Controlled ring-opening polymerization of ε-caprolactone initiated by in situ formed yttrium trisalicylaldimine complexes, and their study by density functional theory

Polymer International

Volumn 60, Issue 12, 2011, Pages 1745-1752

  Ni, Xufeng ^a   Liang, Zhenhua ^a   Ling, Jun ^a   Li, Xue ^a   Shen, Zhiquan ^a  

^a ZHEJIANG UNIVERSITY   (China)

Author keywords

caprolactone; Catalysts; DFT calculations; Ring opening polymerization; Yttrium salicylaldimine complex

Indexed keywords

ACTIVE CENTER; CAPROLACTONE; CATALYTIC PROPERTIES; DENSITY FUNCTIONAL THEORY CALCULATIONS; DFT CALCULATION; HIGH MOLECULAR WEIGHT; IN-SITU; OPTIMIZED GEOMETRIES; SALICYLALDIMINE LIGANDS; SALICYLALDIMINES; STERIC EFFECT; TETRA-HYDROFURAN; YTTRIUM COMPLEXES;

CATALYSTS; DENSITY FUNCTIONAL THEORY; LIGANDS; MOLECULAR WEIGHT DISTRIBUTION; ORGANIC SOLVENTS; PHENOLS; POLYMERS; RING OPENING POLYMERIZATION; YTTRIUM;

YTTRIUM ALLOYS;

EID: 81855196995     PISSN: 09598103     EISSN: 10970126     Source Type: Journal    
DOI: 10.1002/pi.3145     Document Type: Article

References (52)

1. Okada M, Prog Polym Sci 27: 87-133 (2002).
2. Labet M and Thielemans W, Chem Soc Rev 38: 3484-3504 (2009).
3. Sudesh K, Abe H and Doi Y, Prog Polym Sci 25: 1503-1555 (2000).
4. Kamber NE, Jeong W, Waymouth RM, Pratt RC, Lohmeijer BGG and Hedrick JL, Chem Rev 107: 5813-5840 (2007).
5. Khan JH, Schuea F and Georgea GA, Polym Int 58: 296-301 (2009).
6. Ajellal N, Carpentier J-F, Guillaume C, Guillaume SM, Helou M, Poirier V et al, Dalton Trans 39: 8363-8376 (2010).
7. Yasuda H, Prog Polym Sci 25: 573-626 (2000).
8. Hou ZM and Wakatsuki Y, Coord Chem Rev 231: 1-22 (2002).
9. McLain SJ and Drysdale NE, Yttrium and rare earth compounds catalyzed lactone polymerization, US Patent 5028667 (1991).
10. McLain SJ and Drysdale NE, Polym Prep 33: 174 (1992).
11. Evans JW, Shreeve JL and Doedens RJ, Inorg Chem 32: 245-246 (1993).
12. Shen YQ, Shen ZQ, Zhang YF and Yao KM, Macromolecules 29: 8289-8295 (1996).
13. Zhang J, Gan ZH, Zhong ZY and Jing XB, Polym Int 45: 60-66 (1998).
14. Agarwal S, Mast C, Dehnicke K and Greiner A, Macromol Rapid Commun 21: 195-212 (2000).
15. Kunioka M, Wang Y and Onozawa S, Polym J 35: 422-429 (2003).
16. Fan L, Zhang LF and Shen ZQ, Polym J 36: 91-95 (2004).
17. Yu CP, Zhang LF and Shen ZQ, Polym Int 53: 1485-1490 (2004).
18. Xue MQ, Sun HM, Zhou H, Yao YM, Shen Q and Zhang Y, J Polym Sci, Part A: Polym Chem 44: 1147-1152 (2006).
19. Sheng HT, Zhou LY, Zhang Y, Yao YM and Shen Q, J Polym Sci, Part A: Polym Chem 45: 1210-1218 (2007).
20. Palard I, Schappacher M, Belloncle B, Soum A and Guillaume SM, Chem Eur J 13: 1511-1521 (2007).
21. Oshimura M and Takasu A, Macromolecules 43: 2283-2290 (2010).
22. Wu GM, Liu JC, Sun WL, Shen ZQ and Ni XF, Polym Int 59: 431-436 (2010).
23. Xu X, Chen YF and Sun H, Organometallics 27: 758-763 (2008).
24. Gao W, Cui DM, Liu XM, Zhang Y and Mu Y, Organometallics 27: 5889-5893 (2008).
25. Li SH, Cui DM, Li DF and Hou ZM, Organometallics 28: 4814-4822 (2009).
26. Li XF, Nishiura M, Hu LH, Mori K and Hou ZM, J Am Chem Soc 131: 13870-13882 (2009).
27. Xu X, Chen YF, Feng J, Zou G and Sun J, Organometallics 29: 549-553 (2010).
28. Martin E, Dubois P and Jérôme R, Macromolecules 33: 1530-1535 (2000).
29. Martin E, Dubois P and Jérôme R, Macromolecules 36: 5934-5941 (2003).
30. Martin E, Dubois P and Jérôme R, Macromolecules 36: 7094-7099 (2003).
31. Martin E, Dubois PH and Jérôme R, J Polym Sci, Part A: Polym Chem 41: 569-578 (2003).
32. Emslie DJH, Piers WE, Parvez M and McDonald R, Organometallics 21: 4226-4240 (2002).
33. Nomura N, Aoyama T, Ishii R and Kondo T, Macromolecules 38: 5363-5366 (2005).
34. Ten Breteler MR, Zhong ZY, Dijkstra PJ, Palmans ARA, Peeters J and Feijen J, J Polym Sci, Part A: Polym Chem 45: 429-436 (2007).
35. Iwasa N, Fujiki M and Nomura K, J Mol Catal A: Chem 292: 67-75 (2008).
36. Li BY, Wang YR, Yao YM, Zhang Y and Shen Q, J Organ Chem 694: 2409-2414 (2009).
37. Tessier-Youngs C, Beachley OT, Oliver JP and Butcher K, Inorg Synth 24: 95-97 (2007).
38. Netopilík M and Kratochvíl P, Polymer 44: 3431 (2003).
39. Cameron PA, Gibson VC, Redshaw C, Segal JA, White AJP and Williams DJ, J Chem Soc, Dalton Trans 3: 415-422 (2002).
40. Lee C, Yang W and Parr RG, Phys Rev B 37: 785-789 (1988).
41. Becke AD, J Chem Phys 98: 5648-5652 (1993).
42. Frisch MJ, Trucks GW, Schlegel HB, Scuseria GE, Robb MA, Cheeseman JR et al, Gaussian03. Gaussian Inc., Wallingford, CT (2004).
43. Liu JZ, Ling J, Li X and Shen ZQ, J Mol Catal A-Chem 300: 59-64 (2009).
44. Huang CH, Wang FC, Ko BT, Yu TL and Lin CC, Macromolecules 43: 356-361 (2001).
45. Báez JE, Martínez-Rosales M and Martínez-Richa A, Polymer 44: 6767-6772 (2003).
46. Cayuela J, Bounor-Legaré V, Cassagnau P and Michel A, Macromolecules 39: 1338-1346 (2006).
47. Ling J and Shen ZQ, Macromol Chem Phys 203: 735-738 (2002).
48. Ling J, Zhu WP and Shen ZQ, Macromolecules 37: 758-763 (2004).
49. Peng F, Ling J, Shen ZQ and Zhu WW, J Mol Catal A: Chem 230: 135-141 (2005).
50. Nishiura M, Hou ZM, Koizumi T, Imamoto T and Wakatsuki Y, Macromolecules 32: 8245-8251 (1999).
51. Barros N, Mountford P, Guillaume SM and Maron L, Chem Eur J 14: 5507-5518 (2008).
52. Ling J, Shen JG and Hogen-Esch TE, Polymer 50: 3575-3581 (2009).