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dc.contributor.authorChiang, CLen_US
dc.contributor.authorShu, CFen_US
dc.contributor.authorChen, CTen_US
dc.date.accessioned2014-12-08T15:18:37Z-
dc.date.available2014-12-08T15:18:37Z-
dc.date.issued2005-08-18en_US
dc.identifier.issn1523-7060en_US
dc.identifier.urihttp://dx.doi.org/10.1021/ol0513591en_US
dc.identifier.urihttp://hdl.handle.net/11536/13396-
dc.description.abstract[graphics] Pure 2,2'-Dibromo-9,9'-spirobifluorene was synthesized by a method that did not involve troublesome dibromination of 9,9'-spirobifluorene or Sandmeyer reaction of 2,2'-diamino-9,9'-spirobifluorene. A series of donor-acceptor orthogonally substituted 9,9'-spirobifluorene was subsequently prepared showing rich variation of fluorescence in solution and in solid state.en_US
dc.language.isoen_USen_US
dc.titleImproved synthesis of 2,2'-dibromo-9,9'-spirobifluorene and its 2,2'-bisdonor-7,7'-bisacceptor-substituted fluorescent derivativesen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/ol0513591en_US
dc.identifier.journalORGANIC LETTERSen_US
dc.citation.volume7en_US
dc.citation.issue17en_US
dc.citation.spage3717en_US
dc.citation.epage3720en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000231294400030-
dc.citation.woscount46-
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