博碩士論文 962203020 完整後設資料紀錄

DC 欄位 語言
DC.contributor化學學系zh_TW
DC.creator陳宣尹zh_TW
DC.creatorHsuan-Yin Chenen_US
dc.date.accessioned2010-1-22T07:39:07Z
dc.date.available2010-1-22T07:39:07Z
dc.date.issued2010
dc.identifier.urihttp://ir.lib.ncu.edu.tw:88/thesis/view_etd.asp?URN=962203020
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鈀觸媒應用於Suzuki反應時,金屬的電子密度愈大愈有利於催化反應中的氧化加成作用進行。而碳烯化合物(carbene)是一種具有強供電子能力的配位基(ligand),因此我們在觸媒(PA2UF40)中直接加入carbene,希望藉以提升鈀金屬的電子密度,進而在催化鈴木反應上,我們觀察出其反應性已成功地產生了活化的現象。隨後,我們又合成出不同鈀金屬顆粒大小的觸媒(PA2US20、PA2UF20、PA2US58),在交叉比對的實驗中,可以發現影響反應的因素除了金屬的電子密度之外,決定活性點多寡的表面積大小亦是需要考量的重點之一。而在觸媒的鑑定方面,我們利用到原位-紅外線光譜儀針對金屬的電子密度特性作為分析。 zh_TW
dc.description.abstractIn Palladium-catalyzed Suzuki coupling, the higher electron density of the catalytic metal possesses the much higher active reaction will undergo. Since carbene is a well-known electron-donating ligand, herein, we describe an innovation of that versatile ligand directly loaded onto the heterogeneous Palladium catalyst which we expected to increase the electron property of the metal. Afterward, the novel catalysts turned out to exhibit a certain promotion while testing the coupling reaction of the 4-bromotoluene with phenylboronic acid. Moreover, a series of different particle size of the heterogeneous catalytic metals were also synthesized. In our crossover experiments, we find that not only the electron density of the metal dominates the reaction proceeding but the amount of the active sites affects the reactive efficiency which is determined by the surface area of the metal. Furthermore, the characterization of the catalysts was confirmed by in-situ IR analysis. en_US
DC.subject碳碳鍵結zh_TW
DC.subject鈴木反應zh_TW
DC.subject異相觸媒zh_TW
DC.subject鈀金屬zh_TW
DC.subjectC-C couplingen_US
DC.subjectpalladiumen_US
DC.subjectheterogeneousen_US
DC.subjectSuzuki reactionen_US
DC.title含有碳烯化合物之鈀金屬異相觸媒催化碳碳鍵生成反應之研究zh_TW
dc.language.isozh-TWzh-TW
DC.type博碩士論文zh_TW
DC.typethesisen_US
DC.publisherNational Central Universityen_US

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