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[null,"1.","Record Nr.",null,"UNINA9910139922203321"]
[null,null,"Autore",null,"Perepichka Igor F"]
[null,null,"Titolo",null,"Handbook of thiophene-based materials [[electronic resource] ] : applications in organic electronics and photonics / / Igor F. Perepichka, Dmitrii F. Perepichka"]
[null,null,"Pubbl/distr/stampa",null,"Hoboken, : Wiley, 2009"]
[null,null,"ISBN",null,"1-282-34950-3"]
[{"$nulls":4},"9786612349508"]
[{"$nulls":4},"0-470-74553-3"]
[{"$nulls":4},"0-470-74554-1"]
[null,null,"Descrizione fisica",null,"1 online resource (887 p.)"]
[null,null,"Disciplina",null,"661.8"]
[{"$nulls":4},"661/.8"]
[null,null,"Soggetti",null,"Thiophenes - Electric properties"]
[{"$nulls":4},"Conjugated polymers"]
[{"$nulls":4},"Organic compounds - Synthesis"]
[null,null,"Lingua di pubblicazione",null,"Inglese"]
[null,null,"Formato",null,"Materiale a stampa"]
[null,null,null,"Livello bibliografico","Monografia"]
[null,null,null,"Note generali","Description based upon print version of record."]
[{"$nulls":4},"Print version published in 2-volume set."]
[null,null,null,"Nota di bibliografia","Includes bibliographical references and index."]
[null,null,"Nota di contenuto",null,"Handbook of Thiophene-based Materials; Contents; Volume One: Synthesis and Theory; Volume Two: Properties and Applications; Foreword by Professor Fred Wudl; Preface; List of Contributors; 1 Functional oligothiophene-based materials: nanoarchitectures and applications; 1.1 Introduction; 1.2 Functionalized oligothiophenes; 1.2.1 Oligothiophenes containing surface-active groups; 1.2.2 Self-assembling hybrid oligothiophenes; 1.2.3 Oligothiophenes as pendant groups grafted to polymer backbones; 1.2.4 Oligothiophenes as liquid crystalline materials; 1.2.5 π-Dimeric model system"]
[{"$nulls":4},"1.2.6 Donor, acceptor and donor-acceptor (D-A) mixed systems1.2.7 Dye-functionalized oligothiophenes; 1.2.8 Oligothiophenes containing redox active groups; 1.2.9 Oligothiophenes containing recognition groups; 1.2.10 Biologically active oligothiophenes; 1.3 Fused thiophenes; 1.3.1 Benzothiophene analogues; 1.3.2 Heteroaromatic ring-fused oligothiophenes; 1.3.3 Thienothiophenes and higher homologues; 1.4 Macrocyclic thiophenes; 1.4.1 Macrocycles based only on thiophenes; 1.4.2 Mixed macrocycles based on thiophenes and other unsaturated units; 1.4.3 Thiophene-based porphyrinoid "]
[{"$nulls":4},"macrocycles"]
[{"$nulls":4},"1.5 Dendritic and hyperbranched oligothiophenes1.5.1 Star-shaped structures; 1.5.2 Tetrahedral oligothiophenes; 1.5.3 Functionalization of dendrimers with oligothiophenes at the periphery; 1.5.4 Oligothiophenes used as cores in dendrimers; 1.5.5 Functionalized all-thiophene dendrimers; 1.6 Conclusions and prospects; Acknowledgments; References; 2 Synthesis, characterization and properties of regioregular polythiophene-based materials; 2.1 Introduction; 2.1.1 Scope of the chapter; 2.1.2 Development of polythiophenes; 2.1.3 Nomenclature; 2.2 Consequences of regiochemistry"]
[{"$nulls":4},"2.3 Synthesis of regioregular polythiophenes2.3.1 Survey of regioregular syntheses; 2.3.2 Mechanism of nickel-mediated cross-coupling polymerization; 2.3.3 Polymer modification: chain and termini; 2.3.4 Polymer modification: substituent; 2.4 Purification and fractionation; 2.5 Molecular characterization; 2.5.1 NMR spectroscopy; 2.5.2 UV-Vis spectroscopy; 2.5.3 MALDI-TOF-MS; 2.5.4 Light scattering studies of aggregates; 2.6 Solid-state studies; 2.6.1 Solid-state NMR spectroscopy; 2.6.2 Solid-state UV-Vis spectroscopy; 2.6.3 Solid-state vibrational spectroscopy (IR, Raman)"]
[{"$nulls":4},"2.6.4 Solid-state X-ray studies2.6.5 Anisotropy; 2.6.6 Microscopy (AFM, STM); 2.6.7 Thermal analysis (DSC, TGA); 2.6.8 Charge carrier mobility; 2.7 Block copolymers containing regioregular polythiophenes; 2.8 Conclusions; References; 3 Fused oligothiophenes; 3.1 Introduction; 3.2 Synthesis and molecular properties of fused oligothiophenes; 3.2.1 Thienothiophenes; 3.2.2 Dithienothiophenes; 3.2.3 Linked bithiophenes; 3.2.4 Higher fused and linear oligothiophenes; 3.2.5 Cyclic and helical fused oligothiophenes; 3.3 Conclusion; References"]
[{"$nulls":4},"4 Thiophene-S,S-dioxides as a class of electron-deficient materials for electronics and photonics"]
[null,null,null,"Sommario/riassunto","This essential resource consists of a series of critical reviews written by leading scientists, summarising the progress in the field of conjugated thiophene materials. It is an application-oriented book, giving a chemists' point of view on the state-of-art and perspectives of the field. While presenting a comprehensive coverage of thiophene-based materials and related applications, the aim is to show how the rational molecular design of materials can bring a new breadth to known device applications or even aid the development of novel application concepts. The main topics covered include synthetic methodologies to thiophene-based materials (including the chemistry of thiophene, preparation of oligomers and polymerisation approaches) and the structure and physical properties of oligo- and polythiophenes (discussion of structural effects on electronic and optical properties). Part of the book is devoted to the optical and semiconducting properties of conjugated thiophene materials for electronics and photonics, and the role of thiophene-based materials in nanotechnology."]