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Record Nr. |
UNINA9910819818103321 |
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Titolo |
Functional polymers by post-polymerization modification : concepts, guidelines, and applications / / edited by Patrick Theato and Harm-Anton Klok |
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Pubbl/distr/stampa |
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Weinheim an der Bergstrasse, Germany, : Wiley-VCH Verlag GmbH, c2013 |
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ISBN |
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3-527-65542-5 |
1-299-31353-1 |
3-527-65545-X |
3-527-65544-1 |
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Edizione |
[1st ed.] |
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Descrizione fisica |
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1 online resource (438 p.) |
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Altri autori (Persone) |
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TheatoPatrick |
KlokHarm-Anton |
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Disciplina |
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Soggetti |
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Polymer engineering |
Polymers - Industrial applications |
Polymerization |
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Lingua di pubblicazione |
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Formato |
Materiale a stampa |
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Livello bibliografico |
Monografia |
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Note generali |
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Description based upon print version of record. |
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Nota di bibliografia |
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Includes bibliographical references and index. |
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Nota di contenuto |
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Functional Polymers by Post-Polymerization Modification; Contents; List of Abbreviations; List of Contributors; 1 History of Post-polymerization Modification; 1.1 Introduction; 1.2 Post-polymerization Modification via Thiol-ene Addition; 1.3 Post-polymerization Modification of Epoxides, Anhydrides, Oxazolines, and Isocyanates; 1.4 Post-polymerization Modification of Active Esters; 1.5 Post-polymerization Modification via Thiol-Disulfide Exchange; 1.6 Post-polymerization Modification via Diels-Alder Reactions; 1.7 Post-polymerization Modification via Michael-Type Addition |
1.8 Post-polymerization Modification via Azide Alkyne Cycloaddition Reactions 1.9 Post-polymerization Modification of Ketones and Aldehydes; 1.10 Post-polymerization Modifications via Other Highly Efficient Reactions; 1.11 Concluding Remarks; References; 2 Post-polymerization Modifications via Active Esters; 2.1 Introduction; 2.2 Active Esters in the Side Group; 2.2.1 Homopolymers; 2.2.1.1 General; |
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2.2.1.2 Stimuli-Responsive Polymers; 2.2.1.3 Biologically Active Polymers; 2.2.1.4 Thin Films; 2.2.1.5 Polymeric Ligands for Nanoparticles; 2.2.1.6 Miscellaneous Uses of Active Ester Polymers |
2.2.2 Block Copolymers 2.2.2.1 General; 2.2.2.2 Block Copolymers and Inorganic Moieties; 2.2.2.3 Amphiphilic Block Copolymers; 2.2.2.4 Stimuli-Responsive Block Copolymers; 2.3 Star Polymers; 2.4 Active Esters at the End Groups; 2.5 Controlled Positioning of Active Ester Moieties; 2.6 Summary; References; 3 Thiol-ene Based Functionalization of Polymers; 3.1 Introduction; 3.2 General Considerations and Mechanisms; 3.2.1 Radical Thiol-ene Addition; 3.2.2 Nucleophilic Thiol-ene Addition; 3.3 Functionalization of Polymers; 3.3.1 Endfunctionalization; 3.3.1.1 Polymer-ene/Thiol |
3.3.1.2 Polymer-SH/Olefin 3.3.2 Polymer-Analog Reactions; 3.3.2.1 Polyene/Thiol; 3.3.2.2 Polythiol/Olefin; 3.3.3 Bioconjugation; 3.4 Summary; Acknowledgments; References; 4 Thiol-yne Chemistry in Polymer and Materials Science; 4.1 Introduction; 4.2 The Thiol-yne Reaction in Small-Molecule Chemistry; 4.3 The Thiol-yne Reaction in Polymer and Material Synthesis; 4.3.1 Network Polymers; 4.3.2 Surface-Initiated Polymerizations and Modifications; 4.3.3 Polymer Beads; 4.3.4 Hyperbranched Polymers; 4.3.5 Dendrimers and Dendritic Polymers; 4.3.6 Main chain a- and w-Functional (co)Polymers |
4.3.7 Nonradical Thiol-yne Click Polymerization 4.3.8 Summary and Outlook; References; 5 Design and Synthesis of Maleimide Group Containing Polymeric Materials via the Diels-Alder/Retro Diels-Alder Strategy; 5.1 Introduction; 5.2 Maleimide Functional Group Containing Polymeric Materials; 5.3 The Diels-Alder/Retro Diels-Alder Cycloaddition-Cycloreversion Reactions; 5.4 Application of Diels-Alder/Retro Diels-Alder Reaction to Synthesize Maleimide-Containing Polymers; 5.4.1 Synthesis of Polymers Containing the Maleimide Group at the Chain Termini |
5.4.2 Polymers Containing Maleimide Groups as Side Chains |
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Sommario/riassunto |
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Filling the gap for a book dealing with synthetic strategies and recent developments, this volume provides a comprehensive and up-to-date overview of the field of post-polymerization modification. As such, the international team of expert authors covers a wide range of topics, including new synthetic techniques utilizing different reactive groups for post-polymerization modifications of synthetic polymers, as well as modification of biomimetic and biological polymers. Furthermore, industrial applications of polymers that are synthesized by post-polymerization techniques are included. |
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