完整後設資料紀錄
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.author | Chiang, CL | en_US |
dc.contributor.author | Shu, CF | en_US |
dc.contributor.author | Chen, CT | en_US |
dc.date.accessioned | 2014-12-08T15:18:37Z | - |
dc.date.available | 2014-12-08T15:18:37Z | - |
dc.date.issued | 2005-08-18 | en_US |
dc.identifier.issn | 1523-7060 | en_US |
dc.identifier.uri | http://dx.doi.org/10.1021/ol0513591 | en_US |
dc.identifier.uri | http://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.iso | en_US | en_US |
dc.title | Improved synthesis of 2,2'-dibromo-9,9'-spirobifluorene and its 2,2'-bisdonor-7,7'-bisacceptor-substituted fluorescent derivatives | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1021/ol0513591 | en_US |
dc.identifier.journal | ORGANIC LETTERS | en_US |
dc.citation.volume | 7 | en_US |
dc.citation.issue | 17 | en_US |
dc.citation.spage | 3717 | en_US |
dc.citation.epage | 3720 | en_US |
dc.contributor.department | 應用化學系 | zh_TW |
dc.contributor.department | Department of Applied Chemistry | en_US |
dc.identifier.wosnumber | WOS:000231294400030 | - |
dc.citation.woscount | 46 | - |
顯示於類別: | 期刊論文 |