Synthesis and characterization of organoaluminum compounds containing quinolin-8-amine derivatives and their catalytic behaviour for ring-opening polymerization of ε-caprolactone

Dalton Transactions

Volumn , Issue 41, 2009, Pages 9000-9009

  Shen, Miao ^a   Zhang, Wenjuan ^a   Nomura, Kotohiro ^b   Sun, Wen Hua ^a  

^a INSTITUTE OF CHEMISTRY   (China)

^b NARA INSTITUTE OF SCIENCE AND TECHNOLOGY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

AMINE DERIVATIVES; BENZYL ALCOHOL; BIDENTATE LIGANDS; CAPROLACTONE; CATALYTIC ACTIVITY; CATALYTIC BEHAVIOUR; ELEMENTAL ANALYSIS; HIGH MOLECULAR WEIGHT; IMIDAZOL; ORGANOALUMINUM COMPOUNDS; REACTION CONDITIONS; REPRESENTATIVE COMPOUND; SQUARE-PYRAMIDAL GEOMETRY; STOICHIOMETRIC REACTION; SYNTHESIS AND CHARACTERIZATION; TETRADENTATE LIGANDS; TETRAHEDRON GEOMETRY;

ALUMINA; ALUMINUM; ALUMINUM COMPOUNDS; AMINES; LIGANDS; LIVING POLYMERIZATION; MOLECULAR WEIGHT; ORGANIC COMPOUNDS; PHENOLS; POLYMERS; X RAY CRYSTALLOGRAPHY;

RING OPENING POLYMERIZATION;

EID: 70349972296     PISSN: 14779226     EISSN: 14779234     Source Type: Journal    
DOI: 10.1039/b910155a     Document Type: Article

References (51)

1. For example: K. Ishihara, in Lewis Acids in Organic Synthesis, ed., H. Yamamoto, Wiley-VCH, Weinheim, Germany, 2000, vol. 1, p. 89
2. T. Ooi and K. Maruoka, in Lewis Acids in Organic Synthesis, ed., H. Yamamoto, Wiley-VCH, Weinheim, Germany, 2000, p. 191
3. D. W. Wulff, in Lewis Acids in Organic Synthesis, ed., H. Yamamoto, Wiley-VCH, Weinheim, Germany, 2000, p. 283
4. E. Y.-X. Chen T. J. Marks Chem. Rev. 2000 100 1391
5. J.-N. Pedeutour K. Radhakrishnan H. Cramail A. Deffieux Macromol. Rapid Commun. 2001 22 1095
6. W. E. Piers Adv. Organomet. Chem. 2004 52 1
7. D. Mecerreyes R. Jerome P. Dubois Adv. Polym. Sci. 1999 147 1
8. B. J. O'Keefe M. A. Hillmyer W. B. Tolman J. Chem. Soc., Dalton Trans. 2001 2215
9. K. M. Stridsberg M. Ryner A.-C. Albertsson Adv. Polym. Sci. 2002 157 41
10. A.-C. Albertsson I. Varma Biomacromolecules 2003 4 1466
11. O. Dechy-Cabaret B. Martin-Vaca D. Bourissou Chem. Rev. 2004 104 6147
12. M. Okada Prog. Polym. Sci. 2002 27 87
13. E. Chiellini R. Solaro Adv. Mater. 1996 8 305
14. T. Hayashi Prog. Polym. Sci. 1994 19 663
15. C. E. Radzewich M. P. Coles R. F. Jordon J. Am. Chem. Soc. 1998 120 9384
16. C. E. Radzewich I. A. Guzei R. F. Jordon J. Am. Chem. Soc. 1999 121 8673
17. S. Gong H. Ma Dalton Trans. 2008 3345
18. N. Nomura T. Aoyama R. Ishii T. Kondo Macromolecules 2005 38 5363
19. J. Liu N. Iwasa K. Nomura Dalton Trans. 2008 3978
20. N. Iwasa M. Fujiki K. Nomura J. Mol. Catal. A: Chem. 2008 292 67
21. N. Iwasa S. Katao J. Y. Liu M. Fujiki Y. Furukawa K. Nomura Organometallics 2009 28 2179
22. A. Arbaoui C. Redshaw D. L. Hughes Chem. Commun. 2008 4717
23. Z. Zhong P. J. Dijkstra J. Feijen Angew. Chem., Int. Ed. 2002 41 4510
24. N. Spassky M. Wisniewski C. Pluta A. Le Borgne Macromol. Chem. Phys. 1996 197 2627
25. T. M. Ovitt G. W. Coates J. Am. Chem. Soc. 2002 124 1316
26. C. P. Radano G. L. Baker M. R. Smith J. Am. Chem. Soc. 2000 122 1552
27. T. M. Ovitt G. W. Coates J. Polym. Sci., Part A: Polym. Chem. 2000 38 4686
28. Z.-Y. Chai C. Zhang Z.-X. Wang Organometallics 2008 27 1626
29. C. Zhang Z.-X. Wang Appl. Organomet. Chem. 2009 23 9
30. K. Wang P. Hao D. Zhang W.-H. Sun J. Mol. Struct. 2008 890 95
31. W.-H. Sun K. Wang K. Wedeking D. Zhang S. Zhang J. Cai Y. Li Organometallics 2007 26 4781
32. K. Wang K. Wedeking W. Zuo D. Zhang W.-H. Sun J. Organomet. Chem. 2008 693 1073
33. K. Wang M. Shen W.-H. Sun Dalton Trans. 2009 4085
34. C. A. Harbert J. J. Plattner W. M. Welch A. Weissman B. K. Koe J. Med. Chem. 1980 23 635
35. H. Lexy T. Kauffmann Chem. Ber. 1980 113 2755
36. P. C. Unangst D. T. Connor S. R. Stabler R. J. Weikert J. Heterocycl. Chem. 1987 24 811
37. Y. Kato M. M. Conn J. Rebek, Jr. J. Am. Chem. Soc. 1994 116 3279
38. J. P. Collman M. Zhong Org. Lett. 2000 2 1233
39. J. C. Antilla J. M. Baskin T. E. Barder S. L. Buchwald J. Org. Chem. 2004 69 5578
40. P. Hormnirun E. L. Marshall V. C. Gibson A. J. P. White D. J. Williams J. Am. Chem. Soc. 2004 126 2688
41. W. Dittrich R. C. Shultz Angew. Makromol. Chem. 1971 15 109
42. W. Yao Y. Mu A. Gao W. Gao L. Ye Dalton Trans. 2008 3199
43. W. Zhang W. Katao W.-H. Sun K. Nomura Organometallics 2009 28 1558
44. D. Chakraborty E. Y.-X. Chen Organometallics 2002 21 1438
45. S. Milione F. Grisi R. Centore A. Tuzi Organometallics 2006 25 266
46. K. C. Hultzsch T. P. Spaniol J. Okuda Organometallics 1997 16 4845
47. R.-C. Yu C.-H. Hung J.-H. Huang H.-Y. Lee J.-T. Chen Inorg. Chem. 2002 41 6450
48. P. T. Beurskens, G. Beurskens, R. de Gelder, S. Garcia-Granda, R. O. Gould, R. Israel and J. M. M. Smits, The DIRDIF-94 program system, Crystallography Laboratory, University of Nijmegen, The Netherlands, 1998
49. Crystal Structure 3.6.0: Crystal Structure Analysis Package, Rigaku and Rigaku/MSC, 9009 New Trails Dr., The Woodlands, 77381 TX, USA, 2000-2004
50. D. J. Watkin, C. K. Prout, J. R. Carruthers and P. W. Betteridge, CRYSTALS Issue 10, Crystallography Laboratory- Oxford, UK, 1996
51. G. M. Sheldrick, SHELXL-97, Program for the Refinement of Crystal Structure, University of Göttingen, Göttingen, Germany, 1997