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Strongly Phase-Segregating Block Copolymers with Sub-20 nm Features

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dc.contributor.authorKempe, Kristian-
dc.contributor.authorKillops, Kato L.-
dc.contributor.authorPoelma, Justin E.-
dc.contributor.authorJung, Hyunjung-
dc.contributor.authorBang, Joona-
dc.contributor.authorHoogenboom, Richard-
dc.contributor.authorTran, Helen-
dc.contributor.authorHawker, Craig J.-
dc.contributor.authorSchubert, Ulrich S.-
dc.contributor.authorCampos, Luis M.-
dc.date.accessioned2021-09-05T23:16:07Z-
dc.date.available2021-09-05T23:16:07Z-
dc.date.created2021-06-14-
dc.date.issued2013-08-
dc.identifier.issn2161-1653-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/102576-
dc.description.abstractThe modular synthesis and lithographic potential of diblock copolymers based on polystyrene-block-poly(2-ethyl-2-oxazoline) (PS-b-PEtOx) are highlighted herein. Controlled radical and living cationic polymerization techniques were utilized to synthesize hydrophobic PS and hydrophilic PEtOx building block of varying molar mass. Subsequently, "click" chemistry was used to couple the blocks and obtain a family of PS-b-PEtOx polymers. The influence of molar mass, composition, and thin-film thickness on the microphase-segregated morphology and orientation were investigated with atomic force microscopy (AFM) and grazing incidence small-angle X-ray scattering (GISAXS). Dense hexagonal arrays of cylindrical nanodomains normal to the substrate, having a periodicity of less than 2,0 run were obtained.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherAMER CHEMICAL SOC-
dc.subjectRING-OPENING POLYMERIZATION-
dc.subjectCYCLIC IMINO ETHERS-
dc.subjectTRIBLOCK COPOLYMERS-
dc.subjectTERMINAL ALKYNES-
dc.subjectLITHOGRAPHY-
dc.subjectPOLY(2-OXAZOLINE)S-
dc.subjectFUNCTIONALIZATION-
dc.subject2-OXAZOLINES-
dc.subjectBIOMOLECULES-
dc.subjectOXAZOLINES-
dc.titleStrongly Phase-Segregating Block Copolymers with Sub-20 nm Features-
dc.typeArticle-
dc.contributor.affiliatedAuthorBang, Joona-
dc.identifier.doi10.1021/mz400309d-
dc.identifier.scopusid2-s2.0-84883078747-
dc.identifier.wosid000323472100009-
dc.identifier.bibliographicCitationACS MACRO LETTERS, v.2, no.8, pp.677 - 682-
dc.relation.isPartOfACS MACRO LETTERS-
dc.citation.titleACS MACRO LETTERS-
dc.citation.volume2-
dc.citation.number8-
dc.citation.startPage677-
dc.citation.endPage682-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPolymer Science-
dc.relation.journalWebOfScienceCategoryPolymer Science-
dc.subject.keywordPlusRING-OPENING POLYMERIZATION-
dc.subject.keywordPlusCYCLIC IMINO ETHERS-
dc.subject.keywordPlusTRIBLOCK COPOLYMERS-
dc.subject.keywordPlusTERMINAL ALKYNES-
dc.subject.keywordPlusLITHOGRAPHY-
dc.subject.keywordPlusPOLY(2-OXAZOLINE)S-
dc.subject.keywordPlusFUNCTIONALIZATION-
dc.subject.keywordPlus2-OXAZOLINES-
dc.subject.keywordPlusBIOMOLECULES-
dc.subject.keywordPlusOXAZOLINES-
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