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Substituent effect of the ester moiety of epoxysuccinates on the polycondensation with diamine

✍ Scribed by Taiqi Liu; Fumio Sanda; Takeshi Endo


Publisher
John Wiley and Sons
Year
2000
Tongue
English
Weight
124 KB
Volume
38
Category
Article
ISSN
0887-624X

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✦ Synopsis


Di-2,2,2-trichloroethyl cis-epoxysuccinate, di-2-cyanoethyl cis-epoxysuccinate, and di-2-methoxyethyl cis-epoxysuccinate were synthesized, and the substituent effect of the epoxysuccinates on the polycondensation with diamine was studied. The order of reactivities of the epoxysuccinates with m-xylylenediamine was as follows: di-trichloroethyl ester Σ· di-cyanoethyl ester ΟΎ di-methoxyethyl ester, such was also confirmed by the model reaction of the epoxysuccinate with benzylamine. 1 H NMR and IR spectroscopic study and ab initio calculation also well explained the reactivity order.


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