Ring-opening polymerization of 1,5-dioxepan-2-one initiated by 1,1,6,6tetra-n-butyl-1,6-distanna-2,5,7,10-tetraoxacyclodecane was carried out in chloroform, dichloromethane, or 1,2-dichloroethane. Effects of reaction temperature, solvent, and monomer-to-initiator ratio were investigated. Polymerizat
On the difference of reactivities of various aggregated forms of aluminium triisopropoxide in initiating ring-opening polymerizations
✍ Scribed by Andrzej Duda; Stanislaw Penczek
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 487 KB
- Volume
- 16
- Category
- Article
- ISSN
- 1022-1336
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✦ Synopsis
Abstract
The polymerization of ε‐caprolactone (εCL) initiated with aluminium triisopropoxide (Al(O^i^Pr)~3~) trimer (A~3~) and/or tetramer (A~4~) was studied. The rate of A~3~ ⇔︁ A~4~ interconversions in the diluted (≤0,1 mol · L^‐1^) C~6~D~6~, C~6~D~6~/εCL, and THF/εCL solutions were found to be slow, when compared with the rate of propagation. Comparison of the ^1^H NMR spectra of the initiators with those of the polymerization mixtures revealed that A~3~ is much more reactive than A~4~ in their reactions with εCL. From the initiator reacted with εCL all threeO^i^Pr groups from Al(O^i^Pr)~3~ are transferred into the poly(εCL) as end groups. Kinetic studies of polymerization confirmed the large reactivity difference between A~3~ and A~4~.
📜 SIMILAR VOLUMES
Time dependence of the yields in c-acryloyloxyethyl-c-butyrolactone and poly(c-acryloyloxy-e-caprolactone) in toluene at 0 8C. Conditions: [ACL] 0 = 1 m, [ACL] 0 /[Al(O i Pr) 3 ] 0 = 50 (ACL: c-acryloyloxy-e-caprolactone). Scheme 1.