TY - JOUR
T1 - Polymerization of N-carboxy anhydrides by organotin catalysts
AU - Freireich, S.
AU - Gertner, D.
AU - Zilkha, A.
PY - 1974/5
Y1 - 1974/5
N2 - Organotin compounds were found to lead to polymerization of N-carboxy anhydrides. The polymerization was studied in detail using γ-benzyl N-carboxyl-t-glutamate anhydride (BGA). Compounds such as tributyltin methoxide, bis(tributyltin)oxide, and N-tributyltin imidazole polymerized BGA while others like dibutyltin dichloride, which are Lewis acids, failed. Polymerization of BGA in dioxane at various monomer to dibutyltin dimethoxide ratios showed a first order reaction to monomer. The plot of In M0/M1 vs time showed two stage kinetics, the second one being faster. The pseudo first order rate constants were smaller than those for primary amine initiated polymerizations and much smaller than that for polymerization initiated by sodium methoxide. The molecular weights were independent of the monomer to initiator ratio both in dioxane and in DMF. In the reaction of an equimolar amount of tributyltin methoxide with NCA, the methyl ester of the amino acid was formed. The mechanism suggested is that of addition of the organotin compound to the NCA forming an organotin carbamate which decarboxylates, leaving an active -N-Sn-group which adds to another NCA molecule. This process is repeated in every step of the propagation.
AB - Organotin compounds were found to lead to polymerization of N-carboxy anhydrides. The polymerization was studied in detail using γ-benzyl N-carboxyl-t-glutamate anhydride (BGA). Compounds such as tributyltin methoxide, bis(tributyltin)oxide, and N-tributyltin imidazole polymerized BGA while others like dibutyltin dichloride, which are Lewis acids, failed. Polymerization of BGA in dioxane at various monomer to dibutyltin dimethoxide ratios showed a first order reaction to monomer. The plot of In M0/M1 vs time showed two stage kinetics, the second one being faster. The pseudo first order rate constants were smaller than those for primary amine initiated polymerizations and much smaller than that for polymerization initiated by sodium methoxide. The molecular weights were independent of the monomer to initiator ratio both in dioxane and in DMF. In the reaction of an equimolar amount of tributyltin methoxide with NCA, the methyl ester of the amino acid was formed. The mechanism suggested is that of addition of the organotin compound to the NCA forming an organotin carbamate which decarboxylates, leaving an active -N-Sn-group which adds to another NCA molecule. This process is repeated in every step of the propagation.
UR - http://www.scopus.com/inward/record.url?scp=0343598274&partnerID=8YFLogxK
U2 - 10.1016/0014-3057(74)90209-2
DO - 10.1016/0014-3057(74)90209-2
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???
AN - SCOPUS:0343598274
SN - 0014-3057
VL - 10
SP - 439
EP - 443
JO - European Polymer Journal
JF - European Polymer Journal
IS - 5
ER -