Design Strategies for Functionalized Poly(2-oxazoline)s and Derived Materials

The polymer class of poly(2-oxazoline)s currently is under intensive investigation due to the versatile properties that can be tailor-made by the variation and manipulation of the functional groups they bear. In particular their utilization in the biomedic(in)al field is the subject of numerous stud...

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Main Authors: Frank Wiesbrock, Verena Schenk, Elisabeth Rossegger
Format: Article
Language:English
Published: MDPI AG 2013-07-01
Series:Polymers
Subjects:
Online Access:http://www.mdpi.com/2073-4360/5/3/956
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spelling doaj-1645a2d1521e4778b89130ec3af589b92020-11-25T01:37:50ZengMDPI AGPolymers2073-43602013-07-0153956101110.3390/polym5030956Design Strategies for Functionalized Poly(2-oxazoline)s and Derived MaterialsFrank WiesbrockVerena SchenkElisabeth RosseggerThe polymer class of poly(2-oxazoline)s currently is under intensive investigation due to the versatile properties that can be tailor-made by the variation and manipulation of the functional groups they bear. In particular their utilization in the biomedic(in)al field is the subject of numerous studies. Given the mechanism of the cationic ring-opening polymerization, a plethora of synthetic strategies exists for the preparation of poly(2-oxazoline)s with dedicated functionality patterns, comprising among others the functionalization by telechelic end-groups, the incorporation of substituted monomers into (co)poly(2-oxazoline)s, and polymeranalogous reactions. This review summarizes the current state-of-the-art of poly(2-oxazoline) preparation and showcases prominent examples of poly(2-oxazoline)-based materials, which are retraced to the desktop-planned synthetic strategy and the variability of their properties for dedicated applications.http://www.mdpi.com/2073-4360/5/3/956poly(2-oxazoline)scationic ring-opening polymerizationtelechelic end-group functionalizationpolymeranalogous reactions
collection DOAJ
language English
format Article
sources DOAJ
author Frank Wiesbrock
Verena Schenk
Elisabeth Rossegger
spellingShingle Frank Wiesbrock
Verena Schenk
Elisabeth Rossegger
Design Strategies for Functionalized Poly(2-oxazoline)s and Derived Materials
Polymers
poly(2-oxazoline)s
cationic ring-opening polymerization
telechelic end-group functionalization
polymeranalogous reactions
author_facet Frank Wiesbrock
Verena Schenk
Elisabeth Rossegger
author_sort Frank Wiesbrock
title Design Strategies for Functionalized Poly(2-oxazoline)s and Derived Materials
title_short Design Strategies for Functionalized Poly(2-oxazoline)s and Derived Materials
title_full Design Strategies for Functionalized Poly(2-oxazoline)s and Derived Materials
title_fullStr Design Strategies for Functionalized Poly(2-oxazoline)s and Derived Materials
title_full_unstemmed Design Strategies for Functionalized Poly(2-oxazoline)s and Derived Materials
title_sort design strategies for functionalized poly(2-oxazoline)s and derived materials
publisher MDPI AG
series Polymers
issn 2073-4360
publishDate 2013-07-01
description The polymer class of poly(2-oxazoline)s currently is under intensive investigation due to the versatile properties that can be tailor-made by the variation and manipulation of the functional groups they bear. In particular their utilization in the biomedic(in)al field is the subject of numerous studies. Given the mechanism of the cationic ring-opening polymerization, a plethora of synthetic strategies exists for the preparation of poly(2-oxazoline)s with dedicated functionality patterns, comprising among others the functionalization by telechelic end-groups, the incorporation of substituted monomers into (co)poly(2-oxazoline)s, and polymeranalogous reactions. This review summarizes the current state-of-the-art of poly(2-oxazoline) preparation and showcases prominent examples of poly(2-oxazoline)-based materials, which are retraced to the desktop-planned synthetic strategy and the variability of their properties for dedicated applications.
topic poly(2-oxazoline)s
cationic ring-opening polymerization
telechelic end-group functionalization
polymeranalogous reactions
url http://www.mdpi.com/2073-4360/5/3/956
work_keys_str_mv AT frankwiesbrock designstrategiesforfunctionalizedpoly2oxazolinesandderivedmaterials
AT verenaschenk designstrategiesforfunctionalizedpoly2oxazolinesandderivedmaterials
AT elisabethrossegger designstrategiesforfunctionalizedpoly2oxazolinesandderivedmaterials
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