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Produktbild: Synthesis and Applications of Copolymers

Synthesis and Applications of Copolymers

Fr. 183.00

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Beschreibung

Produktdetails

Einband

Gebundene Ausgabe

Erscheinungsdatum

23.06.2014

Verlag

John Wiley & Sons

Seitenzahl

400

Maße (L/B/H)

23.6/16.3/2.8 cm

Gewicht

703 g

Auflage

1. Auflage

Sprache

Englisch

ISBN

978-1-118-05746-9

Beschreibung

Produktdetails

Einband

Gebundene Ausgabe

Erscheinungsdatum

23.06.2014

Verlag

John Wiley & Sons

Seitenzahl

400

Maße (L/B/H)

23.6/16.3/2.8 cm

Gewicht

703 g

Auflage

1. Auflage

Sprache

Englisch

ISBN

978-1-118-05746-9

Herstelleradresse

Libri GmbH
Europaallee 1
36244 Bad Hersfeld
DE

Email: gpsr@libri.de

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  • Produktbild: Synthesis and Applications of Copolymers
  • Preface xii

    Contributors xv

    SECTION I SYNTHESIS OF COPOLYMERS 1

    1 Trends in Synthetic Strategies for Making (CO)Polymers 3
    Anbanandam Parthiban

    1.1 Background and Introduction, 3

    1.2 Significance of Control Over Arrangement of Monomers in Copolymers, 5

    1.3 Chain-Growth Condensation Polymerization, 5

    1.3.1 Sequential Self-Repetitive Reaction (SSRR), 6

    1.3.2 Poly(phenylene Oxide)s by Chain-Growth Condensation Polymerization, 8

    1.3.3 Hydroxybenzoic Acids as AA' Type Monomer in Nucleophilic Aliphatic Substitution Polymerization, 8

    1.4 Sequence-Controlled Polymerization, 9

    1.4.1 Sequence-Controlled Copolymers of N-Substituted Maleimides, 10

    1.4.2 Alternating Copolymers by Ring-Opening Polymerization, 10

    1.4.3 Selective Radical Addition Assisted by a Template, 11

    1.4.4 Alternating AB-Type Sequence-Controlled Polymers, 11

    1.4.5 Metal-Templated ABA Sequence Polymerization, 11

    1.4.6 Sequence-Controlled Vinyl Copolymers, 12

    1.4.7 Sequence-Regulated Polymerization Induced by Dual-Functional Template, 13

    1.5 Processing of Thermoset Polymers: Dynamic Bond Forming Processes and Self-Healing Materials, 13

    1.5.1 Plasticity of Networked Polymers Induced by Light, 14

    1.5.2 Radically Exchangeable Covalent Bonds, 14

    1.5.3 Self-Repairing Polyurethane Networks, 15

    1.5.4 Temperature-Induced Self-Healing in Polymers, 15

    1.5.5 Diels-Alder Chemistry at Room Temperature, 15

    1.5.6 Trithiocarbonate-Centered Responsive Gels, 16

    1.5.7 Shuffling of Trithiocarbonate Units Induced by Light, 16

    1.5.8 Processable Organic Networks, 17

    1.6 Miscellaneous Developments, 17

    1.6.1 Atom Transfer Radical Polymerization (ATRP) Promoted by Unimolecular Ligand-Initiator Dual-Functional Systems (ULIS), 17

    1.6.2 Unsymmetrical Ion-Pair Comonomers and Polymers, 20

    1.6.3 Imidazole-Derived Zwitterionic Polymers, 21

    1.6.4 Post-Modification of Polymers Bearing Reactive Pendant Groups, 22

    1.7 Conclusion, 23

    References, 24

    2 Functional Polyolefins from the Coordination Copolymerization of Vinyl Monomers 29
    Fabio Di Lena and Jo?ao A. S. Bomfim

    2.1 Molecular Aspects of Olefin Coordination to Metals, 29

    2.2 Fundamentals of Homopolymerization of Alkenes, 30

    2.3 Copolymerization of Ethene and other Alkenes, 34

    2.4 Copolymerization of Alkenes and Carbon Monoxide, 35

    2.5 Copolymerization of Alkenes and Polar Vinyl Monomers, 37

    2.5.1 Migratory Insertion Polymerization, 37

    2.5.2 Polymerization via a Dual Radical/Migratory Insertion Pathway, 40

    2.5.3 Coordinative Group Transfer Polymerization, 41

    2.6 Copolymerization of Polar Vinyl Monomers and Carbon Monoxide, 41

    2.7 Why are Phosphine-Sulfonate Ligands so Special? 43

    2.8 Telechelic and End-Capped Macromolecules, 44

    2.9 On the Use of Chemoinformatics for a More Rapid Development of the Field, 44

    2.10 Conclusion and Outlook, 45

    References, 46

    3 General Aspects of Copolymerization 54
    Alex Van Herk

    3.1 Copolymerization in Chain Reactions, 54

    3.1.1 Derivation of the Copolymerization Equation, 55

    3.1.2 Types of Copolymers, 57

    3.1.3 Polymerization Rates in Copolymerizations, 59

    3.2 Measuring Copolymerization Parameters, 60

    3.3 Influence of Reaction Conditions, 63

    3.4 Short-Chain Effects in Copolymerization, 63

    3.5 Synthesis of Block Copolymers With Controlled Chain Architecture, 64

    References, 66

    4 Polymers Bearing Reactive, Pendant Cyclic Carbonate (CC) Group: Syntheses, Post-Polymerization Modifications, and Applications 67
    Satyasankar Jana

    4.1 Introduction, 67

    4.2 Cyclic Carbonate (CC) Monomers and Polymers, 68

    4.2.1 Cyclic Carbonate (CC) Monomers and Their Synthesis, 68

    4.2.2 Polymerization of Cyclic Carbonate (CC) Monomers, 75

    4.2.3 Alternative Route to Synthesize Pendant CC (Co)polymers by CO2 Addition/Fixation Reaction, 83

    4.3 Chemical Modification of Pendant CC Polymers, 85

    4.4 Applications of Pendant CC Polymers, 88

    4.4.1 Fixing CO2 into Polymer, 88

    4.4.2 Surface Coating, 90

    4.4.3 Solid or Gel Polymer Electrolyte for Lithium-Ion Batteries, 90

    4.4.4 Enzyme Immobilization, 91

    4.4.5 Photopolymerization, 91

    4.4.6 Polymer Blends, 92

    4.5 Conclusion, 92

    References, 93

    5 Monomers and Polymers Derived from Renewable or Partially Renewable Resources 101
    Anbanandam Parthiban

    5.1 Building Blocks from Renewable Resources, 101

    5.2 Polyesters Incorporated with Isosorbide, 105

    5.2.1 Poly(hydroxy ester)s Derived from Macrolides, 106

    5.2.2 Semicrystalline Polymers from Fatty Acids, 107

    5.2.3 Cyclic Ester Derived from a Natural Precursor, 107

    5.2.4 Polymerization of Dilactone Derived from 12-Hydroxy Stearic Acid, 107

    5.2.5 Thermoplastic Elastomers Derived from Polylactide and Polymenthide, 108

    5.3 Rosin and Developments Associated with Rosin, 110

    5.3.1 Polyamides and Polyesters Derived from Modified Levopimeric Acid, 110

    5.3.2 Radical Polymerization of Modified Dehydroabietic Acid, 112

    5.3.3 ATRP of Vinyl Monomers Derived from Dehydroabietic Acid, 112

    5.3.4 Block Copolymers Derived from Dehydroabietic Acid Derivative, 112

    5.4 Polyurethanes from Vegetable Oils, 113

    5.4.1 Polyurethanes Derived from Plant Oil Triglycerides, 114

    5.4.2 Long-Chain Unsaturated Diisocyanates Derived from Fatty Acids of Vegetable Origin, 114

    5.5 CO2 as Renewable Resource Comonomer, 115

    5.6 Renewable Triblock Copolymer-Based Pressure-Sensitive Adhesives (PSA), 115

    5.7 Photocurable Renewable Resource Polyester, 116

    5.8 Renewable Resource-Derived Waterborne Polyesters, 116

    5.8.1 Polyesters Made Up of Isosorbide and Succinic Acid, 117

    5.8.2 Polyesters Modified with Citric Acid, 117

    5.9 Polymers Formed by Combining Renewable Resource Monomers with that Derived from Petroleum Feedstock, 117

    5.10 Conclusion and Outlook, 120

    References, 121

    6 Microporous Organic Polymers: Synthesis, Types, and Applications 125
    Shujun Xu and Bien Tan

    6.1 Introduction, 125

    6.2 Preparations of MOPS, 126

    6.2.1 Polymers of Intrinsic Microporosity, 126

    6.2.2 Hypercrosslinked Polymer, 132

    6.2.3 Covalent Organic Frameworks, 134

    6.2.4 Conjugated Microporous Polymers, 138

    6.3 Hydrogen Adsorption, 141

    6.3.1 HCPs for Hydrogen Adsorption, 142

    6.3.2 PIMs for Hydrogen Adsorption, 144

    6.3.3 COFs for Hydrogen Adsorption, 145

    6.3.4 CMPs for Hydrogen Adsorption, 145

    6.4 Carbon Dioxide Capture, 145

    6.5 Separations, 149

    6.5.1 HCPs for Separations, 150

    6.5.2 PIMs for Separations, 153

    6.5.3 CMPs for Separations, 153

    6.6 Catalysis, 153

    6.7 Prospect, 155

    References, 156

    7 Dendritic Copolymers 165
    Srinivasa Rao Vinukonda

    7.1 Introduction, 165

    7.2 Synthesis Approaches or Strategies, 166

    7.2.1 AB2 + A2 Approach, 166

    7.2.2 AB2 + AB Approach, 167

    7.2.3 B3 + A2 + B2 Approach (Biocatalyst), 167

    7.2.4 Macromonomers Approach, 167

    7.2.5 Dendrigraft Approach, 171

    7.2.6 Linear-Dendritic Copolymers, 173

    7.2.7 Living Anionic Polymerization, 178

    7.2.8 Controlled Living Radical Polymerization, 185

    7.2.9 Click Chemistry, 194

    7.3 Properties of Dendritic Copolymers, 198

    7.3.1 Molecular Weight and Molecular Weight Distribution, 198

    7.3.2 Degree of Branching (DB), 200

    7.3.3 Intrinsic Viscosity, 202

    7.4 Applications of Dendritic Copolymers, 203

    References, 204

    SECTION II APPLICATIONS OF COPOLYMERS 215

    8 A New Class of Ion-Conductive Polymer Electrolytes: CO2/Epoxide Alternating Copolymers With Lithium Salts 217
    Yoichi Tominaga

    8.1 Introduction, 217

    8.2 Experimental, 220

    8.2.1 Preparation of Monomers and Catalyst, 220

    8.2.2 Copolymerization of Epoxides with CO2, 220

    8.2.3 Preparation of Electrolyte Membranes, 222

    8.2.4 Measurements, 222

    8.3 Results and Discussion, 222

    8.3.1 NMR Characterization, 222

    8.3.2 Characteristics of Polycarbonates, 224

    8.3.3 Thermal Analysis of Polycarbonates, 225

    8.3.4 Impedance Measurement of Copolymers, 228

    8.3.5 FT-IR Measurement, 231

    8.3.6 PEC System: Effect of Salt Concentration, 232

    8.4 Conclusion, 235

    References, 236

    9 Block Copolymer Nanopatterns as Enabling Platforms for Device Applications--Status, Issues, and Challenges 239
    Sivashankar Krishnamoorthy

    9.1 Introduction, 239

    9.2 Block Copolymer Templates for Pattern Transfer Applications, 240

    9.2.1 Dimensional Scalability and Fine-Tunability Down to Sub-10 nm Length Scales, 240

    9.2.2 Directing Self-Assembly of Block Copolymers, 241

    9.2.3 Block Copolymers for Directed Nanoscale Synthesis and Self-Assembly, 244

    9.2.4 High Resolution Nanolithography, 244

    9.2.5 Nanomanufacturing Material Patterns for Applications, 245

    9.2.6 Top-Down Patterning of Block Copolymer Nanostructures, 249

    9.3 Specific Instances in Exploitation of Block Copolymers in Device Applications, 251

    9.3.1 Memory Devices, 251

    9.3.2 Integrated Circuit Elements, 254

    9.3.3 Photovoltaic and Optoelectronics Applications, 255

    9.3.4 Sensors, 256

    9.3.5 Nanoporous Membranes for Size-Exclusive Filtration or Sensing, 261

    9.4 Conclusions, 263

    References, 263

    10 Stimuli-Responsive Copolymers and Their Applications 274
    He Tao

    10.1 Introduction, 274

    10.2 Temperature-Responsive Copolymers and Applications, 275

    10.2.1 Temperature-Responsive Copolymers Based on LCST, 276

    10.3 pH-Responsive Copolymers and Applications, 284

    10.3.1 pH-Responsive Segments, 285

    10.3.2 Polymer Nanoparticles/Micelles Prepared from pH-Responsive Copolymers, 287

    10.3.3 pH-Responsive Surfaces and Hydrogels, 287

    10.3.4 Typical Applications of pH-Responsive Copolymers, 289

    10.4 Biologically Responsive Copolymers and Applications, 290

    10.4.1 Glucose-Responsive Copolymers and Applications, 290

    10.5 Field-Responsive Copolymers and Applications, 293

    10.5.1 Electric-Responsive Copolymers, 294

    10.5.2 Magneto-Responsive Copolymers, 294

    10.5.3 Light-Responsive Copolymers, 295

    10.6 Conclusion, 297

    References, 297

    11 Pharmaceutical Polymers 307
    Natarajan Venkatesan and Hideki Ichikawa

    11.1 Introduction to Pharmaceutical Polymers, 307

    11.2 Applications of Pharmaceutical Polymers, 308

    11.2.1 Polymers as Excipients, 308

    11.2.2 Functional Excipients, 317

    11.2.3 Drug Delivery Agents, 320

    11.2.4 Solubility and Bioavailability Enhancement, 322

    11.2.5 Transdermal Drug Delivery, 324

    11.2.6 Novel Polymeric Hydrogels for Drug Delivery Applications, 324

    11.3 Summary, 329

    References, 329

    12 Polymer Conjugates of Proteins and Drugs to Improve Therapeutics 334
    Parijat Kanaujia and Ajazuddin

    12.1 Introduction, 334

    12.2 Polymers for Therapeutic Conjugation, 335

    12.2.1 Poly(ethylene Glycol) Protein Conjugate, 336

    12.2.2 Significance of PEG, 337

    12.2.3 Chemistry of Protein-PEG Conjugation, 338

    12.2.4 Biofate of PEGylated Proteins, 348

    12.3 PEGylated Proteins in Clinical Practice, 351

    12.3.1 PEG Conjugate with Low Molecular Weight Drugs, 351

    12.3.2 PEG Structures for Small-Molecule PEGylation, 351

    12.3.3 Advantages of PEGylated Drugs, 355

    12.4 N-(2-Hydroxypropyl) Methacrylamide (HPMA) Copolymer Conjugate, 358

    12.5 Poly(l-Glutamic Acid) Conjugates, 362

    12.6 Polysialic Acid (PSA) Conjugates, 363

    12.7 Conclusion, 364

    References, 365

    Index 373