Two-photon absorption properties of 9,10-disubstituted 2,6-Bis(p-dihexylaminostyryl)Anthracene derivatives. Effect of 9,10-substituents
DC Field | Value | Language |
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dc.contributor.author | Yang, Wen Jun | - |
dc.contributor.author | Seo, Mun Sik | - |
dc.contributor.author | Wang, Xiao Qing | - |
dc.contributor.author | Jeon, Seung-Joon | - |
dc.contributor.author | Cho, Bong Rae | - |
dc.date.accessioned | 2021-09-09T10:49:55Z | - |
dc.date.available | 2021-09-09T10:49:55Z | - |
dc.date.created | 2021-06-10 | - |
dc.date.issued | 2008-03 | - |
dc.identifier.issn | 1053-0509 | - |
dc.identifier.uri | https://scholar.korea.ac.kr/handle/2021.sw.korea/124000 | - |
dc.description.abstract | A series of 2,6-bis(p-dihexylaminostyryl)anthracence derivatives having phenyl, styryl, and phenylethynyl groups at 9,10-positions (1-4) have been synthesized and their two-photon cross-sections were determined. Overall, the wavelengths of the longest wavelength absorption band and emission spectra increase with increase in the conjugation length and the electron withdrawing ability of the 9,10-substituents. All compounds show two-photon cross sections in the range of 740-3940 GM at 780-960 nm, which increase significantly by the donor and acceptor groups at 9,10-positions. In addition, Ph and phenylethynyl groups are better when compared to the styryl group at the 9,10-positions in terms of the two-photon action cross section. From a practical perspective, 1a, 2a-c, and 4b showed significant two-photon action cross-section and are most useful for applications that use two-photon excited fluorescence. | - |
dc.language | English | - |
dc.language.iso | en | - |
dc.publisher | SPRINGER/PLENUM PUBLISHERS | - |
dc.subject | CROSS-SECTIONS | - |
dc.subject | FLUOROPHORES | - |
dc.subject | ACCEPTOR | - |
dc.subject | DESIGN | - |
dc.subject | DYES | - |
dc.title | Two-photon absorption properties of 9,10-disubstituted 2,6-Bis(p-dihexylaminostyryl)Anthracene derivatives. Effect of 9,10-substituents | - |
dc.type | Article | - |
dc.contributor.affiliatedAuthor | Jeon, Seung-Joon | - |
dc.contributor.affiliatedAuthor | Cho, Bong Rae | - |
dc.identifier.doi | 10.1007/s10895-007-0280-3 | - |
dc.identifier.scopusid | 2-s2.0-40549123742 | - |
dc.identifier.wosid | 000253896400019 | - |
dc.identifier.bibliographicCitation | JOURNAL OF FLUORESCENCE, v.18, no.2, pp.403 - 411 | - |
dc.relation.isPartOf | JOURNAL OF FLUORESCENCE | - |
dc.citation.title | JOURNAL OF FLUORESCENCE | - |
dc.citation.volume | 18 | - |
dc.citation.number | 2 | - |
dc.citation.startPage | 403 | - |
dc.citation.endPage | 411 | - |
dc.type.rims | ART | - |
dc.type.docType | Article | - |
dc.description.journalClass | 1 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Biochemistry & Molecular Biology | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.relation.journalWebOfScienceCategory | Biochemical Research Methods | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Analytical | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Physical | - |
dc.subject.keywordPlus | CROSS-SECTIONS | - |
dc.subject.keywordPlus | FLUOROPHORES | - |
dc.subject.keywordPlus | ACCEPTOR | - |
dc.subject.keywordPlus | DESIGN | - |
dc.subject.keywordPlus | DYES | - |
dc.subject.keywordAuthor | two-photon absorption | - |
dc.subject.keywordAuthor | anthracene derivatives | - |
dc.subject.keywordAuthor | structure-property relationship | - |
dc.subject.keywordAuthor | two-photon fluorescence | - |
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