The Resource Conjugated polymer synthesis : methods and reactions, edited by Yoshiki Chujo

Conjugated polymer synthesis : methods and reactions, edited by Yoshiki Chujo

Label
Conjugated polymer synthesis : methods and reactions
Title
Conjugated polymer synthesis
Title remainder
methods and reactions
Statement of responsibility
edited by Yoshiki Chujo
Contributor
Subject
Genre
Language
  • eng
  • eng
Summary
Edited and authored by top international experts, this first book on conjugated polymers with a focus on synthesis provides a detailed overview of all modern synthetic methods for these highly interesting compounds
Cataloging source
MiAaPQ
Dewey number
547.70457
Illustrations
illustrations
Index
index present
Language note
English
LC call number
QD382.C66
LC item number
C69 2010
Literary form
non fiction
Nature of contents
  • dictionaries
  • bibliography
http://library.link/vocab/relatedWorkOrContributorName
Chujo, Y.
http://library.link/vocab/subjectName
Conjugated polymers
Label
Conjugated polymer synthesis : methods and reactions, edited by Yoshiki Chujo
Instantiates
Publication
Copyright
Note
Description based upon print version of record
Bibliography note
Includes bibliographical references and index
Carrier category
online resource
Carrier category code
  • cr
Content category
text
Content type code
  • txt
Contents
  • Conjugated Polymer Synthesis: Methods and Reactions; Contents; Preface; List of Contributors; 1 Organometallic Polycondensation for Conjugated Polymers; 1.1 Basic Organometallic C-C Coupling; 1.2 Syntheses of π-Conjugated Polymers; 1.3 Optical Properties; 1.3.1 UV-Vis Data; 1.3.2 Photoluminescence; 1.3.3 Other Optical Properties; 1.4 Redox Behavior and Electrical Conductivity; 1.5 Linear Structure and Alignment on the Surface of Substrates; 1.6 Stacking in the Solid and Colloid; 1.7 Chemical Reactivity and Catalysis; 1.7.1 Metal Complexes and Modification of Nitrogen
  • 1.8 Electronic and Optical Devices (ECD, Battery, EL, Diode, Transistor, Nonlinear Optical Device, etc.)1.8.1 Redox Functions; 1.8.2 Electronic and Optical Devices; 1.9 Conclusions; References; 2 Catalyst-Transfer Condensation Polymerization for Precision Synthesis of π-Conjugated Polymers; 2.1 Introduction; 2.2 Kumada-Tamao Coupling Polymerization with Ni Catalyst; 2.2.1 Polythiophene; 2.2.1.1 Discovery and Mechanism of Catalyst-Transfer Condensation Polymerization; 2.2.1.2 A Variety of Monomers; 2.2.1.3 Block Polythiophenes; 2.2.1.4 Block Copolymers of Polythiophene and Other Polymers
  • 2.2.1.5 Graft Copolymers2.2.2 Polyphenylenes; 2.2.3 Polypyrroles; 2.2.4 Polyfluorenes and Polycarbazoles; 2.3 Suzuki-Miyaura Coupling Polymerization with Pd Catalyst; 2.3.1 Polyfluorenes; 2.3.2 Polyphenylenes; 2.4 Conclusion; References; 3 Regioregular and Regiosymmetric Polythiophenes; 3.1 Introduction; 3.2 Synthesis of Polythiophene and Regioirregular Polythiophenes; 3.3 Head-to-Tail Coupled Regioregular Poly(3-Alkylthiophene)s; 3.3.1 Design and Synthesis of rrP3ATs; 3.3.1.1 McCullough Method; 3.3.1.2 Rieke Method; 3.3.1.3 GRIM Method; 3.3.1.4 Palladium-Catalyzed Polymerization Methods
  • 3.3.2 Mechanism of the Nickel-Catalyzed Polymerization3.4 Side Chain Functionalized HT Regioregular Polythiophenes; 3.4.1 Heteroatom-Containing Groups; 3.4.2 Aromatic-Containing Group; 3.4.3 Chiral Groups; 3.4.4 γ-Functionalized Groups; 3.5 End Group Functionalized HT Regioregular Polythiophenes; 3.5.1 Postpolymerization End Group Functionalization; 3.5.2 In Situ End Group Functionalization; 3.6 Block Copolymers Derived from HT Regioregular Polythiophenes; 3.6.1 All-Conjugated Block Copolymers; 3.6.2 Conjugated-Non-Conjugated Block Copolymers; 3.7 Universal Use of the GRIM Method
  • 3.8 Regiosymmetric Polythiophenes3.9 Summary; References; 4 Functional Hyperbranched Polymers Constructed from Acetylenic An-Type Building Blocks; 4.1 Introduction; 4.2 Hyperbranched Polymers Constructed from Acetylenic An-Type Building Blocks; 4.2.1 Hyperbranched Poly(Alkylenephenylene)s (hb-PAPs); 4.2.1.1 Synthesis; 4.2.1.2 Structures; 4.2.1.3 Properties; 4.2.2 Hyperbranched Poly(Arylenephenylene)s (hb-PArPs); 4.2.2.1 Synthesis; 4.2.2.2 Structures; 4.2.2.3 Properties; 4.2.3 Hyperbranched Poly(Aroylphenylene)s (hb-PAkPs) and Poly(Aroxycarbonylphenylene)s (hb-PAePs); 4.2.3.1 Synthesis
  • 4.2.3.2 Structures
Dimensions
unknown
Edition
4th ed.
Extent
1 online resource (331 p.)
Form of item
online
Isbn
9783527632671
Media category
computer
Media type code
  • c
Specific material designation
remote
System control number
  • (CKB)2550000001123267
  • (EBL)700885
  • (OCoLC)774065416
  • (SSID)ssj0000506311
  • (PQKBManifestationID)11337703
  • (PQKBTitleCode)TC0000506311
  • (PQKBWorkID)10515625
  • (PQKB)10593918
  • (MiAaPQ)EBC700885
  • (EXLCZ)992550000001123267
Label
Conjugated polymer synthesis : methods and reactions, edited by Yoshiki Chujo
Publication
Copyright
Note
Description based upon print version of record
Bibliography note
Includes bibliographical references and index
Carrier category
online resource
Carrier category code
  • cr
Content category
text
Content type code
  • txt
Contents
  • Conjugated Polymer Synthesis: Methods and Reactions; Contents; Preface; List of Contributors; 1 Organometallic Polycondensation for Conjugated Polymers; 1.1 Basic Organometallic C-C Coupling; 1.2 Syntheses of π-Conjugated Polymers; 1.3 Optical Properties; 1.3.1 UV-Vis Data; 1.3.2 Photoluminescence; 1.3.3 Other Optical Properties; 1.4 Redox Behavior and Electrical Conductivity; 1.5 Linear Structure and Alignment on the Surface of Substrates; 1.6 Stacking in the Solid and Colloid; 1.7 Chemical Reactivity and Catalysis; 1.7.1 Metal Complexes and Modification of Nitrogen
  • 1.8 Electronic and Optical Devices (ECD, Battery, EL, Diode, Transistor, Nonlinear Optical Device, etc.)1.8.1 Redox Functions; 1.8.2 Electronic and Optical Devices; 1.9 Conclusions; References; 2 Catalyst-Transfer Condensation Polymerization for Precision Synthesis of π-Conjugated Polymers; 2.1 Introduction; 2.2 Kumada-Tamao Coupling Polymerization with Ni Catalyst; 2.2.1 Polythiophene; 2.2.1.1 Discovery and Mechanism of Catalyst-Transfer Condensation Polymerization; 2.2.1.2 A Variety of Monomers; 2.2.1.3 Block Polythiophenes; 2.2.1.4 Block Copolymers of Polythiophene and Other Polymers
  • 2.2.1.5 Graft Copolymers2.2.2 Polyphenylenes; 2.2.3 Polypyrroles; 2.2.4 Polyfluorenes and Polycarbazoles; 2.3 Suzuki-Miyaura Coupling Polymerization with Pd Catalyst; 2.3.1 Polyfluorenes; 2.3.2 Polyphenylenes; 2.4 Conclusion; References; 3 Regioregular and Regiosymmetric Polythiophenes; 3.1 Introduction; 3.2 Synthesis of Polythiophene and Regioirregular Polythiophenes; 3.3 Head-to-Tail Coupled Regioregular Poly(3-Alkylthiophene)s; 3.3.1 Design and Synthesis of rrP3ATs; 3.3.1.1 McCullough Method; 3.3.1.2 Rieke Method; 3.3.1.3 GRIM Method; 3.3.1.4 Palladium-Catalyzed Polymerization Methods
  • 3.3.2 Mechanism of the Nickel-Catalyzed Polymerization3.4 Side Chain Functionalized HT Regioregular Polythiophenes; 3.4.1 Heteroatom-Containing Groups; 3.4.2 Aromatic-Containing Group; 3.4.3 Chiral Groups; 3.4.4 γ-Functionalized Groups; 3.5 End Group Functionalized HT Regioregular Polythiophenes; 3.5.1 Postpolymerization End Group Functionalization; 3.5.2 In Situ End Group Functionalization; 3.6 Block Copolymers Derived from HT Regioregular Polythiophenes; 3.6.1 All-Conjugated Block Copolymers; 3.6.2 Conjugated-Non-Conjugated Block Copolymers; 3.7 Universal Use of the GRIM Method
  • 3.8 Regiosymmetric Polythiophenes3.9 Summary; References; 4 Functional Hyperbranched Polymers Constructed from Acetylenic An-Type Building Blocks; 4.1 Introduction; 4.2 Hyperbranched Polymers Constructed from Acetylenic An-Type Building Blocks; 4.2.1 Hyperbranched Poly(Alkylenephenylene)s (hb-PAPs); 4.2.1.1 Synthesis; 4.2.1.2 Structures; 4.2.1.3 Properties; 4.2.2 Hyperbranched Poly(Arylenephenylene)s (hb-PArPs); 4.2.2.1 Synthesis; 4.2.2.2 Structures; 4.2.2.3 Properties; 4.2.3 Hyperbranched Poly(Aroylphenylene)s (hb-PAkPs) and Poly(Aroxycarbonylphenylene)s (hb-PAePs); 4.2.3.1 Synthesis
  • 4.2.3.2 Structures
Dimensions
unknown
Edition
4th ed.
Extent
1 online resource (331 p.)
Form of item
online
Isbn
9783527632671
Media category
computer
Media type code
  • c
Specific material designation
remote
System control number
  • (CKB)2550000001123267
  • (EBL)700885
  • (OCoLC)774065416
  • (SSID)ssj0000506311
  • (PQKBManifestationID)11337703
  • (PQKBTitleCode)TC0000506311
  • (PQKBWorkID)10515625
  • (PQKB)10593918
  • (MiAaPQ)EBC700885
  • (EXLCZ)992550000001123267

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