http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-2.xsd
Functional polymers by post-polymerization modification
1 online resource (xx, 414 pages) : illustrations
"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. With its guidelines this is an indispensable reference for the daily lab work of polymer chemists in both academia and industry researching the field of polymer synthesis."--
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; 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
edited by Patrick Theato and Harm-Anton Klok.
Includes bibliographical references and index.