中大機構典藏-NCU Institutional Repository-提供博碩士論文、考古題、期刊論文、研究計畫等下載:Item 987654321/71288
English  |  正體中文  |  简体中文  |  全文筆數/總筆數 : 78728/78728 (100%)
造訪人次 : 34363081      線上人數 : 682
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
搜尋範圍 查詢小技巧:
  • 您可在西文檢索詞彙前後加上"雙引號",以獲取較精準的檢索結果
  • 若欲以作者姓名搜尋,建議至進階搜尋限定作者欄位,可獲得較完整資料
  • 進階搜尋


    請使用永久網址來引用或連結此文件: http://ir.lib.ncu.edu.tw/handle/987654321/71288


    題名: 含quinoxaline桿狀分子之液晶行為探討
    作者: 柯婉平;Ko,Wan-Ping
    貢獻者: 化學學系
    關鍵詞: 氫鍵;桿狀液晶;層列型液晶;向列型液晶;quinoxaline;schiff base;benzoxazole;pyrazole;isoxazole;oxadiazole
    日期: 2016-07-13
    上傳時間: 2016-10-13 12:40:28 (UTC+8)
    出版者: 國立中央大學
    摘要: 本篇論文主要包含具有quinoxaline結構之有機液晶。所有化合物經由1H-NMR、13C-NMR、元素分析以鑑定其結構及純度,液晶相性質則是利用偏光顯微鏡(POM)來觀測相種類及熱差式掃描分析儀(DSC)測量相變化時之溫度與熱焓值,也藉由氫譜的訊號位移去探討分子內雜環的推拉電子性質,並進一步與UV—可見光光譜的訊號位移相互佐證,最後以變溫粉末X光繞射儀確認相的種類及單晶X光繞射得到的單晶數據去探討其分子的作用力與排列。
    在本篇論文中,以分子中心的quinoxaline分別接上長碳鏈、帶有imine的基團或benzoxazole雜環去合成系列一的1a、1b、1c及1d四種化合物,並對其液晶相、排列還有UV—可見光吸收所造成的影響。而在系列二將探討以quinoxaline為中心但具有不同imine位向的Schiff Base化合物1c及2,我們發現由於分子連結基部份的C = N位置差異,產生不同種類的氫鍵進而對相變化、液晶性質、推拉電子效應及分子排列造成影響。系列三則是將quinoxaline雜環各別與isoxazole、pyrazole及oxadiazole做連結即化合物3a、3b與3c,探討此三者雜環對液晶相的影響以及不同雜環下推拉電子特性對其吸收光譜的差異討論。;In this three series , new compounds were prepared and their
    mesomorphic properties were investigated. All organic derivatives were
    characterized by 1H-NMR and 13C-NMR spectroscopy. The mesomorphic
    behavior of these compounds were investigated by polarized optical microscopy (POM), differential scanning calorimetry (DSC), and powder X-ray diffraction (XRD) measurement.
    In series I, rod-like molecules based on quinoxalines 1a was synthesized. Furthermore, the similar compounds containing an imine moiety 1b 、 1c and its cyclized product, Benzoxazoles 1d are also described and their mesomorphic properties examined.
    In series II, heterocyclic quinoxaline Schiff Base 2 were prepared, characterized and their mesomorphic properties investigated. These compounds 1c and 2 are in fact geometric isomers in which an inime moiety (e.g. –C=N) is inversely incorporated into quinoxaline, leading to an opposite local dipole. Intra- and intermolecular H-bonds were found in both crystals.
    In series III, Both Quinoxaline and three different kinds of five membered rings contained molecules, 3a、3b and 3c, were synthesized. All compounds are rod-lke mesogens. Due to the different five-membered ring, the electron-withdrawing abilities were examined by NMR spectrum.
    顯示於類別:[化學研究所] 博碩士論文

    文件中的檔案:

    檔案 描述 大小格式瀏覽次數
    index.html0KbHTML299檢視/開啟


    在NCUIR中所有的資料項目都受到原著作權保護.

    社群 sharing

    ::: Copyright National Central University. | 國立中央大學圖書館版權所有 | 收藏本站 | 設為首頁 | 最佳瀏覽畫面: 1024*768 | 建站日期:8-24-2009 :::
    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - 隱私權政策聲明