Handbook of Aggregation-Induced Emission, Volume 2. Группа авторов

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      23  16 Aggregation‐induced Emission in Coinage Metal Clusters 16.1 Introduction 16.2 AIE‐active Gold Cluster 16.3 AIE‐active Silver Cluster 16.4 AIE‐active Copper Cluster 16.5 AIE‐active Bimetallic Cluster 16.6 Conclusions References

      24  17 Activated Alkynes in Metal‐free Bioconjugation 17.1 Introduction 17.2 Alkyne–Azide‐based Bioconjugation 17.3 Activated Alkyne–Amine‐based Bioconjugation 17.4 Activated Alkyne–Thiol‐based Bioconjugation 17.5 Activated Alkyne–Hydroxyl‐based Bioconjugation 17.6 Activated Alkyne‐based Bioconjugation and Polymerization in Living Cells and Pathogens 17.7 Conclusion References

      25  18 AIE‐active BODIPY Derivatives 18.1 Introduction 18.2 Structures of BODIPY Derivatives 18.3 Structural–property Relationship 18.4 Application 18.5 Conclusion References

      26  19 Photochemistry‐regulated AIEgens and Their Applications 19.1 Introduction 19.2 Photocleavage Reaction 19.3 Photoreduction Reaction 19.4 Photocyclodehydrogenation Reaction 19.5 Photooxidative Dehydrogenation Reaction 19.6 Spiropyran‐merocyanine Reversible Conversion 19.7 Dithienylethene‐based Ring‐open/‐closing Reaction 19.8 Enol–Keto Isomerization Reaction 19.9 E/Z Isomerization Reaction 19.10 Photo‐induced [2 + 2] Cycloaddition 19.11 Combinational Photoreactions 19.12 Conclusion and Outlook References

      27  20 Design and Development of Naphthalimide Luminogens 20.1 Introduction 20.2 Naphthalimides with N‐Functionalization (I) 20.3 Naphthalimides Substituted at the 4th Position with Oxygen Atom (II) 20.4 Naphthalimides Substituted at the 4th Position with Nitrogen Atom (III) 20.5 Naphthalimides with C−C Aromatic Substitution (IV) 20.6 Naphthalimides with C−C Double‐ and Triple‐Bond Substitutions (V and VI) 20.7 Naphthalimides with the Significant Role of Multifunctionalization (VII) 20.8 Conclusion and Outlooks References

      28  Index

      29  End User License Agreement

      List of Tables

      List of Illustrations