English  |  正體中文  |  简体中文  |  Items with full text/Total items : 67621/67621 (100%)
Visitors : 23044677      Online Users : 234
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
  • Adv. Search
    HomeLoginUploadHelpAboutAdminister Goto mobile version

    Please use this identifier to cite or link to this item: http://ir.lib.ncu.edu.tw/handle/987654321/76654

    Title: 含氮氧原子之硼錯合物液晶性質探討
    Authors: 雷子暘;Lei, Zih-Yang
    Contributors: 化學學系
    Keywords: 液晶;liquid crystal
    Date: 2018-07-10
    Issue Date: 2018-08-31 11:32:09 (UTC+8)
    Publisher: 國立中央大學
    Abstract: 在系列一中成功合成出以salicylideneamines或B-enaminoketonates為配位基1a-c,並與boron difluoride (BF2)形成錯合物1a-c-BF2其中1a-c-BF2皆有液晶相的生成,藉由改變中心結構的共振長度以及增加推電子基,來觀察對液晶行為表現及光學性質的影響。並且由化合物1c-BF2 (n = 10)單晶結構可得知,中心的硼原子為四面體,並且兩苯環之間的兩面角為81.3˚,這也導致了化合物1c-BF2大多缺乏液晶相。化合物1b-BF2擁有SmC的桿狀型液晶相而化合物1a-BF2和1c-BF2則為SmA相。三化合物的放光波長在溶液態λmax = 476-541 nm而在固態時其放光則在λmax = 488-550 nm,而化合物1c-BF2在固態時則具有AIEE (Aggregation induced enhanced emission),可做為一良好的發光材料 。
    第二系列成功以B-enaminoketonates作為主體,以不同的連接基做置換並與boron difluoride (BF2)形成錯合物2-3-BF2,其中化合物2b-BF2 (n = 12, m = 2, 3)和2c-BF2並無液晶相產生,而以萘環取代苯環的化合物3b-BF2 (m = 2, 3)和3c-BF2因為擁有較平整的分子平面,分子間的堆疊較好因此可誘導出液晶相。經由偏光紋理圖與powder X-ray diffraction實驗結果判定2a-BF2、2b-BF2 (n = 12, m = 0)、3a-BF2、3b-BF2 (m =2)為SmC桿狀液晶,而3b-BF2 (m =3)和3c-BF2為SmA桿狀液晶。另外從培養出的化合物2a-BF2 (n = 12)單晶探討分子之排列情形與作用力多寡。化合物23-BF2以UV可見光光譜、螢光光譜探討該分子的光學性質,從結果可得知中心結構以苯環或者直接相連接時,因延伸其共振使得最大的放光波長紅移,即 max = 523 (2a-BF2), 518 (2b-BF2 (m = 0)), 538 (3a-BF2)。放光為黃綠色光。;In the first part, Three new families of borondifluoride complexes 1a-c-BF2 derived from salicylideneamines 1a and B-enaminoketonates 1b-c were reported, and their mesomorphic and optical properties were also investigated. One single crystal and molecular structure of nonmesogenic BF2 complex 1c-BF2 (n = 10) was resolved and the geometry of the central boron atom was tetrahedron. A larger dihedral angle of 81.3˚ between the two phenyl rings observed in crystal lattice was contributed to the lack of liquid crystallinity. Boron complexes 1a-BF2 formed monotropic SmA phases, while boron complexes 1b-BF2 exhibited enantiotropic SmC mesophases. The optical property of the boron complexes was dependent on their molecular structures, and they emitted a blue-to-green emission at max = 476-541 nm in the solution and 488-550 nm in the solid state. The
    1c-BF2 have the property of AIEE (Aggregation-induced enhanced emission), and it can be a protential material of luminescence. In the second part, two new series of bis-(boron difluoride) complexes 2-3-BF2 derived from substituted B-enaminoketonates 2-3 were reported, and their mesomorphic and optical properties were also investigated. 2b-BF2 (n = 12, m = 2, 3) and 2c-BF2 were not mesogens. The single crystal of mesogenic boron complex 2a-BF2 (n = 12) was obtained, and its single crystal and molecular structures were resolved. Results appeared that bis-(BF2) complexes 2a-BF2, 2b-BF2 (n = 12, m = 0), 3a-BF2 and 3b-BF2 (m =2) exhibited smectic C phases. However, 3b-BF2 (m =3) and 3c-BF2 exhibited smectic A phases. In the result, the emission of 2a-BF2, 2b-BF2 and 3a-BF2 red shift to 523, 518 and 538 nm respectively because of their resonance structure. Also, their colors of emission are yellow-green.
    Appears in Collections:[化學研究所] 博碩士論文

    Files in This Item:

    File Description SizeFormat

    All items in NCUIR are protected by copyright, with all rights reserved.

    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 ©   - Feedback  - 隱私權政策聲明