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Conjugated Polymers: Perspective, Theory, and New Materials
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Contents
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Contributors
1. Early History of Conjugated Polymers: From Their Origins to the Handbook of Conducting Polymers
Seth C. Rasmussen
1.1 Introduction
1.2 Basic Synthesis and Doping Processes of Conjugated Polymers
1.3 Polyaniline
1.3.1 Early Reports of the Oxidation of Aniline
1.3.2 Determination of the Structure of Aniline Oxidation Products
1.3.3 Buvet, Jozefowicz, and Conducting Polyaniline
1.4 Polypyrrole
1.4.1 Angeli and Pyrrole Black
1.4.2 Ciusa and ‘Graphite’ from Pyrrole
1.4.3 Weiss and Conducting Polypyrrole
1.4.4 Pyrrole Black at the University of Parma
1.4.5 Diaz and Electropolymerized Polypyrrole Films
1.5 Polyacetylene
1.5.1 Natta and the Polymerization of Acetylene
1.5.2 Tokyo Institute of Technology and Continued Studies of Polyacetylene
1.5.3 Shirakawa and Polyacetylene Films
1.5.4 Smith, Berets, and Doped Polyacetylene
1.5.5 MacDiarmid, Heeger, and Poly(sulfur nitride)
1.5.6 Doped Polyacetylene Films
1.6 Polythiophene
1.6.1 Yamamoto and Polythiophene via Catalytic Cross-Coupling
1.6.2 Lin and Related Catalytic Cross-Coupling Methods
1.6.3 Polythiophene via Electropolymerization
1.6.4 Polythiophenes via Chemical Oxidation
1.7 The Rise of Synthetic Metals and a Developing Field of Conductive Polymers
1.7.1 Synthetic Metals
1.7.2 Dedicated Literature
References
2. Recent Advances in the Computational Characterization of π-Conjugated Organic Semiconductors
Jean-Luc Brédas, Xiankai Chen, Thomas Körzdörfer, Hong Li, Chad Risko, Sean M. Ryno, and Tonghui Wang
2.1 Introduction
2.2 Density Functional Theory for Organic Electronics
2.2.1 The Electronic-Structure Method of Choice for Organic Electronic Materials
2.2.2 A Brief Introduction to DFT and TD-DFT
2.2.3 Challenges in DFT Applications and Recent Advances in Functional Development
2.2.3.1 Condensed Phases and the Problem of Dispersion Corrections in DFT
2.2.3.2 Self-Interaction Errors and Tuned Long-Range Corrected Hybrid Functionals
2.2.3.3 Charged Excitation Energies and the Physical Interpretation of Gaps in DFT
2.2.3.4 Optical Excitation Energies, Charge-Transfer Excitations, and Triplet States
2.3 Noncovalent Interactions and Polarization in the Condensed Phase
2.3.1 Noncovalent Interactions: Solid-State Packing, Miscibility, and Processing
2.3.2 Polarization and Site Energies in the Bulk and at Interfaces: Impact on Charged-State Characteristics
2.4 A Theoretical Description of Organic Emitters for Light-Emitting Diodes Exploiting Thermally Assisted Delayed Fluorescence
2.4.1 Theoretical Description of Reverse Intersystem Crossing
2.4.2 Relationships of the Spin-Orbit Couplings with the Excitation Characteristics
2.4.3 Role of Non-Adiabatic Coupling in the Reverse Intersystem Crossing Process
2.4.4 Novel Molecular-Design Strategies for TADF Emitters
2.5 Molecular Dynamics Description of Organic-OrganicInterfaces and Polymer Pure Phases
2.5.1 Interfaces Between Layers of Small Molecules: Interfacial Mixing
2.5.2 π-Conjugated Polymer Pure Phases: Main-Chain Conformation and Inter-Chain Packing
2.5.3 Polymer-Fullerene Packing and Interfaces in the Mixed Regions
2.6 Characterization of the Interfaces between an Organic Layer and a Metal or Conducting Oxide Surface
2.6.1 Description of the Change in Surface Workfunction upon Deposition of an Organic Layer
2.6.2 Brief Description of the Computational Methodology
2.6.3 Surface Defects
2.6.4 Charge-Transfer Characteristics for Donor/Acceptor Molecules Physisorbed on Metal-Oxide Surfaces
2.6.5 Characterization of the Binding Modes of the Surface Modifiers
Acknowledgments
References
3. Perspective on the Advancements in Conjugated Polymer Synthesis, Design, and Functionality over the Past Ten Years
3.1 Introduction to this Perspective
3.1.1 Polymer Structures
3.1.1.1 Polythiophene and Derivatives
3.1.1.2 Poly(arylene vinylenes)
3.1.1.3 Poly(arylene ethynylenes)
3.1.1.4 Narrow Bandgap Polymers
3.1.2 Polymer Synthesis
3.1.2.1 Transition Metal Catalyzed Polymerizations
3.1.2.2 Electrochemical Oxidative Polymerization
3.1.2.3 McMurry Polymerization
3.1.2.4 Knoevenagel Polycondensation
3.1.2.5 Gilch Polymerization
3.1.2.6 Wittig Type Polycondensations
3.2 Advancements in Conjugated Polymer Syntheses
3.2.1 Emerging Repeat Units
3.2.1.1 Amide and Imide Functionalized Repeat Units
3.2.1.2 Benzothiadiazole, Quinoxaline, and Analogs
3.2.1.3 Fused Donors
3.2.1.4 Heteroatom Modification
3.2.2 New Synthetic Strategies in Conjugated Polymer Chemistry
3.2.2.1 Polymerizations via C–H Activation
3.2.2.2 GRIM/Chain Transfer Polymerization (CTP) Synthetic Strategies
3.2.2.3 Continuous Flow Synthesis
3.2.2.4 Click-Chemistry and Multi-Component Reactions
3.2.2.5 Molecular Weight and Dispersity Effects
3.2.3 Structure Property Modification of Conjugated Polymers
3.2.3.1 Random and Block Copolymers
3.2.3.2 Side Chain Engineering
3.2.3.3 n-Type Conjugated Polymers
3.2.3.4 Metallopolymers
3.2.3.5 Conjugated Porous Polymers
3.3 Future Direction and Outlook
3.3.1 Efficient Monomer and Polymer Synthesis
3.3.2 Polymer Properties and Applications
Acknowledgments
References
4. Advances in Discrete Length and Fused Conjugated Oligomers
Shanshan Chen, So-Huei Kang, Sang Myeon Lee, Tanya Kumari, and Changduk Yang
4.1 Introduction
4.2 Oligothiophenes
4.2.1 End-group Modification
4.2.2 Conjugation Length Extension
4.3 Cyclopentadithiophene Derivatives
4.3.1 Heteroatom Modification
4.3.2 Regiochemistry Studies
4.3.3 Conjugation Length Extension
4.3.4 End-group Modification
4.4 Benzodithiophene Derivatives
4.4.1 Conjugated Length Extension
4.4.2 Core Unit Modification
4.4.3 End-Group Modification
4.5 Indacenodithiophene Derivatives
4.5.1 Core Unit or π-Bridge Modification
4.5.2 Conjugation Length Extension
4.5.3 End-Group Modification
4.6 Rylene Diimide Derivatives
4.6.1 Conjugation Length Extension
4.7 Others
4.8 Conclusion
Acknowledgments
References
5. Direct (Hetero)Arylation Polymerization for the Preparation of Conjugated Polymers
J. Terence Blaskovits and Mario Leclerc
5.1 Introduction
5.2 Direct C–H Activation and Arylation of Small Molecules
5.2.1 History and Development
5.2.2 Proposed Mechanisms and Implications
5.3 Direct Arylation Applied to Polymers
5.3.1 Early Examples
5.3.2 Synthetic Considerations of DHAP
5.4 Defects in DHAP-Prepared Polymers
5.4.1 Regioregularity
5.4.2 Homocoupling
5.4.3 β-Defects
5.5 Considerations for a Successful Polymerization
5.5.1 Optimizing Reaction Conditions
5.5.2 Solvent
5.5.3 Ligand
5.5.4 Catalyst
5.5.5 Base, Acid, and Other Additives
5.5.6 Heating Source
5.6 Conclusions and Outlook
References
6. Living Polymerizations of π-Conjugated Semiconductors
6.1 Introduction
6.2 Poly(3-hexylthiophene)
6.3 Kumada Catalyst-Transfer Polymerization (KCTP)
6.3.1 Mechanistic Details of KCTP
6.3.2 External Initiation of KCTP
6.3.3 Termination and Endcapping in KCTP
6.3.4 Modulation of Electronic and Steric Effects in KCTP
6.4 Synthesis of Semiconducting π-Conjugated Polymers
6.4.1 Other Semiconducting Scaffolds
6.4.2 Block Copolymers
6.4.3 Alternating Copolymers
6.4.4 Synthesis of Advanced Topologies
6.5 Conclusions
References
7. Controlled Synthesis of Polyfurans, Polyselenophenes, and Polytellurophenes
Shuyang Ye, Emily L. Kynaston, and Dwight S. Seferos
7.1 Introduction
7.2 Synthesis of Furan, Selenophene, and Tellurophene Monomers
7.3 Furan, Selenophene, and Tellurophene Homopolymers
7.3.1 Preparation of Polyfurans
7.3.2 Preparation of Polyselenophenes
7.3.3 Preparation of Polytellurophenes
7.4 Properties and Applications of O, Se-, and Te- Polymers
7.4.1 Structure and Rigidity
7.4.2 Optoelectronic Properties
7.5 Furan, Selenophene, and Tellurophene Copolymers and Self-Assembly Behavior
7.6 Summary and Outlook
References
8. Donor-Acceptor Polymers for Organic Photovoltaics
Desta Gedefaw and Mats R. Andersson
8.1 Introduction
8.2 Donor-Acceptor Conjugated Polymers
8.2.1 Fluorene, Silafluorene, Carbazole, and Cyclopentadithiophene-Containing Donor-Acceptor Polymers
8.2.2 Thiophene and Derivatives as a Donor Unit in Donor-Acceptor Polymers
8.2.2.1 Thiophene/Thienothiophene/Selenophene-Quinoxaline
8.2.2.2 Thiophene-Isoindigo Donor-Acceptor Polymers
8.2.3 Benzodithiophene as a Donor Unit for the Synthesis of Donor-Acceptor Polymers
8.2.3.1 Benzodithiophene-Thienothiophene-Based Donor-Acceptor Polymers
8.2.3.2 Benzodithiophene-TPD-Based Donor-Acceptor Polymers
8.2.3.3 BDT-Quinoxaline-Based Donor-Acceptor Polymers
8.2.3.4 BDT with Benzodithiophene-dione
8.2.3.6 BDT-triazole Polymers
8.2.4 Indacenodithiophene and its Derivatives as a Donor Unit in the Construction of Donor-Acceptor Polymers
8.2.4.1 Functionalization of the Bridging Atom
8.2.4.2 Further Extension of the Fused System
8.2.5 Summary and Outlook
Acknowledgments
References
9. Conjugated Polymers for n- and p-Type Charge Transport
Zachary S. Parr, Zhijie Guo, and Christian B. Nielsen
9.1 Introduction
9.2 p-Type Charge Transport
9.2.1 Polythiophene-Based Systems
9.2.2 Donor-Acceptor Systems
9.2.2.1 CPDT-Based Systems
9.2.2.2 IDT-Based Systems
9.2.2.3 Diketopyrrolopyrrole-Based Polymers
9.2.2.4 Isoindigo-Based Polymers
9.2.2.5 Other Donor Acceptor Systems
9.2.3 Molecule:Polymer Blends
9.3 n-Type Charge Transport
9.3.1 Indigo- and Isoindigo-Based Systems
9.3.2 Diketopyrrolopyrrole-Based Systems
9.3.3 Rylene Diimide-Based Systems
9.3.4 Other Structural Systems
9.4 Ambipolar Charge Transport
9.5 Conclusions and Outlook
References
10. Conjugated Block Copolymers: Synthesis, Self-Assembly, and Device Applications
Jessica Shaw and Malika Jeffries-EL
10.1 Introduction
10.2 Synthesis of Conjugated Block Copolymers
10.3 Self-Assembly of Conjugated Block Copolymers
10.4 Device Applications
10.5 Conclusions and Future Perspective
References
11. Metal-Containing Conjugated Polymers
Christopher M. Brown and Michael O. Wolf
11.1 General Introduction
11.2 Group 8 – Fe, Ru, Os
11.2.1 Introduction
11.2.2 Type I
11.2.3 Type III
11.3 Group 9 – Co, Rh, Ir
11.3.1 Introduction
11.3.2 Type I
11.3.3 Type II
11.3.4 Type III
11.4 Group 10 – Ni, Pd, Pt
11.4.1 Introduction
11.4.2 Type II
11.4.3 Type III
11.5 Group 11 – Coinage Metals
11.5.1 Introduction
11.5.2 Type I
11.5.3 Type II
11.5.4 Type III
11.6 Lanthanides
11.6.1 Introduction
11.6.2 Type I
11.6.3 Type II
11.6.4 Type III
11.7 Other Metals/Mixed-Metal Systems
11.7.1 Introduction
11.7.2 Rhenium
11.7.3 Zinc
11.7.4 Mixed Zn-Ln Systems
11.8 Conclusions
Abbreviations
References
12. Recent Progress in the Development of Optoelectronic Materials Based on Group 13 Element-containing Conjugated Polymers
Shunichiro Ito, Masayuki Gon, Kazuo Tanaka, and Yoshiki Chujo
12.1 Introduction
12.2 Boron-Containing π-Conjugated Polymers
12.2.1 Overview
12.2.2 π-Conjugated Polymers Containing Three-Coordinate Boron
12.2.2.1 Hydroboration Polymerization
12.2.2.2 Metal–Boron Exchange Polymerization
12.2.2.3 Transition Metal-Catalyzed Coupling
12.2.2.4 π-Conjugated Polymers Containing B–N Units
12.2.3 π-Conjugated Polymers Containing Four-Coordinate Boron
12.2.3.1 BODIPY and Aza-BODIPY
12.2.3.2 Boron Diketonates, Ketiminates, and Diketiminates
12.2.4 π-Conjugated Polymers Containing Carboranes
12.3 Aluminum-Containing π-Conjugated Polymers
12.3.1 Overview
12.3.2 Aluminum Quinolinolate Complex
12.4 Gallium-Containing π-Conjugated Polymers
12.4.1 Overview
12.4.2 Organogallium Compounds Stabilized by Supporting Ligand
12.4.3 Gallium Complexes Stabilized by π-Conjugated Supporting Ligand
12.5 Conclusion
References
13. Multifunctional Conjugated Polymers: Helically Assembled Spherulites, Photo-Controllable Illuminants, and Helical Graphites
Kazuo Akagi
13.1 Introduction
13.1.1 Conjugated Polymers
13.1.2 Helical π-Conjugated Polymers
13.1.3 Polymer Spherulites
13.1.4 Dynamic Control of Luminescence
13.1.5 Polymer Nanospheres
13.1.6 Chiral Liquid Crystal Field
13.1.7 Carbon and Graphitic Materials
13.2 Polymer Spherulites Consisting of Hierarchical Helical Assemblies
13.2.1 Cationic Conjugated Polymer and Anionic Chiral Compound
13.2.2 Circular Polarized Luminescence
13.2.3 Stoichiometry of Assembly
13.2.4 Spheres Consisting of Polymer Assemblies
13.3 Photochemically Color-Tunable Fluorescence Illuminants Consisting of Conjugated Polymer Nanospheres
13.3.1 Photoswitching of Emission and Quenching
13.3.2 Photoresponsive Polymer Nanospheres
13.3.3 Photoswitching Between White Fluorescence and Quenching
13.3.4 Photoswitching between White and RGB Fluorescence
13.4 Helical Carbon and Graphites Prepared from Helical Conjugated Polymers
13.4.1 Iodine-Doped Helical Polyacetylene
13.4.2 Morphologies of Helical Carbon Films
13.4.3 XRD Intensity Curves and Raman Scattering Spectra
13.4.4 Mechanism of Morphology-Retaining Carbonization
13.4.5 Graphitization of Helical Carbon
13.5 Conclusion
Acknowledgments
References
14. Conjugated Polyelectrolytes Designed for Biological Applications
Pradeepkumar Jagadesan, Yun Huang, and Kirk S. Schanze
14.1 Introduction—Structure and Properties of Conjugated Polyelectrolytes
14.2 Classifications of Conjugated Polyelectrolytes
14.2.1 Cationic Conjugated Polyelectrolytes
14.2.2 Anionic Conjugated Polyelectrolytes
14.2.3 Zwitterionic Conjugated Polymers
14.3 Optical Properties of Conjugated Polyelectrolytes
14.3.1 Background and History of Fluorescence Sensing with Conjugated Polyelectrolytes
14.3.2 Aggregation Based Fluorescence Sensing
14.4 Biosensing with Conjugated Polyelectrolytes
14.4.2 DNA Sensing with Conjugated Polyelectrolytes
14.5 Selective Imaging of Microbial Pathogens with Conjugated Polyelectrolytes
14.6 Application of Machine Learning to Nonspecific Conjugated Polyelectrolyte Sensors
14.7 Cationic Conjugated Polyelectrolytes as Antimicrobials
14.8 Application of Conjugated Polyelectrolytes in Mammalian Cell Investigations
14.8.1 Cell Imaging Studies—Penetration into Mammalian Cells
14.8.2 Localization of Conjugated Polyelectrolytes in Lysosomes and pH-triggered Escape
14.8.3 Gene Transfection Using Conjugated Polyelectrolytes
14.9 Summary, Conclusion, and Perspectives
Acknowledgments
References
15. Oxidative Chemical Vapor Deposition for Conjugated Polymers: Theory and Applications
Karen K. Gleason and Xiaoxue Wang
15.1 Introduction
15.2 Chemistry of Film Growth and Grafting
15.3 Reactors and Processing
15.4 Polymers and their Applications
15.5 The Properties of oCVD PEDOT and Its Applications
15.5.1 Optimization of Electrical Conductivity
15.5.2 Optical Properties
15.5.3 Scale-up and Applications of oCVD PEDOT
15.6 The Properties and Applications of oCVD Copolymers with EDOT
15.7 The Properties and Applications of other oCVD-conjugated Polymers
15.7.1 Polyaniline (PANI)
15.7.2 Polythiophene
15.7.3 Low Band Gap Semiconducting Polymers Polyisothianaphthene (PITN) and Polyselenophene (pSe)
15.7.4 Other Conjugated Polymer Films Deposited using oCVD
15.8 Conclusion and Outlook
Acknowledgments
References
16. Flow Synthesis: A Better Way to Conjugated Polymers?
James H. Bannock, Martin J. Heeney, and John C. de Mello
16.1 Introduction to Flow Chemistry
16.1.1 Flow reactors
16.1.2 Automation
16.1.3 Translating Chemical Reactions from Flash to Flow
16.1.4 Injection Valves
16.2 Flow Synthesis of Conjugated Polymers
16.2.1 Single-Phase Synthesis of Conjugated Polymers
16.2.2 Droplet Synthesis
16.3 Challenges for the Future
16.4 Conclusion
References
Index