{"product_id":"aggregationinduced-emission-9781118701768","title":"AggregationInduced Emission","description":"\u003cb\u003eBook Synopsis\u003c\/b\u003e\u003cbr\u003e\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\u003cbr\u003e\u003cbr\u003e\u003cb\u003eTable of Contents\u003c\/b\u003e\u003cbr\u003eList 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","brand":"John Wiley \u0026 Sons Inc","offers":[{"title":"Default Title","offer_id":49528835211607,"sku":"9781118701768","price":999.99,"currency_code":"GBP","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0817\/1739\/5799\/files\/9781118701768.jpg?v=1731873208","url":"https:\/\/bookcurl.com\/products\/aggregationinduced-emission-9781118701768","provider":"Book Curl","version":"1.0","type":"link"}