LEADER 05343nam 2200673Ia 450 001 9911018819603321 005 20200520144314.0 010 $a9786612783821 010 $a9781282783829 010 $a1282783823 010 $a9783527629787 010 $a3527629785 010 $a9783527629794 010 $a3527629793 035 $a(CKB)2670000000047175 035 $a(EBL)584983 035 $a(OCoLC)644165891 035 $a(SSID)ssj0000415712 035 $a(PQKBManifestationID)11929416 035 $a(PQKBTitleCode)TC0000415712 035 $a(PQKBWorkID)10411186 035 $a(PQKB)10985685 035 $a(MiAaPQ)EBC584983 035 $a(Perlego)2757416 035 $a(EXLCZ)992670000000047175 100 $a20091218d2010 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 00$aDesign and synthesis of conjugated polymers /$fedited by Mario Leclerc, Jean-Francois Morin 210 $aWeinheim $cWiley-VCH$dc2010 215 $a1 online resource (381 p.) 300 $aDescription based upon print version of record. 311 08$a9783527324743 311 08$a3527324747 320 $aIncludes bibliographical references and index. 327 $aDesign and Synthesis of Conjugated Polymers; Contents; Preface; List of Contributors; 1 Synthesis and Functionality of Substituted Polyacetylenes; 1.1 Introduction; 1.2 Polymer Syntheses; 1.2.1 Catalysts; 1.2.2 Polymerization Behaviors; 1.2.3 Polymer Reactions; 1.3 Functional Properties; 1.3.1 Electrical Conductivity and Photoconductivity; 1.3.2 Liquid Crystallinity; 1.3.3 Luminescence; 1.3.4 Fluorescence Sensing; 1.3.5 Patterning and Imaging; 1.3.6 Chromism; 1.3.7 Optical Activity; 1.3.8 Supramolecular Assembly; 1.3.9 Optical Nonlinearity; 1.3.10 Biological Compatibility 327 $a1.4 Conclusions and ProspectsAcknowledgments; References; 2 Suzuki Polycondensation: A Powerful Tool for Polyarylene Synthesis; 2.1 Introduction; 2.2 General Remarks; 2.3 How to Do an SPC and Aspects of Characterization; 2.3.1 Monomer Purity, Stoichiometry, and Solvents; 2.3.2 Brief Note on Optimization; 2.3.3 Reduced Catalyst Amount and Product Purification; 2.3.4 Molar Mass Determination; 2.4 Methodological Developments; 2.4.1 Boronic Acid/Boronate Monomers; 2.4.2 Boron-Based Ate Complexes; 2.4.3 Halo and Related Monomers; 2.4.4 Catalysts; 2.4.5 Chain Growth SPC 327 $a2.4.6 Microwave and Technical Scale Microreactor Applications2.5 Selected Classes of Polyarylenes and Related Polymers; 2.5.1 Poly(para-phenylene)s; 2.5.2 Polyfluorenes; 2.5.3 Poly(para-meta-phenylene)s; 2.5.4 Shielded Polyarylenes; 2.5.5 Miscellaneous; 2.6 Conclusions and Outlook; Acknowledgments; References; 3 Advanced Functional Regioregular Polythiophenes; 3.1 Introduction; 3.2 Unsubstituted Polythiophene; 3.3 Poly(3-alkylthiophene)s; 3.4 Head-to-Tail Regioregular Poly(3-alkylthiophene)s (rrP3ATs); 3.4.1 Design and Synthesis of rrP3ATs; 3.4.1.1 McCullough Method; 3.4.1.2 Rieke Method 327 $a3.4.1.3 GRIM Method3.4.1.4 Other Methods; 3.4.2 Mechanism of the Nickel-Catalyzed Polymerization; 3.4.3 End Group Functionalization; 3.4.3.1 Postpolymerization End Group Functionalization; 3.4.3.2 In situ End Group Functionalization; 3.4.4 Fundamental Properties of rrP3ATs; 3.4.4.1 UV-vis Absorption; 3.4.4.2 Microstructure and Morphology in Thin Films; 3.4.4.3 Electrical Conductivity; 3.4.5 rrP3ATs in Electronic Devices; 3.4.5.1 rrP3ATs in PLEDs; 3.4.5.2 rrP3ATs in OFETs; 3.4.5.3 rrP3ATs in OPVs; 3.5 Regiosymmetric Poly(alkylthiophene)s 327 $a3.5.1 Head-to-Head-, Tail-to-Tail-Coupled Poly(alkylthiophene)s3.5.2 Regiosymmetric Alkylthiophene-Thiophene Copolymers; 3.6 Regiosymmetric Polythiophenes with (Hetero)aromatic Rings; 3.7 Polythiophene Block Copolymers; 3.7.1 All-Conjugated rrP3AT-Based Block Copolymers; 3.7.2 Conjugated-Nonconjugated rrP3AT-Based Block Copolymers; 3.8 Conclusion; References; 4 Poly(phenylenevinylenes); 4.1 Introduction; 4.2 Poly(p-phenylenevinylene)s via Polymerization Methods; 4.2.1 Gilch Approach; 4.2.2 The Wessling Method; 4.3 Poly(p-phenylenevinylene)s via Polycondensation 327 $a4.3.1 Wittig and Horner-Wadsworth-Emmons Reaction 330 $aThis first systematic compilation of synthesis methods for different classes of polymers describes well-tested and reproducible procedures, thus saving time, money and chemicals.Each chapter presents the latest method for a specific class of conjugated polymers with a particular emphasis on the design aspects for organo-electronic applications. In this concise and practically oriented manner, readers are introduced to the strategies of influencing and controlling the polymer properties with respect to their use in the desired device.This style of presentation quickly helps researchers 606 $aPolymers$xElectric properties 606 $aPolymers$vLaboratory manuals 615 0$aPolymers$xElectric properties. 615 0$aPolymers 676 $a620.19204297 701 $aLeclerc$b Mario$f1961-$01837309 701 $aMorin$b Jean-Franc ois$f1978-$01837310 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9911018819603321 996 $aDesign and synthesis of conjugated polymers$94416008 997 $aUNINA