LEADER 05021nam 2200637 450 001 9910831100203321 005 20230422044852.0 010 $a1-282-01020-4 010 $a9786612010200 010 $a3-527-61171-1 010 $a3-527-61170-3 035 $a(CKB)1000000000377519 035 $a(EBL)481992 035 $a(OCoLC)311135073 035 $a(SSID)ssj0000167978 035 $a(PQKBManifestationID)11924611 035 $a(PQKBTitleCode)TC0000167978 035 $a(PQKBWorkID)10178920 035 $a(PQKB)10917201 035 $a(MiAaPQ)EBC481992 035 $a(EXLCZ)991000000000377519 100 $a20160816h19991999 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aHandbook of oligo- and polythiophenes /$fDenis Fichou 210 1$aWeinheim, [Germany] :$cWiley-VCH,$d1999. 210 4$d©1999 215 $a1 online resource (560 p.) 300 $aDescription based upon print version of record. 311 $a3-527-29445-7 320 $aIncludes bibliographical references at the end of each chapters and index. 327 $aHandbook of Oligo- and Polythiophenes; Contents; 1 The Chemistry of Conducting Polythiophenes: from Synthesis to Self-Assembly to Intelligent Materials; 1.1 Introduction; 1.2 Chemical Synthesis of Unsubstituted Polythiophene (PT); 1.3 Chemcial Synthesis of Polyalkylthiophenes (PATs); 1.3.1 Straight Alkyl Side Chains; 1.3.1.1 Chemical Synthesis of PATs; 1.3.1.1.1 Metal Catalyed Cross-coupling Polymerizations; 1.3.1.1.2 FeCl3 Method for the Polymerization of PATs; 1.3.1.2 Comparison of the Above Methods; 1.3.1.3 Regioregular PATs; 1.3.1.3.1 Regioregular HH-TT and TT-HH PATs 327 $a1.3.1.4 Regioregular, Head-to-Tail Coupled PATs1.3.1.4.1 The McCullough Method; 1.3.1.4.2 The Rieke Method; 1.3.1.4.3 The Mechanism and Catalyst Choice; 1.3.1.4.4 NMR Characterization of HT-PAT; 1.3.1.4.5 IR and UV-Vis; 1.3.1.4.6 Self-Assembly, X-ray, and Electrical Conductivity in HT-PATs; 1.3.1.4.7 Other Methods; 1.3.1.4.8 Random Copolymers of Alkyl Thiophenes; 1.3.1.4.9 Head-to-Tail Coupled, Random Copolymers of Alkyl Thiophenes; 1.3.1.5 Branched Alkyl PATs; 1.3.1.6 PTs with Phenyl Sidechains 327 $a1.4 Chemical Synthesis of Heteroatomic Functionalized Substituents on PTs: Recognition Sites for Self-Assembly and Chemical Sensing1.4.1 Chemical Synthesis of Alkoxy Polythiophenes; 1.4.2 Chemical Prepared Alkoxy PTs as Conducting Polymer Sensors; 1.4.3 Chiral Substituents on PT; 1.4.4 Carboxylic Acid Derivatives: Self-Assembly and Sensors; 1.4.5 Other Derivatives of PT; 1.5 Fused Rings Systems; 1.6 Conclusion; References; 2 Electronic Properties of Polythiophenes; 2.1 General Aspects of Conducting Polymers; 2.2 Structure and Conformation of Polythiophenes 327 $a2.2.1 Morphology and Crystal Structure2.2.2 Conformational Features; 2.3 Electronic Processes of Polythiophenes; 2.3.1 Charge Excitations in Polythiophenes; 2.3.2 Charge Transport in Polythiophenes; 2.3.3 Carrier Recombination: Photoluminescence and Electroluminescence; 2.3.4 Spectroscopic Studies of the Charged States; 2.3.4.1 Charge Storage Configurations in Solids and their Anisotropic Properties; 2.3.4.2 Properties in Solutions; 2.4 Concluding Remarks and Future Outlook; Acknowledgments; References; 3 The Synthesis of Oligothiphenes; 3.1 Introduction; 3.2 Synthesis of Oligothiophenes 327 $a3.2.1 Unsubstituted Oligothiphenes3.2.1.1 Arene/arene-Coupling Methods by Oxidative Couplings; 3.2.1.2 Transition Metal Catalyzed Coupling Methods; 3.2.1.3 Ring Closure Reactions from Acyclic Precursors; 3.2.1.4 Physical Properties of ?-Oligothiophenes and Isomers; 3.2.2 Substituted Oligothiophenes; 3.2.2.1 ß,ß-Substituted Oligothiophenes; 3.2.2.2 ?,?'-Substituted Oligothiophenes; 3.2.2.3 ?,?-Substituted Oligothiophenes; 3.2.2.4 Functionalized Oligothiophenes; 3.2.2.5 Amphiphilic Oligothiophenes; 3.2.2.6 Transition Metal Complexes of Oligothiophenes; 3.3 Conclusion; Acknowledgement 327 $aReferences 330 $aThis first concise handbook on this important new class of organic conducting materials gives a broad survey over this emerging field of research.The physical background is covered as well as the synthesis, electronic and nonlinear optical properties and applications of these advanced materials. This information will be of high value for graduate students, researchers and practitioners working in the interdisciplinary field of materials science, polymer and organic chemistry and applied physics. 606 $aThiophenes 606 $aPolythiophenes 615 0$aThiophenes. 615 0$aPolythiophenes. 676 $a547.594 676 $a547.7 700 $aFichou$b Denis$01638977 701 $aFichou$b Denis$01638977 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910831100203321 996 $aHandbook of oligo- and polythiophenes$93981687 997 $aUNINA