<div class="csl-bib-body">
<div class="csl-entry">Pieringer, F., Catel, Y., Liska, R., Moszner, N., & Knaack, P. (2023). Group transfer polymerization in bulk methacrylates. <i>Journal of Polymer Science</i>, <i>61</i>(22), 2922–2931. https://doi.org/10.1002/pol.20230132</div>
</div>
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dc.identifier.issn
2642-4150
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dc.identifier.uri
http://hdl.handle.net/20.500.12708/192092
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dc.description.abstract
Group transfer polymerization (GTP) is a polymerization method developed to obtain targeted (meth)acrylic polymers in solution at ambient temperatures. In this work, it is employed with methacrylic monomers to obtain low Ð polymers in bulk. In this regard, different initiator systems that exhibit different mechanisms are compared concerning the molecular weight, the polydispersity and double bond conversion of the resulting bulk polymers. The respective systems were chosen carefully to give a broad overview of earlier developed initiator-catalyst combinations 1-methoxy-1-(trimethylsiloxy)-2-methylprop-1-ene (MTS) & tetrabutylammonium cyanide (TBACN) and more recently investigated initiating systems MTS & trityl tetrakis(pentafluorophenyl)borate (TTPB) or dimethyl phenyl silane (DMPS) & tris(pentafluorophenyl)borate (BCF). The described initiating systems are applied as a two-component (2K) system to ensure a homogeneous distribution of the respective initiator and catalyst in the bulk monomer. In addition to the 2K experiments, photochemical initiation is also applied to bulk formulations. Therefore, a photoacid generator (PAG) and MTS is used to trigger the polymerization reaction by irradiation with UV light. A highly controlled photopolymerization method in bulk was developed that way achieving a low polydispersity polymer with high double bond conversion.
en
dc.description.sponsorship
Ivoclar Vivadent AG
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dc.language.iso
en
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dc.publisher
Wiley
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dc.relation.ispartof
Journal of Polymer Science
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dc.rights.uri
http://creativecommons.org/licenses/by-nc/4.0/
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dc.subject
bulk polymerization
en
dc.subject
group transfer polymerization
en
dc.subject
living polymerization
en
dc.subject
photopolymers
en
dc.title
Group transfer polymerization in bulk methacrylates
en
dc.type
Article
en
dc.type
Artikel
de
dc.rights.license
Creative Commons Attribution-NonCommercial 4.0 International
en
dc.rights.license
Creative Commons Namensnennung - Nicht kommerziell 4.0 International
Schlagzähe Photopolymere mit Viscosity on Demand Funktion auf Basis von IPNs unter Nutzung der Gruppen Transfer Polymerisation & 2 K Redox-Initiatorsysteme für die radikalische Polymerisation von Dentalformulierungen
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tuw.researchTopic.id
M2
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tuw.researchTopic.id
M8
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tuw.researchTopic.id
M4
-
tuw.researchTopic.name
Materials Characterization
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tuw.researchTopic.name
Structure-Property Relationsship
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tuw.researchTopic.name
Non-metallic Materials
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tuw.researchTopic.value
20
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tuw.researchTopic.value
10
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tuw.researchTopic.value
70
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dcterms.isPartOf.title
Journal of Polymer Science
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tuw.publication.orgunit
E163-02-1 - Forschungsgruppe Polymerchemie und Technologie
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tuw.publisher.doi
10.1002/pol.20230132
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dc.date.onlinefirst
2023-08-19
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dc.identifier.eissn
2642-4169
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dc.identifier.libraryid
AC17202864
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dc.description.numberOfPages
10
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tuw.author.orcid
0000-0002-3337-7088
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tuw.author.orcid
0000-0001-7865-1936
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tuw.author.orcid
0000-0002-9854-1838
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tuw.author.orcid
0000-0001-9984-9087
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dc.rights.identifier
CC BY-NC 4.0
en
dc.rights.identifier
CC BY-NC 4.0
de
wb.sci
true
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wb.sciencebranch
Chemie
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wb.sciencebranch.oefos
1040
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wb.sciencebranch.value
100
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application/pdf
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research article
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item.openairecristype
http://purl.org/coar/resource_type/c_2df8fbb1
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item.openaccessfulltext
Open Access
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item.grantfulltext
open
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item.cerifentitytype
Publications
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item.fulltext
with Fulltext
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item.languageiso639-1
en
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crisitem.author.dept
E163-02-1 - Forschungsgruppe Polymerchemie und Technologie