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Photopolymerisation initiating systems /
An update on the latest developments in the research of photoinitiating systems along with their applications.
| Clasificación: | Libro Electrónico |
|---|---|
| Otros Autores: | , |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
Cambridge :
Royal Society of Chemistry,
2018
|
| Colección: | RSC polymer chemistry series ;
29. |
| Temas: | |
| Acceso en línea: | Texto completo |
MARC
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| 245 | 0 | 0 | |a Photopolymerisation initiating systems / |c editors: Jacques Lalevée, Jean-Pierre Fouassier. |
| 264 | 1 | |a Cambridge : |b Royal Society of Chemistry, |c 2018 | |
| 300 | |a 1 online resource (586 pages) | ||
| 336 | |a text |b txt |2 rdacontent | ||
| 337 | |a computer |b c |2 rdamedia | ||
| 338 | |a online resource |b cr |2 rdacarrier | ||
| 490 | 1 | |a Polymer chemistry series ; |v 29 | |
| 500 | |a Includes index. | ||
| 500 | |a Title from title details screen. | ||
| 505 | 0 | |a Cover; Preface; References; Contents; Chapter 1 Thioxanthone Photoinitiators with Heterocyclic Extended Chromophores; 1.1 Introduction; 1.2 Photophysical Properties of Heterocyclic Extended Thioxanthones; 1.3 Reactivity of Heterocyclic Extended Thioxanthones; 1.4 Photopolymerization of Acrylates UsingHeterocyclic Extended Thioxanthones as Photoinitiators for Free Radical Polymerization; 1.5 Conclusions; References; Chapter 2 Long-wavelength-sensitive Radical Photoinitiators; 2.1 Introduction; 2.2 Long-wavelength Chromophores Acting via Photoreducible Mechanism | |
| 505 | 8 | |a 2.2.1 Photosensitization of Borate Salts2.2.2 Photosensitization of Amines; 2.3 Long-wavelength Chromophores Acting via Photooxidizable Mechanism; 2.3.1 Photosensitization of Borate Salts; 2.3.2 Photosensitization of Iodonium Salts; 2.3.3 Photosensitization of N-Alkoxypyridinium Salts; 2.3.4 Photosensitization of 1,3,5-Triazine Derivatives; 2.3.5 Photosensitization of Silane Compounds; 2.3.6 Long-wavelength Chromophore-UV Photoinitiator Dyads; 2.3.7 Panchromatic Chromophores; 2.3.8 Electron-transfer Photosensitization; 2.4 Conclusions; Abbreviations; References | |
| 505 | 8 | |a Chapter 3 Cationic Photoinitiators3.1 Introduction; 3.2 Application of Photopolymerization Processes; 3.3 Comparison of Cationic Photopolymerization with Different Types of Photochemically Initiated Processes; 3.4 Monomers Used in the Process of Cationic Polymerization; 3.5 Cationic Photoinitiators; 3.5.1 Onium Salts as Cationic Photoinitiators; 3.5.2 Other Initiators of Cationic Polymerization; 3.5.3 Indirect Photoinitiation of Cationic Photopolymerization Processes; 3.6 Conclusion; Acknowledgements; References; Chapter 4 Monomeric and Polymeric Photoinitiators; 4.1 Motivation and Overview | |
| 505 | 8 | |a 4.1.1 Why Monomeric and Polymeric Photoinitiators?4.1.2 Overview: Photoinitiating and Polymerizable Groups; 4.2 Photoinitiators Derived from (Meth)acrylates; 4.2.1 RHMA-based MPIs and PPIs; 4.2.2 More (Meth)acrylate-based MPIs and PPIs; 4.3 Photoinitiators Derived from Maleimides; 4.4 Photoinitiators Derived from Polysiloxanes; 4.5 Photoinitiators Derived from Polyalkylethers; 4.6 Photoinitiators Derived from Biodegradable Polymers; 4.7 Potoinitiators Derived from Dendrimers/Hyperbranched Polymers; 4.8 Others; 4.9 Conclusion; References; Chapter 5 Photoinitiators for Blue to Red LED Exposures | |
| 505 | 8 | |a 5.1 Introduction5.2 Photoinitiators for Blue LED Exposure; 5.2.1 Camphorquinone; 5.2.2 Naphthalimide Derivatives; 5.2.3 Metal-based Complexes; 5.3 Photoinitiators for Green to Red LED Exposures; 5.4 Conclusions and Perspectives; Acknowledgements; References; Chapter 6 How to Design Novel Photoinitiators for Blue Light; 6.1 Introduction; 6.2 Molecular Orbital Calculations and Light Absorption Properties; 6.3 Free Radical Polymerization of Methacrylates Under Blue Light; 6.4 Stability of the Studied PISs in the Formulations; 6.5 Photobleaching of the Studied Formulations Under Blue Light | |
| 520 | |a An update on the latest developments in the research of photoinitiating systems along with their applications. | ||
| 590 | |a Knovel |b ACADEMIC - Chemistry & Chemical Engineering | ||
| 650 | 0 | |a Photopolymerization. | |
| 650 | 6 | |a Photopolymérisation. | |
| 650 | 7 | |a Polymer chemistry. |2 bicssc | |
| 650 | 7 | |a Materials science. |2 bicssc | |
| 650 | 7 | |a TECHNOLOGY & ENGINEERING |x Chemical & Biochemical. |2 bisacsh | |
| 650 | 7 | |a Photopolymerization. |2 fast |0 (OCoLC)fst01062090 | |
| 700 | 1 | |a Lalevée, Jacques, |e editor. | |
| 700 | 1 | |a Fouassier, Jean-Pierre, |d 1947- |e editor. | |
| 776 | 0 | 8 | |i Print version: |t Photopolymerisation initiating systems. |d Cambridge : Royal Society of Chemistry, 2018 |z 1782629629 |z 9781782629627 |w (OCoLC)1027810087 |
| 830 | 0 | |a RSC polymer chemistry series ; |v 29. | |
| 856 | 4 | 0 | |u https://appknovel.uam.elogim.com/kn/resources/kpPIS00001/toc |z Texto completo |
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| 938 | |a ProQuest Ebook Central |b EBLB |n EBL5509709 | ||
| 938 | |a EBSCOhost |b EBSC |n 1886882 | ||
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| 994 | |a 92 |b IZTAP | ||