帳號:guest(3.133.116.55)          離開系統
字體大小: 字級放大   字級縮小   預設字形  

詳目顯示

以作者查詢圖書館館藏以作者查詢臺灣博碩士論文系統以作者查詢全國書目
作者(中文):林義登
作者(外文):Lin, Yi Deng
論文名稱(中文):雙鉻五重鍵錯合物與腈類的活化及硼烷反應研究
論文名稱(外文):Nitriles Activation and Borane Reaction of Quintuply-Bonded Dichromium Complexes
指導教授(中文):蔡易州
指導教授(外文):Tsai, Yi Chou
口試委員(中文):尤禎祥
劉瑞雄
口試委員(外文):Yu, Jen Shiang
Liu, Rai Shung
學位類別:碩士
校院名稱:國立清華大學
系所名稱:化學系
學號:102023542
出版年(民國):104
畢業學年度:103
語文別:中文
論文頁數:84
中文關鍵詞:雙鉻五重鍵腈類活化硼烷反應
外文關鍵詞:Quintuply-Bonded DichromiumNitriles ActivationBorane Reaction
相關次數:
  • 推薦推薦:0
  • 點閱點閱:565
  • 評分評分:*****
  • 下載下載:4
  • 收藏收藏:0
本實驗室使用雙氮基脒為配基與鉻金屬成功合成出雙鉻金屬五重鍵錯合物Cr2[μ-κ2-HC(N-2,6-iPr2C6H3)2]2 (1),其具有低配位數以及低價數的特性,我們嘗試著利用錯合物 1 與小分子進行反應,由於雙鉻金屬五重鍵錯合物具有δ鍵,可與碳-碳多重鍵的π鍵作比較,觀察與碳-碳多重鍵與小分子間的反應性有何異同。
將錯合物 1 與四當量的乙腈反應,可得到錯合物{Cr2[μ-κ2-HC(NDipp)2][μ-HC(NDipp)2][η2-NC(CH3)C(CH3)N]}2 (2) 以及錯合物(μ-η2,η2-MeCN)2(MeCN)2Cr2[μ-κ2-HC(NDipp)2]2 (3) ,而與丙腈和異丁腈反應可得與錯合物 3 相似結構的錯合物(μ-η2,η2-EtCN)2(EtCN)2Cr2[μ-κ2-HC(NDipp)2]2 (4) 以及錯合物(μ-η2,η2-iPrCN)2(iPrCN)2Cr2[μ-κ2-HC(NDipp)2]2 (5),其中令人意外的是與三甲基腈甲矽烷的反應,與上述所得到的結果完全不同,得到鉻零價單核錯合物Cr(Me3SiNC)6 (6) ,六鉻金屬環化錯合物{Cr(μ-CN)2[μ-HC(NDipp)2]}2{[Cr(CN(TMS)2)(μ-HC(NDipp)2)]2(μ-CN)4[Cr(CN)]2} (7) 以及四個三甲基腈甲矽烷配位在鉻上的錯合物Cr[μ-HC(NDipp)2][CN(TMS)2](CNTMS)3 (8) ,錯合物 6-8 鉻鉻五重鍵皆被打斷,三甲基腈甲矽烷的碳-氮鍵反轉,以碳配位在鉻金屬上。
而將錯合物 1 與9-borabicyclo[3.3.1]nonane進行反應,成功的得到十分少見的鉻硼鍵錯合物,最後合成出錯合物Cr2[HC(NDipp)2](9-borabicyclo[3.3.1]nonyl)2(μ2-O-9-borabicyclo[3.3.1]nonyl)(μ2-THF) (9) 。
另外,我們嘗試著用錯合物 1 和疊氮化合物進行反應,與兩當量的叠氮苯甲酰反應,卻無法得到推測中的雙核金屬錯合物,而是形成一單核的錯合物Cr{[HC(NDipp)2]C(NPh)O}2 (10) 。
除了利用雙氮基脒外,本實驗室還嘗試其他配基與不同金屬進行反應,實驗能否能合成出相似的燈籠型金屬多重鍵錯合物,我們利用Li2[HB(N-2,6-iPr2C6H3)2]配基,與鉻、鉬、鎢等金屬進行反應,嘗試其可行性。
The low-coordinate and low-valent quintuply-bonded dichromium complex Cr2[μ-κ2-HC(N-2,6-iPr2C6H3)2]2 (1) characterized by our group behaves like alkynes, so we further examine reactivity of 1 with small molecules. Treatment of 1 with four equiv of acetonitrile respectively results in a complexation product {Cr2[μ-κ2-HC(NDipp)2][μ-HC(NDipp)2][η2-NC(CH3)C(CH3)N]}2 (2) and (μ-η2,η2-MeCN)2(MeCN)2Cr2[μ-κ2-HC(NDipp)2]2 (3).Complex 2 is formed via C-C coupling of two molecules of MeCN. On the other hand, the C-N triple bond of MeCN is activated via coordination to the Cr2 unit in 3. Treatment of 1 with propiononitrile or isobutyronitrile gives complexes (μ-η2,η2-EtCN)2(EtCN)2Cr2[μ-κ2-HC(NDipp)2]2 (4) and (μ-η2,η2-iPrCN)2(iPrCN)2Cr2[μ-κ2-HC(NDipp)2]2 (5). Both structures of 4 and 5 are similar to that of complex 3. Surprisingly, reaction of complex 1 with trimethylsilyl cyanide (Me3SiCN) is complicated and results in three products: Cr(Me3SiNC)6 (6), {Cr(μ-CN)2[μ-HC(NDipp)2]}2 {[Cr(CN(TMS)2)(μ-HC(NDipp)2)]2(μ-CN)4[Cr(CN)]2} (7) and Cr[μ-HC(NDipp)2][CN(TMS)2](CNTMS)3 (8). The characterization of complexes 6-8 indicates this reaction proceeds through cleavage of Cr-Cr quintuple bond, inversion of C-N functionality of Me3SiCN and Si-N bond cleavage. In all complexes 6, 7 and 8, trimethylsilyl cyanide binds the metal center through its C instead of N atom. Treatment of 1 with 9-borabicyclo[3.3.1]nonane(9-BBN) gives Cr2[HC(NDipp)2] (9-borabicyclo[3.3.1]nonyl)2(μ2-O-9-borabicyclo[3.3.1]nonyl)(μ2-THF) (9).Treatment of the 1 with benzoyl azide results in the formation of the mononuclear complex Cr{[HC(NDipp)2]C(NPh)O}2 (10).
We recently succeeded in characterizing boron-containing diamido transition-metal complexes. Therefore, we tried to employ the boron-containing diamido ligand Li2[HB(N-2,6-iPr2C6H3)2] to react with chromium, molybdenum and tungsten species.
中文摘要...................................................I
Abstract................................................III
謝誌......................................................V
目錄.....................................................VI
圖目錄.................................................VIII
流程圖目錄...............................................IX
第一章 緒論................................................1
1-1 金屬多重鍵.............................................1
1-2 小分子活化.............................................4
1-3 金屬五重鍵的反應性......................................7
1-4 實驗目的...............................................9
第二章 雙鉻五重鍵錯合物與腈類反應性研究.......................12
2-1 前言..................................................12
2-2 腈類化合物............................................13
2-3 錯合物{Cr2[μ-κ2-HC(NDipp)2][μ-HC(NDipp)2][η2-NC(CH3)C(CH3)N]}2 (2)與(μ-η2,η2-N-MeCN)2(MeCN)2Cr2[μ-κ2-HC(NDipp)2]2 (3)的合成與鑑定..........................................17
2.4 (μ-η2,η2-EtCN)2(EtCN)2Cr2[μ-κ2-HC(NDipp)2]2 (4) 的合成與鑑定......................................................21
2.5 (μ-η2,η2-iPrCN)2(iPrCN)2Cr2[μ-κ2-HC(NDipp)2]2 (5) 的合成與鑑定....................................................24
2.6 Cr(Me3SiNC)6 (6)的合成與鑑定...........................26
2.7{Cr(μ-CN)2[μ-HC(NDipp)2]}2{[Cr(CN(TMS)2)(μ-HC(NDipp)2)]2(μ-CN)4[Cr(CN)]2} (7) 和Cr[μ-HC(NDipp)2][CN(TMS)2](CNTMS)3 (8)的合成與鑑定............................................30
2.8 小結..................................................37
第三章雙鉻五重鍵錯合物與其他化合物反應性研究...................38
3-1 金屬多重鍵與硼的反應....................................38
3-2 Cr2[HC(NDipp)2](9-borabicyclo[3.3.1]nonyl)2(μ2-O-9-borabicyclo[3.3.1]nonyl)(μ2-THF) (9) 的合成與鑑定..........40
3-3 小結..................................................44
3-4 金屬多重鍵與疊氮化合物反應...............................45
3-5錯合物Cr{[HC(NDipp)2]C(NPh)O}2 (10) 的合成與鑑定.........48
3-6 小結..................................................50
第五章 其他嘗試............................................51
4-1 Cr(CO)3{η6-[μ-κ2-HC(NDipp)2]} (11) 的合成.............51
4-2 Cr2(μ-Br)2[μ-κ2-HC(NDipp)2]2(THF)2 (12) 的合成與鑑定...53
4-3 Cr(N-2,6-iPr2C6H3)2(NH-2,6-iPr2C6H3)2 (13) 的合成與鑑定........................................................55
4-4 [K(18-crown-6)]{(μ-η2-CH3COO)Cr2[μ-η2-HC(N-2,6-Et2C6H3)2]2}與S8反應研究...........................................57
4-5 Cr2[μ-κ2-HC(N-2,6-iPr2C6H3)2]2與diisocyano之反應研究...57
4-6 雙鉻五重鍵與NHCs Carbene之反應研究......................57
4-7 Li2[HB(N-2,6-iPr2C6H3)2]與chromium(II) chloride反應...58
4-8 (TMS)2[HB(N-2,6-iPr2C6H3)2]與WCl3DME反應..............58
第五章 實驗步驟與晶體結構資料................................59
5-1 實驗儀器與溶劑.........................................59
5-1-1 一般操作............................................59
5-1-2實驗使用儀器..........................................59
5-1-3 使用溶劑及藥品.......................................60
5-2 實驗步驟...............................................62
5-2-1{Cr2[μ-κ2-HC(NDipp)2][μ-HC(NDipp)2][η2-N(C)C(C)N]}2 (2) 的合成................................................62
5-2-2(μ-κ1C:κ2N-MeCN)2(η1-MeCN)2Cr2[μ-κ2-HC(NDipp)2]2 (3) 的合成......................................................62
5-2-3 (μ-κ1C:κ2N-EtCN)2(η1-EtCN)2Cr2[μ-κ2-HC(NDipp)2]2 (4) 的合成....................................................63
5-2-4(μ-κ1C:κ2N-iPrCN)2(η1-iPrCN)2Cr2[μ-κ2-HC(NDipp)2]2 (5) 的合成....................................................64
5-2-5 Cr(Me3SiNC)6 (6) 的合成.............................65
5-2-6 {Cr(μ-CN)2[μ-HC(NDipp)2]}2{[Cr(CN(TMS)2)(μ-HC(NDipp)2)]2.....................................................65
(μ-CN)4[Cr(CN)]2} (7) 的合成..............................65
5-2-7 Cr[μ-HC(NDipp)2][CN(TMS)2](CNTMS)3 (8) 的合成.......66
5-2-8 Cr2[HC(NDipp)2](9-BBN)2(μ2-O-9-BBN)(μ-THF) (9) 的合成.......................................................67
5-2-9 Cr{[HC(NDipp)2]C(NPh)O}2 (10) 的合成................68
5-2-10 Cr(CO)3{η6-[μ-κ2-HC(NDipp)2]} (11) 的合成..........68
5-2-11 Cr2(μ-Br)2[μ-κ2-HC(NDipp)2]2(THF)2 (12) 的合成.....69
5-2-12 Cr(N-2,6-iPr2C6H3)2(NH-2,6-iPr2C6H3)2 (13) 的合成..70
5-3晶體結構資料表..........................................71
第六章 參考文獻............................................81


1. Kauffman, G. B. Coord. Chem. Rev. 1973, 9,339.
2. Kauffman, G. B. Coord. Chem. Rev. 1974, 12,105.
3. Kauffman, G. B. Coord. Chem. Rev. 1975, 15,1.
4. Cotton, F. A. ; Curtis, N. F. ; Harris, C. B. .; Johnson, B. F. G.; Lippard, S. J.; Mague, J. T.; Robinsom, W. R.; Wood, J. S.Science. 1964, 145, 1305.
5. Casey, S. M.; Villata, P. W.;Bengali, A. A.; Cheng, C. L.; Dick, J. P.; Fenn, P. T.; Leopard, D. G. J. Am. Chem. Soc. 1991, 113, 6688.
6. Casey, S. M.; Leopard, D. G. J. Phys. Chem. B. 1993, 97,816.
7. Casey, S. M.; Leopard, D. G. Chem. Phys.Lett. 1993, 201, 205.
8. Kuending, E. P.; Moskovits, M.; Ozin. G. A. Nature (London) ,1975, 254, 503.
9. Morse, M. D. Chem. Rev. 1986, 86, 1049.
10. Kant, A.; Strauss, B. H. J. Chem. Phys. 1966, 45, 3161
11. Gupta, S. K.; Atkins, R. M.; Gingerich, K. A. Inorg. Chem. 1978, 17, 3211.
12. Efremov, Y. M.; Samoilova, A. N.; Kozhuhkovskii, V. B.; Gurvich, L. V. J. Mol. Spectrosc. 1978, 73, 430.
13. Kraus, D.; Lorenz, M.; Bondybey, V. E. Phys. Chem. Comm. 2001, 4, 44.
14. Klotzbuecer, W.; Ozin, G. A. Inorg. Chem. 1977, 16, 984.
15. W. Weltner, J.; Zee, R. J. V. Annu. Rev. Phys. Chem. 1984, 35, 291.
16. Chisholm, M. H. Chem. Rev. 2005, 105, 2949.
17. Nguyen, T.; Sutton, A. D.; Brynda, M.;Fettinger, J. C.; Long, G. J.; Power, P. P. Science, 2005, 310, 844.
18. Nguyen, T.;Sutton, A.D.; Brynda, M.; Fettinger, J. C.; Long, G. J.; Power, P. P. Scinece, 2005, 310, 844.
19. Hsu, C. –W.; Yu, J.-S. K. ; Yen, C.-H.; Lee, G.-H.; Wang, Y.; Tsai, Y.-C. Angew Chem. Int. Ed.2008, 47, 9933.
20. Hsu, C.-W.; Yu, J.-S.K.; Yen, C.-H.; Lee, G.-H.; Wang, Y.; Kuo, T.-S.Angew. Chem. Int. Ed. 2008, 47, 7250.
82
21. Noor, A. ; Wagner, F. R.; Kempe, R.Angew. Chem. Int. Ed. 2008, 47, 7246.
22. Noor, A. ; Glatz, G.; Muller, R.; Kaupp, M.; Demeshko, S.; Kempe, R. Z. Anorg. Allg. Chem.2009,635, 1149.
23. Laplaza, C. E.; Cummins, C. C. Science 1995, 268, 861.
24. Laplaza, C. E.; Johnson, M. J. A.; Peters, J. C.; Odom, A. L.; Kim,E.; Cummins, C. C.; George, G. N.; Pickering, I. J. J. Am. Chem. Soc.1996, 118, 8623.
25. Cummins, C. C. Chem. Commun. 1998, 1777.
26. Peters, J. C.; Cherry, J-P. F.; Thomas, J. C.; Baraldo, L.; Mindiola, D. J.; Davis, W.M.; Cummins, C. C. J. Am. Chem. Soc. 1999, 121, 10053-10067.
27. Fickes, M. G.; Odom, A. L.; Cummins, C. C. Chem. Commun. 1997, 1993–1994.
28. Figueroa, J. S.; Piro, N. A.; Clough, C. R.; Cummins, C. C. J. Am. Chem.Soc. 2006, 128, 940–950.
29. Clough, C. R.; Greco, J. B.; Figueroa, J. S.; Diaconescu, P. L.; Davis, W. M.;Cummins, C. C. J. Am. Chem. Soc. 2004, 126, 7742–7743.
30. Silvia, J. S.; Cummins, C. C. J. Am. Chem. Soc. 2009, 131, 446–447.
31. Silvia, J.S.; Cummins, C. C. J. AM. CHEM. SOC. 2010, 132, 2169–2171.
32. Lee, Y.; Mankad, N. P.; Peters, J. C. Nat. Chem. 2010, 2, 558.
33. Moret, M.-E.; Peters, J. C. Angew. Chem. Int. Ed. 2011,50, 2063.
34. Moret, M.-E.; Peters, J. C. J. Am. Chem. Soc. 2011, 133,18118.
35. Betley, T. A.; Peters, J. C. J. Am. Chem. Soc. 2004, 126, 6252
36. Ung, G.; Peters, J. C. Angew. Chem. Int. Ed. 2015, 54, 532 –535.
37. 陳思妏, 國立清華大學化學研究所碩士論文. 2011.
38. Tsai , Y. C.; Chen, H. Z.; Chang, C. C.; Yu, J. S. K.; Lee, G. H.; Wang, Y.; Kuo, T. S. J. Am. Chem. Soc. 2009, 131, 12534.
39. Noor, A.; Qayyum, S.; Bauer, T.; Schwarz, S.; Weber, B.; Kempe, R. Chem. Commun., 2014, 50, 13127—13130.
40. Tamne, E. S.; Noor, A.; Qayyum, S.; Bauer, T.; Kempe, R. Inorg. Chem. 2013, 52, 329−336.
83
41. Schwarzmaier, C.; Noor, A.; Glatz, G.; Zabel, M.; Timoshkin, A. Y.; Cossairt, B. M.; Cummins, C. C.; Kempe, R.; Scheer, M. Angew. Chem. Int. Ed. 2011, 50, 7283 –7286.
42. Noor, A.; Tamne, E. S.; Qayyum, S.; Bauer, T.; Kempe, R. Chem. Eur. J. 2011, 17, 6900 – 6903
43. 顏君旭, 國立清華大學化學研究所碩士論文. 2010.
44. 謝昀蓁, 國立清華大學化學研究所碩士論文. 2011.
45. 薛翔文, 國立清華大學化學研究所碩士論文. 2013.
46. Wang, B.; Li, B.; Xu, S.; Song, H. J. Organomet. Chem. 2008, 693, 87.
47. 劉士誠, 國立清華大學化學研究所碩士論文. 2010.
48. 陳思妏, 國立清華大學化學研究所碩士論文. 2011.
49. 王韻涵, 國立清華大學化學研究所碩士論文. 2012.
50. Filippou, A. C.; Grunleitner, W. Journal of Organmnetailic Chemistrv. 1990. 398. 99-115.
51. Baranoff, E.; Orselli, E.; Allouche, L.; Censo, D. D.; Scopelliti, R.; Gratzel, M.; Nazeeruddin, M. K. Chem. Commun., 2011, 47, 2799–2801
52. Bose, M.; Moula, G.; Sarkar, S. Inorg. Chem. 2014, 53, 6−8
53. Chatani, N.; Hanafusa, T. J. Org. Chem. 1987. 52. 4408
54. 林亨菕, 國立清華大學化學研究所碩士論文. 2012.
55. 林怡慶, 國立清華大學化學研究所碩士論文. 2011
56. Kong, L.; Li, Y.; Ganguly, R.; Vidovic, D.; Kinjo, R. Angew. Chem. Int. Ed. 2014, 53, 9280 –9283.
57. Kalemos, A.; Mavridis, A. J. Chem. Phys. 2000. 113. 2270.
58. Cenini, S.; Gallo, E.; Caselli, A.; Ragaini, F.; Fantauzzi, Cenini, S.; Gallo, E.; Caselli, A.; Ragaini, F.; Fantauzzi, Cenini, S.; Gallo, E.; Caselli, A.; Ragaini, F.; Fantauzzi, Cenini, S.; Gallo, E.; Caselli, A.; Ragaini, F.; Fantauzzi, Cenini, S.; Gallo, E.; Caselli, A.; Ragaini, F.; Fantauzzi, Cenini, S.; Gallo, E.; Caselli, A.; Ragaini, F.; Fantauzzi, Cenini, S.; Gallo, E.; Caselli, A.; Ragaini, F.; Fantauzzi, Cenini, S.; Gallo, E.; Caselli, A.; Ragaini, F.; Fantauzzi, Cenini, S.; Gallo, E.; Caselli, A.; Ragaini, F.; Fantauzzi, Cenini, S.; Gallo, E.; Caselli, A.; Ragaini, F.; Fantauzzi, Cenini, S.; Gallo, E.; Caselli, A.; Ragaini, F.; Fantauzzi, Cenini, S.; Gallo, E.; Caselli, A.; Ragaini, F.; Fantauzzi, Cenini, S.; Gallo, E.; Caselli, A.; Ragaini, F.; Fantauzzi, Cenini, S.; Gallo, E.; Caselli, A.; Ragaini, F.; Fantauzzi, Cenini, S.; Gallo, E.; Caselli, A.; Ragaini, F.; Fantauzzi, Cenini, S.; Gallo, E.; Caselli, A.; Ragaini, F.; Fantauzzi, Cenini, S.; Gallo, E.; Caselli, A.; Ragaini, F.; Fantauzzi, Cenini, S.; Gallo, E.; Caselli, A.; Ragaini, F.; Fantauzzi, Cenini, S.; Gallo, E.; Caselli, A.; Ragaini, F.; Fantauzzi, Cenini, S.; Gallo, E.; Caselli, A.; Ragaini, F.; Fantauzzi, Cenini, S.; Gallo, E.; Caselli, A.; Ragaini, F.; Fantauzzi, Cenini, S.; Gallo, E.; Caselli, A.; Ragaini, F.; Fantauzzi, Piangiolino, C., Piangiolino, C., Piangiolino, C., Piangiolino, C., Piangiolino, C., Piangiolino, C., Piangiolino, C., Coord. Chem. Rev. Coord. Chem. Rev. Coord. Chem. Rev. Coord. Chem. Rev. Coord. Chem. Rev. 2006 , 250 , 1234. , 1234.
84
59. Figueroa, J. S.; Piro, N. A.; Clough, C. R.; Cummins, C., Figueroa, J. S.; Piro, N. A.; Clough, C. R.; Cummins, C., Figueroa, J. S.; Piro, N. A.; Clough, C. R.; Cummins, C., Figueroa, J. S.; Piro, N. A.; Clough, C. R.; Cummins, C., Figueroa, J. S.; Piro, N. A.; Clough, C. R.; Cummins, C., Figueroa, J. S.; Piro, N. A.; Clough, C. R.; Cummins, C., Figueroa, J. S.; Piro, N. A.; Clough, C. R.; Cummins, C., Figueroa, J. S.; Piro, N. A.; Clough, C. R.; Cummins, C., Figueroa, J. S.; Piro, N. A.; Clough, C. R.; Cummins, C., Figueroa, J. S.; Piro, N. A.; Clough, C. R.; Cummins, C., Figueroa, J. S.; Piro, N. A.; Clough, C. R.; Cummins, C., Figueroa, J. S.; Piro, N. A.; Clough, C. R.; Cummins, C., Figueroa, J. S.; Piro, N. A.; Clough, C. R.; Cummins, C., Figueroa, J. S.; Piro, N. A.; Clough, C. R.; Cummins, C., Figueroa, J. S.; Piro, N. A.; Clough, C. R.; Cummins, C., Figueroa, J. S.; Piro, N. A.; Clough, C. R.; Cummins, C., Figueroa, J. S.; Piro, N. A.; Clough, C. R.; Cummins, C., Figueroa, J. S.; Piro, N. A.; Clough, C. R.; Cummins, C., Figueroa, J. S.; Piro, N. A.; Clough, C. R.; Cummins, C., Figueroa, J. S.; Piro, N. A.; Clough, C. R.; Cummins, C., Figueroa, J. S.; Piro, N. A.; Clough, C. R.; Cummins, C., J. Am. J. Am. J. Am. Chem. Soc. Chem. Soc. 2005 , 128 , 940. , 940.
60. Curley, J. J.; Sceats, E. L.; Cummins, C. C., Curley, J. J.; Sceats, E. L.; Cummins, C. C., Curley, J. J.; Sceats, E. L.; Cummins, C. C., Curley, J. J.; Sceats, E. L.; Cummins, C. C., Curley, J. J.; Sceats, E. L.; Cummins, C. C., Curley, J. J.; Sceats, E. L.; Cummins, C. C., Curley, J. J.; Sceats, E. L.; Cummins, C. C., Curley, J. J.; Sceats, E. L.; Cummins, C. C., Curley, J. J.; Sceats, E. L.; Cummins, C. C., Curley, J. J.; Sceats, E. L.; Cummins, C. C., Curley, J. J.; Sceats, E. L.; Cummins, C. C., Curley, J. J.; Sceats, E. L.; Cummins, C. C., Curley, J. J.; Sceats, E. L.; Cummins, C. C., Curley, J. J.; Sceats, E. L.; Cummins, C. C., Curley, J. J.; Sceats, E. L.; Cummins, C. C., J. Am. Chem. Soc. J. Am. Chem. Soc. J. Am. Chem. Soc. J. Am. Chem. Soc. J. Am. Chem. Soc. J. Am. Chem. Soc. 2006 , 128 , 14036.
61. Silvia, J. S.; Cummins, C. C., Silvia, J. S.; Cummins, C. C., Silvia, J. S.; Cummins, C. C., Silvia, J. S.; Cummins, C. C., Silvia, J. S.; Cummins, C. C., Silvia, J. S.; Cummins, C. C., J. Am. Chem. Soc. J. Am. Chem. Soc. J. Am. Chem. Soc. J. Am. Chem. Soc. 2010 , 132 , 2169. , 2169. , 2169.
62. Cantrell, G. K.; Meyer, T. Y., Cantrell, G. K.; Meyer, T. Y., Cantrell, G. K.; Meyer, T. Y., Cantrell, G. K.; Meyer, T. Y., Cantrell, G. K.; Meyer, T. Y., Cantrell, G. K.; Meyer, T. Y., Cantrell, G. K.; Meyer, T. Y., Cantrell, G. K.; Meyer, T. Y., Cantrell, G. K.; Meyer, T. Y., Cantrell, G. K.; Meyer, T. Y., Cantrell, G. K.; Meyer, T. Y., Organometallics Organometallics Organometallics Organometallics Organometallics 1997 1997 , 16 , 5381.
63. K. Cantrell, G.; Y. Meyer, T., K. Cantrell, G.; Y. Meyer, T., K. Cantrell, G.; Y. Meyer, T., K. Cantrell, G.; Y. Meyer, T., K. Cantrell, G.; Y. Meyer, T., K. Cantrell, G.; Y. Meyer, T., K. Cantrell, G.; Y. Meyer, T., K. Cantrell, G.; Y. Meyer, T., K. Cantrell, G.; Y. Meyer, T., Chem. Commun. Chem. Commun. Chem. Commun. Chem. Commun. Chem. Commun. Chem. Commun. 1997 , 1551. , 1551.
64. Musch Long, A. K.; Yu, R. P.; Timmer, G. H.; Berry, J. F., J. Am. Chem. Soc. 128 .2010, 132, 12228.
65. Ni, C. B.; Ellis, B. D.; Long, G. J.; Power, P. P. Chemical Communications. 2009. 2332-2334
 
 
 
 
第一頁 上一頁 下一頁 最後一頁 top
* *