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研究生: 彭威智
Peng, Wei-Chih
論文名稱: 三取代基苯衍生物3,5-二氟苯酚之第一電子激態暨離子態振動光譜
3,5-Difluorophenol Studied by Resonant Two-Photon Ionization and Mass- Analyzed Threshold Spectroscopy
指導教授: 曾文碧
Tzeng, Wen-Bih
林震煌
Lin, Cheng-Huang
學位類別: 碩士
Master
系所名稱: 化學系
Department of Chemistry
論文出版年: 2016
畢業學年度: 104
語文別: 中文
論文頁數: 128
中文關鍵詞: 3,5-二氟苯酚質量解析臨界游離光譜術共振游離雙光子游離光譜術
英文關鍵詞: 3,5-Difluorophenol, Mass analyzed threshold ionization, Resonance-enhanced multiphoton ionization
DOI URL: https://doi.org/10.6345/NTNU202204532
論文種類: 學術論文
相關次數: 點閱:75下載:8
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  • 本論文研究著重於探討3,5二氟苯酚的特性,所使用的實驗技術包括單色共振雙光子游離(1C-R2PI)光譜術、雙色共振雙光子游離(2C-R2PI)光譜術和質量臨界游離(MATI)光譜術,利用以上技術可得知分子的第一電子激發能量、絕熱游離能和電子激發態與離子態分子振動光譜。本次的實驗,我們使用單光共振雙光子游離術精準地測量出3,5二氟苯酚的第一激發態能量為 37 614 ± 2 cm-1 且第一激發態的分子振動光譜訊雜比非常良好,可以很明顯地分辨出是否為真實訊號及雜訊。擁有完整的第一激發態資訊後我們利用質量臨界游離光譜術以S100、S110b1、S19b1為中間態得到準確的絕熱游離能 72 468 ± 5 cm-1 以及離子態分子振動光譜。而在數據分析上,我們參考Varsanyi所著的Assignments for Vibrational Spectra of Seven Hundred Benzene Derivatives書中所列的實驗數據再搭配理論計算所得的結果做譜線標定。相較於實驗室之前所測量的二氟苯酚的位置同分異構物, 3,5-二氟苯酚的第一激發能與游離能都為最高。除了電子躍遷能和電子激發態與離子態分子振動的討論之外,我們也會利用量子化學計算探討3,5-二氟苯酚在基態(S0)、第一激發態(S1)與游離態(D0)時的結構變化,發現在電子躍遷時苯環的結構發生改變,此結果與實驗所見到的現象符合。

    The thesis focuses on investigateing the cationic properties of 3,5-difluorophenol in the D0 state by several intermediate vibrational levels in S1 state. Our laboratory utilizes resonant two-photon ionization (R2PI), mass-analyzed threshold ionization (MATI) to get the vibrational spectra that can also determine the excitation energy (E1) and adiabatic ionization energy (IE).
    In this project, I use the 1C-R2PI technique to obtain the vibronic spectrum that provides the accurate first electronic excitation energy and some vibrational modes in first electronically excited (S1) state. In the vibronic (1C-R2PI) spectrum the band origin of S1←S0 transition appears at 37 614 cm-1. The signal/noise ratio is so excellent that we can easily to distinguish vibronic bands of molecular vibrations 10b, 15, 9b, 14.
    The ionic spectrum recorded by MATI technique. The cationic ground (D0) state of 3,5-difluorophenol is 72 468 ± 5 cm-1. In MATI spectra, the molecule is different from other case. We use the 10b and 9b levels in the S1 to be intermediate states to record the cation spectra. However, spectral features corresponding to the 10b and 9b cation vibrations do not appear in the MATI spectra. This indicates that the transition does not follow the Franck-Condon principle. Our theoretical calculations show that the geometry of 3,5-difluorophenol is changed upon D0←S1 transition. Therefore, the calculated results support our experimental findings.

    目錄......................................................1 圖目錄....................................................4 表目錄....................................................7 中文摘要..................................................8 英文摘要..................................................9 一、簡介..................................................10 二、研究目的..............................................14 三、光譜技術..............................................16 1. 單色共振雙光子游離光譜術.............................16 2. 雙色共振雙光子游離光譜術.............................20 3. 質量解析臨界游離光譜術...............................26 四、儀器介紹..............................................34 1.真空系統..............................................34 a.束源氣室.............................................38 b.分子與雷射作用區.....................................41 c.飛行導管.............................................44 d.離子偵測區...........................................45 2.雷射系統..............................................47 a.固態銣釔鋁石榴石雷射.................................47 b.染料雷射.............................................49 3.時序控制與信號收集....................................56 五、實驗過程..............................................62 1.實驗進行前............................................62 2.實驗進行中............................................64 六、結果分析與理論計算....................................74 1.概論..................................................74 a.優化最穩定的構型.....................................75 b.分子振動頻率.........................................77 2.基底函數..............................................83 3. 光譜判定.............................................87 七、實驗結果..............................................92 1. 3,5-二氟苯酚之第一電子激態振動光譜....................92 2. 3,5-二氟苯酚光游離效率曲線............................95 3. 3,5-二氟苯酚質量解析臨界游離光譜......................98 八、結果討論.............................................104 1. 躍遷能量與游離能....................................104 2. 振動頻率與分子結構探討..............................109 九、結論................................................114 十、參考文獻.............................................115 圖目錄 圖一、3,5二氟苯酚之結構圖..............................14 圖二、單色共振雙光子游離光譜術..........................17 圖三、無法使用單色共振雙光子游離光譜術..................18 圖四、較不適合使用單色共振雙光子游離光譜術..............19 圖五、雙色共振雙光子游離光譜術(1).......................21 圖六、雙色共振雙光子游離光譜術(2)........................22圖七、雙色共振雙光子游離光譜術(3) .......................23 圖八、質量解析臨界游離光譜術............................27 圖九、MATI光譜技術實驗操作.............................28 圖十、雷德堡態分子......................................30 圖十一、高主量子數的雷德堡態............................31 圖十二、遲滯電場........................................33 圖十三、真空腔體外部構造................................36 圖十四、儀器內部構造....................................37 圖十五、脈衝閥剖面構造..................................40 圖十六、鏡組相對距離....................................42 圖十七、MCP剖面圖.....................................46 圖十八、Nd3+能階圖......................................48 圖十九、C500染料........................................52 圖二十、R590染料........................................53 圖二十一、C500使用情況..................................54 圖二十二、系統光路.......................................55 圖二十三、延遲/脈衝產生器.................................57 圖二十四、延遲時間示意圖.................................59 圖二十五、實驗設備示意圖..................................60 圖二十六、3,5-二氟苯酚吸收能量推測........................63 圖二十七、質譜轉光譜示意圖...............................66 圖二十八、1C-R2PI實驗記錄................................67 圖二十九、PIE curve實驗記錄...............................69 圖三十、MATI實驗記錄....................................70 圖三十一、3,5-二氟苯原子標號圖............................74 圖三十二、位能曲面圖......................................76 圖三十三、3,5-二氟苯酚之四項參數示意圖....................74 圖三十四、最佳化後所得振動頻率...........................78 圖三十五、3,5-二氟苯酚在第一電子激發態振動模式............87 圖三十六、苯環的30種振動模式............................89 圖三十七、1,3,5-tri-light系統................................91 圖三十八、3,5-二氟苯酚的第一電子激發態光譜..............94 圖三十九、3,5-二氟苯酚的光游離效率曲線(1)...............96 圖四十、3,5-二氟苯酚的光游離效率曲線(1).................97 圖四十一、3,5-二氟苯酚質量解析臨界游離光譜.............100 圖四十二、3,5-二氟苯酚各個離子態振動模式................101 圖四十三、3,5-二氟苯酚過多的能量........................106 圖四十四、PIE curve與MATI spectrum比較圖...............107 圖四十五、3,5-二氟苯酚標示圖............................110 圖四十六、3,5-二氟苯酚在S0、D0態之結構.................111 圖四十七、3,5-二氟苯酚在S1態之結構.....................112 表目錄 表一、譜峰頻率、理論計算數值、光譜指派及運動模式概述......93 表二、離子態振動光譜中譜峰頻率、理論計算數值、光譜指派及運動 模式概述..........................................101 表三、S0、S1、D0的譜峰頻率、理論計算(CIS/6-311++G**)數值、光 譜標定以及運動模式................................102 表四、3,5-二氟苯酚及其他相關苯酚衍生物之第一分子躍遷能與游離 能比較.............................................108 表五、以理論計算(CIS/6-311++G**)方式預測3,5-二氟苯酚在基態S0、 激發態S1及離子態D0的結構........................113

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