研究生: |
蔡宜興 Y.-S. Tsai |
---|---|
論文名稱: |
多磷配子的合成與十二羰基四銠衍生物的合成及結構研究 Sytheses of Multidentate Phosphine Ligands ;Syntheses and Crystal Structure of Tetrarhodium Dodeccarbonyl Derivatives |
指導教授: |
翁春和
Ueng, Chuen-Her |
學位類別: |
碩士 Master |
系所名稱: |
化學系 Department of Chemistry |
畢業學年度: | 87 |
語文別: | 中文 |
論文頁數: | 80 |
中文關鍵詞: | 多磷配子 |
英文關鍵詞: | Multidentate Phosphine Ligands |
論文種類: | 學術論文 |
相關次數: | 點閱:288 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 |
十二羰四銠[Rh4(CO)12]與含磷雙牙配子Ph2P(CH2)nPPh2(n = 2,dppe;n = 4,dppb),經由熱裂法反應共得到三個錯合物:[Rh4(CO)8(Ph2PCH2CH2CH2CH2PPh2)2 (1)、[Rh4(CO)10(Ph2PCH2CH2PPh2)] (2)、[Rh4-(CO)8(Ph2PCH2CH2CH2CH2PPh2)2] (3);其中(1)、(2)已由X射線單晶繞射獲得晶體結構,錯合物(3)則由紅外線光譜推測其結構。
化合物(1),三個橋鍵羰基維持不變,磷原子取代了兩個銠原子的終端羰基;化合物(2)、(3),每一個銠原子的終端羰基均被磷原子取代。晶體數據:(1)為單斜晶系,空間群 P21/a,a = 23.061(3)A,b =11.956(2) A,c =24.945(2) A,β= 95.742(9)°,最後 Rf = 0.04 (7947個繞射點);(2)為單斜晶系,空間群P21/n,a = 12.651(2) A,b =18.879(2) A,c =18.748(3) A,β=98.752(3)°最後Rf = 0.033 (5258個繞射點)。
根據R.B.King合成多磷配子的方法,合成新的五磷配子
(Ph)(Ph2PCH2CH2)P(CH2)2P(CH2CH2PPh2)2以及六磷配子 (Ph2PCH2CH2)2P(CH2)5P(CH2CH2PPh2)2。
Reactions of [Rh4(CO)12] with Ph2P(CH2)nPPh2 (n = 2 , dppe ; n = 4 , dppb) by the thermolytic method yield three complexes :
[Rh4(CO)10(Ph2PCH2CH2CH2CH2PPh2)] (1), [Rh4(CO)8(Ph2PCH2CH2PPh2)2 (2), [Rh4(CO)8 (Ph2PCH2CH2CH2CH2PPh2)2] (3) . Crystal structures of complexes (1) and (2) have been determined by X-ray diffraction method .
For compound (1) , the set of three bridging CO groups along one triangular set of edges are retained , but two terminal CO groups on two rhodium atoms are replaced by two phosphorus atoms . For compound (2) and (3) , one terminal carbonyl group on each rhodium atom is replaced by a phosphorus atom . Crystal data : (1), monoclinic space group P21/a , a = 23.061(3) A, b = 11.956(2) A,c = 24.945(2) A,β= 95.742(9)°. Final Rf = 0.049 for 7947 reflections . (2), monoclinic space group P21/n , a = 12.651(2) A, b = 18.879(2) A, c = 18.748(3) A, β= 98.752(3)°. Final Rf = 0.033 for 5258 reflections .
The compounds , (Ph)(Ph2PCH2CH2)P(CH2)2P(CH2CH2PPh2)2 and (Ph2PCH2CH2)2P(CH2)5P(CH2CH2PPh2)2] were synthesized according to the published method .
1. M. R. Churchill and J. P. Hutchinson, Inorg. Chem., 1978, 17, 3528.
2. C. H. Wei, Inorg. Chem., 1969, 2384.
3. S. P. Tunik, A. V. Vlasov, N. I. Gorshkov, G. L. Starova, A. B. Nikol’skii, M. I. Rybinskaya, A. S. Batsanov and Yu. T. Struchkov, J. Organomet. Chem., 1992, 433, 189.
4. F. H. Carre, F. A. Cotton and B. A. Frenz, Inorg. Chem., 1976, 15, 380.
5. D. F. Foster, B. S. Nicholls and A. K. Smith, J. Organomet. Chem., 1983, 244, 159.
6. D. F. Foster, B. S. Nicholls and A. K. Smith, J. Organomet. Chem., 1985, 295, 99.
7. C. Allevi, M. Golding, B. T. Heaton, C. A. Ghilardi, S. M. A. Orlandini, D. F. Foster, B. S. Nicholls and A. K. Smith, J. Organomet. Chem., 1987, 326, C19.
8. J. R. Kennedy, P. Selz, A. L. Rheingold, W. C. Trogler, and F. Basolo, J. Am. Chem. Soc. 1989, 111, 3615.
9. E. D. Bergmann, D. Ginsburg, and R. Pappo, Org. React., 1959, 10, 179.
10. R. B. King and J. C. Cloyd, Jr., J. Am. Chem. Soc., 1975, 97, 53.
11. L. Malatesta and G. Caglio, J. Chem. Soc., Chem. Commun., 1967, 420.
12. M. Baack, S. Hietkamp, S. Morton, and O. Stelzar, Chem. Ber., 1981, 114, 3691.
13. J. L. Bookham and W. McFarlane, Polyhedron, 1988, 7, 129.
14. R. B. King and M. S. Saren, Inorg. Chem., 1971, 10, 1861.
15 賴政國,師大化研所博士論文,1999.
16. F. J. Welcher, "The Analytical Uses of Ethylenediamine Tetraacetic Acid" Van Nostran, Princeton, N. J., 1958.
17. C. Giacovazzo, "Fundamentals of Crystallography" Oxford
University Press, New York, 1992.
18. G. H. Stout and L. H. Jensen, "X-ray Structure DeterminationŖrd., Wiley, N. Y., 1989.
19. D. F. Foster, B. S. Nicholls and A. K. Smith, J. Organomet. Chem., 1983, 244, 159.