博碩士論文 108223013 完整後設資料紀錄

DC 欄位 語言
DC.contributor化學學系zh_TW
DC.creator陳婉菁zh_TW
DC.creatorWan-Ching Chenen_US
dc.date.accessioned2021-8-25T07:39:07Z
dc.date.available2021-8-25T07:39:07Z
dc.date.issued2021
dc.identifier.urihttp://ir.lib.ncu.edu.tw:88/thesis/view_etd.asp?URN=108223013
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本論文採用有助於建立化合物具方向性之四苯基(-4Ph)基團鍵結二氧化硫與三嗪為電子受體,並與spiroAC、DMAC、DPAC、4MeCz之電子予體分別合成出一系列化合物,共計有8種化合物。期望當化合物具方向性時,能夠有效提升效率。 在利用二氧化硫為電子受體時,為了加以分析量測結果,我們合成出不具有四苯基之二氧化硫結構對照組,分別與上述四種不同電子予體配合,共計有4種化合物來進行比較及討論。然而,在三嗪的部分,由於合成上遇到困難,因此本篇論文僅討論其化合物之合成,並無其他物性等量測結果之探討。zh_TW
dc.description.abstractIn this thesis, a tetraphenyl (-4Ph) group that helps to induce the horizontal orientation alignment in the OLEDs device is introduced to the designed compound where sulfur dioxide and triazine as the electron acceptor while spiroAC, DMAC, DPAC, and 4MeCz are electron donors. There are a total of 8 compounds. It is expected that when the compound is horizontally aligned on substrate, the efficiency of OLEDs can be effectively improved. When using sulfur dioxide as the electron acceptor, in order to analyze the performance of compound with -4Ph, we synthesized a control group without -4Ph, which was matched with the above four different electron donors, and a total of 4 control compounds were synthesized and compared. However, in the part of triazine, due to difficulties in synthesizing, this thesis only discusses the synthesis process of its compounds but no other analytical measurement results due to insufficient amount of materials. en_US
DC.subject熱活化藍色螢光材料zh_TW
DC.subject四苯基結構zh_TW
DC.subject水平方向排列zh_TW
DC.subjectthermally activated delayed blue fluorescent materialen_US
DC.subjecttetraphenyl structureen_US
DC.subjecthorizontal alignmenten_US
DC.title具有水平方向排列特性四苯基結構之二氧化硫與三嗪架構的熱活化延遲藍色螢光材料合成與鑑定zh_TW
dc.language.isozh-TWzh-TW
DC.titleSynthesis and characterization of a thermally activated delayed blue fluorescent material of a sulfur oxide and a triazine structures with a tetraphenyl structure induced horizontal alignmenten_US
DC.type博碩士論文zh_TW
DC.typethesisen_US
DC.publisherNational Central Universityen_US

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