簡易檢索 / 詳目顯示

研究生: 簡靜瑜
Jian, Jing-Yu
論文名稱: 含三原子螯合配位基銥(Ⅲ)價錯合物的合成,構造,與特性之研究
A Study on Synthesis, Structures, and Properties of Iridium(Ⅲ) Complexes containing Three-Atom Chelates
指導教授: 許拱北
Shiu, Kom-Bei
學位類別: 碩士
Master
系所名稱: 理學院 - 化學系
Department of Chemistry
論文出版年: 2008
畢業學年度: 96
語文別: 中文
論文頁數: 89
中文關鍵詞: 銥金屬三原子
外文關鍵詞: iridium, three-atom
相關次數: 點閱:71下載:1
分享至:
查詢本校圖書館目錄 查詢臺灣博碩士論文知識加值系統 勘誤回報
  • 一系列含3原子螯合的4員環bis-cyclometallated Ir(III)化合物被合成與鑑定,將[Ir( 2-C^N)2Cl]2 1和AgNO3反應可以得到化合物 [Ir(2-C^N)2(MeCN)2]NO3 (C^N= 2-phenylpyridine (ppy, S1)、2-p-tolylpyridine (tpy, S2)、和ethyl 4-(pyridin-2-yl)benzoate (epbo, S3))。在三乙基胺存在時以S1和benzoic acid (bz), 2-methylacrylic acid (ma), 1,1,1- trimethylacetic acid (tma), acetic acid (ac) 反應得到[Ir(2-ppy)2(2-X)] (X= bz (1a), ma (1b), tma (1c),和 ac (1d))。以S1、S2、和S3個別和Na(Et2NCS2) 、K(MeOCS2)、 K(EtOCS2)、 K[(CH3)2CHOCS2]等配位基在MeCN中迴流反應,也同樣得到化合物[Ir(2-ppy)2(2-Y)] (Y= Et2NCS2 (1e)、 MeOCS2 (1f)、EtOCS2 (1g)、(Me)2CHOCS2 (1h));[Ir(2-tpy)2(2-Y)] (Y= Et2NCS2 (2e)、MeOCS2 (2f)、EtOCS2 (2g)、(Me)2CHOCS2 (2h)),和[Ir(2-epbo)2(2-Y)] (Y= Et2NCS2 (3e)、MeOCS2 (3f)、EtOCS2 (3g))。所有的錯合物,均利用元素分析、IR及NMR光譜進行鑑定,其中1a、1b、1c、1g、1h、2g、2h也進一步得到X光繞射數據,並解出構造,此外所有化合物的光物理性質也被研究。

    A series of bis-cyclometallated Ir(III) compounds containing 3 atom chelates has been prepared and characterized. Reaction of [Ir(h2-C^N)2Cl]2 1 with AgNO3 produced [Ir(h2-C^N)2(MeCN)2]NO3 (C^N= 2-phenylpyridine ( ppy, S1), 2-p-tolylpyridine ( tpy, S2), ethyl 4-(pyridin-2-yl)benzoate (epbo, S3)). Further reaction of S1 with benzoic acid(bz), 2-methylacrylic acid (ma), 1,1,1-trimethylacetic Acid (tma), acetic acid (ac) in the presence of excess Et3N yieled [Ir(h2-ppy)2(h2-X)] (X= bz(1a), ma (1b), tma (1c), ac (1d)). Reaction of (S1), tpy (S2), epbo(S3) with Na(Et2NCS2) , K(MeOCS2), K(EtOCS2), and K[(CH3)2CHOCS2] produced likewise [Ir(h2-ppy)2(h2-Y)] (Y= Et2NCS2 (1e), MeOCS2 (1f), EtOCS2 (1g), (Me)2CHOCS2 (1h)) , and [Ir(h2-tpy)2(h2-Y)] (Y= Et2NCS2 (2e), MeOCS2 (2f), EtOCS2 (2g), (Me)2CHOCS2 (2h)) , and [Ir(h2-epbo)2(h2-Y)] (Y= Et2NCS2 (3e), MeOCS2 (3f), EtOCS2 (3g)). All compounds have been characterized by EA, IR, and NMR spectroscopy. Compounds 1a, 1b, 1c, 1g, 1h, 2g, and 2h have been further collecting the respective X-ray diffraction data and solved for the solid state structure. The photophysical properties of all new complexes were also studued.

    目錄 摘要 I Abstract II 致謝 III 第一章緒論 1 1-1. 引言 1 1-2. OLED發光原理 3 1-3. 螢光(Fluorescence)材料與磷光材料8 5 1-4. Ir(III) 化合物 7 1-4-1 含6員環的bis-cyclometallated Ir(III)錯合物 8 1-4-2 含5員環的bis-cyclometallated Ir(III)錯合物 10 1-4-3 含4員環的bis-cyclometallated Ir(III)錯合物 13 1-4-4 Ir化合物軌域理論計算 15 1-5. 實驗動機 16 第二章實驗部份 17 2-1. 實驗與儀器操作 17 2-2. 實驗藥品 21 2-3. 實驗儀器/軟體 22 2-4. 實驗合成 23 第三章結果與討論 35 3-1. 雙氧基金屬化合物 35 3-1-1. 晶體結構的探討 35 3-1-2. 物理光學性質 38 3-2. 雙硫基金屬化合物 42 3-2-1 晶體結構的探討 42 3-2-2 光學性質 44 3-2-3 MeOCS2配位的Ir化合物 49 第四章結論 53 參考資料 54 附錄 56

    1.R. J. Watts., J. Am. Chem. Soc., 106, 6647, 1984
    2.M.E. Thompson, J. Am. Chem. Soc., 123, 4304, 2001
    3.Watts, R. J., J. Am. Chem. Soc., 107, 1431, 1985
    4.Crutchley, R. J., J. Am. Chem. Soc., , 126, 7619, 2004
    5.F. Sato, Appl. Phys. Lett., 83, 2459, 2003
    6.Tang, C. W. and VanSlyke, S. A., Appl. Phys. Lett., 51, 913, 1987
    7.Tang, C. W.; VanSlyke; S. A. and Chen, C. H., J. Appl. Phys., 65, 3610, 1989
    8.吳麗嵐,苯基吡啶銥金屬及苯基仳唑銥金屬於有機發光元件的應用,95年成功大學化學所碩士論文
    9.Baldo, M. A.; O’Brien, D. F.; You, Y.; Shoustikov, A.; Sibley, S.; Thompson, M. E.; Forrest, S. R., Nature, 395, 151, 1998
    10.Thompson, M. E.; Shoustikov, A.; You, Y.; Sibley, S.; Baldo, M.; Koslov, V.; Burrows, E. P.; Forrest, S. R. MRS Abstract, G2.4, Spring Meeting, 1998.
    11.O’Brien, D. F.; Baldo, M. A.; Thompson, M. E.; Forrest, S. R., Appl. Phys. Lett, 74, 442, 1999
    12.Baldo, M. A.; O’Brien, D. F.; Thompson, M. E.; Forrest, S. R., Phys. Rev. B, 60, 14422, 1999.
    13.Jiang, X; Liu, Y.; Song, X. and Zhu D., Synth. Met., 87, 175, 1997.
    14.Pielichowski, J.; Chrzszcz, R.; Nizio, S.; Barta, P. and Sanetra, J., Synth. Met., 94, 123, 1998.
    15.Hanai, N.; Sumitomo, M. and Yanag, H., Thin Solid Films, 331, 106, 1998.
    16.Vestweber, H. and Rieβ, W., Synth. Met., 91, 181, 1997.
    17.Riel, H.; Brütting, W.; Bererlein, T.; Haskal, E.; Müller, P. and Riess, W., Synth. Met., 111, 303, 2000.
    18.Zhilin, Z.; Xueyin, J. and Shaohong, X., Thin Solid Films, 363, 61, 2000.
    19.Era, M.; Tsutsi, T. and Saito, S., Appl. Phys. Lett., 67, 2436, 1995.
    20.Aminaka, E. I.; Tsutsui, T. and Saito, S., J. Appl. Phys., 79, 8808, 1996.
    21.Era, M.; Tsutsi, T.; Takehara, K.; Isomura, K. and Taniguchi, H., Thin Solid Films, 363, 229, 2000.
    22.Hung, L. S.; Tang, C. W. and Mason, M. G., Appl. Phys. Lett., 70, 152, 1997.
    23.Staudigel, J.; Stöβel, M.; Steuber, F.; Blässing, J. and Simmerer, J., Synth. Met., 111-112, 69-73, 2000.
    24.Mark E. Thompson, Inorg. Chem., 40, 1704, 2001
    25.Jian Li, Peter I. Djurovich, Bert D. Alleyne, Muhammed Yousufuddin, Nam N. Ho, J. Christopher Thomas, Jonas C. Peters, Robert Bau, and Mark E. Thompson , Inorg. Chem., 44, 1713, 2005
    26.Qiang Zhao, Shujuan Liu, Mei Shi, Chuanming Wang, Mengxiao Yu, Lei Li, Fuyou Li, Tao Yi, and Chunhui Huang, Inorg. Chem., 45, 6152, 2006
    27.Arnold B. Tamayo, Bert D. Alleyne, Peter I. Djurovich, Sergey Lamansky,Irina Tsyba, Nam N. Ho, Robert Bau, and Mark E. Thompson, J. Am. Chem. Soc., 125, 7377, 2003
    28.Kari A. McGee and Kent R. Mann, Inorg. Chem., 46, 7800, 2007
    29.Wa-Hung Leung, J. Organomet. Chem., 689, 2401, 2004
    30.Shao-Pin Wang, and I-Wen Sun, Organometallics , 25, 4514, 2006
    31.Heinz Bassler, Adv. Mater., 7, 551, 1995
    32.J. A. Cronin and M. E. Thompson., J. Appl. Phys. 79, 7991, 1996

    下載圖示 校內:2018-07-08公開
    校外:2018-07-08公開
    QR CODE