Cited 8 time in
Synthesis and Characterization of Highly Conjugated Cyclopenta[def]phenanthrene-Based Polymers
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Jang, Sang Hun | - |
| dc.contributor.author | Tai, Truong Ba | - |
| dc.contributor.author | Park, Ji Hee | - |
| dc.contributor.author | Jeong, Hee Jeong | - |
| dc.contributor.author | Chun, Eun Jeong | - |
| dc.contributor.author | Kim, Yun-Hi | - |
| dc.contributor.author | Lee, Sang-Gyeong | - |
| dc.contributor.author | Singh, Okram Mukherjee | - |
| dc.contributor.author | Yoon, Yong Jin | - |
| dc.contributor.author | Kwon, Soon Ki | - |
| dc.date.accessioned | 2024-12-03T03:30:48Z | - |
| dc.date.available | 2024-12-03T03:30:48Z | - |
| dc.date.issued | 2010-02 | - |
| dc.identifier.issn | 1598-5032 | - |
| dc.identifier.issn | 2092-7673 | - |
| dc.identifier.uri | https://scholarworks.gnu.ac.kr/handle/sw.gnu/73812 | - |
| dc.description.abstract | Three blue light-emitting cyclopenta[def]phenanthrene-based conjugated polymers were synthesized using the Yamamoto coupling reaction and their optical, thermal, and electrochemical properties were examined. The results indicated that the number-average molecular weights of compounds 11, 12, and 13 were 16,400, 11,000, and 10,400, respectively. The polymers were soluble in common solvents, such as toluene, chloroform, etc. Their structures were confirmed using H-1 NMR, mass, and FTIR spectroscopy. Homopolymer 11 showed stable blue emission with a photoluminescence peak at 408 nm in solution and at 456 nm in thin film form. Moreover, polymers 11, 12, and 13 exhibited high thermal stability up to 340 degrees C, 333 degrees C, and 380 degrees C, respectively. | - |
| dc.format.extent | 7 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | 한국고분자학회 | - |
| dc.title | Synthesis and Characterization of Highly Conjugated Cyclopenta[def]phenanthrene-Based Polymers | - |
| dc.type | Article | - |
| dc.publisher.location | 대한민국 | - |
| dc.identifier.doi | 10.1007/s13233-009-0167-z | - |
| dc.identifier.scopusid | 2-s2.0-77955893495 | - |
| dc.identifier.wosid | 000275800700011 | - |
| dc.identifier.bibliographicCitation | Macromolecular Research, v.18, no.2, pp 185 - 191 | - |
| dc.citation.title | Macromolecular Research | - |
| dc.citation.volume | 18 | - |
| dc.citation.number | 2 | - |
| dc.citation.startPage | 185 | - |
| dc.citation.endPage | 191 | - |
| dc.type.docType | Article | - |
| dc.identifier.kciid | ART001421747 | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | sci | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.description.journalRegisteredClass | kci | - |
| dc.relation.journalResearchArea | Polymer Science | - |
| dc.relation.journalWebOfScienceCategory | Polymer Science | - |
| dc.subject.keywordPlus | LIGHT-EMITTING-DIODES | - |
| dc.subject.keywordPlus | OXADIAZOLE | - |
| dc.subject.keywordAuthor | PCPP | - |
| dc.subject.keywordAuthor | Yamamoto coupling | - |
| dc.subject.keywordAuthor | organic light-emitting diode | - |
| dc.subject.keywordAuthor | photoluminescence | - |
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