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Initiators Based on Benzaldoximes: Bimolecular and Covalently Bound Systems
[Image: see text] Typical bimolecular photoinitiators (PIs) for radical polymerization of acrylates show only poor photoreactivity because of the undesired effect of back electron transfer. To overcome this limitation, PIs consisting of a benzaldoxime ester and various sensitizers based on aromatic...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3558022/ https://www.ncbi.nlm.nih.gov/pubmed/23378672 http://dx.doi.org/10.1021/ma301959n |
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author | Griesser, Markus Rosspeintner, Arnulf Dworak, Claudia Höfer, Michael Grabner, Gottfried Liska, Robert Gescheidt, Georg |
author_facet | Griesser, Markus Rosspeintner, Arnulf Dworak, Claudia Höfer, Michael Grabner, Gottfried Liska, Robert Gescheidt, Georg |
author_sort | Griesser, Markus |
collection | PubMed |
description | [Image: see text] Typical bimolecular photoinitiators (PIs) for radical polymerization of acrylates show only poor photoreactivity because of the undesired effect of back electron transfer. To overcome this limitation, PIs consisting of a benzaldoxime ester and various sensitizers based on aromatic ketones were introduced. The core of the photoinduced reactivity was established by laser flash photolysis, photo-CIDNP, and EPR experiments at short time scales. According to these results, the primarily formed iminyl radicals are not particularly active. The polymerization is predominantly initiated by C-centered radicals. Photo-DSC experiments show reactivities comparable to that of classical monomolecular type I PIs like Darocur 1173. |
format | Online Article Text |
id | pubmed-3558022 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-35580222013-01-31 Initiators Based on Benzaldoximes: Bimolecular and Covalently Bound Systems Griesser, Markus Rosspeintner, Arnulf Dworak, Claudia Höfer, Michael Grabner, Gottfried Liska, Robert Gescheidt, Georg Macromolecules [Image: see text] Typical bimolecular photoinitiators (PIs) for radical polymerization of acrylates show only poor photoreactivity because of the undesired effect of back electron transfer. To overcome this limitation, PIs consisting of a benzaldoxime ester and various sensitizers based on aromatic ketones were introduced. The core of the photoinduced reactivity was established by laser flash photolysis, photo-CIDNP, and EPR experiments at short time scales. According to these results, the primarily formed iminyl radicals are not particularly active. The polymerization is predominantly initiated by C-centered radicals. Photo-DSC experiments show reactivities comparable to that of classical monomolecular type I PIs like Darocur 1173. American Chemical Society 2012-11-01 2012-11-13 /pmc/articles/PMC3558022/ /pubmed/23378672 http://dx.doi.org/10.1021/ma301959n Text en Copyright © 2012 American Chemical Society Terms of Use (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) |
spellingShingle | Griesser, Markus Rosspeintner, Arnulf Dworak, Claudia Höfer, Michael Grabner, Gottfried Liska, Robert Gescheidt, Georg Initiators Based on Benzaldoximes: Bimolecular and Covalently Bound Systems |
title | Initiators Based on Benzaldoximes:
Bimolecular and
Covalently Bound Systems |
title_full | Initiators Based on Benzaldoximes:
Bimolecular and
Covalently Bound Systems |
title_fullStr | Initiators Based on Benzaldoximes:
Bimolecular and
Covalently Bound Systems |
title_full_unstemmed | Initiators Based on Benzaldoximes:
Bimolecular and
Covalently Bound Systems |
title_short | Initiators Based on Benzaldoximes:
Bimolecular and
Covalently Bound Systems |
title_sort | initiators based on benzaldoximes:
bimolecular and
covalently bound systems |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3558022/ https://www.ncbi.nlm.nih.gov/pubmed/23378672 http://dx.doi.org/10.1021/ma301959n |
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