博碩士論文 104223605 完整後設資料紀錄

DC 欄位 語言
DC.contributor化學學系zh_TW
DC.creator雅格婷zh_TW
DC.creatorRachmawati Dwi Agustinen_US
dc.date.accessioned2016-7-27T07:39:07Z
dc.date.available2016-7-27T07:39:07Z
dc.date.issued2016
dc.identifier.urihttp://ir.lib.ncu.edu.tw:88/thesis/view_etd.asp?URN=104223605
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本研究著重於開發新三併環噻吩(DTT)衍生物的材料,希望該材料具備良好的溶解度,使其可以用在OTFT。DTT外掛SBT的結構可以延伸DTT的共軛長度並維持整個結構平面性,並擁有好的溶解度,因此,我將DTT分別結合SBT14和SBT18,成功合成出DDTT-SBT14 和DTT-SBT18。兩者主要骨架相同,差異在於碳鏈的不同,因此我將兩個材料做物性及化性的比較,並量測其光學、電化學、熱性質,發現兩者的結果相當類似,而DTT-SBT14的溶解度則優於DTT-SBT18。zh_TW
dc.description.abstracthis research focused on the development of soluble dithienothiophene (DTT) derivatives for organic thin film transistor (OTFT) application. Two new highly soluble dithienothiophene derivatives, DDTT-SBT14 and DDTT-SBT18 were synthesized by Stille Coupling. The fused thiophene (Bithiophene) enhancement of - molecular conjugation with Dithienothiophene (DDT) group and the comparison of the solubility by the addition of alkyl side chains were investigated. The chemical and physical characterization which included characterizing theirs optical, electrochemical and thermal properties shows that DDTT-SBT14 have the similar results to DDTT-SBT18 for the OTFT applications, but the mobility of DDTT-SBT14 is µ = 1.7 cm2/Vs more higher than than DDTT-SBT18 is µ = 0.3 cm2/Vs.en_US
DC.subjectorganic thin film transistoren_US
DC.subjectdithienothiopheneen_US
DC.subjectfused thiopheneen_US
DC.subjectalkyl side chainsen_US
DC.subjectsolubleen_US
DC.titleSoluble Dithienothiophene (DTT) Derived Small Molecules for Organic Thin Film Transistor (OTFT) Applicationen_US
dc.language.isoen_USen_US
DC.type博碩士論文zh_TW
DC.typethesisen_US
DC.publisherNational Central Universityen_US

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