研究生: |
鄒文力 Wen-li Tzou |
---|---|
論文名稱: |
偶氮吡唑哢衍生物之合成及性質探討 Synthesis and properties of azopyrazolones derivatives |
指導教授: |
王英靖
Ing-Jing Wang |
口試委員: |
陳耿明
Keng-Ming Chen 許應舉 Ying-Gev Hsu |
學位類別: |
碩士 Master |
系所名稱: |
工程學院 - 材料科學與工程系 Department of Materials Science and Engineering |
論文出版年: | 2006 |
畢業學年度: | 94 |
語文別: | 中文 |
論文頁數: | 97 |
中文關鍵詞: | 吡唑哢〔15-a〕嘧啶 、偶氮吡唑哢 |
外文關鍵詞: | pyrazolo〔15-a〕pyrimidine, azopyrazolone |
相關次數: | 點閱:283 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 |
本研究以聯胺衍生物(hydrazine derivatives)與氰基乙酸乙酯(Ethyl cyanoacetate)為起始原料,在乙醇中進行縮合反應製備吡唑哢中間体(3);再以芳香族胺行偶合反應形成4-苯偶氮基-3-胺基-吡唑哢的單偶氮染料(6),或以氰基乙酸乙酯與芳香胺先行偶合反應,再以聯胺衍生物反應形成上述相同吡唑哢偶氮染料。隨後,將其吡唑哢偶氮染料(6)與二酮類衍生物進行反應形成一系列吡唑哢〔1,5-a〕嘧啶化合物。所合成之化合物均經(MS、FT-IR、1H-NMR等)光譜鑑定及元素分析(EA)來確定其化學結構。
In this study, pyrazolone intermediate(3) have been synthesized by the cyclization of ethyl cyanoacetate with hydrazine derivatives. 4-Arylazo-3-amino-2-pyrazolin-5-one monoazo dyes(6) were prepared by the coupling reaction of pyrazolone intermediates with aniline derivatives,or obtained from cyanoarylhydrazono-acetic acid ethyl ester with hydrazine derivatives, respectively. The compounds(6) were reacted with diketone derivatives to give pyrazolo〔1,5-a〕pyrimidine azodyes. All the structures were determined by MS, FT-IR, and1H-NMR.
1. A. Cee, B. Horakova and A. Lycka,; Dyes and Pigments; 9(1988)375.
2. C. C. Chen and I. J. Wang,; Dyes and Pigments; 15(1991)69.
3. Japanese Patent 7881780.
4. Patent EP 413,229.
5. A. Weissberger, and H. D. Porter,; J. Am. Chem. Soc.; 64 (1942) 2133.
6. A. Weissberger, and H. D. Porter,; J. Am. Chem. Soc.; 71(1949) 983.
7. M. S. A. EI-Gaby, A. A. Atalla, A. M. Gaber, and K. A. Abd Al-Wahab,; Il Farmaco; 55 (2000) 596.
8. A. A. Nada, N. R. Mohamed, A. M. Mahran, and Y. A. Ibrahim,; Heterocycl. commun.; 4(3) (1998) 271-276.
9. T.Ishimaru; Chem. Abstr.; 51 (1957) 17892.
10. E. M. Abd-Allah, N. M. Rageh, and H. M. A. Salman; J. Chem. Eng. Data.; 48 (2003) 652.
11. H. Zollinger,; Color Chemistry; 8 (1988) 401.
12. B. Trathnigg, G. Uray, and H. Junek,; Angew. Makromol. Chem; 79 (1979) 207.
13. L. A. Ltutlya, V. F. Morina, A. E. Shevchenko and Yu. N. surov,; Zh. Prikl. Speltr; 27 (1977) 76.
14. B. M. Krasovitslii, D. G. Peeyaslova, V. T.Skripkina,; Dyes and Pigments; 9 (1988) 21.
15. R. Pariser, and R. Parr,; J. Chem. Phys; 21 (1953) 466.
16. S. F. Nelsen, T. B. Frigo, Y. Kim, and T. Colon,; J. Am. Chem. Soc. 108 (1986) 7926.
17. M. J. S. Dewar, E. G. Zoebisxj, E. F. Healy, and J. J. P. Stewart,; J. Am. Chem. Soc; 107 (1985) 39021.
18. S. F. Nelsen, P. A. Petillom, H. Chang, T. B. Frigo, D. A. Dougherty and M. Kaftory,; J. Org. Chem; 566 (1991) 1054.
19. A. I. M. Koraiem, Z. H. Khalil and R. M. AbuEI-Hamd,; Dyes and Pigments; 13 (1990) 289.
20. A. I. M. Koraiem, M. A. EI-Maghraby and R. M. AbuEI-Hamd,; Dyes and Pigments; 14 (1990) 59.
21. A. I. M. Koraiem, M. M. Girgis, Z. H.Khalil and R. M. AbuEI-Hamd,; Dyes and Pigments; 15 (1991) 89.
22. Y. W. Ho,; Dyes and Pigments; 64 (2005) 223.
23. F. Karci, A. Demircali,; Dyes and Pigments; xx; 2006; 1.
24. N. M. Rageh,; Spectrochimica Acta Part A; 60 (2004) 1917.
25. M. S. A. El-Gaby, A. A. Atalla, A. M. Gaber, K. A. Abd Al-Wahab,; Il Farmaco; 55 (2000) 596.
26. A. Krishnaiah, B. Narsaiah,; J. Fluorine Chem.; 109 (2001) 183.
27. A. Chandra Sheker Reddy, B.Narsaiah, R. V. Venkataratnam,; J. Fluorine Chem.; 86 (1997) 127.
28. E. M. Abd-Allah, N. M. Rageh, and H. M. A. Salman,; J. Chem. Eng. Data.; 48 (2003) 652.
29. K. C. Joshi, V. N. Pathak, and U. Garg,; J. Indian Chem. Soc.; (1981) 1180.
30. G. E. H. Elgemeie, A. H. Elghandour, A. M. Elzanate, and A. M. Hussein,; J. Chem. Research(S); (1997) 256.
31. P. C. Tsia, I. J. Wang,; Dyes and Pigments; 64 (2005) 259.