Poly--pbenzyl-cglutamate prepared by polymerization of 7-benzyl-Lglutamate NCA in dimethylformamide (DMF) with the use of diisopropylamine as the initiator was precipitated from the polymerization mixture under different conditions. A portion of the almost completely polymerized solution was treated
Molecular weight distribution of polymers of γ-benzyl-L-glutamate
✍ Scribed by Ernesto Scoffone; Evaristo Peggion; Alessandro Cosani; Maria Terbojevich
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1965
- Tongue
- English
- Weight
- 356 KB
- Volume
- 3
- Category
- Article
- ISSN
- 0006-3525
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✦ Synopsis
The molecular weight distribution of poly-ybenzyl-cglutamate prepared by N-carboxy anhydride (NCA) polymerization with the use of die-butylamine, diisopropylamine, and sodium methoxide aa initiators waa investigated. In every case, narrow distributions were fcund. Moreover the results allow us to conclude that the same polymerization mechanism is operative with each of the above initiators. The experimental distribution curves show fairly good agreement with the theoretical distributions expected for a polymerization process without termination.
📜 SIMILAR VOLUMES
## Synopsis llotatory dispersion and circular dichroism of low-molecular-weight poly-7-benzyl-Lglutamate, which was prepared from the ,V-carboxyanhydride by n-hexylamine initiation a t [A]/[I] 3, 4, and 8, have been nieasured in ethylene dichloride and dioxane a t difierent concentrations. The rot
Four samples of copolymeix of -&enzyl bgliitamic (BLG) and 0-benzyl-L-wrine (BLS) were syntheriized by changing the mixing ratio of two monomer anhydrides. The conformations of these copolymers in CHCb, containing very small amount of dichloroacetic acid (DCA) necessary to dissolve the sample, were
0 1 1 leave from the Iiihli(,riLe for Rubber aiid Plastics Technology, (httwaldov, Cxec.hoslovaki:i. 271 0 1972 I)y Joliii W h y & SOII\, 1 1 1 ~.