Crosslinked Poly(2-oxazoline)s as “Green” Materials for Electronic Applications
Poly(2-nonyl-2-oxazoline)80-stat-poly(2-dec-9′-enyl-2-oxazoline)20 and poly(2-dec-9′-enyl-2-oxazoline)100 can be synthesized from the cationic ring-opening polymerization of monomers that can be derived from fatty acids from renewable resources. These (co)poly(2-oxazoline)s can be crosslinked with d...
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doaj-22f8c2e75c47487c8fc370c48bbc43182020-11-25T00:25:00ZengMDPI AGPolymers2073-43602015-12-0181610.3390/polym8010006polym8010006Crosslinked Poly(2-oxazoline)s as “Green” Materials for Electronic ApplicationsMartin Fimberger0Ioannis-Alexandros Tsekmes1Roman Kochetov2Johan J. Smit3Frank Wiesbrock4Polymer Competence Center Leoben, Rosseggerstrasse 12, Leoben 8700, AustriaDepartment of Electrical Sustainable Energy, Delft University of Technology, Mekelweg 4, 2628 CD Delft, The NetherlandsDepartment of Electrical Sustainable Energy, Delft University of Technology, Mekelweg 4, 2628 CD Delft, The NetherlandsDepartment of Electrical Sustainable Energy, Delft University of Technology, Mekelweg 4, 2628 CD Delft, The NetherlandsPolymer Competence Center Leoben, Rosseggerstrasse 12, Leoben 8700, AustriaPoly(2-nonyl-2-oxazoline)80-stat-poly(2-dec-9′-enyl-2-oxazoline)20 and poly(2-dec-9′-enyl-2-oxazoline)100 can be synthesized from the cationic ring-opening polymerization of monomers that can be derived from fatty acids from renewable resources. These (co)poly(2-oxazoline)s can be crosslinked with di- and trifunctional mercapto compounds using the UV-induced thiol-ene reaction. The complex permittivity of the corresponding networks increases with the temperature and decreases with the network density. In a frequency range from 10−2 to 106 Hz and at temperatures ranging from −20 to 40 °C, the changes of the real part of the complex permittivity as well as the loss factor can be explained by interfacial polarization within the material. At a temperature of 20 °C and a frequency of 50 Hz, the permittivity of the crosslinked (co)poly(2-oxazoline)s covers a range from 4.29 to 4.97, and the loss factors are in the range from 0.030 to 0.093. The electrical conductivities of these polymer networks span a range from 5 × 10−12 to 8 × 10−9 S/m, classifying these materials as medium insulators. Notably, the values for the permittivity, loss factor and conductivity of these copoly(2-oxazoline)s are in the same range as for polyamides, and, hence, these copoly(2-oxazoline)-based networks may be referred to as “green” alternatives for polyamides as insulators in electronic applications.http://www.mdpi.com/2073-4360/8/1/6poly(2-oxazoline)scrosslinked polymersthiol-ene click chemistrypermittivityloss factorinterfacial polarizationelectrical conductivity |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Martin Fimberger Ioannis-Alexandros Tsekmes Roman Kochetov Johan J. Smit Frank Wiesbrock |
spellingShingle |
Martin Fimberger Ioannis-Alexandros Tsekmes Roman Kochetov Johan J. Smit Frank Wiesbrock Crosslinked Poly(2-oxazoline)s as “Green” Materials for Electronic Applications Polymers poly(2-oxazoline)s crosslinked polymers thiol-ene click chemistry permittivity loss factor interfacial polarization electrical conductivity |
author_facet |
Martin Fimberger Ioannis-Alexandros Tsekmes Roman Kochetov Johan J. Smit Frank Wiesbrock |
author_sort |
Martin Fimberger |
title |
Crosslinked Poly(2-oxazoline)s as “Green” Materials for Electronic Applications |
title_short |
Crosslinked Poly(2-oxazoline)s as “Green” Materials for Electronic Applications |
title_full |
Crosslinked Poly(2-oxazoline)s as “Green” Materials for Electronic Applications |
title_fullStr |
Crosslinked Poly(2-oxazoline)s as “Green” Materials for Electronic Applications |
title_full_unstemmed |
Crosslinked Poly(2-oxazoline)s as “Green” Materials for Electronic Applications |
title_sort |
crosslinked poly(2-oxazoline)s as “green” materials for electronic applications |
publisher |
MDPI AG |
series |
Polymers |
issn |
2073-4360 |
publishDate |
2015-12-01 |
description |
Poly(2-nonyl-2-oxazoline)80-stat-poly(2-dec-9′-enyl-2-oxazoline)20 and poly(2-dec-9′-enyl-2-oxazoline)100 can be synthesized from the cationic ring-opening polymerization of monomers that can be derived from fatty acids from renewable resources. These (co)poly(2-oxazoline)s can be crosslinked with di- and trifunctional mercapto compounds using the UV-induced thiol-ene reaction. The complex permittivity of the corresponding networks increases with the temperature and decreases with the network density. In a frequency range from 10−2 to 106 Hz and at temperatures ranging from −20 to 40 °C, the changes of the real part of the complex permittivity as well as the loss factor can be explained by interfacial polarization within the material. At a temperature of 20 °C and a frequency of 50 Hz, the permittivity of the crosslinked (co)poly(2-oxazoline)s covers a range from 4.29 to 4.97, and the loss factors are in the range from 0.030 to 0.093. The electrical conductivities of these polymer networks span a range from 5 × 10−12 to 8 × 10−9 S/m, classifying these materials as medium insulators. Notably, the values for the permittivity, loss factor and conductivity of these copoly(2-oxazoline)s are in the same range as for polyamides, and, hence, these copoly(2-oxazoline)-based networks may be referred to as “green” alternatives for polyamides as insulators in electronic applications. |
topic |
poly(2-oxazoline)s crosslinked polymers thiol-ene click chemistry permittivity loss factor interfacial polarization electrical conductivity |
url |
http://www.mdpi.com/2073-4360/8/1/6 |
work_keys_str_mv |
AT martinfimberger crosslinkedpoly2oxazolinesasgreenmaterialsforelectronicapplications AT ioannisalexandrostsekmes crosslinkedpoly2oxazolinesasgreenmaterialsforelectronicapplications AT romankochetov crosslinkedpoly2oxazolinesasgreenmaterialsforelectronicapplications AT johanjsmit crosslinkedpoly2oxazolinesasgreenmaterialsforelectronicapplications AT frankwiesbrock crosslinkedpoly2oxazolinesasgreenmaterialsforelectronicapplications |
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