{"product_id":"handbook-of-aggregationinduced-emission-volume-1-9781119642916","title":"Handbook of AggregationInduced Emission Volume 1","description":"\u003cb\u003eBook Synopsis\u003c\/b\u003e\u003cbr\u003e\u003cp\u003e\u003cb\u003eThefirstvolume of the ultimate reference on the science and applications of aggregation-induced emission\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e\u003ci\u003eTheHandbook of Aggregation-Induced Emission\u003c\/i\u003eexplores foundational and advanced topics in aggregation-induced emission, as well as cutting-edge developments in the field,celebratingtwenty years of progress and achievement in this important and interdisciplinary field.The three volumes combine to offer readers a comprehensive and insightful interpretation accessible to both new and experiencedresearchersworking onaggregation-induced emission.\u003c\/p\u003e \u003cp\u003eIn thisfirst volume of three, theeditorssurveythe subjectofaggregation-induced emissionwith afocus on the fundamentals of various branches of the discipline, such ascrystallization-induced emission,room temperature phosphorescence,aggregation-induced delayed fluorescence, and more.Thisbook coversthe new properties of materials endowed by molecular aggregates. It also includes:\u003c\/p\u003e \u003cul\u003e \u003cli\u003eA thorough introduction tot\u003cbr\u003e\u003cbr\u003e\u003cb\u003eTable of Contents\u003c\/b\u003e\u003cbr\u003e\u003cp\u003eList of Contributors xv\u003c\/p\u003e \u003cp\u003ePreface to Handbook of Aggregation-Induced Emission xxi\u003c\/p\u003e \u003cp\u003ePreface to Volume 1: Fundamentals xxiii\u003c\/p\u003e \u003cp\u003e\u003cb\u003e1 The Mechanistic Understanding of the Importance of Molecular Motions to Aggregation-induced Emission 1\u003cbr\u003e\u003c\/b\u003e\u003ci\u003eJunkai Liu and Ben Zhong Tang\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e1.1 Introduction 1\u003c\/p\u003e \u003cp\u003e1.2 Restriction of Intramolecular Motion 2\u003c\/p\u003e \u003cp\u003e1.2.1 Restriction of Intramolecular Rotation 3\u003c\/p\u003e \u003cp\u003e1.2.2 Restriction of Intramolecular Vibration 4\u003c\/p\u003e \u003cp\u003e1.2.3 Ultrafast Insights into Tetraphenylethylene Derivatives 6\u003c\/p\u003e \u003cp\u003e1.2.4 Theoretical Insights into Restriction of Intramolecular Motion 8\u003c\/p\u003e \u003cp\u003e1.3 Restricted Access to Conical Intersection 12\u003c\/p\u003e \u003cp\u003e1.4 Restriction of Access to the Dark State 14\u003c\/p\u003e \u003cp\u003e1.5 Suppression of Kasha’s Rule 15\u003c\/p\u003e \u003cp\u003e1.6 Through Space Conjugation 17\u003c\/p\u003e \u003cp\u003e1.6.1 Clusterization-Triggered Emission 18\u003c\/p\u003e \u003cp\u003e1.6.2 Polymerization-induced Emission 19\u003c\/p\u003e \u003cp\u003e1.6.3 Excited-state Through-space Conjugation 19\u003c\/p\u003e \u003cp\u003e1.7 Perspective 21\u003c\/p\u003e \u003cp\u003eReferences 23\u003c\/p\u003e \u003cp\u003e\u003cb\u003e2 Understanding the AIE Mechanism at the Molecular Level \u003c\/b\u003e\u003cb\u003e27\u003cbr\u003e\u003c\/b\u003e\u003ci\u003eXiaoyan Zheng and Qian Peng\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e2.1 Introduction 27\u003c\/p\u003e \u003cp\u003e2.2 Theoretical Methods 28\u003c\/p\u003e \u003cp\u003e2.2.1 Radiative and Nonradiative Rate Constants 28\u003c\/p\u003e \u003cp\u003e2.2.2 Computational Details 29\u003c\/p\u003e \u003cp\u003e2.3 Revealed AIE Mechanism 31\u003c\/p\u003e \u003cp\u003e2.3.1 Rotating Vibrations of Intramolecular Aromatic Ring 31\u003c\/p\u003e \u003cp\u003e2.3.2 Stretching Vibrations of Bonds 33\u003c\/p\u003e \u003cp\u003e2.3.3 Bending Vibration of Bonds 34\u003c\/p\u003e \u003cp\u003e2.3.4 Flipping Vibrations of Molecular Skeletons 35\u003c\/p\u003e \u003cp\u003e2.3.5 Twisting Vibration of Molecular Skeletons 36\u003c\/p\u003e \u003cp\u003e2.4 Visualize Calculated Parameters in Experiments 37\u003c\/p\u003e \u003cp\u003e2.4.1 Stokes Shift vs Reorganization Energy 37\u003c\/p\u003e \u003cp\u003e2.4.2 Resonance Raman Spectroscopy (RSS) vs Reorganization Energy 38\u003c\/p\u003e \u003cp\u003e2.4.3 Isotope Effect vs DRE 40\u003c\/p\u003e \u003cp\u003e2.4.4 Linear Relationship between Fluorescence Intensity and Amorphous Aggregate Size 42\u003c\/p\u003e \u003cp\u003e2.4.5 Pressure-induced Enhanced Emission (PIEE) 44\u003c\/p\u003e \u003cp\u003e2.5 Molecular Design Based on AIE Mechanism 45\u003c\/p\u003e \u003cp\u003e2.6 Summary and Outlook 46\u003c\/p\u003e \u003cp\u003eAcknowledgments 48\u003c\/p\u003e \u003cp\u003eReferences 48\u003c\/p\u003e \u003cp\u003e\u003cb\u003e3 Aggregation-induced Emission from the Restriction of Double Bond Rotation at the Excited State \u003c\/b\u003e\u003cb\u003e55\u003cbr\u003e\u003c\/b\u003e\u003ci\u003eMing Hu and Yan-Song Zheng\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e3.1 Introduction 55\u003c\/p\u003e \u003cp\u003e3.2 AIE Phenomena and Applications from RDBR Mechanism 58\u003c\/p\u003e \u003cp\u003e3.2.1 Evolvement and Development of AIE Mechanisms 58\u003c\/p\u003e \u003cp\u003e3.2.2 Investigation of RDBR AIE Mechanism by \u003ci\u003eE\/Z \u003c\/i\u003eisomerization 64\u003c\/p\u003e \u003cp\u003e3.2.3 Investigating of RDBR AIE Mechanism by Immobilization of TPE Propeller-like Conformation 69\u003c\/p\u003e \u003cp\u003e3.2.4 Research of Theoretical Calculation on RDBR 78\u003c\/p\u003e \u003cp\u003e3.2.5 Other AIEgens Involving RBDR Process 84\u003c\/p\u003e \u003cp\u003e3.3 Conclusions 93\u003c\/p\u003e \u003cp\u003eReferences 94\u003c\/p\u003e \u003cp\u003e\u003cb\u003e4 The Expansion of AIE Thought: From Single Molecule to Molecular Uniting \u003c\/b\u003e\u003cb\u003e99\u003cbr\u003e\u003c\/b\u003e\u003ci\u003eQiuyan Liao, Qianqian Li, and Zhen Li\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e4.1 Aggregation-Induced Emission 99\u003c\/p\u003e \u003cp\u003e4.2 Photoluminescence Materials Based on Molecular Set 101\u003c\/p\u003e \u003cp\u003e4.3 Mechanoluminescence Materials Based on Molecular Set 106\u003c\/p\u003e \u003cp\u003e4.3.1 Mechanoluminescence Materials with Fluorescence Emission 106\u003c\/p\u003e \u003cp\u003e4.3.2 Mechanoluminescence Materials with Mechanical Induced Dual-or Tri-color Emission 115\u003c\/p\u003e \u003cp\u003e4.3.3 Quantitative Research of Mechanoluminescence Property 121\u003c\/p\u003e \u003cp\u003e4.4 Mechanochromism Materials 122\u003c\/p\u003e \u003cp\u003e4.4.1 Mechanochromism Materials Based on Polymorphs 122\u003c\/p\u003e \u003cp\u003e4.4.2 Mechanochromism Materials Based on Excimer Emission 125\u003c\/p\u003e \u003cp\u003e4.4.3 Other Kinds of Mechanochromism Materials 128\u003c\/p\u003e \u003cp\u003e4.5 Room Temperature Phosphorescence Materials Based on Molecular Uniting 131\u003c\/p\u003e \u003cp\u003e4.5.1 Room Temperature Phosphorescence Materials with Aromatics 131\u003c\/p\u003e \u003cp\u003e4.5.2 Room Temperature Phosphorescence Materials with Simple or Nonaromatic Structure 140\u003c\/p\u003e \u003cp\u003e4.5.3 Room Temperature Phosphorescence Materials with Multiple Emission 142\u003c\/p\u003e \u003cp\u003e4.5.4 Photoinduced Room Temperature Phosphorescence Materials 144\u003c\/p\u003e \u003cp\u003e4.6 Conclusion and Perspectives 147\u003c\/p\u003e \u003cp\u003eReferences 147\u003c\/p\u003e \u003cp\u003e\u003cb\u003e5 Clusterization-Triggered Emission \u003c\/b\u003e\u003cb\u003e153\u003cbr\u003e\u003c\/b\u003e\u003ci\u003eHaoke Zhang and Ben Zhong Tang\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e5.1 Introduction 153\u003c\/p\u003e \u003cp\u003e5.2 Pure \u003ci\u003en\u003c\/i\u003e-Electron Systems 156\u003c\/p\u003e \u003cp\u003e5.3 Pure \u003ci\u003eπ\u003c\/i\u003e-Electron Systems 160\u003c\/p\u003e \u003cp\u003e5.4 (\u003ci\u003en\u003c\/i\u003e, \u003ci\u003eπ\u003c\/i\u003e)-Electrons Systems 164\u003c\/p\u003e \u003cp\u003e5.5 Other Systems 166\u003c\/p\u003e \u003cp\u003e5.6 Summary 167\u003c\/p\u003e \u003cp\u003eReferences 168\u003c\/p\u003e \u003cp\u003e\u003cb\u003e6 Crystallization-induced Emission Enhancement \u003c\/b\u003e\u003cb\u003e177\u003cbr\u003e\u003c\/b\u003e\u003ci\u003eYong Qiang Dong, Yingying Liu, Mengyang Liu, Qian Wang, and Kang Wang\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e6.1 Introduction 177\u003c\/p\u003e \u003cp\u003e6.2 Tetraphenylethylene Derivatives 178\u003c\/p\u003e \u003cp\u003e6.3 CIEE Active Luminogens with Bulky Conjugation Core 183\u003c\/p\u003e \u003cp\u003e6.3.1 Dibenzofulvene (DBF) Derivatives (Chart 6.2) 183\u003c\/p\u003e \u003cp\u003e6.3.2 9-([1,1\u003cb\u003e′\u003c\/b\u003e-Biphenyl]-4-ylphenylmethylene)-9H-xanthene 185\u003c\/p\u003e \u003cp\u003e6.3.3 Dicyanomethylenated Acridones 186\u003c\/p\u003e \u003cp\u003e6.3.4 Bis(diarylmethylene)dihydroanthracene [31] 187\u003c\/p\u003e \u003cp\u003e6.4 Other High-contrast CIEE Luminogens 190\u003c\/p\u003e \u003cp\u003e6.4.1 4-Dimethylamino-2-Benzylidene Malonic Acid Dimethyl Ester 190\u003c\/p\u003e \u003cp\u003e6.4.2 Diphenyl Maleimide Derivatives [33] 191\u003c\/p\u003e \u003cp\u003e6.4.3 3,4-Bisthienylmaleic Anhydride [34] 192\u003c\/p\u003e \u003cp\u003e6.4.4 Boron-containing CIEE Luminogens 193\u003c\/p\u003e \u003cp\u003e6.5 Potential Applications 196\u003c\/p\u003e \u003cp\u003e6.5.1 Volatile Organic Compounds (VOCs) Sensor 196\u003c\/p\u003e \u003cp\u003e6.5.2 OLED 196\u003c\/p\u003e \u003cp\u003e6.5.3 High-density Data Storage 197\u003c\/p\u003e \u003cp\u003e6.5.4 Mechanochromic (MC) Luminescent Sensor 198\u003c\/p\u003e \u003cp\u003e6.6 Summary and Perspective 198\u003c\/p\u003e \u003cp\u003eReferences 198\u003c\/p\u003e \u003cp\u003e\u003cb\u003e7 Surface-fixation Induced Emission \u003c\/b\u003e\u003cb\u003e203\u003cbr\u003e\u003c\/b\u003e\u003ci\u003eYohei Ishida and Shinsuke Takagi\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e7.1 Introduction 203\u003c\/p\u003e \u003cp\u003e7.2 What Happened to the Characteristics of Molecules on the Clay Mineral Nanosheets 205\u003c\/p\u003e \u003cp\u003e7.3 Clay–Molecular Complexes 206\u003c\/p\u003e \u003cp\u003e7.4 Absorption Spectra of Clay–Molecular Complexes 207\u003c\/p\u003e \u003cp\u003e7.5 Emission Enhancement Phenomenon in Clay–Molecular Complexes: S-FIE 208\u003c\/p\u003e \u003cp\u003e7.6 Mechanism of Surface-Fixation Induced Emission 211\u003c\/p\u003e \u003cp\u003e7.7 Summary and Outlook 214\u003c\/p\u003e \u003cp\u003eAcknowledgment 215\u003c\/p\u003e \u003cp\u003eReferences 215\u003c\/p\u003e \u003cp\u003e\u003cb\u003e8 Aggregation-induced Delayed Fluorescence \u003c\/b\u003e\u003cb\u003e221\u003cbr\u003e\u003c\/b\u003e\u003ci\u003eYan Fu, Hao Chen, Zujin Zhao, and Ben Zhong Tang\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e8.1 Introduction 221\u003c\/p\u003e \u003cp\u003e8.2 Novel Aggregation-induced Delayed Fluorescence Luminogens 222\u003c\/p\u003e \u003cp\u003e8.3 Conclusion and Outlook 247\u003c\/p\u003e \u003cp\u003eReferences 247\u003c\/p\u003e \u003cp\u003e\u003cb\u003e9 Homogeneous Systems to Induce Emission of AIEgens \u003c\/b\u003e\u003cb\u003e251\u003cbr\u003e\u003c\/b\u003e\u003ci\u003eKenta Kokado and Kazuki Sada\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e9.1 Introduction 251\u003c\/p\u003e \u003cp\u003e9.2 Homogeneous Solution 252\u003c\/p\u003e \u003cp\u003e9.2.1 Complexation with Anions 253\u003c\/p\u003e \u003cp\u003e9.2.2 Complexation with Cations 254\u003c\/p\u003e \u003cp\u003e9.2.3 Inclusion Complexes 256\u003c\/p\u003e \u003cp\u003e9.2.4 Adhesion on Macromolecules 257\u003c\/p\u003e \u003cp\u003e9.2.5 Steric Hindrance 258\u003c\/p\u003e \u003cp\u003e9.2.6 Covalent Linkage 259\u003c\/p\u003e \u003cp\u003e9.3 Liquid 260\u003c\/p\u003e \u003cp\u003e9.4 Gels and Network Polymers 261\u003c\/p\u003e \u003cp\u003e9.4.1 Chemically Crosslinked Gels 261\u003c\/p\u003e \u003cp\u003e9.4.2 Physically Crosslinked Gels 262\u003c\/p\u003e \u003cp\u003e9.5 Crystalline Materials 264\u003c\/p\u003e \u003cp\u003e9.6 Outlook and Future Perspectives 266\u003c\/p\u003e \u003cp\u003eReferences 266\u003c\/p\u003e \u003cp\u003e\u003cb\u003e10 Hetero-aggregation-induced Tunable Emission (HAITE) Through Cocrystal Strategy \u003c\/b\u003e\u003cb\u003e273\u003cbr\u003e\u003c\/b\u003e\u003ci\u003eYinjuan Huang and Qichun Zhang\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e10.1 Introduction 273\u003c\/p\u003e \u003cp\u003e10.2 Interactions Within Organic Cocrystals 274\u003c\/p\u003e \u003cp\u003e10.3 Preparation of Organic Cocrystals 275\u003c\/p\u003e \u003cp\u003e10.4 Molecular Stacking Modes Within Organic Cocrystals 276\u003c\/p\u003e \u003cp\u003e10.5 Characterization of Organic Cocrystals 277\u003c\/p\u003e \u003cp\u003e10.6 HAITE Through Cocrystal Strategy 277\u003c\/p\u003e \u003cp\u003e10.6.1 HAITE with Tunable Color and Enhanced Emission 278\u003c\/p\u003e \u003cp\u003e10.6.1.1 Insignificant Changed Intensity but Tuned Color 278\u003c\/p\u003e \u003cp\u003e10.6.1.2 Enhanced Emission and Tuned Color 287\u003c\/p\u003e \u003cp\u003e10.6.2 HAITE with Increased PLQY but Intrinsic Color 291\u003c\/p\u003e \u003cp\u003e10.6.3 HAITE: Thermally Activated Delayed Fluorescence 297\u003c\/p\u003e \u003cp\u003e10.6.4 HAITE-phosphorescence 300\u003c\/p\u003e \u003cp\u003e10.7 Summary and Outlook 302\u003c\/p\u003e \u003cp\u003eReferences 304\u003c\/p\u003e \u003cp\u003e\u003cb\u003e11 Anti-Kasha Emission from Organic Aggregates \u003c\/b\u003e\u003cb\u003e311\u003cbr\u003e\u003c\/b\u003e\u003ci\u003eWenbin Huang and Zikai He\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e11.1 Introduction 311\u003c\/p\u003e \u003cp\u003e11.2 Anti-Kasha Emission from Aromatic Carbonyl Compounds in Aggregates 312\u003c\/p\u003e \u003cp\u003e11.3 Anti-Kasha Emission from Azulene Compounds in Aggregate 322\u003c\/p\u003e \u003cp\u003e11.4 Anti-Kasha Emission from Other Unconventional Aromatic Compounds in Aggregates 324\u003c\/p\u003e \u003cp\u003e11.5 Conclusions 327\u003c\/p\u003e \u003cp\u003eReferences 327\u003c\/p\u003e \u003cp\u003e\u003cb\u003e12 Aggregation-enhanced Emission: From Flexible to Rigid Cores \u003c\/b\u003e\u003cb\u003e333\u003cbr\u003e\u003c\/b\u003e\u003ci\u003eHarnimarta Deol, Gurpreet Singh, Vandana Bhalla, and Manoj Kumar\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e12.1 Introduction 333\u003c\/p\u003e \u003cp\u003e12.2 Freely Moving Rotors-induced Emission Enhancement 334\u003c\/p\u003e \u003cp\u003e12.3 Guest-induced Emission Enhancement 344\u003c\/p\u003e \u003cp\u003e12.4 Conclusion 366\u003c\/p\u003e \u003cp\u003eAcknowledgment 367\u003c\/p\u003e \u003cp\u003eReferences 367\u003c\/p\u003e \u003cp\u003e\u003cb\u003e13 Room-temperature Phosphorescence of Pure Organics \u003c\/b\u003e\u003cb\u003e371\u003cbr\u003e\u003c\/b\u003e\u003ci\u003eTianwen Zhu, Zihao Zhao, Tianjia Yang, and Wang Zhang Yuan\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e13.1 Introduction 371\u003c\/p\u003e \u003cp\u003e13.2 Fundamental Mechanism in Organic Phosphorescence 372\u003c\/p\u003e \u003cp\u003e13.2.1 Photophysical Process for Phosphorescence 372\u003c\/p\u003e \u003cp\u003e13.2.2 Theoretical Study on Phosphorescent Process 373\u003c\/p\u003e \u003cp\u003e13.3 Recent Progress in Organic RTP Materials 375\u003c\/p\u003e \u003cp\u003e13.3.1 Crystallization-induced RTP 375\u003c\/p\u003e \u003cp\u003e13.3.1.1 Heavy Atom Effect 376\u003c\/p\u003e \u003cp\u003e13.3.1.2 Molecular Interaction 380\u003c\/p\u003e \u003cp\u003e13.3.1.3 H-aggregation 380\u003c\/p\u003e \u003cp\u003e13.3.2 Doping in Rigid Matrix-induced RTP 382\u003c\/p\u003e \u003cp\u003e13.3.2.1 Host–Guest System 385\u003c\/p\u003e \u003cp\u003e13.3.2.2 Doping in Polymer Matrix 387\u003c\/p\u003e \u003cp\u003e13.3.3 Clustering-triggered RTP 389\u003c\/p\u003e \u003cp\u003e13.3.3.1 Natural Products 389\u003c\/p\u003e \u003cp\u003e13.3.3.2 Synthetic Compounds 394\u003c\/p\u003e \u003cp\u003e13.3.4 Other Systems 399\u003c\/p\u003e \u003cp\u003e13.3.4.1 Amorphous Organics 399\u003c\/p\u003e \u003cp\u003e13.3.4.2 Organic Framework 399\u003c\/p\u003e \u003cp\u003e13.3.4.3 Supramolecular Organics 402\u003c\/p\u003e \u003cp\u003e13.3.4.4 Hybrid Perovskites 403\u003c\/p\u003e \u003cp\u003e13.3.5 Applications 405\u003c\/p\u003e \u003cp\u003e13.4 Conclusions and Perspectives 405\u003c\/p\u003e \u003cp\u003eReferences 407\u003c\/p\u003e \u003cp\u003e\u003cb\u003e14 A Global Potential Energy Surface Approach to the Photophysics of AIEgens: The Role of Conical Intersections \u003c\/b\u003e\u003cb\u003e411\u003cbr\u003e\u003c\/b\u003e\u003ci\u003eRachel Crespo-Otero and Lluís Blancafort\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e14.1 Introduction 411\u003c\/p\u003e \u003cp\u003e14.2 Methodological Aspects 412\u003c\/p\u003e \u003cp\u003e14.2.1 Intramolecular Restriction Models and the FGR-based Approach 412\u003c\/p\u003e \u003cp\u003e14.2.2 A PES-based Description of Photochemical Mechanisms 412\u003c\/p\u003e \u003cp\u003e14.2.3 Computational Approaches for Excited States 416\u003c\/p\u003e \u003cp\u003e14.2.3.1 Electronic Structure Methods for Excited States 416\u003c\/p\u003e \u003cp\u003e14.2.3.2 Dynamics Simulations in the Context of AIE 420\u003c\/p\u003e \u003cp\u003e14.2.4 Methods for Large Systems 420\u003c\/p\u003e \u003cp\u003e14.3 CI-centered Global PES for AIEgens 424\u003c\/p\u003e \u003cp\u003e14.3.1 Double-bond Torsion 424\u003c\/p\u003e \u003cp\u003e14.3.2 Double-bond Torsion \u003ci\u003evs \u003c\/i\u003eCyclization in TPE Derivatives 428\u003c\/p\u003e \u003cp\u003e14.3.3 Excited-state Intramolecular Proton Transfer (ESIPT) Compounds 431\u003c\/p\u003e \u003cp\u003e14.3.4 Ring Puckering 432\u003c\/p\u003e \u003cp\u003e14.3.5 Bond Stretching 435\u003c\/p\u003e \u003cp\u003e14.3.6 A View of AIE Based on the RACI Model and the Global PES 436\u003c\/p\u003e \u003cp\u003e14.4 Crystallization-induced Phosphorescence 436\u003c\/p\u003e \u003cp\u003e14.5 Effect of Intermolecular and Intramolecular Interactions on the Photophysics of AIEgens 437\u003c\/p\u003e \u003cp\u003e14.5.1 Excitonic Effects in AIE 437\u003c\/p\u003e \u003cp\u003e14.5.2 Effect of Intramolecular and Intermolecular Interactions on Emission Color 439\u003c\/p\u003e \u003cp\u003e14.6 New Challenges 439\u003c\/p\u003e \u003cp\u003e14.6.1 The Role of Dark States in AIE 439\u003c\/p\u003e \u003cp\u003e14.6.2 Pressure-induced Emission Enhancement 440\u003c\/p\u003e \u003cp\u003e14.6.3 AIE in Transition Metal (TM) Compounds 442\u003c\/p\u003e \u003cp\u003e14.7 Conclusions and Outlook 443\u003c\/p\u003e \u003cp\u003eReferences 444\u003c\/p\u003e \u003cp\u003e\u003cb\u003e15 Multicomponent Reactions as Synthetic Design Tools of AIE and Emission Solvatochromic Quinoxalines \u003c\/b\u003e\u003cb\u003e455\u003cbr\u003e\u003c\/b\u003e\u003ci\u003eLukas Biesen and Thomas J. J. Müller\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e15.1 Introduction 455\u003c\/p\u003e \u003cp\u003e15.2 Synthetic Approaches to Quinoxalines via Multicomponent Reactions and One-Pot Processes 456\u003c\/p\u003e \u003cp\u003e15.3 Photophysical Properties and Emission Solvatochromicity of Quinoxalines 462\u003c\/p\u003e \u003cp\u003e15.4 AIE Characteristics and Effects of Quinoxalines 468\u003c\/p\u003e \u003cp\u003e15.5 Conclusion 476\u003c\/p\u003e \u003cp\u003eAcknowledgments 476\u003c\/p\u003e \u003cp\u003eReferences 476\u003c\/p\u003e \u003cp\u003e\u003cb\u003e16 Aggregation-induced Emission Luminogens with Both High-luminescence Efficiency and Charge Mobility \u003c\/b\u003e\u003cb\u003e485\u003cbr\u003e\u003c\/b\u003e\u003ci\u003eYing Yu, Zheng Zhao, and Ben Zhong Tang\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e16.1 Introduction 485\u003c\/p\u003e \u003cp\u003e16.2 p-Type OSCs 487\u003c\/p\u003e \u003cp\u003e16.3 n-Type OSCs 495\u003c\/p\u003e \u003cp\u003e16.4 Ambipolar OSCs 500\u003c\/p\u003e \u003cp\u003e16.5 Conclusion and Perspective 505\u003c\/p\u003e \u003cp\u003eReferences 505\u003c\/p\u003e \u003cp\u003e\u003cb\u003e17 Morphology Modulation of Aggregation-induced Emission: From Thermodynamic Self-assembly to Kinetic Controlling \u003c\/b\u003e\u003cb\u003e509\u003cbr\u003e\u003c\/b\u003e\u003ci\u003eKaizhi Gu, Chenxu Yan, Zhiqian Guo, and Wei-Hong Zhu\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e17.1 Introduction 509\u003c\/p\u003e \u003cp\u003e17.2 Aggregation Modulation of AIE Bioprobes via Hydrophilicity Improvement 511\u003c\/p\u003e \u003cp\u003e17.2.1 Molecular Modification 511\u003c\/p\u003e \u003cp\u003e17.2.2 Polymerization with Hydrophilic Matrix 515\u003c\/p\u003e \u003cp\u003e17.3 Thermodynamic Self-assembly of AIE Materials 519\u003c\/p\u003e \u003cp\u003e17.4 Morphology Tuning of AIE Nanoaggregates 519\u003c\/p\u003e \u003cp\u003e17.5 Kinetic-driven Preparation of AIE NPs 523\u003c\/p\u003e \u003cp\u003e17.6 Conclusion and Outlook 527\u003c\/p\u003e \u003cp\u003eReferences 527\u003c\/p\u003e \u003cp\u003e\u003cb\u003e18 AIE-active Polymer \u003c\/b\u003e\u003cb\u003e531\u003cbr\u003e\u003c\/b\u003e\u003ci\u003eRong Hu, Anjun Qin, and Ben Zhong Tang\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e18.1 Introduction 531\u003c\/p\u003e \u003cp\u003e18.2 Photophysical Properties 532\u003c\/p\u003e \u003cp\u003e18.2.1 Quantum Yield 532\u003c\/p\u003e \u003cp\u003e18.2.2 Photosensitization 536\u003c\/p\u003e \u003cp\u003e18.2.3 Two-photon Absorption and Emission 538\u003c\/p\u003e \u003cp\u003e18.2.4 Circularly Polarized Luminescence 540\u003c\/p\u003e \u003cp\u003e18.3 Applications 541\u003c\/p\u003e \u003cp\u003e18.3.1 Chem-sensor 541\u003c\/p\u003e \u003cp\u003e18.3.2 Bioimaging 543\u003c\/p\u003e \u003cp\u003e18.3.3 Therapy Applications 546\u003c\/p\u003e \u003cp\u003e18.4 Conclusion and Perspective 549\u003c\/p\u003e \u003cp\u003eAcknowledgments 550\u003c\/p\u003e \u003cp\u003eReferences 550\u003c\/p\u003e \u003cp\u003e\u003cb\u003e19 Liquid-crystalline AIEgens: Materials and Applications \u003c\/b\u003e\u003cb\u003e555\u003cbr\u003e\u003c\/b\u003e\u003ci\u003eKyohei Hisano, Supattra Panthai, and Osamu Tsutsumi\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e19.1 Introduction 555\u003c\/p\u003e \u003cp\u003e19.2 Materials: Molecular Design 556\u003c\/p\u003e \u003cp\u003e19.2.1 Discotic LC AIEgen 556\u003c\/p\u003e \u003cp\u003e19.2.2 Calamitic LC AIEgens 561\u003c\/p\u003e \u003cp\u003e19.2.3 Polymeric LC AIEgens 566\u003c\/p\u003e \u003cp\u003e19.3 Applications of LC AIEgens 567\u003c\/p\u003e \u003cp\u003e19.3.1 Linearly Polarized Luminescence 567\u003c\/p\u003e \u003cp\u003e19.3.2 Circularly Polarized Luminescence 568\u003c\/p\u003e \u003cp\u003e19.4 Conclusion 571\u003c\/p\u003e \u003cp\u003eReferences 571\u003c\/p\u003e \u003cp\u003e\u003cb\u003e20 Push–Pull AIEgens \u003c\/b\u003e\u003cb\u003e575\u003cbr\u003e\u003c\/b\u003e\u003ci\u003eAndrea Nitti and Dario Pasini\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e20.1 Introduction 575\u003c\/p\u003e \u003cp\u003e20.2 Basic Concept of Molecular Design 576\u003c\/p\u003e \u003cp\u003e20.2.1 Photophysical Excited States in Aggregates 576\u003c\/p\u003e \u003cp\u003e20.2.2 Fundamental Molecular Design to Achieve Push–Pull AIEgens 579\u003c\/p\u003e \u003cp\u003e20.3 Push–Pull AIEgens from Rotor Structure 581\u003c\/p\u003e \u003cp\u003e20.3.1 Double Bond Stator 582\u003c\/p\u003e \u003cp\u003e20.3.2 Point-restricted Rotors from Atoms or Functional Groups 584\u003c\/p\u003e \u003cp\u003e20.3.3 Aromatic Rotors 587\u003c\/p\u003e \u003cp\u003e20.4 Push–Pull AIEgens from ACQ Chromophores 589\u003c\/p\u003e \u003cp\u003e20.4.1 BT-based AIEgens 589\u003c\/p\u003e \u003cp\u003e20.4.2 Cyanine and DCM-based AIEgens 594\u003c\/p\u003e \u003cp\u003e20.4.3 QM-based AIEgens 595\u003c\/p\u003e \u003cp\u003e20.4.4 DPP-based AIEgens 597\u003c\/p\u003e \u003cp\u003e20.4.5 Rylene-based AIEgens 599\u003c\/p\u003e \u003cp\u003e20.5 Concluding Remarks 602\u003c\/p\u003e \u003cp\u003eReferences 602\u003c\/p\u003e \u003cp\u003eIndex 609\u003c\/p\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e","brand":"John Wiley \u0026 Sons Inc","offers":[{"title":"Default Title","offer_id":49407107400023,"sku":"9781119642916","price":178.16,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0817\/1739\/5799\/files\/9781119642916.jpg?v=1730498202","url":"https:\/\/bookcurl.com\/products\/handbook-of-aggregationinduced-emission-volume-1-9781119642916","provider":"Book Curl","version":"1.0","type":"link"}