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A Soluble, Low-Temperature Thermochromic and Chemically Reactive Polydiacetylene
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Park, In Sung | - |
| dc.contributor.author | Park, Hye Jin | - |
| dc.contributor.author | Kim, Jong-Man | - |
| dc.date.accessioned | 2022-07-16T08:31:29Z | - |
| dc.date.available | 2022-07-16T08:31:29Z | - |
| dc.date.issued | 2013-09 | - |
| dc.identifier.issn | 1944-8244 | - |
| dc.identifier.issn | 1944-8252 | - |
| dc.identifier.uri | https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/162083 | - |
| dc.description.abstract | The majority of polydiacetylenes (PDAs) described to date display thermochromic transitions above room temperature. By following a strategy that employs headgroups that do not participate in strong interactions, we have designed and prepared a liquid diacetylene (DA) that solidifies at a temperature near 0 degrees C. The isocyanate-containing DA monomer, DA-NCO, having this property does not Undergo polymerization in its liquid state at room temperature. However, UV irradiation of frozen DA-NCO at 0 degrees C causes the instantaneous formation of a blue PDA (PDA-NCO). Interestingly, PDA-NCO was found to display a sharp blue-to-red color transition at a temperature near 11 degrees C. By taking advantage of its room temperature liquid-phase property, we were able to readily transfer the DA monomer to solid substrates by using common stamping and writing methods used for creating patterned PDA images. In addition, PDA-NCO dissolves in chloroform, giving a yellow solution that becomes red and simultaneously generates polymer aggregates when hexane is added. Finally, the isocyanate moieties present in PDA-NCO have been utilized to differentiate 1 degrees from 2 degrees and 3 degrees amines owing to the fact that a chloroform solution of PDA-NCO undergoes a rapid yellow-to-red color change associated with an insoluble urea-forming reaction with primary amines. | - |
| dc.format.extent | 8 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | American Chemical Society | - |
| dc.title | A Soluble, Low-Temperature Thermochromic and Chemically Reactive Polydiacetylene | - |
| dc.type | Article | - |
| dc.publisher.location | 미국 | - |
| dc.identifier.doi | 10.1021/am402701n | - |
| dc.identifier.scopusid | 2-s2.0-84884246585 | - |
| dc.identifier.wosid | 000330017100072 | - |
| dc.identifier.bibliographicCitation | ACS Applied Materials & Interfaces, v.5, no.17, pp 8805 - 8812 | - |
| dc.citation.title | ACS Applied Materials & Interfaces | - |
| dc.citation.volume | 5 | - |
| dc.citation.number | 17 | - |
| dc.citation.startPage | 8805 | - |
| dc.citation.endPage | 8812 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | sci | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Science & Technology - Other Topics | - |
| dc.relation.journalResearchArea | Materials Science | - |
| dc.relation.journalWebOfScienceCategory | Nanoscience & Nanotechnology | - |
| dc.relation.journalWebOfScienceCategory | Materials Science, Multidisciplinary | - |
| dc.subject.keywordPlus | CONJUGATED POLYMER | - |
| dc.subject.keywordPlus | TURN-ON | - |
| dc.subject.keywordPlus | SENSING MATERIALS | - |
| dc.subject.keywordPlus | SIDE-CHAIN | - |
| dc.subject.keywordPlus | SUPRAMOLECULES | - |
| dc.subject.keywordPlus | INTERCALATION | - |
| dc.subject.keywordPlus | REVERSIBILITY | - |
| dc.subject.keywordPlus | ALKYLAMINES | - |
| dc.subject.keywordPlus | LIPOSOME | - |
| dc.subject.keywordPlus | CRYSTALS | - |
| dc.subject.keywordAuthor | polydiacetylene | - |
| dc.subject.keywordAuthor | thermochromism | - |
| dc.subject.keywordAuthor | solvatochromism | - |
| dc.subject.keywordAuthor | conjugated polymer | - |
| dc.subject.keywordAuthor | sensor | - |
| dc.identifier.url | https://pubs.acs.org/doi/10.1021/am402701n | - |
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