含雙金屬無機液晶之設計與物性探討

以作者查詢圖書館館藏

、以作者查詢臺灣博碩士

、以作者查詢全國書目

、勘誤回報

、線上人數：21

、訪客IP：3.136.19.124

姓名

鄭元輔(Yuan-Fu Cheng) 查詢紙本館藏

畢業系所

化學學系

論文名稱

含雙金屬無機液晶之設計與物性探討
(The studies of bimetallmesogens)

相關論文

★ 具有benzoxazole結構之無機液晶材料	★ 以1,3,4-thiadiazole為架構之不對稱無機液晶材料
★ 新穎香蕉形液晶及對稱含萘環之液晶分子	★ 香蕉形無機液晶
★ 具有benzoxazole結構之有機及無機液晶材料	★ 以1,3,4-thiadiazole為架構之無機盤狀液晶材料
★ 以benzoxazole為架構之無機桿狀液晶	★ 具有Quinoxaline結構之雙金屬無機液晶材料
★ 星型液晶材料及磷光發光材料之合成與研究	★ 含pyrazole及isoxazole之有機桿狀液晶
★ 矽咔哚與矽螺旋雙笏物質之放光性質研究	★ 具有Benzobisthiazoles和Benzobisoxazoles結構之盤狀液晶材料
★ 含 Benzoxazole 之對稱二聚物其奇偶效應的探討	★ 以電腦模擬研究香蕉型液晶元的分子交互作用力
★ 極性取代基對於彎曲型液晶分子的影響	★ 由彎曲型分子形成盤狀液晶之探討

檔案

[Endnote RIS 格式]

[Bibtex 格式]

[相關文章]

[文章引用]

[完整記錄]

[館藏目錄]

[檢視]

[下載]

本電子論文使用權限為同意立即開放。
已達開放權限電子全文僅授權使用者為學術研究之目的，進行個人非營利性質之檢索、閱讀、列印。
請遵守中華民國著作權法之相關規定，切勿任意重製、散佈、改作、轉貼、播送，以免觸法。

摘要(中)

本篇論文以合成三系列具不同結構形式之配位基及其金屬錯合物，與分別探考其可能之液晶相行為及性質。此三系列分為：系列一dicopper (II) complexes of 3, 4, 5-trialkoxybenzoicacid-(2-hydroxy-4- alkoxybenzyidine)hydrazides，系列二dicopper (II) complexes of 4-(tetra decanoxy-benzoicacid4-[(3,4-dialkoxybenzoyl)hydrazonomethy]-3- hydroxyphenyl esters，以及系列三2, 6-bis-(3, 4, 5-trialkoxyphenyl)- benzo[1, 2-d; 5, 4-d’]bisoxazoles。
於分子結構設計中，我們藉著改變兩邊側鏈柔軟支鏈之碳鏈長度、支鏈數目與配位基中段連接基種類，來探討其對液晶相形成所產生之影響。實驗藉1H及13C-NMR光譜來鑑定合成化合物之結構，並由元素分析值以確定錯合物之純度。於液晶相行為之探討部分，我們藉偏光顯微鏡下對不同相溫度變化範圍及液晶相種類作一初步觀察，再以DSC熱分析儀對相變化溫度及熱含量變化判別。
實驗結果得知，系列一之dicopper (II) complexes of 3,4,5-tri alkoxybenzoicacid -(2-hydroxy-4-alkoxybenzyidine)hydrazides，當其側鏈基數目為六或八根時，此系列之化合物皆為盤狀液晶，液晶相結構為Colh phase。於系列二dicopper (II) complexes of 4-(tetradecanoxy- benzoicacid4-[(3,4-dialkoxybenzoyl)-hydrazonomethy]-3-hydroxyphenyl esters；當化合物中間連接基為醚化基時，側邊只需六根側鏈基便具液晶相，然而，中間連接基為酯化基時，側邊則需增加至十根側鏈基才具液晶相，其二者之液晶相結構皆為Colh phase。系列三2, 6-bis(3, 4, 5-trialkoxphenyl)benzo[1, 2-d; 5, 4-d’]bisoxazoles，側鏈基之alkoxy groups碳數為n = 8、10、12或14時，皆具有Colh之液晶相。

摘要(英)

This thesis describes the synthesis, characterization and meso- morphic properties of three series (Series I , II , III) of organic ligands and their copper(II) complexes. These compounds include; Series I dicopper (II) complexes of 3, 4, 5-trialkoxybenzoic acid-(2-hydroxy-4- alkoxybenzyidine)hydrazides; Series II dicopper (II) complexes of 4-(tetradecanoxybenzoicacid4-[(3, 4-dialkoxybenzoyl)hydrazonomethy] -3-hydroxyphenyl esters and Series III: 2, 6-bis-(3,4,5-trialkoxphenyl) benzo[1, 2-d; 5, 4-d’]bisoxazoles.
By molecular modification of the carbon chain lengths, the number of the terminal flexible side chains and/or the linkers, the mesomorphic properties observed by these compounds were characterized and also studied in detail. For the spectroscopic characterization of all compounds, 1H and 13C NMR spectra were used to identify the structure and the purity of the compounds, and elemental analysis was also used to confirm the purity. DSC thermal analysis and optical polarised microscopy were used to characterize and confirm the structure of the liquid crystalline mesophases.
The data indicated that for the Series I, dicopper (II) complexes of 3, 4, 5-trialkoxybenzoic acid-(2-hydroxy-4-alkoxybenzyidine)hydrazides, when the numbers of the terminal flexible side chains were either six or eight these copper complexes exhibited Colh phase. The Colh phases were observed for the Series II, dicopper (II) complexes of 4-(tetradeca noxybenzoic acid 4-[(3, 4-dialkoxybenzoyl)hydrazonomethy]-3-hydroxy phenyl esters with the ether group as linker, when the carbon numbers is six, however, the same Colh phases were also formed for the copper(II) complexes with ester group as linker and side chains of ten. For the series III, 2, 6-bis-(3,4,5-trialkoxphenyl)benzo[1,2-d; 5, 4-d’]bisoxazole, these compounds exhibited Colh phases when the carbon numbers of the terminal flexible side chains are 8, 10, 12 and 14

關鍵字(中)

★ 雙金屬
★ 液晶

關鍵字(英)

★ bimetallmesogens

論文目次

中文摘要……………………………………………………I
英文摘要………………………………………………………………...II
謝誌……………………………………………………………………III
目錄……………………………………………………………………..IV
圖目錄……………………………………………………………VII
表目錄…………………………………………………………………..XI
附圖目錄……………………………………………………………XII
第一章緒論
1-1 前言……………………………………………………………2
1-2 液晶之發現與形成…………………………………………2
1-3 液晶形成之要件……………………………………………4
1-4 液晶之性質……………………………………………………4
1-5 無機液晶之特性………………………………………………6
1-6 無機液晶的設計………………………………………………8
1-7 研究動機………………………………………………………8
第二章實驗部份
2-1 實驗藥品……………………………………………………21
2-2 儀器設備……………………………………………………22
2-3 實驗流程……………………………………………………23
2-4 實驗步驟……………………………………………………29
2-4-1 系列一之合成步驟…………………………………………29
2-4-1-1 Methyl-3, 4, 5-trialkoxybenzoates之合成………………29
2-4-1-2 Ethyl-3, 4-dialkoxybenzoates之合成…………31
2-4-1-3 3, 4, 5-Trialkoxybenzoic acids之合成…………………32
2-4-1-4 3, 4-Dialkoxybenzoic acid之合成………………………34
2-4-1-5 3, 4, 5-Trialkoxybenzoic acid hydrazides之合成………35
2-4-1-6 3, 4-Dialkoxybenzoic acid hydrazide之合成…………37
2-4-1-7 4-Alkoxy -2-hydroxybenzaldehyde之合成……………...38
2-4-1-8 3, 4-Dialkoxybenzoicacid-(2-hydroxy-4-dodecanoxybenzyidine)hydrazides之合成………………………………..39
2-4-1-9 3, 4, 5-Trialkoxybenzoicacid-(2-hydroxy-4-dodecanoxybenzyidine)hydrazides之合成……………………………..42
2-4-1-10 Dicopper (II) complexes of 3, 4, 5-trialkoxybenzoicacid -(2-hydroxy-4-alkoxybenzyidine)hydrazides之合成…47
2-4-2 系列二之合成步驟………………………………………50
2-4-2-1 Methyl-4-alkoxybenzoates之合成………………………50
2-4-2-2 4-Tetradecanoxybenzoic acid之合成……………………50
2-4-2-3 4-Tetradecanoxybenzoyloxy salicylaldehyde…………….51
2-4-2-4 3, 4, 5-Tritetradecyloxy 4-acetyl-3-hydroxy-phenyl ester52
2-4-2-5 4-Tetradecanoxybenzyl alcohol…………………………52
2-4-2-6 4-Tetradecanoxybenzyl chloride…………………………53
2-4-2-7 2-Hydroxy-4-(tetradecanoxybenzyloxy)benzaldehyde…..53
2-4-2-8 4-(Tetradecanoxy-benzoicacid4-[(3,4-dialkoxybenzoyl)hydazonomethy]-3-hydroxyphenyl ester…………………….54
2-4-2-9 3, 4, 5-Tritetradecanoxybenzoicacid4-[3, 4-dialkoxyben zoyl]hydrazonomethy]-3-hydroxyphenylester…………56
2-4-2-10 4-(Tetradecanoxybenzoicacid4-[(3,4-dialkoxybenzoyl) hydrazonomethy]-3-hydroxyphenyl ester……………….57
2-4-2-11 Dicopper(II) complexes of 4-(tetradecanoxybenzoicac
id4-[(3,4-dialkoxybenzoyl)hydrazonomethy]-3-hydroxyphenyl ester之合成………………………………………….60
2-4-3 系列三之合成步驟………………………………………...62
2-4-3-1 2, 6-Bis-(3, 4, 5-trialkox-phenyl)-benzo[1, 2-d; 5, 4-d’]bisoxazole之合成…………………………………62
第三章實驗結果與討論
3-1 實驗合成與反應機構之探討………………………………67
3-2 結果討論…………………………………………………….70
3-3 結論………………………………………………………….99
參考文獻……………………………………………………………...101
附圖

參考文獻

[1] S. Pal, V. Manivannan, Polyhedron, 1999, 18, 1425.
[2] N. Hoshino, H. Murakami, Inorg. Chem. 1990, 29, 1177.
[3] T. M. Swager, C. K. Lai, Chem. Mater. 1994, 6, 2252.
[4] J. L. Serrano, M. Marcos, Chem. Mater. 2003, 15, 958.
[5] C. K. Lai, Y. F. Leu, Liq. Cryst., 1998, 25, 689.
[6] C. K. Lai, M. Yi Lu, Liq. Cryst., 1997, 23, 313.
[7] J. L. Serrano, M. Marcos, Liq. Cryst., 2003, 30, 651.
[8] R. Paschke, E. Sinn, Inorg. Chem., 2002, 41, 1949.
[9] C. K. Lai, H. D. Lin, J. Chem. Soc., Dalton Trans, 2001, 2383
[10] M. Ghedini, S. Morrone, Chem. Mater. 1991, 3, 752.
[11] M. F. Iskander, T. E. Khalil, Polyhedron, 2001, 20, 2787.
[12] C. K. Lai, S. M. Ku, J. Chem. Soc., Dalton Trans, 2001, 2383.
[13] C. Tschierske, T. Hegmann, J. Mater. Chem. 2003, 13, 991.
[14] K. Binnemans, Chem. Rev. 2002, 93, 861
[15] T. M. Swager, C.K. Lai, J. Am. Chem. Soc. 1992, 114,7948.
[16] C. K. Lai, F. J. Lin, J. Chem. Soc., Dalton Trans., 1996, 17.
[17] C. K. Lai, F. G. Che, J. Chem. Soc., Dalton Trans.,
1997, 4683.
[18] A. M. D. C. Ferreira, M. L. P. Santos, Inorg. Chem, 2003, 42, 8230.
[19] C. K. Lai, C. H. Tsai, J. Mater. Chem., 1998, 8, 1355.
[20] C. K. Lai, C. H. Chang, J. Mater. Chem., 1998, 8, 599.
[21] R. Ziessel, L. Douce, J. Mater. Chem., 1998, 8, 599.
[22] T. M. Swager, H. Zheng, Chem. Mater. 1996, 8, 907.
[23] Y. Shimizu, N. Terasawa, CHEM. COMMUN., 2003, 1678.
[24] G. F. Liu, M. H. Qi, J. Mater. Chem., 2003, 13, 2479.
[25] C. K. Lai, R. Lin, J. Mater. Chem., 2001, 11, 359.
[26] P. M. Maitlis, S. A. Hudsont, Chem. Rev. 1993, 93, 861
[27] M. Marcos, P. Romero, Chem. Mater. 1990, 2, 495
[28] M. Ghedini, S. Morrone, Chem. Mater. 1993, 5, 876.
[29] M. Marcos, J. L. Serrano, Chem. Mater. 1993, 5, 1332.
[30] M. Marcos, E. Campillos, Chem. Mater. 1993, 5, 1518.
[31] T. M. Swager, C. K. Lai, Chem. Mater. 1996, 7, 2067
[32] T. M. Swager, A. Serrette, J. Am. Chem. Soc. 1992, 114, 1889.
[33] B. Blanzat, J. Simon, J. Am. Chem. Soc. 1987, 109, 6194.
[34] J. T. Va´zquez, M. A. Pe´rez-Jubindo, J. Am. Chem. Soc. 1998, 120, 2908.
[35] Jose Luis Serrano, Mercedes Marcos, Macromolecules, 1990, 23, 5187.
[36] M. Lee, Y.S.Yoo, J. Mater. Chem., 2002, 12, 2161.
[37] M. M. Naoum, R.Nessim, Liq. Cryst. 2003, 30, 165
[38] K. B., J. Sleven, Liq. Cryst. 2002, 29, 1425.
[39] S. Kumar, J. J. Naidu, Liq. Cryst. 2002, 29, 1369.
[40] C. V. Yelamaggad, S. A. Nagamani, Liq. Cryst. 2002, 29, 1181.
[41] K. Kishikawa, S. Furusawa, J. Am. Chem. Soc. 2002, 124, 1597.
[42] H. Gallardo, E. Meyer, J. Mater. Chem., 1998, 8, 1351.
[43] A. J. Attias, P. Hapiot, Chem. Mater. 2000, 12, 461.
[44] R. V. Deun, T. N. P.Vogt, J. Mater. Chem., 2003, 13, 1639.
[45] V. F. Petrov, Liquid Cryst, 2000, 27, 393.
[46] C. K. Lai, W. R. Li, J. Mater. Chem., 2001, 11, 1763.
[47] D. Velasco, E. Perea, Liquid Cryst, 2002, 29, 421.
[48] V. F. Petrov, Liquid Cryst, 2001, 28, 217.
[49] C. ZUÂNÄIGA, J. Belmar, Liquid Cryst, 1999, 26, 389.
[50] E. T. Samulski, K. J. K. Semmler, Liquid Cryst, 1998, 24, 799.
[51] J. L. Serrano, J. Barbera´, Chem. Mater. 2003, 15, 958
[52] C. K. Lai, Y. S. Pang, J. Mater. Chem., 1998, 8, 2605.
[53] S. Kumar, J. J. Naidu, Liquid Cryst, 2003, 30, 319.
[54] A. M. D. C. Ferreira, M. L. P. Santos, J. Chem. Soc., Dalton Trans., 2001, 838.
[55] P. Berrdague, J. P. Bayle, Liquid Cryst, 2001, 28, 197.
[56] S. Mery, D. Haristoy, J. Mater. Chem., 2003, 13, 1622.
[57] P. J. Alonso, J. I. Martinez, Liquid Cryst, 1999, 26, 649.
[58] M. Bellwood, C. M. Buckley, Liquid Cryst, 1998, 25, 13.
[59] J. P. Bayle, P. Berdague, Bull Soc Chim Fr, 1994, 131, 335

指導教授

賴重光(C. K. Lai)

審核日期

2004-7-6

推文