Info
- Utilizzare la checkbox di selezione a fianco di ciascun documento per attivare le funzionalità di stampa, invio email, download nei formati disponibili del (i) record.
Aggregation-induced emission : applications / / edited by Anjun Qin and Ben Zhong Tang
| Aggregation-induced emission : applications / / edited by Anjun Qin and Ben Zhong Tang |
| Pubbl/distr/stampa | Chichester, West Sussex : , : John Wiley & Sons, , 2013 |
| Descrizione fisica | 1 online resource (293 p.) |
| Disciplina | 620.11295 |
| Altri autori (Persone) |
QinAnjun
TangBen Zhong |
| Soggetto topico |
Electroluminescent devices
Optoelectronic devices |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-118-70177-1
1-118-70161-5 1-118-70158-5 |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| 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 |
| Record Nr. | UNINA-9910452505503321 |
| Chichester, West Sussex : , : John Wiley & Sons, , 2013 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Aggregation-induced emission : fundamentals / / edited by Anjun Qin and Ben Zhong Tang
| Aggregation-induced emission : fundamentals / / edited by Anjun Qin and Ben Zhong Tang |
| Pubbl/distr/stampa | Chichester, West Sussex, United Kingdom : , : John Wiley & Sons, , 2013 |
| Descrizione fisica | 1 online resource (442 p.) |
| Disciplina | 620.1/1295 |
| Altri autori (Persone) |
QinAnjun
TangBen Zhong |
| Soggetto topico |
Aggregation (Chemistry)
Electroluminescent devices Organosilicon compounds - Optical properties Photoemission |
| Soggetto genere / forma | Electronic books. |
| ISBN |
1-118-65395-5
1-118-65393-9 1-118-65394-7 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
""Aggregation-Induced Emission: Fundamentals""; ""Contents""; ""List of Contributors""; ""Preface""; ""1 Synthesis of Siloles (and Germoles) that Exhibit the AIE Effect""; ""1.1 Introduction""; ""1.2 Background""; ""1.3 Synthesis of Siloles""; ""1.3.1 Reductive dimerization of tolan""; ""1.3.2 Intramolecular cyclization of dialkynylsilanes""; ""1.3.3 Intramolecular cyclization of dialkynylsilanes utilizing borane reagents""; ""1.3.4 Synthesis of siloles using transition metal reagents""; ""1.4 Modification of Preformed Siloles""; ""1.4.1 Reactions at silicon centers""
""1.4.2 Reactions of a ring carbon center""""1.5 Related Germole Methodology""; ""1.5.1 Germoles produced by metathesis and exchange reactions""; ""1.5.2 Germoles from other methods""; ""1.5.3 Photoluminescence and AIE of germoles""; ""1.6 Metallaindenes and Metallafluorenes of Si and Ge""; ""1.6.1 Methods for the formation of silaindenes and germaindenes""; ""1.6.2 Methods for the formation of metallafluorenes""; ""1.7 Oligomers and Polymers of Metalloles and Benzene-Annulated Metalloles""; ""1.7.1 Oligomers that contain silole units connected at the 1,1- and 2,5-positions"" ""1.7.2 Polysiloles and silole polymers connected through 2,5-positions""""1.7.3 Polymers with silole pendants and hyperbranched polymers""; ""1.7.4 Polybenzosiloles and ladder polymers""; ""1.7.5 Polymers that contain silafluorenes""; ""1.7.6 Germoles in oligomers and polymers""; ""1.8 Summary and Future Directions""; ""References""; ""2 Aggregation-Induced Emission in Group 14 Metalloles (Siloles, Germoles, and Stannoles): Spectroscopic Considerations, Substituent Effects, and Applications""; ""2.1 Introduction""; ""2.1.1 The group 14 metalloles"" ""2.2 Characteristics of AIE in the Group 14 Metalloles""""2.2.1 Aryl-substituted siloles""; ""2.2.2 Aryl-substituted germoles and stannoles""; ""2.3 Origins of AIE in Group 14 Metalloles: Restricted Intramolecular Rotation""; ""2.3.1 Effect of solvent viscosity""; ""2.3.2 Effect of temperature""; ""2.3.3 Room-temperature glasses""; ""2.3.4 Effect of pressure""; ""2.3.5 Excited-state lifetimes""; ""2.3.6 Molecular geometry""; ""2.3.7 Aggregate nanoparticle morphology""; ""2.3.8 Internal structural control of intramolecular rotations""; ""2.4 Polymer Films and Polymerized Siloles"" ""2.5 Applications of AIE-Active Metalloles""""2.5.1 Electrooptical devices""; ""2.5.2 Chemical sensors""; ""References""; ""3 Aggregation-Induced Emission of 9,10-Distyrylanthracene Derivatives and Their Applications""; ""3.1 Introduction""; ""3.2 AIE Molecules Based on 9,10-Distyrylanthracene""; ""3.2.1 Small molecules""; ""3.2.2 Macromolecules""; ""3.3 AIE Mechanism of 9,10-Distyrylanthracene Molecule Systems""; ""3.4 Application of AIE Luminogens Based on 9,10-Distyrylanthracene""; ""3.4.1 Solid-state emitters""; ""3.4.2 Piezochromism""; ""3.4.3 Fluorescent sensors and probes"" ""3.4.4 Bioimaging"" |
| Record Nr. | UNINA-9910452889803321 |
| Chichester, West Sussex, United Kingdom : , : John Wiley & Sons, , 2013 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Aggregation-induced emission : fundamentals / / edited by Anjun Qin and Ben Zhong Tang
| Aggregation-induced emission : fundamentals / / edited by Anjun Qin and Ben Zhong Tang |
| Pubbl/distr/stampa | Chichester, West Sussex, United Kingdom : , : John Wiley & Sons, , 2013 |
| Descrizione fisica | 1 online resource (442 p.) |
| Disciplina | 620.1/1295 |
| Altri autori (Persone) |
QinAnjun
TangBen Zhong |
| Soggetto topico |
Aggregation (Chemistry)
Electroluminescent devices Organosilicon compounds - Optical properties Photoemission |
| ISBN |
1-118-65395-5
1-118-65393-9 1-118-65394-7 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
""Aggregation-Induced Emission: Fundamentals""; ""Contents""; ""List of Contributors""; ""Preface""; ""1 Synthesis of Siloles (and Germoles) that Exhibit the AIE Effect""; ""1.1 Introduction""; ""1.2 Background""; ""1.3 Synthesis of Siloles""; ""1.3.1 Reductive dimerization of tolan""; ""1.3.2 Intramolecular cyclization of dialkynylsilanes""; ""1.3.3 Intramolecular cyclization of dialkynylsilanes utilizing borane reagents""; ""1.3.4 Synthesis of siloles using transition metal reagents""; ""1.4 Modification of Preformed Siloles""; ""1.4.1 Reactions at silicon centers""
""1.4.2 Reactions of a ring carbon center""""1.5 Related Germole Methodology""; ""1.5.1 Germoles produced by metathesis and exchange reactions""; ""1.5.2 Germoles from other methods""; ""1.5.3 Photoluminescence and AIE of germoles""; ""1.6 Metallaindenes and Metallafluorenes of Si and Ge""; ""1.6.1 Methods for the formation of silaindenes and germaindenes""; ""1.6.2 Methods for the formation of metallafluorenes""; ""1.7 Oligomers and Polymers of Metalloles and Benzene-Annulated Metalloles""; ""1.7.1 Oligomers that contain silole units connected at the 1,1- and 2,5-positions"" ""1.7.2 Polysiloles and silole polymers connected through 2,5-positions""""1.7.3 Polymers with silole pendants and hyperbranched polymers""; ""1.7.4 Polybenzosiloles and ladder polymers""; ""1.7.5 Polymers that contain silafluorenes""; ""1.7.6 Germoles in oligomers and polymers""; ""1.8 Summary and Future Directions""; ""References""; ""2 Aggregation-Induced Emission in Group 14 Metalloles (Siloles, Germoles, and Stannoles): Spectroscopic Considerations, Substituent Effects, and Applications""; ""2.1 Introduction""; ""2.1.1 The group 14 metalloles"" ""2.2 Characteristics of AIE in the Group 14 Metalloles""""2.2.1 Aryl-substituted siloles""; ""2.2.2 Aryl-substituted germoles and stannoles""; ""2.3 Origins of AIE in Group 14 Metalloles: Restricted Intramolecular Rotation""; ""2.3.1 Effect of solvent viscosity""; ""2.3.2 Effect of temperature""; ""2.3.3 Room-temperature glasses""; ""2.3.4 Effect of pressure""; ""2.3.5 Excited-state lifetimes""; ""2.3.6 Molecular geometry""; ""2.3.7 Aggregate nanoparticle morphology""; ""2.3.8 Internal structural control of intramolecular rotations""; ""2.4 Polymer Films and Polymerized Siloles"" ""2.5 Applications of AIE-Active Metalloles""""2.5.1 Electrooptical devices""; ""2.5.2 Chemical sensors""; ""References""; ""3 Aggregation-Induced Emission of 9,10-Distyrylanthracene Derivatives and Their Applications""; ""3.1 Introduction""; ""3.2 AIE Molecules Based on 9,10-Distyrylanthracene""; ""3.2.1 Small molecules""; ""3.2.2 Macromolecules""; ""3.3 AIE Mechanism of 9,10-Distyrylanthracene Molecule Systems""; ""3.4 Application of AIE Luminogens Based on 9,10-Distyrylanthracene""; ""3.4.1 Solid-state emitters""; ""3.4.2 Piezochromism""; ""3.4.3 Fluorescent sensors and probes"" ""3.4.4 Bioimaging"" |
| Record Nr. | UNINA-9910790420203321 |
| Chichester, West Sussex, United Kingdom : , : John Wiley & Sons, , 2013 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Aggregation-induced emission : applications / / edited by Anjun Qin and Ben Zhong Tang
| Aggregation-induced emission : applications / / edited by Anjun Qin and Ben Zhong Tang |
| Pubbl/distr/stampa | Chichester, West Sussex : , : John Wiley & Sons, , 2013 |
| Descrizione fisica | 1 online resource (293 p.) |
| Disciplina | 620.11295 |
| Altri autori (Persone) |
QinAnjun
TangBen Zhong |
| Soggetto topico |
Electroluminescent devices
Optoelectronic devices |
| ISBN |
1-118-70177-1
1-118-70161-5 1-118-70158-5 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| 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 |
| Record Nr. | UNINA-9910790546203321 |
| Chichester, West Sussex : , : John Wiley & Sons, , 2013 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Aggregation-induced emission : applications / / edited by Anjun Qin and Ben Zhong Tang
| Aggregation-induced emission : applications / / edited by Anjun Qin and Ben Zhong Tang |
| Pubbl/distr/stampa | Chichester, West Sussex : , : John Wiley & Sons, , 2013 |
| Descrizione fisica | 1 online resource (293 p.) |
| Disciplina | 620.11295 |
| Altri autori (Persone) |
QinAnjun
TangBen Zhong |
| Soggetto topico |
Electroluminescent devices
Optoelectronic devices |
| ISBN |
1-118-70177-1
1-118-70161-5 1-118-70158-5 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| 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 |
| Record Nr. | UNINA-9910818071903321 |
| Chichester, West Sussex : , : John Wiley & Sons, , 2013 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Aggregation-induced emission : fundamentals / / edited by Anjun Qin and Ben Zhong Tang
| Aggregation-induced emission : fundamentals / / edited by Anjun Qin and Ben Zhong Tang |
| Pubbl/distr/stampa | Chichester, West Sussex, United Kingdom : , : John Wiley & Sons, , 2013 |
| Descrizione fisica | 1 online resource (442 p.) |
| Disciplina | 620.1/1295 |
| Altri autori (Persone) |
QinAnjun
TangBen Zhong |
| Soggetto topico |
Aggregation (Chemistry)
Electroluminescent devices Organosilicon compounds - Optical properties Photoemission |
| ISBN |
1-118-65395-5
1-118-65393-9 1-118-65394-7 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
""Aggregation-Induced Emission: Fundamentals""; ""Contents""; ""List of Contributors""; ""Preface""; ""1 Synthesis of Siloles (and Germoles) that Exhibit the AIE Effect""; ""1.1 Introduction""; ""1.2 Background""; ""1.3 Synthesis of Siloles""; ""1.3.1 Reductive dimerization of tolan""; ""1.3.2 Intramolecular cyclization of dialkynylsilanes""; ""1.3.3 Intramolecular cyclization of dialkynylsilanes utilizing borane reagents""; ""1.3.4 Synthesis of siloles using transition metal reagents""; ""1.4 Modification of Preformed Siloles""; ""1.4.1 Reactions at silicon centers""
""1.4.2 Reactions of a ring carbon center""""1.5 Related Germole Methodology""; ""1.5.1 Germoles produced by metathesis and exchange reactions""; ""1.5.2 Germoles from other methods""; ""1.5.3 Photoluminescence and AIE of germoles""; ""1.6 Metallaindenes and Metallafluorenes of Si and Ge""; ""1.6.1 Methods for the formation of silaindenes and germaindenes""; ""1.6.2 Methods for the formation of metallafluorenes""; ""1.7 Oligomers and Polymers of Metalloles and Benzene-Annulated Metalloles""; ""1.7.1 Oligomers that contain silole units connected at the 1,1- and 2,5-positions"" ""1.7.2 Polysiloles and silole polymers connected through 2,5-positions""""1.7.3 Polymers with silole pendants and hyperbranched polymers""; ""1.7.4 Polybenzosiloles and ladder polymers""; ""1.7.5 Polymers that contain silafluorenes""; ""1.7.6 Germoles in oligomers and polymers""; ""1.8 Summary and Future Directions""; ""References""; ""2 Aggregation-Induced Emission in Group 14 Metalloles (Siloles, Germoles, and Stannoles): Spectroscopic Considerations, Substituent Effects, and Applications""; ""2.1 Introduction""; ""2.1.1 The group 14 metalloles"" ""2.2 Characteristics of AIE in the Group 14 Metalloles""""2.2.1 Aryl-substituted siloles""; ""2.2.2 Aryl-substituted germoles and stannoles""; ""2.3 Origins of AIE in Group 14 Metalloles: Restricted Intramolecular Rotation""; ""2.3.1 Effect of solvent viscosity""; ""2.3.2 Effect of temperature""; ""2.3.3 Room-temperature glasses""; ""2.3.4 Effect of pressure""; ""2.3.5 Excited-state lifetimes""; ""2.3.6 Molecular geometry""; ""2.3.7 Aggregate nanoparticle morphology""; ""2.3.8 Internal structural control of intramolecular rotations""; ""2.4 Polymer Films and Polymerized Siloles"" ""2.5 Applications of AIE-Active Metalloles""""2.5.1 Electrooptical devices""; ""2.5.2 Chemical sensors""; ""References""; ""3 Aggregation-Induced Emission of 9,10-Distyrylanthracene Derivatives and Their Applications""; ""3.1 Introduction""; ""3.2 AIE Molecules Based on 9,10-Distyrylanthracene""; ""3.2.1 Small molecules""; ""3.2.2 Macromolecules""; ""3.3 AIE Mechanism of 9,10-Distyrylanthracene Molecule Systems""; ""3.4 Application of AIE Luminogens Based on 9,10-Distyrylanthracene""; ""3.4.1 Solid-state emitters""; ""3.4.2 Piezochromism""; ""3.4.3 Fluorescent sensors and probes"" ""3.4.4 Bioimaging"" |
| Record Nr. | UNINA-9910823111503321 |
| Chichester, West Sussex, United Kingdom : , : John Wiley & Sons, , 2013 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||