LEADER 00759nam0-22002891i-450- 001 990004227200403321 005 19990530 010 $a0-521-09201-9 035 $a000422720 035 $aFED01000422720 035 $a(Aleph)000422720FED01 035 $a000422720 100 $a19990530d1985----km-y0itay50------ba 101 0 $aeng 105 $ay-------001yy 200 1 $a<>Elements of drama$fby J. L. Styan 205 $aRepr. 210 $aCambridge$cCambridge University press$d1985 215 $a306 p.$d22 cm 700 1$aStyan,$bJohn L.$0158323 801 0$aIT$bUNINA$gRICA$2UNIMARC 901 $aBK 912 $a990004227200403321 952 $aP.3 BR.C.878$fFLFBC 959 $aFLFBC 996 $aElements of drama$9481859 997 $aUNINA LEADER 11636nam 2200505 450 001 9910830135803321 005 20230630001042.0 010 $a3-527-82380-8 010 $a3-527-82381-6 010 $a3-527-82379-4 035 $a(CKB)4100000011804613 035 $a(MiAaPQ)EBC6523018 035 $a(Au-PeEL)EBL6523018 035 $a(OCoLC)1178868123 035 $a(EXLCZ)994100000011804613 100 $a20211014d2021 uy 0 101 0 $aeng 135 $aurcnu|||||||| 181 $ctxt$2rdacontent 182 $cc$2rdamedia 183 $acr$2rdacarrier 200 00$aSulfur-containing polymers $efrom synthesis to functional materials /$fedited by Xing-Hong Zhang and Patrick Theato 210 1$aWeinheim, Germany :$cWiley-VCH,$d[2021] 210 4$dİ2021 215 $a1 online resource (xxv, 446 pages) $cillustrations 311 $a3-527-34670-8 327 $aCover -- Title Page -- Copyright -- Contents -- Introduction -- Chapter 1 Synthesis of Sulfur?Containing Polymers Through Multicomponent Polymerizations -- 1.1 Introduction -- 1.2 Multicomponent Polymerizations of Elemental Sulfur -- 1.2.1 Multicomponent Polymerization of Sulfur, Dialdehydes, and Diamines -- 1.2.2 Multicomponent Polymerization of Sulfur, Diynes, and Aliphatic Amines -- 1.2.3 Multicomponent Polymerization of Sulfur, Benzyl Diamines, and Aliphatic Diamines -- 1.2.4 Multicomponent Polymerization of Sulfur, Diarylacetic Acids, and Aliphatic/Aromatic Diamines -- 1.2.5 Multicomponent Polymerization of Sulfur, Diisocyanides, and Aliphatic Diamines -- 1.3 Cu(I)?Catalyzed Multicomponent Polymerizations of Sulfonyl Azides/Hydrazides -- 1.3.1 Multicomponent Polymerization of Sulfonyl Azides, Alkynes, and Amines/Alcohols -- 1.3.2 Multicomponent Polymerization of Sulfonyl Azides, Alkynes, and Other Monomers -- 1.3.3 Multicomponent Polymerization of Sulfonyl Hydrazide, Alkynes, and Diphenyl Dichalcogen -- 1.3.4 Topological Polymers Prepared from Sulfonyl Azides and Alkyne?Based MCPs -- 1.4 Multicomponent Polymerizations with Thiol?Related Monomers -- 1.4.1 One?Pot Multicomponent Tandem Polymerization of Alkyne, Carbonyl Chloride, and Thiol -- 1.4.2 Multicomponent Polymerizations with Cyclic Dithiocarbonate -- 1.4.3 Multicomponent Polymerizations with Cyclic Thiolactone -- 1.5 The Applications of Sulfur?Containing Polymers Prepared from MCP -- 1.5.1 Chemosensors -- 1.5.2 Metal Ion Removal/Enrichment -- 1.5.3 Cell Imaging -- 1.6 Conclusion -- Acknowledgments -- References -- Chapter 2 Carbon Disulfide Derived Polymers -- 2.1 Introduction -- 2.2 Synthesis of Thiiranes (Episulfides) -- 2.3 Copolymerization Reactions -- 2.3.1 Copolymerization of Carbon Disulfide and Episulfides -- 2.3.2 Copolymerization of Carbon Disulfide and Epoxides. 327 $a2.3.2.1 Scrambling Mechanism for Sulfur/Oxygen Atoms -- 2.3.2.2 NMR Scrambling Studies -- 2.3.2.3 Mixed Species Scrambling -- 2.4 Other Related CS2?Based Polymers -- 2.5 Concluding Remarks -- Acknowledgments -- References -- Chapter 3 Carbonyl Sulfide Derived Polymers -- 3.1 Introduction -- 3.1.1 Overview of COS -- 3.1.2 Preparation of COS -- 3.1.2.1 Direct Reaction of CO and Sulfur -- 3.1.2.2 Using Carbon Disulfide (CS2) -- 3.1.2.3 Laboratory Preparation of COS -- 3.1.3 Environmental and Safety Considerations -- 3.1.4 COS Chemistry -- 3.1.4.1 Dissociation -- 3.1.4.2 Hydrolysis -- 3.1.4.3 Oxidation -- 3.1.4.4 Reduction -- 3.1.4.5 Reaction with SO2 -- 3.1.4.6 Reaction with Ammonia and Amines -- 3.1.4.7 Miscellaneous Reactions -- 3.1.4.8 The Claus Reaction -- 3.2 Metal Catalysts for COS Copolymerization -- 3.2.1 Zinc?Cobalt(III) Double?Metal Cyanide Complex -- 3.2.2 Catalysts Centered with Chromium (Cr) -- 3.2.3 Catalyst Centered with Iron (Fe) and Cobalt (Co) -- 3.2.4 Alkoxy Metal Salts -- 3.3 Organocatalysts for COS Copolymerization -- 3.3.1 TEB?Organic Base Pair -- 3.3.2 Dual?Site Lewis Pair -- 3.3.3 Thiourea?Organic Base Pairs -- 3.3.4 Supramolecular Anion -- 3.4 Oxygen?Sulfur Exchange Reaction -- 3.5 Utilization of O/S ER for Poly(thioether)s -- 3.5.1 COS?Epoxides Route to Poly(thioether)s -- 3.5.2 CS2?Epoxides Route to Poly(thioether)s -- 3.5.3 Repurposing Poly(monothiocarbonate)s to Poly(thioether)s -- 3.6 Crystalline COS?Derived Polymers -- 3.7 COS?Derived Block Polymers -- 3.8 Properties of COS?Derived Polymers -- 3.8.1 Thermal Properties -- 3.8.2 Crystalline Properties -- 3.8.3 Optical Properties -- 3.8.4 Electronic Properties -- 3.9 Summary and Outlook -- References -- Chapter 4 Thiol?Based Click Polymerizations for Sulfur?Containing Polymers -- 4.1 Introduction -- 4.2 Thiol?Ene Click Polymerization. 327 $a4.2.1 Radical?Initiated Thiol?Ene Click Polymerization -- 4.2.2 Thiol?Ene Michael Addition Click Polymerization -- 4.3 Thiol?Yne Click Polymerization -- 4.3.1 Radical?Initiated Thiol?Yne Click Polymerization -- 4.3.2 Base?Mediated Thiol?Yne Click Polymerization -- 4.3.3 Metal?Catalyzed Thiol?Yne Click Polymerization -- 4.3.4 Spontaneous Thiol?Yne Click Polymerization -- 4.4 Other Thiol?Based Click Polymerizations -- 4.4.1 Thiol?Epoxy Click Polymerization -- 4.4.2 Thiol?Isocyanate Click Polymerization -- 4.4.3 Thiol?Halogen Click Polymerization -- 4.5 Conclusion -- Acknowledgments -- References -- Chapter 5 Synthesis of Polythioesters -- 5.1 Introduction -- 5.2 Synthesis of Aromatic Polythioesters -- 5.3 Synthesis of Semi?aromatic Polythioesters -- 5.4 Synthesis of Aliphatic Polythioesters -- 5.5 Summary and Concluding Remarks -- Acknowledgments -- References -- Chapter 6 Polymers with Sulfur?Nitrogen Bonds -- 6.1 Introduction -- 6.2 Synthesis of Sulfur?Nitrogen Containing Polymers -- 6.2.1 Poly(sulfenamide)s -- 6.2.2 Poly(diaminosulfide)s -- 6.2.3 Poly(aminodisulfide)s and Poly(diaminodisulfide)s -- 6.2.3.1 Poly(aminodisulfide)s -- 6.2.3.2 Poly(diaminodisulfide)s -- 6.2.4 Poly(oxothiazene)s -- 6.2.5 Poly(sulfonylimidate)s -- 6.2.6 Poly(sulfonylamidine)s -- 6.3 Applications of Polymers with Sulfur?Nitrogen Bond -- 6.3.1 Biomedical Applications -- 6.3.2 Metal?Ion Detection -- 6.3.3 Flame Retardant Chemicals Based on Polymers with Sulfur?Nitrogen Bonds -- 6.3.4 Energy Storage Applications -- 6.4 Conclusion and Outlook -- References -- Chapter 7 Thioester Functional Polymers -- 7.1 Introduction -- 7.2 Thioesters: Structural Features, Reactivities, and Reactions -- 7.3 Preparation of Thioester Containing Structures -- 7.3.1 Access to Thioester Containing Polymers: Thioesters in the Side Chain. 327 $a7.3.2 Access to Thioester Containing Polymers: Thioester in the Chain End -- 7.3.3 Access to Thioester Containing Polymers via Polymerization Process -- 7.3.4 Access to Thioester?Bearing Structures via Post?modification Approach -- 7.4 Post?Polymerization Modification of Thioesters -- 7.5 Conclusion and Outlook -- References -- Chapter 8 Thiophene?Based Polymers: Synthesis and Applications -- 8.1 Introduction -- 8.2 Development of Synthetic Methods -- 8.2.1 Oxidative Polymerization and Electrochemical Polymerization -- 8.2.2 Transmetalation Polymerization -- 8.2.2.1 Polymerization with Ni Catalysis -- 8.2.2.2 Polymerization with Pd Catalysis -- 8.2.2.3 Suzuki Coupling Method -- 8.2.2.4 Stille Coupling Method -- 8.2.2.5 Direct Arylation Method -- 8.2.3 Other Polymerization Methods -- 8.2.3.1 Photoinitiated Polymerization -- 8.2.3.2 Solid?State Polymerization -- 8.2.3.3 Acid?Catalyzed Polymerization -- 8.3 Applications of Polythiophene and Its Derivatives -- 8.3.1 Organic Thin?Film Transistors -- 8.3.2 Organic Photovoltaics -- 8.3.3 Organic Light?Emitting Diodes -- 8.3.4 Biological Applications -- 8.4 Conclusions and Future Scope -- References -- Chapter 9 High Refractive Index Sulfur?Containing Polymers (HRISPs) -- 9.1 Introduction -- 9.2 Basics of Optics -- 9.2.1 Absorption and Refraction -- 9.2.2 Refractive Index -- 9.2.2.1 Refractive Index Determination -- 9.2.3 Dispersion -- 9.2.4 Birefringence -- 9.3 High Refractive Index Polymers (HRIPs) -- 9.3.1 General Strategies and Applications -- 9.4 Sulfur?Containing HRIPs -- 9.4.1 Polyimides and Polyamides -- 9.4.2 Poly(meth)acrylates and Polythioacrylates -- 9.4.3 Polycarbonates and Polyesters -- 9.4.4 Thermosets -- 9.4.5 Inverse Vulcanization -- 9.5 Conclusion and Outlook -- References -- Chapter 10 Selenium?Containing Dynamic Polymers: From Synthesis to Functions -- 10.1 Introduction. 327 $a10.2 Synthesis of Selenium?Containing Polymers -- 10.2.1 Step Growth Polymerization -- 10.2.2 Radical Polymerization -- 10.2.3 Ring?Opening Polymerization -- 10.2.4 Synthesis of Dendrimer and Hyperbranched Selenium?Containing Polymer -- 10.3 Selenium?Containing Dynamic Covalent Chemistry -- 10.3.1 Diselenide Bond -- 10.3.2 Se S Bond -- 10.3.3 Se Te Bond -- 10.3.4 Se N Bond -- 10.4 Selenium?Containing Dynamic Materials -- 10.4.1 Selenium?Containing Elastomer -- 10.4.2 Selenium?Containing Surface/Interface Materials -- 10.4.3 Selenium?Containing Nanomaterials -- 10.5 Conclusion and Outlook -- Acknowledgments -- References -- Chapter 11 Poly(disulfide)s -- 11.1 Introduction -- 11.2 Synthesis of Poly(disulfide)s -- 11.2.1 Oxidative Polymerization of Dithiols -- 11.2.2 Ring?Opening Polymerization (ROP) of Cyclic Disulfide -- 11.2.3 Photo?Induced Disulfide Metathesis -- 11.2.4 Fragmentation Polymerization -- 11.2.5 Self?Organizing Surface?Initiated Polymerization (SOSIP) -- 11.2.6 Thiol?Disulfide Exchange Reaction -- 11.3 Amphiphilic PDS and Drug Delivery Application -- 11.4 Cell?Penetrating Poly(disulfide)s -- 11.5 Summary and Outlook -- References -- Chapter 12 Reduction?Responsive Disulfide?Containing Polymers for Biomedical Applications -- 12.1 Introduction -- 12.2 Disulfide?Containing Topological Polymers -- 12.2.1 Systems with the Disulfide Linkages -- 12.2.2 Disulfide?Containing Linear Polymers -- 12.2.2.1 Linear Polymers with Cleavable Backbones -- 12.2.2.2 Linear Polymers with Cleavable Side Chains -- 12.2.3 Disulfide?Containing Dendritic Polymers -- 12.2.3.1 Disulfide?Containing Hyperbranched Polymers -- 12.2.3.2 Disulfide?Containing Dendrimers -- 12.2.4 Disulfide?Containing Polypeptides and Proteins -- 12.2.5 Disulfide?Containing Polymeric Nanoparticles -- 12.2.5.1 Disulfide Linker for Amphiphilic Polymers. 327 $a12.2.5.2 Disulfide Linker for Nano?Assemblies. 330 $a"This book focuses on the state-of-the-art synthesis of various sulfur-containing polymers from low-cost sulfur resources such as elemental sulfur, carbon disulfide (CS2), carbonyl sulfide (COS) and mercaptan. In-depth mechanistic understanding related to the synthesis is presented in each chapter. Importantly, various types of sulfur-containing polymers, including poly(thioester)s, poly(thioether)s and poly(thiocarbonate)s and poly(thiourethane)s with linear or hyperbranched (dendrimer) architectures have also been included. The structure-property relationship and applications of sulfur-containing polymers are also presented. This book provides the latest developments of sulfur-containing polymers in a timely manner, which will be beneficial for both fundamental research and application-oriented development in this area"--$cProvided by publisher. 606 $aOrganosulfur compounds 615 0$aOrganosulfur compounds. 676 $a547.06 702 $aZhang$b Xinghong 702 $aTheato$b Patrick 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910830135803321 996 $aSulfur-containing polymers$94064929 997 $aUNINA