{"product_id":"aggregation-induced-emission-isbn-9781118701768","title":"Aggregation-Induced Emission","description":"\u003cp\u003eEdited by the academic who first discovered this important phenomenon, \u003ci\u003eAggregation-Induced Emission\u003c\/i\u003e is the first book to cover the applications of Aggregation-Induced Emission. This groundbreaking text explores the high-tech applications of AIE materials in optoelectronic devices, chemical sensors, and biological probes. A valuable resource for scientists, physicists, and biological chemists, topics covered include: AIE materials for LEDs and lasers; mechanochromic AIE materials; new chemo- and biosensors based on AIE fluorophores; AIE dye-encapsulated nanoparticles for optical bioimaging; and chiral recognition and enantiomeric excess determination based on AIE.\u003c\/p\u003e  List of Contributors xi  \u003cp\u003ePreface xiii\u003c\/p\u003e \u003cp\u003e1 AIE or AIEE Materials for Electroluminescence Applications 1\u003c\/p\u003e \u003cp\u003eChiao-Wen Lin and Chin-Ti Chen\u003c\/p\u003e \u003cp\u003e1.1 Introduction 1\u003c\/p\u003e \u003cp\u003e1.2 EL Background, EL Efficiency, Color Chromaticity, and Fabrication Issues of OLEDs 2\u003c\/p\u003e \u003cp\u003e1.3 AIE or AIEE Silole Derivatives for OLEDs 7\u003c\/p\u003e \u003cp\u003e1.4 AIE or AIEE Maleimide and Pyrrole Derivatives for OLEDs 10\u003c\/p\u003e \u003cp\u003e1.5 AIE or AIEE Cyano-Substituted Stilbenoid and Distyrylbenzene Derivatives for OLEDs 14\u003c\/p\u003e \u003cp\u003e1.6 AIE or AIEE Triarylamine Derivatives for OLEDs 17\u003c\/p\u003e \u003cp\u003e1.7 AIE or AIEE Triphenylethene and Tetraphenylethene Derivatives for OLEDs 17\u003c\/p\u003e \u003cp\u003e1.8 White OLEDs Containing AIE or AIEE Materials 31\u003c\/p\u003e \u003cp\u003e1.9 Perspectives 36\u003c\/p\u003e \u003cp\u003eReferences 37\u003c\/p\u003e \u003cp\u003e2 Crystallization-Induced Phosphorescence for Purely Organic Phosphors at Room Temperature and Liquid Crystals with Aggregation-Induced Emission Characteristics 42\u003c\/p\u003e \u003cp\u003eWang Zhang Yuan, Yongming Zhang, and Ben Zhong Tang\u003c\/p\u003e \u003cp\u003e2.1 Crystallization-Induced Phosphorescence for Purely Organic Phosphors at Room Temperature 42\u003c\/p\u003e \u003cp\u003e2.1.1 Introduction 42\u003c\/p\u003e \u003cp\u003e2.1.2 Molecular luminogens with crystallization-induced phosphorescence at room temperature 43\u003c\/p\u003e \u003cp\u003e2.2 Liquid crystals with aggregation-induced emission characteristics 51\u003c\/p\u003e \u003cp\u003e2.2.1 Luminescent liquid crystals 51\u003c\/p\u003e \u003cp\u003e2.2.2 Aggregation-induced emission strategy towards high-efficiency luminescent liquid crystals 52\u003c\/p\u003e \u003cp\u003e2.3 Conclusions and Perspectives 56\u003c\/p\u003e \u003cp\u003eReferences 57\u003c\/p\u003e \u003cp\u003e3 Mechanochromic Aggregation-Induced Emission Materials 60\u003c\/p\u003e \u003cp\u003eZhenguo Chi and Jiarui Xu\u003c\/p\u003e \u003cp\u003e3.1 Introduction 60\u003c\/p\u003e \u003cp\u003e3.2 Mechanochromic Non-AIE Compounds 61\u003c\/p\u003e \u003cp\u003e3.3 Mechanochromic AIE Compounds 63\u003c\/p\u003e \u003cp\u003e3.4 Conclusion 81\u003c\/p\u003e \u003cp\u003eReferences 82\u003c\/p\u003e \u003cp\u003e4 Chiral Recognition and Enantiomeric Excess Determination Based on Aggregation-Induced Emission 86\u003c\/p\u003e \u003cp\u003eYan-Song Zheng\u003c\/p\u003e \u003cp\u003e4.1 Introduction to Chiral Recognition 86\u003c\/p\u003e \u003cp\u003e4.2 Chiral Recognition and Enantiomeric Excess Determination of Chiral Amines 87\u003c\/p\u003e \u003cp\u003e4.3 Chiral Recognition and Enantiomeric Excess Determination of Chiral Acids 90\u003c\/p\u003e \u003cp\u003e4.3.1 Enantiomeric excess determination of chiral acids using chiral AIE amines 90\u003c\/p\u003e \u003cp\u003e4.3.2 Enantiomeric excess determination of chiral acids using a chiral receptor in the presence of an AIE compound 97\u003c\/p\u003e \u003cp\u003e4.4 Mechanism of chiral recognition based on AIE 100\u003c\/p\u003e \u003cp\u003e4.4.1 Mechanism of chiral recognition by a chiral AIE monoamine 101\u003c\/p\u003e \u003cp\u003e4.4.2 Mechanism of chiral recognition by a chiral AIE diamine 101\u003c\/p\u003e \u003cp\u003e4.5 Prospects for chiral recognition based on AIE 103\u003c\/p\u003e \u003cp\u003eReferences 104\u003c\/p\u003e \u003cp\u003e5 AIE Materials Towards Efficient Circularly Polarized Luminescence, Organic Lasing, and Superamplified Detection of Explosives 106\u003c\/p\u003e \u003cp\u003eJianzhao Liu, Jacky W.Y. Lam, and Ben Zhong Tang\u003c\/p\u003e \u003cp\u003e5.1 Introduction 106\u003c\/p\u003e \u003cp\u003e5.2 AIE Materials with Efficient Circularly Polarized Luminescence and Large Dissymmetry Factor 106\u003c\/p\u003e \u003cp\u003e5.2.1 Aggregation-induced circular dichroism 107\u003c\/p\u003e \u003cp\u003e5.2.2 AIE, fluorescence decay dynamics and theoretical understanding 109\u003c\/p\u003e \u003cp\u003e5.2.3 Aggregation-induced circularly polarized luminescence 112\u003c\/p\u003e \u003cp\u003e5.2.4 Supramolecular assembly and structural modeling 114\u003c\/p\u003e \u003cp\u003e5.3 AIE Materials for Organic Lasing 117\u003c\/p\u003e \u003cp\u003e5.3.1 Fabrication of nano-structures 117\u003c\/p\u003e \u003cp\u003e5.3.2 Lasing performances 118\u003c\/p\u003e \u003cp\u003e5.4 AIE Materials for Superamplified Detection of Explosives 120\u003c\/p\u003e \u003cp\u003e5.4.1 Hyperbranched polymer-based sensor 121\u003c\/p\u003e \u003cp\u003e5.4.2 Mesoporous material-based sensor 126\u003c\/p\u003e \u003cp\u003e5.5 Conclusion 126\u003c\/p\u003e \u003cp\u003eReferences 127\u003c\/p\u003e \u003cp\u003e6 Aggregation-Induced Emission and Applications of Aryl-Substituted Pyrrole Derivatives 129\u003c\/p\u003e \u003cp\u003eBin Tong and Yuping Dong\u003c\/p\u003e \u003cp\u003e6.1 Introduction 129\u003c\/p\u003e \u003cp\u003e6.2 Luminescence Properties of Triphenylpyrrole Derivatives in the Aggregated State 130\u003c\/p\u003e \u003cp\u003e6.3 Applications 134\u003c\/p\u003e \u003cp\u003e6.4 Aggregation-Induced Emission of Pentaphenylpyrrole 145\u003c\/p\u003e \u003cp\u003e6.5 AIEE Mechanism of Pentaphenylpyrrole 148\u003c\/p\u003e \u003cp\u003e6.6 Conclusion 150\u003c\/p\u003e \u003cp\u003eReferences 150\u003c\/p\u003e \u003cp\u003e7 Biogenic Amine Sensing with Aggregation-Induced Emission-Active Tetraphenylethenes 154\u003c\/p\u003e \u003cp\u003eTakanobu Sanji and Masato Tanaka\u003c\/p\u003e \u003cp\u003e7.1 Introduction 154\u003c\/p\u003e \u003cp\u003e7.1.1 Biogenic amines 154\u003c\/p\u003e \u003cp\u003e7.1.2 Sensing methods for biogenic amines 154\u003c\/p\u003e \u003cp\u003e7.2 Fluorimetric Sensing of Biogenic Amines with AIE-Active TPEs 155\u003c\/p\u003e \u003cp\u003e7.2.1 Design for fluorimetric sensing of biogenic amines 155\u003c\/p\u003e \u003cp\u003e7.2.2 Sensing studies and statistical analysis 155\u003c\/p\u003e \u003cp\u003e7.2.3 Determination of histamine concentration 159\u003c\/p\u003e \u003cp\u003e7.2.4 Fluorimetric sensing of melamine with AIE-active TPEs 160\u003c\/p\u003e \u003cp\u003e7.3 Summary and Outlook 160\u003c\/p\u003e \u003cp\u003eReferences 161\u003c\/p\u003e \u003cp\u003e8 New Chemo-\/Biosensors with Silole and Tetraphenylethene Molecules Based on the Aggregation and Deaggregation Mechanism 162\u003c\/p\u003e \u003cp\u003eMing Wang, Guanxin Zhang, and Deqing Zhang\u003c\/p\u003e \u003cp\u003e8.1 Introduction 162\u003c\/p\u003e \u003cp\u003e8.2 Cation and Anion Sensors 163\u003c\/p\u003e \u003cp\u003e8.3 Fluorimetric Biosensors for Biomacromolecules 166\u003c\/p\u003e \u003cp\u003e8.4 Fluorimetric Assays for Enzymes 170\u003c\/p\u003e \u003cp\u003e8.5 Fluorimetric Detection of Physiologically Important Small Molecules 177\u003c\/p\u003e \u003cp\u003e8.6 Miscellaneous Sensors 180\u003c\/p\u003e \u003cp\u003e8.7 Conclusion and Outlook 182\u003c\/p\u003e \u003cp\u003eReferences 182\u003c\/p\u003e \u003cp\u003e9 Carbohydrate-Functionalized AIE-Active Molecules as Luminescent Probes for Biosensing 186\u003c\/p\u003e \u003cp\u003eQi Chen and Bao-Hang Han\u003c\/p\u003e \u003cp\u003e9.1 Introduction 186\u003c\/p\u003e \u003cp\u003e9.2 Carbohydrate-Bearing AIE-Active Molecules 187\u003c\/p\u003e \u003cp\u003e9.2.1 Carbohydrate-bearing siloles 188\u003c\/p\u003e \u003cp\u003e9.2.2 Carbohydrate-bearing phosphole oxides 189\u003c\/p\u003e \u003cp\u003e9.2.3 Carbohydrate-bearing tetraphenylethenes 190\u003c\/p\u003e \u003cp\u003e9.3 Luminescent Probes for Lectins 192\u003c\/p\u003e \u003cp\u003e9.4 Luminescent Probes for Enzymes 196\u003c\/p\u003e \u003cp\u003e9.5 Luminescent Probes for Viruses and Toxins 200\u003c\/p\u003e \u003cp\u003e9.6 Conclusion 202\u003c\/p\u003e \u003cp\u003eAcknowledgments 202\u003c\/p\u003e \u003cp\u003eReferences 202\u003c\/p\u003e \u003cp\u003e10 Aggregation-Induced Emission Dyes for In Vivo Functional Bioimaging 205\u003c\/p\u003e \u003cp\u003eJun Qian, Dan Wang, and Sailing He\u003c\/p\u003e \u003cp\u003e10.1 Introduction 205\u003c\/p\u003e \u003cp\u003e10.2 AIE Dyes for Macro In Vivo Functional Bioimaging 206\u003c\/p\u003e \u003cp\u003e10.2.1 AIE dye-encapsulated phospholipid–PEG nanomicelles 206\u003c\/p\u003e \u003cp\u003e10.2.2 AIE dye-encapsulated nanomicelles for SLN mapping of mice 206\u003c\/p\u003e \u003cp\u003e10.2.3 AIE dye-encapsulated nanomicelles for tumor targeting of mice 212\u003c\/p\u003e \u003cp\u003e10.2.4 Other types of AIE-nanoparticles for in vivo functional bioimaging 217\u003c\/p\u003e \u003cp\u003e10.3 Multiphoton-Induced Fluorescence from AIE Dyes and Applications in\u003c\/p\u003e \u003cp\u003eIn Vivo Functional Microscopic Imaging 219\u003c\/p\u003e \u003cp\u003e10.3.1 Two- and three-photon-induced fluorescence of AIE dyes 219\u003c\/p\u003e \u003cp\u003e10.3.2 AIE dye-encapsulated nanomicelles for two-photon blood vessel imaging\u003c\/p\u003e \u003cp\u003eof live mice 223\u003c\/p\u003e \u003cp\u003e10.3.3 AIE dye-encapsulated nanomicelles for two-photon brain imaging\u003c\/p\u003e \u003cp\u003eof live mice 226\u003c\/p\u003e \u003cp\u003e10.4 Summary and Perspectives 228\u003c\/p\u003e \u003cp\u003eAcknowledgments 230\u003c\/p\u003e \u003cp\u003eReferences 230\u003c\/p\u003e \u003cp\u003e11 Specific Light-Up Bioprobes with Aggregation-Induced Emission Characteristics for Protein Sensing 234\u003c\/p\u003e \u003cp\u003eJing Liang, Haibin Shi, Ben Zhong Tang, and Bin Liu\u003c\/p\u003e \u003cp\u003e11.1 Introduction 234\u003c\/p\u003e \u003cp\u003e11.2 In Vitro Detection of Integrin avb3 Using a TPS-Based Probe 235\u003c\/p\u003e \u003cp\u003e11.2.1 Detection mechanisms 236\u003c\/p\u003e \u003cp\u003e11.2.2 Synthesis and characterization of the TPS-2cRGD probe 236\u003c\/p\u003e \u003cp\u003e11.2.3 Detection of integrin in solutions 238\u003c\/p\u003e \u003cp\u003e11.2.4 In vitro sensing of integrin in cancer cells 239\u003c\/p\u003e \u003cp\u003e11.3 Real-Time Monitoring of Cell Apoptosis and Drug Screening with a TPE-Based Probe 240\u003c\/p\u003e \u003cp\u003e11.3.1 Design principles 240\u003c\/p\u003e \u003cp\u003e11.3.2 Synthesis and characterization of Ac-DEVEK-TPE probe 241\u003c\/p\u003e \u003cp\u003e11.3.3 Detection of caspase and kinetic study of caspase activities in solutions 242\u003c\/p\u003e \u003cp\u003e11.3.4 Imaging of cell apoptosis and screening of apoptosis-inducing agents 243\u003c\/p\u003e \u003cp\u003e11.4 In Vivo Monitoring of Cell Apoptosis and Drug Screening with PyTPE-Based Probe 246\u003c\/p\u003e \u003cp\u003e11.4.1 Working principles 246\u003c\/p\u003e \u003cp\u003e11.4.2 Synthesis and characterization of DEVD-PyTPE probe 247\u003c\/p\u003e \u003cp\u003e11.4.3 Monitoring of caspase activities in solutions 248\u003c\/p\u003e \u003cp\u003e11.4.4 In vitro and in vivo imaging of cell apoptosis 248\u003c\/p\u003e \u003cp\u003e11.5 Conclusion 250\u003c\/p\u003e \u003cp\u003eAcknowledgments 250\u003c\/p\u003e \u003cp\u003eReferences 251\u003c\/p\u003e \u003cp\u003e12 Applications of Aggregation-Induced Emission Materials in Biotechnology 254\u003c\/p\u003e \u003cp\u003eYuning Hong, Jacky W.Y. Lam, and Ben Zhong Tang\u003c\/p\u003e \u003cp\u003e12.1 Introduction 254\u003c\/p\u003e \u003cp\u003e12.2 AIE Materials for Nucleic Acid Studies 255\u003c\/p\u003e \u003cp\u003e12.2.1 Quantitation and gel visualization of DNA and RNA 255\u003c\/p\u003e \u003cp\u003e12.2.2 Specific probing of G-quadruplex DNA formation 257\u003c\/p\u003e \u003cp\u003e12.3 AIE Materials for Protein Studies 258\u003c\/p\u003e \u003cp\u003e12.3.1 Quantitation and PAGE staining of proteins 258\u003c\/p\u003e \u003cp\u003e12.3.2 Fluorescence immunoassay by AIE materials 261\u003c\/p\u003e \u003cp\u003e12.3.3 Monitoring of the unfolding\/refolding process of human serum albumin 261\u003c\/p\u003e \u003cp\u003e12.3.4 Monitoring and inhibition of amyloid fibrillation of insulin 262\u003c\/p\u003e \u003cp\u003e12.4 AIE Materials for Live Cell Imaging 264\u003c\/p\u003e \u003cp\u003e12.4.1 AIE bioprobes for long-term cell tracking 264\u003c\/p\u003e \u003cp\u003e12.4.2 AIE nanoparticles for cell staining 264\u003c\/p\u003e \u003cp\u003e12.5 Conclusion 266\u003c\/p\u003e \u003cp\u003eReferences 267\u003c\/p\u003e \u003cp\u003eIndex 271\u003c\/p\u003e \u003cp\u003e\u003cb\u003eANJUN QIN,\u003c\/b\u003e Department of Polymer Science and Engineering, Zhejiang University, China.\u003c\/p\u003e \u003cp\u003e\u003cb\u003eBEN ZHONG TANG,\u003c\/b\u003e Department of Chemistry, The Hong Kong University of Science and Technology, China.\u003c\/p\u003e \u003cp\u003eAggregation-Induced Emission (AIE) is a novel photophysical phenomenon which offers a new platform APPLICATIONS for researchers to look into the light-emitting processes from luminogen aggregates, from which useful information on structure–property 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 significantly expand the technological applications of luminescent materials.\u003c\/p\u003e \u003cp\u003e\u003ci\u003eAggregation-Induced Emission: Applications\u003c\/i\u003e is the first book to explore the high-tech applications of AIE luminogens, including technological utilizations of AIE materials in the areas of electroluminescence, mechanochromism, chiral recognition, ionic sensing, biomolecule detection, and cell imaging. Potential applications in room temperature phosphorescence, liquid crystals, circularly polarized luminescence, and organic lasing are also introduced in this volume.\u003c\/p\u003e \u003cp\u003eTopics covered include:\u003c\/p\u003e \u003cul\u003e \u003cli\u003eAIE materials for electroluminescence applications\u003c\/li\u003e \u003cli\u003eLiquid crystals with AIE characteristics\u003c\/li\u003e \u003cli\u003eMechanochromic AIE materials\u003c\/li\u003e \u003cli\u003eChiral recognition and enantiomeric differentiation based on AIE\u003c\/li\u003e \u003cli\u003eAIE and applications of aryl-substituted pyrrole derivatives\u003c\/li\u003e \u003cli\u003eNew chemo-\/biosensors with AIE-active molecules\u003c\/li\u003e \u003cli\u003eAIE luminogens for in vivo functional bioimaging\u003c\/li\u003e \u003cli\u003eApplications of AIE materials in biotechnology\u003c\/li\u003e \u003c\/ul\u003e \u003cp\u003eThis book is essential reading for scientists and engineers who are designing optoelectronic materials and biomedical sensors, and will also be of interest to academic researchers in materials science, physical and synthetic organic chemistry as well as physicists and biological chemists.\u003c\/p\u003e","brand":"Wiley","offers":[{"title":"Default Title","offer_id":47988706771173,"sku":"NP9781118701768","price":190.95,"currency_code":"USD","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1842\/7735\/files\/9781118701768.jpg?v=1761781269","url":"https:\/\/k12savings.com\/es\/products\/aggregation-induced-emission-isbn-9781118701768","provider":"K12savings","version":"1.0","type":"link"}