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完整後設資料紀錄
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.advisor | 林英智(Ying-Chih Lin) | |
dc.contributor.author | Hung-Chih Lin | en |
dc.contributor.author | 林鴻志 | zh_TW |
dc.date.accessioned | 2021-06-13T16:47:24Z | - |
dc.date.available | 2006-07-05 | |
dc.date.copyright | 2005-07-05 | |
dc.date.issued | 2005 | |
dc.date.submitted | 2005-06-28 | |
dc.identifier.citation | 第一部分
1. Schiff, H. Ann. Suppl. 1864, 3, 343. 2. (a) Jacobsen, E. N. in Catalytic Asymmetric Synthesis, Ed. I. Ojima, VCH, New York, 1993, p. 159. (b) Canali, L.; Sherrington, D. C. Chem. Soc. Rev. 1999, 28, 85-93. 3. Shrivastava, H. Y.; Kanthimathi M.; Nair, B. U. Biochem. Biophys.Res. Commun. 1999, 265, 311 4. (a) Johnson, R. A.; Sharpless, K. B. In Catalytic Asymmetric Synthesis; Ojima, I., Ed.; VCH: New York, 1993; Chapter 4.1. (b) Jacobsen, E. N. In Catalytic Asymmetric Synthesis; Ojima, I., Ed.; VCH: New York, 1993; Chapter 4.2. 5. (a) Katsuki, T. Coord. Chem. Rev. 1995, 140, 189-214. (b) Katsuki, T. J. Mol. Catal. A 1996, 113, 87-107. (c) Ito, Y. N.; Katsuki, T. Bull. Chem. Soc. Jpn. 1999, 72, 603-619. 6. (a) Dalton, C. T.; Ryan, K. M.; Wall, V. M.; Bousquet, C.; Gilheany, D. G. Top. Catal. 1998, 5, 75-91. (b) Finney, N. S.; Pospisil, P. J.; Chang, S.; Palucki, M.; Konsler, R. G.; Hansen, K. B.; Jacobsen, E. N. Angew. Chem., Int. Ed. Engl. 1997, 36, 1720-1723. (c) Palucki, M.; Finney, N. S.; Pospisil, P. J.; Guler, M. L.; Ishida, T.; Jacobsen, E. N. J. Am. Chem. Soc. 1998, 120, 948-954. (d) Linker, T. Angew. Chem., Int. Ed. Engl. 1997, 36, 2060-2062. 7. (a) Feichtinger, D.; Plattner, D. A. Angew. Chem., Int. Ed. Engl. 1997, 36, 1718-1719. (b) Feichtinger, D.; Plattner, D. A. J. Chem. Soc., Perkin Trans. 2 2000, 1023-1028. (c) Feichtinger, D.; Plattner, D. A. Chem.-Eur. J. 2001, 7, 591-599. 8. (a) Srinivasan, K.; Michaud, P.; Kochi, J. K. J. Am. Chem. Soc. 1986, 108, 2309-2320. (b) Jacobsen, E. N.; Deng, L.; Furukawa, Y.; Martýnez, L. E. Tetrahedron 1994, 50, 4323-4334. (c) Linde, C. Ph.D. Thesis, Royal Institute of Technology, Stockholm, 1998. 9. Adam, W.; Roschmann, K. J.; Saha-Moller, C. R. Eur. J. Org. Chem. 2000, 3519-3521. 10. Schroder, D.; Shaik, S.; Schwarz, H. Acc. Chem. Res. 2000, 33, 139-145. 11. Martínez, L. E.; Leighton, J. L.; Carsten, D. H.; Jacobsen, E. N. J. Am. Chem. Soc. 1995, 117, 5897. 12. (a) Polymers for Second-Order Nonlinear Optics; Lindsay, G. A., Singer, K. D., Eds.; ACS Symposium Series 601; American Chemical Society: Washington DC, 1995. (b) Molecular Nonlinear Optics; Zyss, J., Ed.; Academic Press: New York, 1994. (c) Prasad, N. P., Willams, D. J. Introduction to Nonlinear Optical Effects in Molecules and Polymers, Wiley: New York, 1991. (d) Materials for Nonlinear Optics: Chemical Perspectives; Marder, S. R., Sohn, J. E., Stucky, G. D., Eds; ACS Symposium Series 455; American Chemical Society: Washington DC, 1991. (e) Nonlinear Optical Properties of Organic Molecules and Crystals; Chemla, D. S., Zyss, J., Eds.; Academic Press: New York, 1987; Vols 1 and 2. 13. (a) Ledoux, I.; Zyss, J. In Novel Optical Materials and Applications; Khoo, I. C., Simoni, F., Umeton, C., Eds.; John Wiley & Sons: New York, 1997. (b) Dalton, L. R.; Harper, A. W.; Ghosn, R.; Steir, W. H.; Ziari, M.; Fetterman, H.; Shi, Y.; Mustacich, R. V.; Jen, A. K. Y.; Shea, K. J. Chem. Mater. 1995, 7, 1060. (c) Marks, T. J.; Ratner, M. A. Angew. Chem. Int. Ed. Engl. 1995, 34, 155. 14. (a) Long, N. J. Angew. Chem. Int. Ed. Engl. 1995, 34, 21. (b) Nalwa, H. S. Appl. Organomet. Chem. 1991, 5, 349. (c) Cummings, S. D.; Cheng, L. T.; Eisenberg, R. Chem. Mater. 1997, 9, 440. (d) Di Bella, S; Fragalà, I.; Marks, T. J.; Ratner, M. A. J. Am. Chem. Soc. 1996, 118, 12747. (e) Lacroix, P. G.; Di Bella, S.; Ledoux, I. Chem. Mater. 1996, 8, 541. (f) Houbrechts, S.; Clays, K.; Persoons, A.; Cadierno, V.; Gamasa, M. P.; Gimeno, J. Organometallics 1996, 15, 5266. (g) Whittall, I. R.; Humphrey, M. G.; Houbrechts, S.; Persoons, A.; Hockless, D. C. R. Organometallics 1996, 15, 5738. (h) Di Bella, S; Fragalà, I.; Ledoux, I.; Marks, T. J. J. Am. Chem. Soc. 1995, 117, 9481. (i) Kanis, D. R.; Lacroix, P. G.; Ratner, M. A.; Marks, T. J. J. Am. Chem. Soc. 1994, 116, 10089. (j) Bourgault, M.; Mountassir, C.; Le Bozec, H.; Ledoux, I.; Puccetti, G.; Zyss, J. J. Chem. Soc., Chem. Commun. 1993, 1623. 15. (a) Di Bella, S; Fragalà, I.; Ledoux, I.; Diaz-Garica, M. A.; Marks, T. J. J. Am. Chem. Soc. 1997, 119, 9550. (b) Di Bella, S; Fragalà, I.; Ledoux, I.; Diaz-Garica, M. A.; Lacroix, P. G. Marks, T. J. Chem. Mater. 1994, 6, 881. 16. Leung, W. H.; Chan, E. Y. Y.; Chow, E. K. F.; Williams, I. D.; Peng, S. M. J. Chem. Soc., Dalton Trans. 1996, 1229. 17. Atwood D. A.; Harvey, M. J. Chem. Rev. 2001, 101, 37. 18. (a) Morris, G. A.; Zhou, H.; Stern, C. L.; Nguyen, S. T. Inorg.Chem. 2001, 40, 3222. (b) Bandini, M.; Cozzi, P. G.; Umani-Ronchi, A. Chem. Commun. 2002, 919 (c) Canali, L.; Sherrington, D. C. Chem. Soc. Rev. 1999, 28, 85. (d) Ito, N. Y.; Katsuki, T. Bull. Chem. Soc. Jpn. 1999, 72, 603. (e) Katsuki, T. Org. Chem., 2001, 5, 663. 19. Briggs, M. S. J.; Fossey, J. S.; Richards, C. J.; Scott B.; Whateley, J. Tetrahedron Lett. 2002, 43, 5169. 20. (a) de Silva, A. P.; Gunaratne, H. Q. N.; Gunnlaugsson, T.; Huxley, A. J. M.; McCoy, C. P.; Rademacher J. T.; Rice, T. E. Chem. Rev. 1997, 97, 1515; (b) Fabbrizzi, L.; Licchelli M.; Pallavicini, P. Acc. Chem. Res. 1999, 32, 846. (c) Prodi, L.; Bolletta, F.; Montalti M.; Zaccheroni, N. Coord. Chem. Rev. 2000, 205, 59 (d) Bargossi, C.; Fiorini, M. C.; Montalti, M.; Prodi, L.; Zaccheroni, N. Coord. Chem. Rev. 2000, 208, 17 (e) Prodi, L.; Bargossi, C.; Montalti, M.; Zaccheroni, N.; Su, N.; Bradshaw, J. S.; Izatt, R. M.; Savage, P. B. J. Am. Chem. Soc., 2000, 122, 6769 (f) Dalley, N. K.; Xue, P. B. G.-P.; Bradshaw, J. S.; Dalley, N. K.; Savage, P. B.; Krakowiak, K. E.; Izatt, R. M.; Prodi, L.; Montalti, M.; Zaccheroni, N. Tetrahedron 2001, 57, 7623 (g) Xue, G.; Bradshaw, J. S.; Dalley, N. K.; Savage, P. B.; Izatt, R. M.; Prodi, L.; Montalti, M.; Zaccheroni, N. Tetrahedron 2002, 58, 4809 (h ) Prodi, L.; Montalti, M.; Zaccheroni, N.; Pickaert, G.; Charbonniere, L.; Ziessel, R. New J. Chem., 2003, 27, 134. 21. (a) Montalti, M.; Prodi, L. Chem. Commun. 1998, 1461 (b) La Monica, L.; Monti, D.; Mancini, G.; Montalti, M.; Prodi, L.; Zaccheroni, N.; Paolesse, R.; D’Arcangelo, G. New J. Chem. 2001, 25, 597. 22. Munoz-Hernandez, M.-A.; McKee, M. L.; Keizer, T. S.; Yearwood, B. C.; Atwood, D. A. J. Chem. Soc., Dalton Trans. 2002, 410. 23. Prodi, L. New J. Chem. 2003, 27, 692–697 24. (a) Gymer, R. W. Endeavour 1996, 20, 115. (b) Rothberg, L. J.; Lovinger, A. J. J. Mater. Res. 1996, 11, 3174. (c) Salbeck, J. Ber. Bunsenges. Phys. Chem. 1996, 100, 1666. (d) Sheats, J. R.; Antoniadis, H.; Hueschen, M.; Leonard, W.; Miller, J.; Moon, R.; Roitman, D.; Stocking, A. Science 1996, 273, 884. (e) Lovinger, A. J.; Rothberg, L. J. J. Mater. Res. 1996, 11, 1581. (f) Deuen, M.; Bässler, H. Chem. Unserer Zeit 1997, 31, 76. (g) Mitschke, U.; Bauerle, P. J. Mater. Chem. 2000, 10, 1471. (h) Kido, J. Phys. World 1999, 12, 27. 25. (a) Kraft, A.; Grimsdale, A. C.; Holmes, A. B. Angew. Chem. Int. Ed. 1998, 37, 402. (b) May, P. Phys. World 1995, 8(3), 52. (c) Friend, R. H.; Bradley, D. D. C.; Holmes, A. B. Phys. World 1992, 5(11), 42. (d) Baigent, D. R.; Greenham, N. C.; Grüner, J; Marks, R. N.; Friend, R. H.; Moratti, S. C.; Holmes, A. B. Synth. Lett. 1994, 67, 3. (e) Yam, P. Sci. Am. 1995, 273(1), 74. (f) Greenham, N. C.; Friend, R. H. Solid State Phys. 1995, 49, 1. (g) Feast, W. J.; Tsibouklis, J.; Pouwer, K. L.; Groenendaal, L.; Meijer, E. W. Polymer 1996, 37, 5017. (h) Friend, R. H.; Gymer, R. W.; Holmes, A. B.; Burroughes, J. H.; Marks, R. N.; Taliani, C.; Bradley, D. D. C.; Dos Santos, D. A.; Bredas, J. L.; Logdlund, M.; Salaneck, W. R. Nature 1999, 397, 121. (i) Wang, Y. Z.; Epstein, A. J. Acc. Chem. Res. 1999, 32, 217. 26. (a) Hosokawa, C.; Tokailin, H.; Higashi, H.; Kusumoto, T. Appl. Phys. Lett. 1992, 60, 1200. (b) Van Slyke, S. A. US 5,151,629, 1992. (c) Bryan, P. S.; Lovecchio, F. V.; Van Slyke, S. A. US 5,141,671, 1992. 27. Hamada, Y.; Adachi, C.; Tsutsui, T.; Saito, S. Optoelectron.-Devices Technol. 1992, 7, 83. 28. Shirota, Y.; Kuwabara, Y.; Inaba, H.; Wakimoto, T.; Nakada, H.; Yonemoto, Y.; Kawami, S.; Imai, K. Appl. Phys. Lett. 1994, 65, 807. 29. Adachi, C.; Tokito, S.; Tsutsui, T.; Saito. S. Jpn. J. Appl. Phys. 1988, 27, L713. 30. Wakimoto, T.; Murayama, R.; Nakada, H.; Imai, K.; Sato, G.; Nomura, M. Polym. Preprint 1991, 40, 3600. 31. Burroughes, J. H.; Bradley, D. D. C.; Brown, A. R.; Marks, R. N.; Mackay, K.; Friend, R. H.; Burns, P. L.; Holmes, A. B. Nature, 1990, 347, 539. 32. Grem, G.; Leditzky, G.; Ullrich, B.; Leising, G. Adv. Mater. 1992, 4, 36. 33. Ohmori, Y.; Uchida, M.; Muro, K.; Yoshino, K. Jpn. J. Appl. Phys. 1991, 30, L1941. 34. Ohmori, Y.; Uchida, M.; Muro, K.; Yoshino, K. Jpn. J. Appl. Phys. 1991, 30, L1938. 35. (a) Hamada, Y.; Sano, T.; Fujita, M.; Fujii, T.; Nishio, Y.; Shibata, K. Jpn. J. Appl. Phys. 1993, 32, L514. (b) Hamada, Y.; Sano, T.; Fujita, M.; Fujii, T.; Nishio, Y.; Shibata, K. Chem. Lett. 1993, 905. (c) Hamada, Y.; Sano, T.; Shibata, K.; Kuroki, K. Jpn. J. Appl. Phys. 1995, 34, L824. (d) Kido, J.; Hongawa, K.; Okuyama, K.; Nagai, K. Appl. Phys. Lett. 1994, 64, 815. 36. Sano, T.; Fujita, M.; Fujii, T.; Hamada, Y.; Shibata, K.; Kuroki, K. Jpn. J. Appl. Phys. 1995, 34, 1883. 37. Kido, J.; Nagai, K.; Okamoto, Y.; Skotheim, T. Chem. Lett. 1991, 1267. 38. Morishige, K. Analytica Chimica Acta 1974, 72, 295. 39. Hamada, Y.; Sano, T.; Fujita, M.; Fujii, T.; Nishio, Y.; Shibata, K. Jpn. J. Appl. Phys. 1993, 32, L511. 40. (a) Baldo, M. A.; O’Brien, D. F.; You, Y.; Shoustikov, A.; Sibley, S.; Thompson, M. E.; Forrest, S. R. Nature 1998, 395, 151.(b) Kido, J.; Hayase, H.; Hongawa, K.; Nagai, K.; Okuyama, K. Appl.Phys. Lett. 1994, 65, 2124. (c) Hoshino, S.; Suzuki, H. Appl. Phys.Lett., 1996, 69, 224. (d) Zhang, X.; Sun, R.; Zheng, Q.; Kobayashi, T.; Li, W. Appl. Phys. Lett. 1997, 71, 2596. (e) Ma, Y.; Zhang, H.; Shen, J.; Che, C.M. Synth. Met. 1998, 94, 245. (f) McGehee, M. D.; Bergstedt, T.; Zhang, C.; Saab, A. P.; O’Regan, M. B.; Bazan, G. C.; Srdanov, V. I.; Heeger, A. J. Adv. Mater. 1999, 11, 1349. 41. (a) O’Brien, D. F.; Baldo, M. A.; Thompson, M. E.; Forrest, S. R. Appl.Phys. Lett. 1999, 74, 442. (b) Cleave, V.; Yahioglu, G.; Le Barny, P.; Friend, R. H.; Tessler, N. Adv. Mater. 1999, 11, 285. (c) Adachi, C.; Baldo, M. A.; Forrest, S. R.; Lamansky, S.; Thompson, M. E.; Kwong, R. C. Appl. Phys. Lett. 2001, 78, 1622. 42. (a) Baldo, M. A.; Lamansky, S.; Burrows, P. E.; Thompson, M. E.; Forrest, S. R. Appl. Phys. Lett. 1999, 75, 4. (b) Baldo, M. A.; Thompson, M. E.; Forrest, S. R. Nature 2000, 403, 750. (c) Wang, Y.; Herron, N.; Grushin, V. V.; LeCloux, D.; Petrov, V. Appl. Phys. Lett. 2001, 79, 449. (d) Adachi, C.; Kwong, R. C.; Djurovich, P.; Adamovich, V.; Baldo, M. A.; Thompson, M. E.; Forrest, S. R. Appl. Phys. Lett. 2001,79, 2082. (e) Lamansky, S.; Djurovich, P.; Murphy, D.; Abdel-Razzaq, F.; Lee, H.-E.; Adachi, C.; Burrows, P. E.; Forrest, S. R.; Thompson, M. E. J. Am. Chem. Soc. 2001, 123, 4304. (f) Gong, X.; Robinson, M. R.; Ostrowski, J. C.; Moses, D.; Bazan, G. C.; Heeger, A. J. Adv. Mater. 2002, 14, 581. 43. (a) Adachi, C.; Baldo, M. A.; Forrest, S. R.; Thompson, M. E. Appl. Phys. Lett. 2000, 77, 904. (b) Adachi, C.; Baldo, M. A.; Thompson, M. E.; Forrest, S. R. J. Appl. Phys. 2001, 90, 5048. (c) Ikai, M.; Tokito, S.; Sakamoto, Y.; Suzuki, T.; Taga, Y. Appl. Phys. Lett. 2001, 79, 156. (d) D’Andrade, B. W.; Brooks, J.; Adamovich, V.; Thompson, M. E.; Forrest, S. R. Adv. Mater. 2002, 14, 1032. 44. Lin, Y. Y.; Chan, S. C.; Michael C. ; Chan, W.; Hou, Y. J.; Zhu, N.; Che, C. M.; Liu, Y.; Wang, Y. Chem. Eur. J. 2003, 9, No. 6, 1263. 45. Chang, K. H.; Huang, C. C.; Liu, Y. H.; Hu, Y. H.; Chou, P. T.; Lin Y. C. Daltons Trans 2004, 1731. 46. Pohl, R.; Anzenbacher, P. Jr. Org. Lett. 2003, 5, No. 16, 2769. 47. Paschke, R.; Balkow, D.; Sinn, E. Inorg. Chem. 2002, 41, 1949. 第二部分 1. Wu, J.; Watson, M. D.; Zhang, L.; Wang, Z.; Mullen, K. J. Am. Chem. Soc. 2004, 126, 177. 2. Silverstain, R. M.; Bassler, G. C.; Morrill, T. C. In Spectrometeric Identification of Organic Compounds; 4th edition, John Wiley & Sons, Inc.: New York, 1981. 3. Chang, K. H.; Huang, C. C.; Liu, Y. H.; Hu, Y. H.; Chou, P. T.; Lin Y. C. Daltons Trans 2004, 1731. 4. Morris, G. A.; Zhou, H.; Stern, C. L.; Nguyen, S. T. Inorg. Chem. 2001, 40, 3222. 5. Hamada, Y.; Sano, T.; Fujita, M.; Fujii, T.; Nishio, Y.; Shibata, K. Jpn. J. Appl. Phys. 1993, 32, L511. 6. Schon, E.; Plattner, D. A.; Chen, P. Inorg. Chem. 2004, 43, 3164. 7. Cozzi, P. G.; Dolci, L. S.; Garelli, A.; Montalti, M.; Prodi, L.; Zaccheroni, N. New J. Chem. 2003, 27, 692. 8. Manna, I. K.; Weier, R. M.; Lentz, K. T.; Swenton, L.; Lankin, D. C. J. Org. Chem. 1995, 60, 960. 9. Li, H.; Powell, D. R.; Hayashi, R. K.; West, R. Macromolecules 1998, 31, 52. 10. CRC Handbook of Chemistry and Physics, 77th ed.; CRC Press: Boca Raton, FL, 1996-1997; pp 8-77. 11. Wang, P.; Hong, Z.; Xie, Z.; Tong, S.; Wong, O.; Lee, C. S.; Wong, N.; Hung, L.; Lee, S. Chem. Commun. 2003, 1664. 12. Hocek, M.; tepnicka, P. S.; LudvIk, J. I.; Votruba, I.; Eha, D. R.; Hobza, P. Chem. Eur. J. 2004, 10, 2058. | |
dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/38813 | - |
dc.description.abstract | 一系列的新穎含炔基之柳酫化合物可以經由sonogashira coupling偶合反應合成。再將柳酫化合物與醋酸鋅、雙胺化合物作用,即可得到一系列的鋅席夫鹼金屬錯合物。上述錯合物皆經由1H-NMR、13C-NMR及Mass的鑑定,再利用UV/vis、fluorescence、TGA之測量,可以得到其光色和熱穩定性。它們所發螢光範圍為橘光,且可藉由改變柳酫化合物的取代與雙胺化合物得到不同光色之金屬錯合物,此錯合物均具有不錯的量子效率。此類化合物具有極高的熱穩定性Td > 400 oC。
單核二價鎂席夫鹼金屬錯合物也是利用類似合成鋅席夫鹼金屬錯合物系統的方法製備,鎂錯合物所發螢光範圍為黃光,且大大提升了量子效率。此外,不對稱的鋅席夫鹼金屬錯合物也可以被合成出來,光物理性質與對稱的錯合物有些許的不同。 | zh_TW |
dc.description.abstract | A new series of substituted-arylethynyl ligands have been synthesized via Sonogashira coupling reaction. A series of Schiff base metal complexes were obtained by a method that the ligands are first treated with metal salt followed by addition of the different diamines. These compounds were characterized by 1H and 13C NMR and mass spectroscopies. The optical properties and the thermal properties of these complexes were measured by UV/vis, PL (photoluminescent) and TGA spectroscopic studies. All of these complexes emit orange fluorescence in THF with good quantum efficiencies. All of these complexes exhibited highly thermal stability in nitrogen (Td > 400℃).
The Mg(II) Schiff base derivatives were synthesized by the same methodology used for the preparation of Zn(II) analogues. These Mg-complexes emit yellow fluorescence in THF and the quantum yield was dramatically enhanced relative to Zn-complexes. Additionally, the unsymmetrical Zn(II) Schiff base complexes also can be prepared. The optical properties of unsymmetrical complexes are some different from that of symmetrical complexes. | en |
dc.description.provenance | Made available in DSpace on 2021-06-13T16:47:24Z (GMT). No. of bitstreams: 1 ntu-94-R92223060-1.pdf: 1686495 bytes, checksum: 8dc8f2c4dcda4c9e5dc55b8cee5d7363 (MD5) Previous issue date: 2005 | en |
dc.description.tableofcontents | 摘 要 5
Abstract 6 Schemes 7 Introduction 11 1. Metal–Salen Schiff base complexes in catalysis 11 2. NLO Properties of Metal–Salen Schiff base complexes 14 3. Photophysical Properties of Metal–Salen Schiff base complexes 16 4. Electroluminescent (EL) materials 18 5. Motivation 26 6. References 29 Results and Discussion 36 1. Synthesis of 5-Substituted Salicylaldehydes 36 2. Synthesis of Alkynyl-Substituted Zn(II) Schiff Base Complexes 41 3. Synthesis of Other Alkynyl-Substituted Zn(II) Schiff Base Complexes 54 4. Synthesis of Mg(II) Schiff Base Complexes 58 5. Synthesis of Unsymmetrical Zn(II) Schiff Base Complexes 64 6. Synthesis of Other Metal Schiff Base Complexes 67 7. Photophysical Properties The Zinc Series Complexes 68 a. Zn(II) Schiff Base Complexes with Alkynyl-Substitutent 68 b. Zn(II) Schiff Base Complexes with Other Alkynyl-Substitutents 72 c. Mg(II) Schiff Base Complexes 74 d. Unsymmetrical Zn(II) Schiff Base Complexes 75 8. TGA Properties of Schiff base Metal Complexes 78 9. Cyclic Voltammetric Study 79 10. Liquid Crystal Properties of Schiff base Metal Complexes 81 11. References 82 Experimental Section 83 Conclusion 116 | |
dc.language.iso | en | |
dc.title | 鋅、鎂系統中含多烷鏈之炔基席夫鹼金屬錯合物:
合成,鑑定及光物理性質 | zh_TW |
dc.title | Alkynylated Schiff Base Metal Complexes Containing Multiple-Alkyl Chains in Zn and Mg System: Synthesis, Characterization, and Photophysical Properties | en |
dc.type | Thesis | |
dc.date.schoolyear | 93-2 | |
dc.description.degree | 碩士 | |
dc.contributor.oralexamcommittee | 梁文傑(Man-Kit Leung),汪根欉(Ken-Tsung Wong) | |
dc.subject.keyword | 席夫,合成,鑑定, | zh_TW |
dc.subject.keyword | Schiff,Synthesis,Characterization, | en |
dc.relation.page | 117 | |
dc.rights.note | 有償授權 | |
dc.date.accepted | 2005-06-28 | |
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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