{"product_id":"aggregationinduced-emission-9781118394304","title":"AggregationInduced Emission","description":"\u003cb\u003eBook Synopsis\u003c\/b\u003e\u003cbr\u003eAggregation-Induced Emission (AIE) is a novel photophysical phenomenon which offers a new platformfor researchers to look into the light-emitting processes from luminogen aggregates, from which useful information on structureproperty relationships may be collected and mechanistic insights may be gained. The discovery of the AIE effect opens a new avenue for the development of new luminogen materials in the aggregate or solid state. By enabling light emission in the practically useful solid state, AIE has the potential to expand significantly the technological applications of luminescent materials.  \u003cp\u003e\u003ci\u003eAggregation-Induced Emission: Fundamentals\u003c\/i\u003e is the first book to explore the fundamental issues of AIE, including the design, synthesis, and photophysical behavior of AIE-active molecules and polymers. The control of the morphological structures of the aggregates of AIE-active materials, and the experimental investigation and theoretical understanding of the AIE mechanism, are also \u003cbr\u003e\u003cbr\u003e\u003cb\u003eTable of Contents\u003c\/b\u003e\u003cbr\u003e\u003c\/p\u003e\u003cp\u003eList of Contributors xiii\u003c\/p\u003e \u003cp\u003ePreface xvii\u003c\/p\u003e \u003cp\u003e\u003cb\u003e1 Synthesis of Siloles (and Germoles) that Exhibit the AIE Effect 1\u003c\/b\u003e\u003cbr\u003e \u003ci\u003eJoyce Y. Corey\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e1.1 Introduction 1\u003c\/p\u003e \u003cp\u003e1.2 Background 2\u003c\/p\u003e \u003cp\u003e1.3 Synthesis of Siloles 4\u003c\/p\u003e \u003cp\u003e1.4 Modification of Preformed Siloles 14\u003c\/p\u003e \u003cp\u003e1.5 Related Germole Methodology 15\u003c\/p\u003e \u003cp\u003e1.6 Metallaindenes and Metallafluorenes of Si and Ge 19\u003c\/p\u003e \u003cp\u003e1.7 Oligomers and Polymers of Metalloles and Benzene-Annulated Metalloles 25\u003c\/p\u003e \u003cp\u003e1.8 Summary and Future Directions 31\u003c\/p\u003e \u003cp\u003e\u003cb\u003e2 Aggregation-Induced Emission in Group 14 Metalloles (Siloles, Germoles, and Stannoles): Spectroscopic Considerations, Substituent Effects, and Applications 39\u003c\/b\u003e\u003cbr\u003e \u003ci\u003eJerome L. Mullin and Henry J. Tracy\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e2.1 Introduction 39\u003c\/p\u003e \u003cp\u003e2.2 Characteristics of AIE in the Group 14 Metalloles 44\u003c\/p\u003e \u003cp\u003e2.3 Origins of AIE in Group 14 Metalloles: Restricted Intramolecular Rotation 48\u003c\/p\u003e \u003cp\u003e2.4 Polymer Films and Polymerized Siloles 51\u003c\/p\u003e \u003cp\u003e2.5 Applications of AIE-Active Metalloles 53\u003c\/p\u003e \u003cp\u003e\u003cb\u003e3 Aggregation-Induced Emission of 9,10-Distyrylanthracene Derivatives and Their Applications 61\u003c\/b\u003e\u003cbr\u003e \u003ci\u003eBin Xu, Jibo Zhang and Wenjing Tian\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e3.1 Introduction 61\u003c\/p\u003e \u003cp\u003e3.2 AIE Molecules Based on 9,10-Distyrylanthracene 63\u003c\/p\u003e \u003cp\u003e3.3 AIE Mechanism of 9,10-Distyrylanthracene Molecule Systems 65\u003c\/p\u003e \u003cp\u003e3.4 Application of AIE Luminogens Based on 9,10-Distyrylanthracene 67\u003c\/p\u003e \u003cp\u003e3.5 Conclusion 80\u003c\/p\u003e \u003cp\u003e\u003cb\u003e4 Diaminobenzene-Cored Fluorophores Exhibiting Highly Efficient Solid-State Luminescence 83\u003c\/b\u003e\u003cbr\u003e \u003ci\u003eMasaki Shimizu\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e4.1 Introduction 83\u003c\/p\u003e \u003cp\u003e4.2 1,4-Bis(alkenyl)-2,5-dipiperidinobenzenes 86\u003c\/p\u003e \u003cp\u003e4.3 1,4-Diamino-2,5-bis(arylethenyl)benzenes 89\u003c\/p\u003e \u003cp\u003e4.4 2,5-Diaminoterephthalates 93\u003c\/p\u003e \u003cp\u003e4.5 2,5-Bis(diarylamino)-1,4-diaroylbenzenes 95\u003c\/p\u003e \u003cp\u003e4.6 Applications 99\u003c\/p\u003e \u003cp\u003e4.7 Conclusion 102\u003c\/p\u003e \u003cp\u003e\u003cb\u003e5 Aggregation-Induced Emission in Organic Ion Pairs 105\u003c\/b\u003e\u003cbr\u003e \u003ci\u003eSuzanne Fery-Forgues\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e5.1 Introduction 105\u003c\/p\u003e \u003cp\u003e5.2 Historical Background 106\u003c\/p\u003e \u003cp\u003e5.3 Preparation and Control of the Fluorophore Arrangement 107\u003c\/p\u003e \u003cp\u003e5.4 AIE-Active Organic Ion Pairs in Nano- and Microparticles 111\u003c\/p\u003e \u003cp\u003e5.5 Applications as Fluorescent Probes and Sensors for Analytical Purposes 115\u003c\/p\u003e \u003cp\u003e5.6 Perspectives 122\u003c\/p\u003e \u003cp\u003e\u003cb\u003e6 Aggregation-Induced Emission Materials: the Art of Conjugation and Rotation 127\u003c\/b\u003e\u003cbr\u003e \u003ci\u003eJing Huang, Qianqian Li and Zhen Li\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e6.1 Introduction 127\u003c\/p\u003e \u003cp\u003e6.2 Rotation and Conjugation in AIE Molecules 128\u003c\/p\u003e \u003cp\u003e6.3 Design of Functional Materials by Tuning the Conjugation Effect and Restricting Rotations 134\u003c\/p\u003e \u003cp\u003e6.4 Outlook 151\u003c\/p\u003e \u003cp\u003e\u003cb\u003e7 Red-Emitting AIE Materials 155\u003c\/b\u003e\u003cbr\u003e \u003ci\u003eXiao Yuan Shen, Anjun Qin and Jing Zhi Sun\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e7.1 Introduction 155\u003c\/p\u003e \u003cp\u003e7.2 Basic Principles of Molecular Design for Red-Emitting Materials 156\u003c\/p\u003e \u003cp\u003e7.3 Acquirement of Red-Emitting AIE Materials by Reconstruction of Traditional Red-Emitting Molecules 158\u003c\/p\u003e \u003cp\u003e7.4 Preparation of Red-Emitting Materials by Introduction of Electron Donors\/Acceptors into AIE-Active Molecules 162\u003c\/p\u003e \u003cp\u003e7.5 Outlook 164\u003c\/p\u003e \u003cp\u003e\u003cb\u003e8 Properties of Triarylamine Derivatives with AIE and Large Two-Photon Absorbing Cross-Sections 169\u003c\/b\u003e\u003cbr\u003e \u003ci\u003eJianli Hua, He Tian and Hao Zhang\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e8.1 Introduction 169\u003c\/p\u003e \u003cp\u003e8.2 Design and Synthesis of Triarylamine Derivatives with AIE and 2PA 170\u003c\/p\u003e \u003cp\u003e8.3 AIE Properties of Triarylamine Derivatives 170\u003c\/p\u003e \u003cp\u003e8.4 One-Photon and Two-Photon Absorption Properties of Triarylamine Derivatives with AIE 176\u003c\/p\u003e \u003cp\u003e8.5 Application of Triarylamine Materials with AIE and 2PA 180\u003c\/p\u003e \u003cp\u003e8.6 Conclusion 181\u003c\/p\u003e \u003cp\u003e\u003cb\u003e9 Photoisomerization and Light-Driven Fluorescence Enhancement of Azobenzene Derivatives 185\u003c\/b\u003e\u003cbr\u003e \u003ci\u003eMina Han and Yasuo Norikane\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e9.1 Introduction 185\u003c\/p\u003e \u003cp\u003e9.2 Photoisomerization and Fluorescence of Azobenzene Derivatives 186\u003c\/p\u003e \u003cp\u003e9.3 Aggregation-Induced Emission (AIE) 191\u003c\/p\u003e \u003cp\u003e9.4 Fluorescence from Azobenzene-Based Aggregates 193\u003c\/p\u003e \u003cp\u003e9.5 Conclusion 199\u003c\/p\u003e \u003cp\u003e\u003cb\u003e10 Supramolecular Structure and Aggregation-Induced Emission 205\u003c\/b\u003e\u003cbr\u003e \u003ci\u003eHongyu Zhang and Yue Wang\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e10.1 Introduction 205\u003c\/p\u003e \u003cp\u003e10.2 Hydrogen Bonding-Based Molecular Dimer and AIE 206\u003c\/p\u003e \u003cp\u003e10.3 Quinacridine Derivatives with 1D Aggregation-Induced Red Emission 210\u003c\/p\u003e \u003cp\u003e10.4 Multi-Stimuli-Responsive Fluorescence Switching of AIE\/AIEE Luminogens 217\u003c\/p\u003e \u003cp\u003e10.5 Pt Pt Interaction-Induced Emissive and Conductive 1D Crystals 222\u003c\/p\u003e \u003cp\u003e10.6 Conclusion 226\u003c\/p\u003e \u003cp\u003e\u003cb\u003e11 Aggregation-Induced Emission in Supramolecular p-Organogels 233\u003c\/b\u003e\u003cbr\u003e \u003ci\u003ePengchong Xue and Ran Lu\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e11.1 Introduction 233\u003c\/p\u003e \u003cp\u003e11.2 Organogels Based on Discotic Molecules with AIE 234\u003c\/p\u003e \u003cp\u003e11.3 Organogels Based on Rod-Like Molecules with AIE 238\u003c\/p\u003e \u003cp\u003e11.4 Organogels Based on Banana-Shaped Molecules with AIE 242\u003c\/p\u003e \u003cp\u003e11.5 Organogels Based on Dendritic Molecules with AIE 246\u003c\/p\u003e \u003cp\u003e11.6 Conclusion 249\u003c\/p\u003e \u003cp\u003e\u003cb\u003e12 AIE-Active Polymers 253\u003c\/b\u003e\u003cbr\u003e \u003ci\u003eRongrong Hu, Jacky W.Y. Lam and Ben Zhong Tang\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e12.1 Introduction 253\u003c\/p\u003e \u003cp\u003e12.2 Polyolefins 254\u003c\/p\u003e \u003cp\u003e12.3 Polyacetylenes 258\u003c\/p\u003e \u003cp\u003e12.4 Polydiynes 259\u003c\/p\u003e \u003cp\u003e12.5 Polyarylenes 263\u003c\/p\u003e \u003cp\u003e12.6 Polytriazoles 269\u003c\/p\u003e \u003cp\u003e12.7 Polysilylenevinylenes 271\u003c\/p\u003e \u003cp\u003e12.8 Poly(Vinylene Sulfide)s 272\u003c\/p\u003e \u003cp\u003e12.9 Other Systems 277\u003c\/p\u003e \u003cp\u003e12.10 Conclusion 280\u003c\/p\u003e \u003cp\u003e\u003cb\u003e13 Enhanced Emission by Restriction of Molecular Rotation 285\u003c\/b\u003e\u003cbr\u003e \u003ci\u003eJin-Long Hong\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e13.1 Background 285\u003c\/p\u003e \u003cp\u003e13.2 Strategy to Restrict Molecular Rotation 286\u003c\/p\u003e \u003cp\u003e13.3 Characterizations of Hindered Molecular Rotations 297\u003c\/p\u003e \u003cp\u003e13.4 Conclusion 302\u003c\/p\u003e \u003cp\u003e\u003cb\u003e14 Restricted Intramolecular Rotations: a Mechanism for Aggregation-Induced Emission 307\u003c\/b\u003e\u003cbr\u003e \u003ci\u003eJunwu Chen and Ben Zhong Tang\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e14.1 Introduction: 2,3,4,5-Tetraphenylsilole, the Prototype Molecule of Aggregation-Induced Emission (AIE) 307\u003c\/p\u003e \u003cp\u003e14.2 Crystal Structures of 2,3,4,5-Tetraphenylsiloles 310\u003c\/p\u003e \u003cp\u003e14.3 Restricted Intramolecular Rotation (RIR) 312\u003c\/p\u003e \u003cp\u003e14.4 Conclusion 320\u003c\/p\u003e \u003cp\u003e\u003cb\u003e15 Crystallization-Induced Emission Enhancement 323\u003c\/b\u003e\u003cbr\u003e \u003ci\u003eYongqiang Dong\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e15.1 Introduction 323\u003c\/p\u003e \u003cp\u003e15.2 Traditional Luminogens 324\u003c\/p\u003e \u003cp\u003e15.3 Crystallization-Induced Emission Enhancement (CIEE) 324\u003c\/p\u003e \u003cp\u003e15.4 Conclusion 333\u003c\/p\u003e \u003cp\u003e\u003cb\u003e16 Time-Resolved Spectroscopic Study of the Aggregation-Induced Emission Mechanism 337\u003c\/b\u003e\u003cbr\u003e \u003ci\u003eBing-rong Gao, Hai-yu Wang, Qi-dai Chen and Hong-bo Sun\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e16.1 Introduction 337\u003c\/p\u003e \u003cp\u003e16.2 Time-Resolved Spectroscopy 338\u003c\/p\u003e \u003cp\u003e16.3 AIE Molecules Without Electron Donor–Acceptor Units 341\u003c\/p\u003e \u003cp\u003e16.4 AIE Molecules with Electron Donor–Acceptor Units 344\u003c\/p\u003e \u003cp\u003e16.5 Conclusion 353\u003c\/p\u003e \u003cp\u003e\u003cb\u003e17 Theoretical Understanding of AIE Phenomena Through Computational Chemistry 357\u003c\/b\u003e\u003cbr\u003e \u003ci\u003eQian Peng, Yingli Niu, Qunyan Wu, Xing Gao and Zhigang Shuai\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e17.1 Introduction 357\u003c\/p\u003e \u003cp\u003e17.2 Fundamental Photophysics Relating to AIE Phenomena 358\u003c\/p\u003e \u003cp\u003e17.3 Computational Approaches to Investigate AIE Molecules 360\u003c\/p\u003e \u003cp\u003e17.4 Computational Results 370\u003c\/p\u003e \u003cp\u003e17.5 Summary and Outlook 389\u003c\/p\u003e \u003cp\u003e\u003cb\u003e18 Recent Theoretical Advances in Understanding the Mechanism of Aggregation-Induced Emission for Small Organic Molecules 399\u003c\/b\u003e\u003cbr\u003e \u003ci\u003eJun-Ling Jin, Yun Geng and Zhong-Min Su\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e18.1 Introduction 399\u003c\/p\u003e \u003cp\u003e18.2 Theoretical Methods 400\u003c\/p\u003e \u003cp\u003e18.3 Recent Theoretical Advances in Understanding the Mechanism of Aggregation-Induced Emission 406\u003c\/p\u003e \u003cp\u003e18.4 Prospects 413\u003c\/p\u003e \u003cp\u003eAcknowledgments 414\u003c\/p\u003e \u003cp\u003eReferences 414\u003c\/p\u003e \u003cp\u003eIndex 419\u003c\/p\u003e","brand":"John Wiley \u0026 Sons Inc","offers":[{"title":"Default Title","offer_id":49528827904343,"sku":"9781118394304","price":158.95,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0817\/1739\/5799\/files\/9781118394304.jpg?v=1731873175","url":"https:\/\/bookcurl.com\/products\/aggregationinduced-emission-9781118394304","provider":"Book Curl","version":"1.0","type":"link"}