Functional polymers by post-polymerization modification : concepts, guidelines, and applications
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Bibliographic Information
Functional polymers by post-polymerization modification : concepts, guidelines, and applications
Wiley-VCH, c2013
Available at 3 libraries
Note
Includes bibliographical references and index
Description and Table of Contents
Description
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.
Table of Contents
List of Abbreviations XIII List of Contributors XIX 1 History of Post-polymerization Modification 1 Kemal Arda Gunay, Patrick Th'eato, and Harm-Anton Klok 1.1 Introduction 1 1.2 Post-polymerization Modification via Thiol-ene Addition 3 1.3 Post-polymerization Modification of Epoxides, Anhydrides, Oxazolines, and Isocyanates 4 1.4 Post-polymerization Modification of Active Esters 13 1.5 Post-polymerization Modification via Thiol-Disulfide Exchange 19 1.6 Post-polymerization Modification via Diels-Alder Reactions 20 1.7 Post-polymerization Modification via Michael-Type Addition 22 1.8 Post-polymerization Modification via Azide Alkyne Cycloaddition Reactions 27 1.9 Post-polymerization Modification of Ketones and Aldehydes 32 1.10 Post-polymerization Modifications via Other Highly Efficient Reactions 35 1.11 Concluding Remarks 39 References 39 2 Post-polymerization Modifications via Active Esters 45 Ryohei Kakuchi and Patrick Theato 2.1 Introduction 45 2.2 Active Esters in the Side Group 46 2.2.1 Homopolymers 47 2.2.1.1 General 47 2.2.1.2 Stimuli-Responsive Polymers 48 2.2.1.3 Biologically Active Polymers 49 2.2.1.4 Thin Films 51 2.2.1.5 Polymeric Ligands for Nanoparticles 52 2.2.1.6 Miscellaneous Uses of Active Ester Polymers 53 2.2.2 Block Copolymers 53 2.2.2.1 General 53 2.2.2.2 Block Copolymers and Inorganic Moieties 53 2.2.2.3 Amphiphilic Block Copolymers 54 2.2.2.4 Stimuli-Responsive Block Copolymers 54 2.3 Star Polymers 55 2.4 Active Esters at the End Groups 55 2.5 Controlled Positioning of Active Ester Moieties 57 2.6 Summary 58 References 59 3 Thiol ene Based Functionalization of Polymers 65 Nikhil K. Singha and Helmut Schlaad 3.1 Introduction 65 3.2 General Considerations and Mechanisms 66 3.2.1 Radical Thiol ene Addition 66 3.2.2 Nucleophilic Thiol ene Addition 68 3.3 Functionalization of Polymers 69 3.3.1 Endfunctionalization 69 3.3.1.1 Polymer ene/Thiol 70 3.3.1.2 Polymer SH/Olefin 72 3.3.2 Polymer-Analog Reactions 75 3.3.2.1 Polyene/Thiol 75 3.3.2.2 Polythiol/Olefin 80 3.3.3 Bioconjugation 81 3.4 Summary 83 Acknowledgments 83 References 84 4 Thiol yne Chemistry in Polymer and Materials Science 87 Andrew B. Lowe and Justin W. Chan 4.1 Introduction 87 4.2 The Thiol yne Reaction in Small-Molecule Chemistry 88 4.3 The Thiol yne Reaction in Polymer and Material Synthesis 95 4.3.1 Network Polymers 96 4.3.2 Surface-Initiated Polymerizations and Modifications 98 4.3.3 Polymer Beads 103 4.3.4 Hyperbranched Polymers 104 4.3.5 Dendrimers and Dendritic Polymers 108 4.3.6 Main chain - and -Functional (co)Polymers 110 4.3.7 Nonradical Thiol yne Click Polymerization 114 4.3.8 Summary and Outlook 115 References 116 5 Design and Synthesis of Maleimide Group Containing Polymeric Materials via the Diels-lder/Retro Diels-Alder Strategy 119 Tugce Nihal Gevrek, Mehmet Arslan, and Amitav Sanyal 5.1 Introduction 119 5.2 Maleimide Functional Group Containing Polymeric Materials 120 5.3 The Diels-Alder/Retro Diels-Alder Cycloaddition-Cycloreversion Reactions 120 5.4 Application of Diels-Alder/Retro Diels-Alder Reaction to Synthesize Maleimide-Containing Polymers 122 5.4.1 Synthesis of Polymers Containing the Maleimide Group at the Chain Termini 122 5.4.2 Polymers Containing Maleimide Groups as Side Chains 141 5.4.3 Synthesis of Maleimide-Containing Hydrogels Obtained Using the Diels Alder/Retro Diels Alder Reaction-Based Strategy 147 5.5 Conclusions 150 References 150 6 The Synthesis of End-Functional Ring-Opening Metathesis Polymers 153 Andreas F. M. Kilbinger 6.1 Introduction 153 6.2 End-Functionalization Methods in General 156 6.3 Functionalization during Initiation 159 6.4 Functionalization after Propagation 160 6.4.1 Reaction with Carbonyl Groups 161 6.4.2 Reaction with Molecular Oxygen 162 6.4.3 Reaction with Functional Vinyl Ethers 162 6.4.4 Reaction with Functional Vinyl Esters 163 6.4.5 Reaction with Nondeactivating Olefins 165 6.5 Functionalization during Propagation 166 6.5.1 Using Chain-Transfer Agents 166 6.5.2 Sacrificial Synthesis 167 6.6 Conclusions and Outlook 168 Acknowledgments 168 References 169 7 Functional Polymers with Controlled Microstructure Based on Styrene and N-Substituted Maleimides 173 Delphine Chan-Seng, Mirela Zamfir, and Jean-Fran,cois Lutz 7.1 Introduction 173 7.2 Background on Radical Copolymerization of Styrene and Maleimides 174 7.2.1 Conventional Radical Polymerization 175 7.2.2 Controlled Radical Polymerization 177 7.3 Precise Incorporation of Maleimide Units on Polystyrene Backbone 179 7.3.1 Strategy 179 7.3.2 Maleimides 180 7.3.3 Styrene Derivatives 181 7.4 Tuning a Simple Technique for the Preparation of Sequence-Controlled Polymers to the Elaboration of Functionalized Well-Defined Macromolecules 182 7.4.1 Incorporation of Different Functionalities on the Same Polymer Backbone of a Well-Defined Polymer Possessing a Controlled Microstructure 183 7.4.2 Designing 1D Periodic Molecular Arrays 183 7.4.3 Elaboration of New Materials by Post-polymerization Modification 185 7.4.3.1 Activated Esters as Precursor of Post-polymerization Modification 186 7.4.3.2 Formation of Positionable Covalent Bridges 186 7.5 Summary and Outlook 189 References 189 8 Temperature-Triggered Functionalization of Polymers 193 Bongjin Moon 8.1 Introduction 193 8.2 Temperature-Triggered Alteration of Polymer Property 194 8.2.1 Thermolysis of t-Butyl Esters, Carbonates, and Carbamates 194 8.2.2 Thermolysis of Miscellaneous Esters, Carbonates, and Carbamates 197 8.2.3 Thermolysis of Acetals 199 8.3 Temperature-Triggered Generation of Reactive Groups 201 8.3.1 Thermolytic Generation of Anhydride Group in Polymers 201 8.3.2 Thermolytic Generation of Ketenes in Polymers 206 8.3.3 Thermolytic Generation of Transient Reactive Groups 211 8.4 Conclusions 213 References 215 9 New Functional Polymers Using Host Guest Chemistry 217 Ryosuke Sakai and Toyoji Kakuchi 9.1 Introduction 217 9.2 Polymers with Responsive Three-Dimensional Structures 218 9.2.1 Helicity Induction 218 9.2.2 Helix Inversion 220 9.3 Polymer Probes for Specific Chemical Sensing 222 9.3.1 Colorimetric Probes 222 9.3.2 Fluorescent Probes 226 9.4 Responsive Soft Materials 228 9.4.1 Responsive Smart Gels 228 9.4.2 Thermoresponsive Materials with Molecular Recognition Ability 230 9.5 Functional Polyrotaxanes 232 References 234 10 Glycopolymers via Post-polymerization Modification Techniques 237 James A. Burns, Matthew I. Gibson, and C. Remzi Becer 10.1 Introduction 237 10.2 Synthesis and Controlled Polymerization of Glycomonomers 238 10.3 Post-polymerization Modification of Polymer Scaffolds to Synthesize Glycopolymers 240 10.4 Azide Alkyne Click Reactions 243 10.5 Utilizing Thiol-Based Click Reactions 252 10.6 Thiol ene Click Reactions 253 10.7 Thiol yne Click Reactions 254 10.8 Thiol Halogen Substitution Reactions 255 10.9 Alkyne/Alkene Glycosides: Backward Click Reactions 258 10.10 Post-polymerization Glycosylation of Nonvinyl Backbone Polymers 259 10.11 Conclusions and Outlook 260 Acknowledgments 262 References 262 11 Design of Polyvalent Polymer Therapeutics 267 Jacob T. Martin and Ravi S. Kane 11.1 Introduction 267 11.2 Polyvalent Polymer Therapeutics 268 11.2.1 Polymer Micelles 269 11.2.2 Controlled-Molecular-Weight Linear Polymers 273 11.2.3 Controlled Ligand Spacing 276 11.2.4 Matching Valency to the Target 280 11.2.5 Biocompatible Polymer Scaffolds 284 11.2.6 Bioengineered Polymer Scaffolds 285 11.3 Conclusions 287 References 288 12 Posttranslational Modification of Proteins Incorporating Nonnatural Amino Acids 291 Haresh More, Ching-Yao Yang, and Jin Kim Montclare 12.1 Posttranslational Modification of Existing Amino Acids within Protein Chain 291 12.1.1 Phosphorylation 291 12.1.2 Acetylation 292 12.1.3 Methylation 292 12.1.4 Glycosylation 293 12.1.5 Hydroxylation 293 12.1.6 Sulfation 294 12.2 Exploiting Biosynthetic Machinery: Cotranslational Approach 294 12.2.1 Site-Specific Incorporation (SSI) 294 12.2.1.1 In vitro SSI 294 12.2.1.2 In vivo SSI 298 12.2.1.3 Applications 306 12.2.2 Residue-Specific Incorporation (RSI) 308 12.2.2.1 Endogenous AARS 310 12.2.2.2 Overexpression of Endogenous AARS 310 12.2.2.3 Shrinking the AARS Editing Pocket 311 12.2.2.4 Enlarging the AARS Binding Pocket 312 12.2.2.5 Applications 312 12.3 Intein-Inspired Ligation Approach 315 12.3.1 Native Chemical Ligation (NCL) 316 12.3.1.1 Sulfur-Based N-Terminal Residue 316 12.3.1.2 Selenocysteine-Based N-Terminal Residue 316 12.3.2 Expressed Protein Ligation (EPL) 318 12.4 Combined Approach 319 12.4.1 RSI and EPL 319 12.4.2 SSI and Intein-Mediated Ligation 319 12.5 Protein and Polymer Conjugates 320 12.5.1 PEGlyation of Proteins via NAA 321 12.6 Modulating the Physicochemical Properties of Protein Polymers via NAA Incorporation 322 12.7 Future in Combined Technologies to Fabricate Tailored Protein-Polymer Conjugates as New Materials 322 12.8 Conclusion and Future Perspectives 323 Acknowledgments 324 References 324 13 Functionalization of Porous Polymers from High-Internal-Phase Emulsions and Their Applications 333 Linda Kircher, Patrick Theato, and Neil R. Cameron 13.1 Introduction 333 13.1.1 Preparation Method of polyHIPEs 334 13.2 Functionalization of polyHIPEs 335 13.2.1 Functionalization of polyHIPEs Based on Copolymerization with Functional Comonomers 337 13.2.2 Functionalization of polyHIPEs by Post-polymerization Modification 342 13.2.3 Functionalization of polyHIPEs Based on Grafting Modification of Porous Materials 343 13.2.3.1 ATRP to Functionalize polyHIPEs 345 13.2.4 Click Chemistry for Functionalization of polyHIPEs 346 13.2.5 Thiol-ene-based polyHIPEs 347 13.2.6 Dicyclopentadiene polyHIPEs 347 13.3 Applications 347 13.3.1 Tissue Engineering 348 13.3.2 Support Materials 348 13.4 Conclusions 349 References 350 14 Post-polymerization Modification of Polymer Brushes 353 Sara Orski, Gareth Sheppard, Rachelle Arnold, Joe Grubbs, and Jason Locklin 14.1 Introduction 353 14.2 Synthesis and Strategies for Functional Polymer Brushes 357 14.2.1 Preparation of Active Ester Polymer Brushes by SI-ATRP 357 14.2.2 Synthesis of Poly(NHS4VB) Block Copolymer Brushes with 2-Hydroxyethyl Acrylate, tert-Butyl Acrylate, or Styrene 360 14.2.3 Functionalization of Poly(NHS4VB) Brushes with Primary Amines 360 14.2.4 Quantification of Active Ester Post-polymerization Modification 361 14.3 Applications of Polymer Brush Modification: Multifunctional Surfaces via Photopatterning 362 14.3.1 Polymer Brush Functionalization with Photoactivated Dibenzocyclooctyne for Catalyst-Free Azide Cycloaddition 362 14.3.2 Copper-Free Click of Dibenzocyclooctyne and Azido-FL/Azido-RB 365 14.4 Conclusions and Future Outlook 366 References 366 15 Covalent Layer-by-Layer Assembly Using Reactive Polymers 371 Adam H. Broderick and David M. Lynn 15.1 Introduction 371 15.2 Overview of Layer-by-Layer Assembly: Conventional versus Covalent Assembly 371 15.3 Scope and Organization 375 15.4 Covalent LbL Assembly Based on Click Chemistry 375 15.5 Reactive LbL Assembly Using Azlactone-Functionalized Polymers 387 15.6 Other Reactions and Other Approaches 396 15.7 Concluding Remarks 401 Acknowledgments 402 References 402 Index 407
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