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

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

      1 Chapter 1Table 1.1 EL performance of devices.

      2 Chapter 7Table 7.1 Photoluminescence data of TT and its derivatives.

      3 Chapter 9Table 9.1 Optimization of reaction conditions for synthesis of TAPP [27].Table 9.2 Optimization of the Sonogashira reaction leading to compound 4 [3...Table 9.3 Photophysical properties of (137–150) dyes measured in tolu...

      4 Chapter 14Table 14.1 Summary of the reported TPE−based ligands.

      List of Illustrations

      1 Chapter 1Chart 1.1 Molecular structures of AIEgens of tetraphenylethene (TPE), triphe...Scheme 1.1 Reaction mechanism of synthesizing TPP with benzoin and ammonia....Scheme 1.2 Current synthetic routes to TPP.Scheme 1.3 Proposed mechanism of synthesizing TPP catalyzed by Mg and Cp₂TiC...Scheme 1.4 Proposed mechanism of preparing TPP catalyzed by RuNPs.Chart 1.2 Molecular structures of TPP–TPA and TPP–PPI.Figure 1.1 Fluorescent detection of H₂S by TPP‐PDCV. (a) Time‐dependent PL s...Figure 1.2 Fluorescent detection of PA and Ru³⁺ by AIE isomers. (a) Molecula...Figure 1.3 TPP‐based chiral cage for self‐assembly to achieve white‐light em...Figure 1.4 Functional MOFs with TPP‐4COOH as ligand for sensing. (a) Intersy...

      2 Chapter 2Figure 2.1 Small molecules of 9,10‐distyrylanthracene (DSA) derivatives exhi...Figure 2.2 Compounds based on DSA exhibiting response luminescence upon exte...Figure