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Diarylethene Molecular Photoswitches. Masahiro IrieЧитать онлайн книгу.

Diarylethene Molecular Photoswitches - Masahiro Irie


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      Table of Contents

      1  Cover

      2  Title Page

      3  Copyright

      4  Preface

      5  1 Introduction 1.1 General Introduction 1.2 Discovery of Diarylethene Molecular Photoswitches References

      6  2 Reaction Mechanism 2.1 Basic Concepts 2.2 Theoretical Study 2.3 Reaction Dynamics References

      7  3 Photoswitching Performance 3.1 Quantum Yield 3.2 Thermal Stability 3.3 Fatigue Resistance 3.4 Fluorescence Property 3.5 Chiral Property References

      8  4 Photoswitchable Crystals 4.1 Dichroism 4.2 X‐Ray Crystallographic Analysis 4.3 Quantum Yield 4.4 Multicolored Systems and Nano‐Layered Periodic Structures 4.5 Fluorescent Crystals 4.6 Photomechanical Response References

      9  5 Memory 5.1 Single‐Molecule Memory 5.2 Near‐Field Optical Memory 5.3 Three‐Dimensional Optical Memory 5.4 Readout Using Infrared Absorption, Raman Scattering, and Refractive Index Changes References

      10  6 Switches 6.1 Single‐Molecule Conductance Photoswitch 6.2 Optical Switch Based on Refractive Index Change 6.3 Magnetism References

      11  7 Surface Properties 7.1 Surface Wettability 7.2 Selective Metal Deposition 7.3 Subwavelength Nanopatterning References

      12  8 Polymers and Liquid Crystals 8.1 Polymers 8.2 Liquid Crystals References

      13  9 Applications 9.1 Organic Field‐Effect Transistors (OFETs) 9.2 Metal Organic Frameworks (MOFs) 9.3 Super‐Resolution Fluorescence Microscopy 9.4 Chemical Reactivity Control 9.5 Biological Activity 9.6 Color Dosimeters References

      14  Appendix A: Appendix ASynthesis Procedures of Typical Diarylethenes A.1 1,2‐Bis(2,4‐dimethyl‐5‐phenyl‐3‐thienyl)perfluorocyclopentene (7) [5–7] A.2 1,2‐Bis(2‐ethyl‐6‐phenyl‐1‐benzothiophene‐1,1‐ dioxide‐3‐yl)‐perfluorocyclopenetene (11) [8–10] References

      15  Index

      16  End User License Agreement

      List of Tables

      1 Chapter 2Table 2.1 Relative ground state energy differences between the open‐ and clos...Table 2.2 Aromatic stabilization energy differences.

      2 Chapter 3Table 3.1 Photocyclization and photocycloreversion quantum yields of typical ...Table 3.2 Ratios of antiparallel and parallel conformers and photocyclization...Table 3.3 Photocyclization and photocycloreversion quantum yields of bisarylb...Table 3.4 Photocyclization and photocycloreversion quantum yields of diarylet...Table 3.5 Photocyclization and photocycloreversion quantum yields of diarylet...Table 3.6 Photocyclization and photocycloreversion quantum yields of diarylet...Table 3.7 T‐type molecular photoswitches. Half‐life times of closed‐ring isom...Table 3.8 Photochemical properties of diarylethenes in acetonitrile upon irra...Table 3.9 Photophysical properties of fluorescent diarylethenes (λ max: a...Table 3.10 Photophysical and


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