博碩士論文 972203030 完整後設資料紀錄

DC 欄位 語言
DC.contributor化學學系zh_TW
DC.creator吳瑛立zh_TW
DC.creatorYing-Li Wuen_US
dc.date.accessioned2010-7-28T07:39:07Z
dc.date.available2010-7-28T07:39:07Z
dc.date.issued2010
dc.identifier.urihttp://ir.lib.ncu.edu.tw:88/thesis/view_etd.asp?URN=972203030
dc.contributor.department化學學系zh_TW
DC.description國立中央大學zh_TW
DC.descriptionNational Central Universityen_US
dc.description.abstract共軛系統化合物,向來備受關注,尤其廣泛被應用在光電材料領域。於共軛化合物上接以推拉電子基,不僅縮小能隙更對其光學、電學性質上造成很大影響,甚至會具有非線性光學的性質。   本論文利用Buchwald –Hartwig 耦合反應合成具有不同胺官能基及雙腈基之并苯衍生物,利用選擇性水解與實驗室新開發加長并苯法來延長共軛系統。合成出以4.4’’-dimethoxydiphenylamine、吡咯啶、正二丁基胺為胺官能基的具雙腈基之三并苯、四并苯衍生物,探討其光學與電學性質,以期望應用在有機光電材料或者雙光子吸收染料上。 zh_TW
dc.description.abstractOrganic conjugated systems have long been the focus of research activities. Recently, their potential applications in optical-electronic devices have added extra momentum to this vital field. By attaching electron donating and electron withdrawing substitutions to this conjugated system, material scientists can easily tune the band gaps in these molecules. Furthermore, this approach is often employed in constructing compounds with non-linear optical properties. The objective of this dissertation is to synthesize acene derivatives substituted with both electron donating and withdrawing groups. The acene skeletons were constructed via iterative elongation reaction. Their preliminary photophysical and electrochemical properties were also investigated. We hope these compounds can find future applications as opto-electronic materials or two-photon-absorbing dyes. en_US
DC.subject多并苯zh_TW
DC.subjectAceneen_US
DC.title合成具推拉電子基并苯化合物及其物性探討zh_TW
dc.language.isozh-TWzh-TW
DC.titleSynthesis of Push-Pull Substituted Acene Derivatives and Investigations of Their Photophysical and Electrochemical Propertiesen_US
DC.type博碩士論文zh_TW
DC.typethesisen_US
DC.publisherNational Central Universityen_US

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