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...
Gespeichert in:
Veröffentlicht in: | Polymers 2013-09, Vol.5 (3), p.956-1011 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1011 |
---|---|
container_issue | 3 |
container_start_page | 956 |
container_title | Polymers |
container_volume | 5 |
creator | Rossegger, Elisabeth Schenk, Verena Wiesbrock, Frank |
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. |
doi_str_mv | 10.3390/polym5030956 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_1537121420</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3338308621</sourcerecordid><originalsourceid>FETCH-LOGICAL-c301t-7581b7be98d3571a046374f6a8a326613063a1f82daca74fe520d7c6f68901033</originalsourceid><addsrcrecordid>eNpNUF1LwzAUDaLgmHvzBwR8UbB6k9sk7aNsToUNBfW5ZG06MrqmJq24_Xoj82H35Vw4HxwOIZcM7hBzuO9cs9sKQMiFPCEjDgqTFCWcHv3nZBLCBuKlQkqmRmQ5M8GuW_ree92btTWB1s7T-dCWvXWtbuzeVPQtZl_zxP3ovWtsa24C1W1FZ8bb70gvo9Vb3YQLclZHMJN_HJPP-ePH9DlZvD69TB8WSYnA-kSJjK3UyuRZhUIxDalEldZSZxp57IUgUbM645UudSSM4FCpUtYyy4EB4phcHXI7774GE_pi4wYf24aCCVSMs5RDVN0eVKV3IXhTF523W-13BYPib7PieDP8BfmxXjs</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1537121420</pqid></control><display><type>article</type><title>Design Strategies for Functionalized Poly(2-oxazoline)s and Derived Materials</title><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>MDPI - Multidisciplinary Digital Publishing Institute</source><creator>Rossegger, Elisabeth ; Schenk, Verena ; Wiesbrock, Frank</creator><creatorcontrib>Rossegger, Elisabeth ; Schenk, Verena ; Wiesbrock, Frank</creatorcontrib><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.</description><identifier>ISSN: 2073-4360</identifier><identifier>EISSN: 2073-4360</identifier><identifier>DOI: 10.3390/polym5030956</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><ispartof>Polymers, 2013-09, Vol.5 (3), p.956-1011</ispartof><rights>Copyright MDPI AG 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c301t-7581b7be98d3571a046374f6a8a326613063a1f82daca74fe520d7c6f68901033</citedby><cites>FETCH-LOGICAL-c301t-7581b7be98d3571a046374f6a8a326613063a1f82daca74fe520d7c6f68901033</cites><orcidid>0000-0002-6459-6136</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>313,314,780,784,792,27921,27923,27924</link.rule.ids></links><search><creatorcontrib>Rossegger, Elisabeth</creatorcontrib><creatorcontrib>Schenk, Verena</creatorcontrib><creatorcontrib>Wiesbrock, Frank</creatorcontrib><title>Design Strategies for Functionalized Poly(2-oxazoline)s and Derived Materials</title><title>Polymers</title><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.</description><issn>2073-4360</issn><issn>2073-4360</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNpNUF1LwzAUDaLgmHvzBwR8UbB6k9sk7aNsToUNBfW5ZG06MrqmJq24_Xoj82H35Vw4HxwOIZcM7hBzuO9cs9sKQMiFPCEjDgqTFCWcHv3nZBLCBuKlQkqmRmQ5M8GuW_ree92btTWB1s7T-dCWvXWtbuzeVPQtZl_zxP3ovWtsa24C1W1FZ8bb70gvo9Vb3YQLclZHMJN_HJPP-ePH9DlZvD69TB8WSYnA-kSJjK3UyuRZhUIxDalEldZSZxp57IUgUbM645UudSSM4FCpUtYyy4EB4phcHXI7774GE_pi4wYf24aCCVSMs5RDVN0eVKV3IXhTF523W-13BYPib7PieDP8BfmxXjs</recordid><startdate>20130901</startdate><enddate>20130901</enddate><creator>Rossegger, Elisabeth</creator><creator>Schenk, Verena</creator><creator>Wiesbrock, Frank</creator><general>MDPI AG</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>JG9</scope><scope>KB.</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><orcidid>https://orcid.org/0000-0002-6459-6136</orcidid></search><sort><creationdate>20130901</creationdate><title>Design Strategies for Functionalized Poly(2-oxazoline)s and Derived Materials</title><author>Rossegger, Elisabeth ; Schenk, Verena ; Wiesbrock, Frank</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c301t-7581b7be98d3571a046374f6a8a326613063a1f82daca74fe520d7c6f68901033</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rossegger, Elisabeth</creatorcontrib><creatorcontrib>Schenk, Verena</creatorcontrib><creatorcontrib>Wiesbrock, Frank</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>SciTech Premium Collection</collection><collection>Materials Research Database</collection><collection>Materials Science Database</collection><collection>Materials Science Collection</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>Polymers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rossegger, Elisabeth</au><au>Schenk, Verena</au><au>Wiesbrock, Frank</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Design Strategies for Functionalized Poly(2-oxazoline)s and Derived Materials</atitle><jtitle>Polymers</jtitle><date>2013-09-01</date><risdate>2013</risdate><volume>5</volume><issue>3</issue><spage>956</spage><epage>1011</epage><pages>956-1011</pages><issn>2073-4360</issn><eissn>2073-4360</eissn><abstract>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.</abstract><cop>Basel</cop><pub>MDPI AG</pub><doi>10.3390/polym5030956</doi><tpages>56</tpages><orcidid>https://orcid.org/0000-0002-6459-6136</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2073-4360 |
ispartof | Polymers, 2013-09, Vol.5 (3), p.956-1011 |
issn | 2073-4360 2073-4360 |
language | eng |
recordid | cdi_proquest_journals_1537121420 |
source | Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; MDPI - Multidisciplinary Digital Publishing Institute |
title | Design Strategies for Functionalized Poly(2-oxazoline)s and Derived Materials |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-11T19%3A33%3A37IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Design%20Strategies%20for%20Functionalized%20Poly(2-oxazoline)s%20and%20Derived%20Materials&rft.jtitle=Polymers&rft.au=Rossegger,%20Elisabeth&rft.date=2013-09-01&rft.volume=5&rft.issue=3&rft.spage=956&rft.epage=1011&rft.pages=956-1011&rft.issn=2073-4360&rft.eissn=2073-4360&rft_id=info:doi/10.3390/polym5030956&rft_dat=%3Cproquest_cross%3E3338308621%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1537121420&rft_id=info:pmid/&rfr_iscdi=true |