LEADER 05615nam 2200709 a 450 001 9910819818103321 005 20240313151718.0 010 $a3-527-65542-5 010 $a1-299-31353-1 010 $a3-527-65545-X 010 $a3-527-65544-1 035 $a(CKB)2670000000337924 035 $a(EBL)1129780 035 $a(OCoLC)829460528 035 $a(SSID)ssj0000855342 035 $a(PQKBManifestationID)11477374 035 $a(PQKBTitleCode)TC0000855342 035 $a(PQKBWorkID)10912938 035 $a(PQKB)11333582 035 $a(OCoLC)828148153 035 $a(MiAaPQ)EBC1129780 035 $a(Au-PeEL)EBL1129780 035 $a(CaPaEBR)ebr10674770 035 $a(CaONFJC)MIL462603 035 $a(PPN)177046880 035 $a(EXLCZ)992670000000337924 100 $a20130419d2013 uy 0 101 0 $aeng 135 $aurcn||||||||| 181 $ctxt 182 $cc 183 $acr 200 00$aFunctional polymers by post-polymerization modification$b[electronic resource] $econcepts, guidelines, and applications /$fedited by Patrick Theato and Harm-Anton Klok 205 $a1st ed. 210 $aWeinheim an der Bergstrasse, Germany $cWiley-VCH Verlag GmbH$dc2013 215 $a1 online resource (438 p.) 300 $aDescription based upon print version of record. 311 $a3-527-33115-8 320 $aIncludes bibliographical references and index. 327 $aFunctional 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 327 $a1.8 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 327 $a2.2.2 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 327 $a3.3.1.2 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 327 $a4.3.7 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 327 $a5.4.2 Polymers Containing Maleimide Groups as Side Chains 330 $aFilling 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. 606 $aPolymer engineering 606 $aPolymers$xIndustrial applications 606 $aPolymerization 615 0$aPolymer engineering. 615 0$aPolymers$xIndustrial applications. 615 0$aPolymerization. 676 $a668.9 701 $aTheato$b Patrick$01684284 701 $aKlok$b Harm-Anton$01684285 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910819818103321 996 $aFunctional polymers by post-polymerization modification$94055698 997 $aUNINA