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完整後設資料紀錄
DC 欄位 | 值 | 語言 |
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dc.contributor.advisor | 劉廣定(Kwang-Ting Liu) | |
dc.contributor.author | Jin-Yi Liau | en |
dc.contributor.author | 廖晉逸 | zh_TW |
dc.date.accessioned | 2021-06-13T06:43:27Z | - |
dc.date.available | 2005-08-01 | |
dc.date.copyright | 2005-08-01 | |
dc.date.issued | 2005 | |
dc.date.submitted | 2005-07-29 | |
dc.identifier.citation | (1) Ringsdorf, H. Angew. Chem. Int. Ed. Engl. 1988, 27, 113.
(2) Finkelmann, H.; Rehang, G. Adv. Polym. Sci. 1984, 60, 99. (3) Niori, T.; Sekine, F.; Watanabe, J.; Furukawa, T.; Takezoe, H. J. Mater. Chem. 1996, 6, 1231. (4) Shen, D.; Pegenau, A.; Diele, S.; Wirth, I.; Tschierske, C. J. Am. Chem. Soc. 2000, 122, 1593. (5) W. Weissflog, C. Lischka, I. Benne, T. Scharf, G. Scharf, G. Pelzl, S. Diele, H. Kruth, Proc. SPIE: Int. Soc. Opt. Eng. 1998, 3319, 12. (6) Pelzl, G.; Shen, D.; Weissflog, W. Adv. Mater. 1999, 11, 707. (7) Shen, D.; Diele, S.; Pelzl, G.; Wirth, I.; Tschierske, C. J. Mater. Chem. 1999, 9, 661. (8) Mieczkowski, J.; Szydlowska, J.; Matraszek, J.; Pociecha, D.; Gorecka, E.; Donnio, B.; Guillon, D. J. Mater. Chem. 2002, 12, 3392. (9) Rouillon, J. C.; Marcerou, J. P.; Laguerre, M.; Nguyen, H. T.; Achard, M. F. J. Mater. Chem. 2001, 11, 2946. (10) Nguyen, H. T.; Rouillon, J. C.; Marcerou, J. P.; Bedel, J. P.; Barois, P.; Sarmento, S. Mol. Cryst. Liq. Cryst. 1999, 177. (11) Bedel, J. P.; Nguyen, H. T.; Rouillon, J. C.; Marcerou, J. P.; Sigaud, G.; Barois, P. Mol. Cryst. Liq. Cryst. 1999, 2673. (12) Jin, J. J.; Kong, C. S.; Kung, B. Y. Bull. Korean. Chem. Soc. 1990, 11, 245. (13) Wirth, I.; Diele, S.; Eremin, A.; Pelzl, G.; Grande, S.; Kovalenko, L.; Pancenko, N.; Weissflog, W. J. Mater. Chem. 2001, 11, 1642. (14) Mieczkowski, J.; Szydlowska, J.; Matraszek, J.; Pociecha, D.; Gorecka, E.; Donnio, B.; Guillon, D. J. Mater. Chem. 2002, 12, 3392. (15) Dantlgraber, G.; Shen, D.; Diele, S.; Tschierske, C. Chem. Mater. 2002, 14, 1149. (16) Keum, C. D.; Kanazawa, A.; Ikeda, T. Adv. Mater. 2001, 13, 321. (17) Sadashiva, B. K.; Shreenivasa Murthy, H. N. J. Mater. Chem. 2004, 14, 2813. (18) 陸勤偉, 碩士論文, 國立台灣大學化學研究所, 2003. (19) Solomons, T. W. G. “Organic Chemistry”, John Wiely & Sons, Inc.,(Sixth Edition)p.823. (20) Arduini, A.; Fabbi, M.; Mantovani, M.; Mirone, L.; Pochini, A.; Secchi, A.; Ungaro, R. J. Org. Chem. 1995, 60, 1454. (21) Karl, J.; Gust, R.; Spruss, T.; Schneider, M. R.; Schonenberger, H.; Engel, J.; Wrobe1, K.-H.; Lux, F.; Haeberlin, S. T. J. Med. Chem. 1988, 31, 72. (22) Lawrence, N. J.; Hepworth, L. A.; Rennison, D.; McGown, A. T.; Hadfield, J. A. J. of Fluorine Chem. 2003, 123, 101. (23) Speicher, A.; Kolz, J.; Sambanjc, R. P. Synthesis 2002, 17, 2503. (24) Rao, M.G. S.; Srikantia, C.; Iyengar, M.S. J. Chem. Soc. 1924, 524. (25) Reddy, R. A.; Sadashiva, B. K. J. Mater. Chem. 2002, 12, 2627. (26) Durrani, A. A.; Tyman, J. H. P. J. Chem. Soc. Perkin Trans. 1, 1980, 1658. | |
dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/35187 | - |
dc.description.abstract | 繼續以前本研究室探討以酯類做為連接基的香蕉形分子的取代基效應。本論文對末端側鏈進行改變,結果顯示改變側鏈長短有可能會影響分子構形,進而造成液晶相的不同。另外採用不同的側鏈連結基,並固定碳鏈長短以比較其異同,數據顯示當連結基由烷氧基改為酯基時,液晶相範圍變大同時澄清點上升,而當改為烷基時,則不利於液晶相的產生。
另在側環(B環)上導入不同的取代基,結果發現B環上含有取代基不利於液晶相的產生,除了取代基為氟的分子有機會產生液晶相外,其他的取代基皆使得液晶相消失。最後我們將C 環改為吡啶環,結果顯示,相較於苯環,吡啶環不利產生液晶相。 | zh_TW |
dc.description.abstract | A series of banana-shaped organic molecules which have a central aromatic ring (C ring) modified by different substituents and four side aromatic rings linked by ester bonds were synthesized and characterized in our earlier work. In this research, we aim toward the modification of terminal side chains on the molecules. Results show that the modification of chain length will alter the mesophases due to different molecule geometry. In addition, we modified the molecules with several different linkages but maintain the same carbon chain length. Results show that molecules with ester linkages prefer a larger mesophase temperature range and higher transition temperature between liquid crystal mesophase and isotropic phase comparing to ether linkages. Molecules with pure alkyl side chains are unfavorable to form liquid crystal mesophases.
On the other hand, the addition of substitents on side ring B will diminish the appearance of liquid crystal mesophases except fluorine. Also, the replacement of central benzene ring (C ring) with a pyridine ring results in the disappearance of liquid crystal mesophases as well. | en |
dc.description.provenance | Made available in DSpace on 2021-06-13T06:43:27Z (GMT). No. of bitstreams: 1 ntu-94-R91223027-1.pdf: 8467249 bytes, checksum: 80a09639d9207795c08771fd58f5e3cb (MD5) Previous issue date: 2005 | en |
dc.description.tableofcontents | 謝誌
摘要 第一章 序論 1 1-1前言 2 1-2 液晶的發現 2 1-3 液晶的分類 3 1-4 熱向型液晶 5 1-4-1 桿狀液晶相 6 1-4-2 盤狀液晶相 11 1-5 液晶相的鑑定 13 1-6 液晶的性質 15 1-7 鐵電性 17 1-8 香蕉形液晶 20 1-9 研究動機 27 1-10 參考文獻 28 第二章合成步驟及光譜數據 30 2-1 目標分子 31 2-2 實驗藥品 33 2-3 儀器設備 35 2-4 合成路徑 38 2-5 實驗流程及結果 40 第三章 討論 95 3-1 合成步驟之討論 96 3-1-1 醚化反應 96 3-1-2 酯化反應 97 3-1-3 氧化反應 98 3-1-4 醯化反應 99 3-1-5 氯化反應 100 3-1-6 硝化反應 100 3-1-7 氫解反應 100 3-1-8以吡啶(pyridine)為中心環之酯化反應 101 3-1-9 不對稱香蕉形分子之合成 102 3-1-10 4-氟-間苯二酚(4-Fluoro-resorcinol)之合成嘗試 102 3-2 香蕉形分子液晶性質之討論 103 3-2-1 側鏈長短對香蕉形分子的影響 103 3-2-1-1 無取代基之香蕉形分子 103 3-2-1-2 中心苯環C-4位置為氯取代基之香蕉形分子 105 3-2-2 側鏈種類對香蕉形分子的影響 108 3-2-3 側環取代基對香蕉形分子的影響 110 3-2-4 雜環中心之香蕉形分子 115 3-3結論 117 3-4參考文獻 118 附圖 | |
dc.language.iso | zh-TW | |
dc.title | 側環取代基與尾端側鏈對香蕉形分子液晶性質影響之研究 | zh_TW |
dc.title | Studies on the Substituent Effects of Side Ring and Side Chain of Banana-Shaped Molecules | en |
dc.type | Thesis | |
dc.date.schoolyear | 93-2 | |
dc.description.degree | 碩士 | |
dc.contributor.oralexamcommittee | 徐秀福(Hsiu-Fu Hsu),邱勝賢(Sheng-Hsien Chiu) | |
dc.subject.keyword | 香蕉型,液晶,側鏈,取代基效應, | zh_TW |
dc.subject.keyword | banana-shape,liquid crystal,side chain,substituent effect, | en |
dc.relation.page | 118 | |
dc.rights.note | 有償授權 | |
dc.date.accepted | 2005-07-30 | |
dc.contributor.author-college | 理學院 | zh_TW |
dc.contributor.author-dept | 化學研究所 | zh_TW |
顯示於系所單位: | 化學系 |
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