Constrained thermoresponsive polymers - new insights into fundamentals and applications

dc.bibliographicCitation.firstPage2123eng
dc.bibliographicCitation.lastPage2163eng
dc.bibliographicCitation.volume17eng
dc.contributor.authorFlemming, Patricia
dc.contributor.authorMünch, Alexander S.
dc.contributor.authorFery, Andreas
dc.contributor.authorUhlmann, Petra
dc.date.accessioned2022-03-17T07:31:14Z
dc.date.available2022-03-17T07:31:14Z
dc.date.issued2021
dc.description.abstractIn the last decades, numerous stimuli-responsive polymers have been developed and investigated regarding their switching properties. In particular, thermoresponsive polymers, which form a miscibility gap with the ambient solvent with a lower or upper critical demixing point depending on the temperature, have been intensively studied in solution. For the application of such polymers in novel sensors, drug delivery systems or as multifunctional coatings, they typically have to be transferred into specific arrangements, such as micelles, polymer films or grafted nanoparticles. However, it turns out that the thermodynamic concept for the phase transition of free polymer chains fails, when thermoresponsive polymers are assembled into such sterically confined architectures. Whereas many published studies focus on synthetic aspects as well as individual applications of thermoresponsive polymers, the underlying structure-property relationships governing the thermoresponse of sterically constrained assemblies, are still poorly understood. Furthermore, the clear majority of publications deals with polymers that exhibit a lower critical solution temperature (LCST) behavior, with PNIPAAM as their main representative. In contrast, for polymer arrangements with an upper critical solution temperature (UCST), there is only limited knowledge about preparation, application and precise physical understanding of the phase transition. This review article provides an overview about the current knowledge of thermoresponsive polymers with limited mobility focusing on UCST behavior and the possibilities for influencing their thermoresponsive switching characteristics. It comprises star polymers, micelles as well as polymer chains grafted to flat substrates and particulate inorganic surfaces. The elaboration of the physicochemical interplay between the architecture of the polymer assembly and the resulting thermoresponsive switching behavior will be in the foreground of this consideration.eng
dc.description.versionpublishedVersioneng
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/8253
dc.identifier.urihttps://doi.org/10.34657/7291
dc.language.isoengeng
dc.publisherFrankfurt, M. : Beilstein-Institut zur Förderung der Chemischen Wissenschafteneng
dc.relation.doihttps://doi.org/10.3762/bjoc.17.138
dc.relation.essn1860-5397
dc.relation.ispartofseriesBeilstein Journal of Organic Chemistry 17 (2021)eng
dc.rights.licenseCC BY 4.0 Unportedeng
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/eng
dc.subjectlower critical solution temperature (LCST)eng
dc.subjectresponsive coatingeng
dc.subjectsmart materialeng
dc.subjectthermoresponsive polymereng
dc.subjectupper critical solution temperature (UCST)eng
dc.subject.ddc540eng
dc.titleConstrained thermoresponsive polymers - new insights into fundamentals and applicationseng
dc.typearticleeng
dc.typeTexteng
dcterms.bibliographicCitation.journalTitleBeilstein journal of organic chemistryeng
tib.accessRightsopenAccesseng
wgl.contributorIPFeng
wgl.subjectChemieeng
wgl.typeZeitschriftenartikeleng
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