Ring-opening polymerization of l-lactide by organotin(IV)alkoxides, R2Sn(OPri)2: Estimation of the activation parameters

Polyhedron

Volumn 26, Issue 15, 2007, Pages 4436-4444

  Chisholm, Malcolm H ^a   Gallucci, Judith C ^a   Krempner, Clemens ^a  

^a OHIO STATE UNIVERSITY   (United States)

Author keywords

Alkoxides; Catalysis; Lactide polymerization; Tin

Indexed keywords

CHEMICAL ACTIVATION; ORGANOMETALLICS;

ACTIVATION PARAMETER; ALKOXIDES; ENTROPY OF ACTIVATION; L-LACTIDE; LACTIDE POLYMERIZATION; ORGANOTINS; POLY (L-LACTIDE); RING-OPENING POLYMERIZATION; SMALL VARIATIONS; TEMPERATURE RANGE;

RING OPENING POLYMERIZATION;

EID: 34548232242     PISSN: 02775387     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.poly.2007.06.002     Document Type: Article

References (27)

1. Dechy-Cabaret O., Martin-Vaca B., and Bourissou D. Chem. Rev. 104 (2004) 6147
2. Neederberg F., Connor E.F., Glausser T., and Hedrick J.L. Chem. Commun. (2001) 2006
3. Neederberg F., Connor E.F., Moeller M., Glauser T., and Hedrick J.L. Angew. Chem., Int. Ed. 40 (2001) 2712
4. Nyce G.W., Glauser T., Connor E.F., Möck A., Waymouth R.M., and Hedrick J.L. J. Am. Chem. Soc. 125 (2003) 3046
5. O'Keefe B.J., Hillmyer M.A., and Tolman W.B. J. Chem. Soc., Dalton Trans. (2001) 2215
6. Chisholm M.H., and Zhou Z. In: Baugh L., and Canich J. (Eds). Stereoselective Polymerization with Single Site Catalysts (2007), Taylor and Francis publishers
7. Spassky N., Wisniewski M., Pluta C., and LeBorgne A. Macromol. Chem. Phys. 197 (1996) 2627
8. Spassky N., Pluta C., Simic V., Thiam M., and Wisniewski M. Macromol. Symp. 128 (1998) 39
9. Radano C.P., Baker G.L., and Smith III M.R. J. Am. Chem. Soc. 122 (2000) 1552
10. Ovitt T.M., and Coates G.W. J. Am. Chem. Soc. 124 (2002) 1316
11. Hormnirun P., Marshall E.L., Gibson V.C., White A.J.P., and Williams D. J. Am. Chem. Soc. 126 (2004) 2688
12. Zhong Z., Dijkstra P.J., and Feijen J. J. Am. Chem. Soc. 125 (2003) 11291
13. Tang Z., Chen X., Pang X., Yang Y., Zhang X., and Jing X. Biomacromolecules 5 (2004) 965
14. Chisholm M.H., and Zhou Z. Chem. Commun. (2005) 127
15. Chisholm M.H., and Delbridge E.E. New J. Chem. 27 (2003) 1167
16. Chisholm M.H., and Delbridge E.E. New J. Chem. 27 (2003) 1177
17. Chisholm M.H., Delbridge E.E., and Gallucci J.C. New J. Chem. 28 (2004) 145
18. DENZO:. Otwinowski Z., and Minor W. In: Carter Jr. C.W., and Sweet R.M. (Eds). Methods in Enzymology, vol. 276: Macromolecular Crystallography, part A (1997), Academic Press 307-326
19. shelxs-86. Sheldrick G.M. Acta Cryst. A46 (1990) 467-473
20. Sheldrick G.M. shelxs-97 (1997), Universitat Gottingen, Germany
21. Sheldrick G.M. shelxl-97 (1997), Universitat Gottingen, Germany
22. wingx-Version 1.64.05. Farrugia L.J. J. Appl. Cryst. 32 (1999) 837-838
23. International Tables for Crystallography, Volume C. Dordrecht: Kluwer Academic Publishers, 1992.
24. Williams C.K., Breyfogle L.E., Choi S.K., Nam W., Young V.G., Hillmyer M.A., and Tolman W.B. J. Am. Chem. Soc. 125 (2003) 11350
25. Woodward R.B., and Hoffmann R. The Conservation of Orbital Symmetry (1969), Academic Press, New York
26. Marshall E.L., Gibson V.C., and Rzepa H.S. J. Am. Chem. Soc. 127 (2005) 6048
27. Dove A.P., Gibson V.C., Marshall E.L., Rzepa H.S., White A.J.P., and Williams D.J. J. Am. Chem. Soc. 128 (2006) 9834