Higly Ordered Self-Assembly of 1D Nanoparticles in Phospholipids Driven by Curvature and Electrostatic Interaction

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dc.contributor.authorKim, Tae-Hwanko
dc.contributor.authorKang, Shin-Hyunko
dc.contributor.authorDoe, Changwooko
dc.contributor.authorYu, Jihyunko
dc.contributor.authorSim, Jun-Boko
dc.contributor.authorKim, Jehanko
dc.contributor.authorKline, Steven R.ko
dc.contributor.authorChoi, SungMinko
dc.date.accessioned2009-09-09T01:44:18Z-
dc.date.available2009-09-09T01:44:18Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2009-06-
dc.identifier.citationJOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v.131, no.21, pp.7456 - 7460-
dc.identifier.issn0002-7863-
dc.identifier.urihttp://hdl.handle.net/10203/11087-
dc.description.abstractSelf-assembly of 1 D nanoparticles such as carbon nanotubes or nanorods into highly ordered superstructures using various interactions has been of great interest as a route toward materials with new functionalities. However, the phase behavior of 1 D nanoparticles interacting with surrounding materials, which is the key information. to design self-assembled superstructures, has not been fully exploited yet. Here, we report for the first time a new phase diagram of negatively charged 1 D nanoparticle and cationic liposome (CLs) complexes in water that exhibit three different highly ordered phases, intercalated lamellar, doubly intercalated lamellar, and centered rectangular phases, depending on particle curvature and electrostatic interactions. The new phase diagram can be used to understand and design new highly ordered self-assemblies of 1 D nanoparticles in soft matter, which provide new functionalities.-
dc.description.sponsorshipThis work is supported by the Ministry of Education, Science and Technology of Korea through the Basic Atomic Energy Research Institute (BAERI) program and the basic science research program (R-01-2008-000-10219-0).en
dc.languageEnglish-
dc.language.isoen_USen
dc.publisherAMER CHEMICAL SOC-
dc.subjectRECTANGULAR COLUMNAR PHASE-
dc.subjectGOLD NANORODS-
dc.subjectDNA COMPLEXES-
dc.subjectNANOWIRES-
dc.subjectDIMENSIONS-
dc.subjectNANOTUBES-
dc.subjectMEMBRANES-
dc.subjectALIGNMENT-
dc.subjectMICELLES-
dc.subjectDELIVERY-
dc.titleHigly Ordered Self-Assembly of 1D Nanoparticles in Phospholipids Driven by Curvature and Electrostatic Interaction-
dc.typeArticle-
dc.identifier.wosid000266484900046-
dc.identifier.scopusid2-s2.0-67650511246-
dc.type.rimsART-
dc.citation.volume131-
dc.citation.issue21-
dc.citation.beginningpage7456-
dc.citation.endingpage7460-
dc.citation.publicationnameJOURNAL OF THE AMERICAN CHEMICAL SOCIETY-
dc.identifier.doi10.1021/ja901810n-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.contributor.localauthorChoi, SungMin-
dc.contributor.nonIdAuthorKim, Jehan-
dc.contributor.nonIdAuthorKline, Steven R.-
dc.type.journalArticleArticle-
dc.subject.keywordPlusRECTANGULAR COLUMNAR PHASE-
dc.subject.keywordPlusGOLD NANORODS-
dc.subject.keywordPlusDNA COMPLEXES-
dc.subject.keywordPlusNANOWIRES-
dc.subject.keywordPlusDIMENSIONS-
dc.subject.keywordPlusNANOTUBES-
dc.subject.keywordPlusMEMBRANES-
dc.subject.keywordPlusALIGNMENT-
dc.subject.keywordPlusMICELLES-
dc.subject.keywordPlusDELIVERY-
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