透過您的圖書館登入
IP:3.21.106.69
  • 學位論文

可溶性含四羧酸-鈷、鎳配位聚合物之自組裝合成與重組

Soluble Metal-Organic Frameworks: Dissolution/Reassembly towards the Structural Rearrangement of Porous Cobalt(II)- and Nickel(II)–Carboxylate Coordination Polymers

指導教授 : 呂光烈 李光華
若您是本文的作者,可授權文章由華藝線上圖書館中協助推廣。

摘要


本論文研究重點在於利用自組裝的方式,將四羧酸benzene-1,2,4,5-tetracarboxylic acid (H4btec)與鈷、鎳金屬離子利用水熱合成法製備具有孔洞結構的金屬-有機配位聚合物。 利用H4btec與鈷、鎳金屬離子經由自組裝的方式合成四個三維孔洞結構{K2[Co3(btec)2(H2O)4]∙6H2O}n (1•6H2O)、{K2[Ni3(btec)2(H2O)4]•4H2O}n (2•4H2O)、{Cs2[Co3(btec)2(H2O)4]•3H2O}n (3•3H2O)與{Cs2[Ni3(btec)2(H2O)4]•3H2O}n (4•3H2O)。此四個化合物皆由具4個連接樞紐之btec4-為節點與具8個連接樞紐之三核金屬簇M3(O2C)8(H2O)4為另一節點構成(4,8)-連接網狀架構,均具有ㄧ維親水通道之三維金屬-有機孔洞配位聚合物,鹼金屬陽離子(KI或CsI)與客分子水都充斥在孔道中。 上述所生成之可溶性三維金屬-有機孔洞配位聚合物均可溶於鹼金屬氯化鹽(LiCl、NaCl、KCl、CsCl)水溶液中。藉由拆解-重組的方式,可溶性金屬-有機配位聚合物(1~4)會溶解而重新組合轉變為新的化合物(5~13)。其結構藉由單晶及粉末繞射技術鑑定,其固態結構之變化頗為豐富有趣,其中化合物1、6、9,之間有結構轉換性,這更是本篇論文最有趣的地方。

並列摘要


The goal of this study was to develop a self-assembly synthetic strategy for the preparation of metal–organic coordination polymers using benzene-1,2,4,5-tetracarboxylic acid (H4btec) and transition-metal ions (CoII, NiII). Four three-dimensional, soluble, porous metal–organic coordination networks {K2[Co3(btec)2(H2O)4]∙6H2O}n (1•6H2O), {K2[Ni3(btec)2(H2O)4]•4H2O}n (2•4H2O), {Cs2[Co3(btec)2(H2O)4]•3H2O}n (3•3H2O), and {Cs2[Ni3(btec)2(H2O)4]•3H2O}n (4•3H2O) with near identical structural features were hydrothermally prepared. These structures adopt a (4,8)-connected net consisting of a four-connected square-planar node of a btec4- ligand and an eight-connected node of trinuclear clusters M3(O2C)8(H2O)4. These three-dimensional frameworks possess hydrophilic channels, where the alkali metal ions (KI or CsI) and free water molecules reside. Ion-exchange studies, by treating 1~4 in an aqueous solution of alkali chloride (LiCl, NaCl, CsCl and KCl), revealed that a surprisingly dissolution/reassembly process occurred, leading to the rearrangement of metal–carboxylate building blocks and the formation of new metal–carboxylate species (5~13). The structural transformations were confirmed by single-crystal and powder X-ray diffraction (PXRD) data

參考文獻


[14](a) Akine, S.; Taniguchi, T.; Nabeshima, T. Inorg. Chem. 2004, 43, 6142. (b) Akine, S.; Taniguchi, T.; Nabeshima, T. J. Am. Chem. Soc. 2006, 128, 15765. (c) Akine, S.; Sunaga, S.; Taniguchi, T.; Miyazaki, H.; Nabeshima, T. Inorg. Chem. 2007, 46, 2959.
[17](a) Kumagai, H.; Kepert, C. J.; Kurmoo, M. Inorg. Chem. 2002, 41, 3410. (b) Shi, X.; Zhu, G.; Wang, X.; Li, G.; Fang, Q.; Wu,G.; Tian, G.; Xue, M.; Zhao, X.; Wang, R.; Qiu, S. Cryst. Growth Des. 2005, 5, 207. (c) Tian, Z.; Song, T.; Fan, Y.; Shi, S.; Wang, L. Inorg. Chim. Acta 2007, 360, 3424. (d) Bo, Q. B.; Sun, Z. X.; Sheng, Y. L.; Zhang, Z.W. Sun, G. X.; Chen, C. L.; Li, Y. X.; Wang, D. Q. Struct. Chem. 2006, 17, 609. (e) Sun, D.; Cao, R.; Liang, Y.; Shi, Q.; Hong, M. J. Chem. Soc., Dalton Trans., 2002, 1847. (f) Hou, Y.; Wang, S.; Shen, E.; Wang, E.; Xiao, D.; Li, Y.; Xu, L.; Hu, C. Inorg. Chim. Acta 2004, 357, 3155. (g) Cao, R.; Shi, Q.; Sun, D.; Hong, M.; Bi, W.; Zhao, Y. Inorg. Chem. 2002, 41, 6161. (h) Li, Y.; Zhang, H.; Wang, E.; Hao, Na.; Hu, C.; Yanc, Y.; Hall, D. New J. Chem., 2002, 26, 1619. (i) Li, Y.; Hao, N.; Lu, Y.; Wang, E.; Kang, Z.; Hu, C. Inorg. Chem. 2003, 42, 3119. (j) Li, Y.-G.; Hao, N.; Wang, E.-B.; Lu, Y.; Hu, C.-W.; Xu, L. Eur. J. Inorg. Chem. 2003, 14, 2567.
[12](a) Jung, O.-S.; Kim, Y. J.; Kim, K. M.; Lee, Y.-A. J. Am. Chem. Soc. 2002, 124, 7906. (b) Jung, O.-S.; Kim, Y. J.; Lee, Y.-A.; Chae, H. K.; Jang, H. G.; Hong, J. Inorg. Chem. 2001, 40, 2105. (c) Min, K. S.; Suh, M. P. J. Am. Chem. Soc. 2000, 122, 6834. (d) Noro, S.-I. ; Kitaura, R.; Kondo, M.; Kitagawa, S.; Ishii, T.; Matsuzaka, H.; Yamashita, M. J. Am. Chem. Soc. 2002, 124, 2568.
[2]Lehn, J.-M. Science 1985, 227, 849.
[3]Lehn, J.-M. Angew. Chem., Int. Ed. Engl. 1988, 27, 90.

延伸閱讀