; 2.3 Addition of Free Radicals; 2.3.1 Diazonium Salt Reaction; 2.3.2 Other Radical Additions; 2.4 Nucleophilic Addition; 2.5 Electrophilic Addition on Graphene 2.6 Organometallic Chemistry of Graphene2.7 Post Functionalization Reactions; 2.8 Conclusion; References; Chapter 3 Addition of Organic Groups through Reactions with Oxygen Species of Graphene Oxide; 3.1 Introduction; 3.1.1 Graphene/Polymer Nanocomposites; 3.2 The Role of Carboxylic Acids of GO; 3.2.1 Organic Functionalization through Amide Bond Formation; 3.2.1.1 Lipophilic Derivatives; 3.2.1.2 Hydrophilic - Biocompatible Derivatives; 3.2.1.3 Addition of Chromophores; 3.2.1.4 Polymer Graphene Composite; 3.2.2 Esterification of GO 3.2.3 Functionalization of GO through Heterocyclic Ring Formation3.3 The Role of Hydroxyl Groups of GO; 3.4 Miscellaneous Additions; 3.4.1 Reaction of Carboxylic Acid and Hydroxyl Groups with Isocyanate Derivatives; 3.4.2 Reaction of Epoxides with Carboxylic Acids or Hydroxyl Groups; 3.4.3 Interaction of Ammonia with Carboxylic Acids and Epoxides of GO; 3.4.4 Enrichment of GO in Carboxylic Acids; 3.4.5 Addition of Gallium-Phthalocyanine (Ga-Pc) to GO through Ga-O Covalent Bond; 3.5 The Role of Epoxide Groups of GO; 3.5.1 Nucleophilic Addition of Amine to Epoxides 3.5.2 Addition of Chromophores3.5.3 Addition of Polymers; 3.6 Post Functionalization of GO; 3.6.1 Post Functionalization of Organically Modified GO via Click Chemistry; 3.6.2 Counter Anion Exchange; 3.7 Conclusions; References; Chapter 4 Chemical Functionalization of Graphene for Biomedical Applications; 4.1 Introduction; 4.2 Covalent Functionalization of Graphene Nanomaterials; 4.2.1 Synthesis of GO and rGO; 4.2.1.1 Synthesis of Graphene Oxide; 4.2.1.2 Reduction of Graphene Oxide; 4.2.2 Functionalization of Graphene Oxide with Polymers; 4.2.2.1 PEGylated-GO Conjugates 4.2.2.2 Covalent Linkage of Biopolymers |
| Record Nr. | UNINA-9910818913603321 |
| Weinheim an der Bergstrasse, Germany : , : Wiley-VCH, , 2014 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||