Chain transfer constants for vinyl monomers polymerized in methyl oleate and methyl stearate

• Published in: Journal of polymer science. Part A-1, Polymer chemistry Polymer chemistry, 1969-09, Vol.7 (9), p.2605-2620
• Main Authors: Jordan Jr, Edmund F., Artymyshyn, Bohdan, Wrigley, A. N.
• Format: Article
• Language: English
• ISSN: 0449-296X; 1542-9350
• DOI: 10.1002/pol.1969.150070912

Chain transfer constants were obtained for styrene, methyl methacrylate, methyl acrylate and vinyl acetate, polymerized in methyl oleate and methyl stearate at 60°C. Transfer constants increased in the order: methyl methacrylate < styrene < methyl acrylate ≪ vinyl acetate in both solvents. Average values of the transfer parameters were: for methyl oleate, Q tr = 2.04 × 10 −4 , e tr = 1.08; for methyl stearate, Q tr = 0.373 × 10 −4 , e tr = 1.01. Indication that polar species predominate in the transition state is supported by the observed order of reactivity. The usual rate dependence appeared to be followed by all of the monomers except vinyl acetate, which was retarded, severely in methyl oleate. Transfer in methyl oleate was about 5.8 times greater than that found in methyl stearate for these four monomers. The internal allylic double bond of methyl oleate had about the same reactivity in transfer as had the terminal unsaturation in N ‐allylstearamide at 90°C. Rough estimates were obtained of the monomer transfer constants for the long side‐chain homologs of these four monomers from the respective monomer transfer constants and the experimental transfer constants, corrected for transfer to the labile groups of the solvent. It was concluded that the rate of polymerization would determine in large measure the degree of polymerization for the reactive 18‐carbon homologs but that the molecular weight of poly(vinyl stearate) and (oleate) will be regulated primarily by transfer to monomer.