Ring-opening polymerization of lactides using heterobimetallic yttrocene complexes
β Scribed by Klaus Beckerle; Kai C. Hultzsch; Jun Okuda
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 77 KB
- Volume
- 200
- Category
- Article
- ISSN
- 1022-1352
No coin nor oath required. For personal study only.
β¦ Synopsis
Structurally characterized, chiral heterobimetallic yttrocene derivatives Li[Y(g 5 : g 1 -C 5 R 4 Si-Me 2 NCH 2 CH 2 OMe) 2 ] (R = Me, H) have been shown to be active in the controlled ring-opening polymerization of L-lactide to give poly(L-lactide)s with high molecular weights and moderately narrow molecular weight distributions (M w /M n a 1.50). Both transesterification and racemization appear to be less prominent. 1 H NMR spectroscopic tetrad analysis of copolymers prepared using a mixture of L-and D-lactide demonstrates the absence of any preference for one enantiomer during the polymerization.
π SIMILAR VOLUMES
Currently there is considerable interest in the controlled ringopening polymerization (ROP) of lactides (LAs) by welldefined metal initiators because of the biodegradable and biocompatible nature of polylactides (PLAs) and their potentially wide-ranging commercial applications. [1, 2] Particularly i
Polyether dendrons have been successfully used as macroinitiators for the living ring-opening polymerization (ROP) of lactones and lactides. A hydroxyl group located at the focal point of dendrimers of different generations was transformed into diethyl aluminum alkoxides by reaction with triethyl al
Ring-opening polymerization of -caprolactone (CL) has been initiated with rare earth phenyl compounds in both bulk and solution. These rare earth phenyl initiators can give polycaprolactone (PCL) with high yield and high molecular weight. The polymerization mechanism is through a coordination-deprot