Aggregation-induced emission : applications / / edited by Anjun Qin and Ben Zhong Tang

• Pubblicazione: Chichester, West Sussex : , : John Wiley & Sons, , 2013
• Descrizione fisica: 1 online resource (293 p.)
• Disciplina: 620.11295
• Soggetto topico: Electroluminescent devices; Optoelectronic devices
• Altri autori: QinAnjun TangBen Zhong
• Note generali: Description based upon print version of record.
• Nota di contenuto: Aggregation-Induced Emission: Applications; Contents; List of Contributors; Preface; 1 AIE or AIEE Materials for Electroluminescence Applications; 1.1 Introduction; 1.2 EL Background, EL Efficiency, Color Chromaticity, and Fabrication Issues of OLEDs; 1.3 AIE or AIEE Silole Derivatives for OLEDs; 1.4 AIE or AIEE Maleimide and Pyrrole Derivatives for OLEDs; 1.5 AIE or AIEE Cyano-Substituted Stilbenoid and Distyrylbenzene Derivatives for OLEDs; 1.6 AIE or AIEE Triarylamine Derivatives for OLEDs; 1.7 AIE or AIEE Triphenylethene and Tetraphenylethene Derivatives for OLEDs ; 1.8 White OLEDs Containing AIE or AIEE Materials1.9 Perspectives; References; 2 Crystallization-Induced Phosphorescence for Purely Organic Phosphors at Room Temperature and Liquid Crystals with Aggregation-Induced Emission Characteristics; 2.1 Crystallization-Induced Phosphorescence for Purely Organic Phosphors at Room Temperature; 2.1.1 Introduction; 2.1.2 Molecular luminogens with crystallization-induced phosphorescence at room temperature; 2.2 Liquid Crystals with Aggregation-Induced Emission Characteristics; 2.2.1 Luminescent liquid crystals ; 2.2.2 Aggregation-induced emission strategy towards high-efficiency luminescent liquid crystals2.3 Conclusions and Perspectives; References; 3 Mechanochromic Aggregation-Induced Emission Materials; 3.1 Introduction; 3.2 Mechanochromic Non-AIE Compounds; 3.3 Mechanochromic AIE Compounds; 3.4 Conclusion; References; 4 Chiral Recognition and Enantiomeric Excess Determination Based on Aggregation-Induced Emission; 4.1 Introduction to Chiral Recognition; 4.2 Chiral Recognition and Enantiomeric Excess Determination of Chiral Amines ; 4.3 Chiral Recognition and Enantiomeric Excess Determination of Chiral Acids4.3.1 Enantiomeric excess determination of chiral acids using chiral AIE amines; 4.3.2 Enantiomeric excess determination of chiral acids using a chiral receptor in the presence of an AIE compound; 4.4 Mechanism of Chiral Recognition Based on AIE; 4.4.1 Mechanism of chiral recognition by a chiral AIE monoamine; 4.4.2 Mechanism of chiral recognition by a chiral AIE diamine; 4.5 Prospects for Chiral Recognition Based on AIE; References ; 5 AIE Materials Towards Efficient Circularly Polarized Luminescence, Organic Lasing, and Superamplified Detection of Explosives5.1 Introduction; 5.2 AIE Materials with Efficient Circularly Polarized Luminescence and Large Dissymmetry Factor; 5.2.1 Aggregation-induced circular dichroism; 5.2.2 AIE, fluorescence decay dynamics and theoretical understanding; 5.2.3 Aggregation-induced circularly polarized luminescence; 5.2.4 Supramolecular assembly and structural modeling; 5.3 AIE Materials for Organic Lasing; 5.3.1 Fabrication of nano-structures; 5.3.2 Lasing performances ; 5.4 AIE Materials for Superamplified Detection of Explosives
• Sommario/riassunto: Aggregation-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
• Titolo autorizzato: Aggregation-induced emission
• ISBN: 1-118-70177-1; 1-118-70161-5; 1-118-70158-5
• Formato: Materiale a stampa
• Livello bibliografico: Monografia
• Lingua di pubblicazione: Inglese
• Record Nr.: 9910818071903321
• Lo trovi qui: Univ. Federico II