Wang Dong, HUANG Zhi-tang. THE THERMO-POLYMERIZATION OF N-PHENYL-BICYCLO [2.2.1] HEPT-S-ENE-2,3-DICARBOXIMIDE. [J]. Acta Polymerica Sinica (3):212-219(1981)
DOI:
Wang Dong, HUANG Zhi-tang. THE THERMO-POLYMERIZATION OF N-PHENYL-BICYCLO [2.2.1] HEPT-S-ENE-2,3-DICARBOXIMIDE. [J]. Acta Polymerica Sinica (3):212-219(1981)DOI:
THE THERMO-POLYMERIZATION OF N-PHENYL-BICYCLO [2.2.1] HEPT-S-ENE-2,3-DICARBOXIMIDE
The crosslinking reaction of bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic anhydride capped polyimide by using N-phenyl-bicyclo[2.2.1]hept-5-ene-dicarboximide (I) as the model compound was studied.It is found from the changes of the conversion and the molecular weight of the polymers with reaction temperature and time that endo-I could be polymerized above 275℃ and the polymerization tended to the completion at 800℃ for 2hr.NMR spectra of endo-I polymers show that the following structural units were present in the pulymer:The contents of different types of double bonds in the polymer could be determined semi-quantitatively by NMR spectroscopy and the bromine addition method.The ex- perimental results indicated that the average molecular weights of the polymer are 800一1000 and the total contents of double bonds are 1.00一1.25 per molecule.while the con-tents of double bonds of cyclopentene type are smaller than 0.5. Under the same reac-tion conditions the structure of the polymers from endo.and exo-I is similar.As a result,the following mechanism of polymerization was proposed.The retro Diels-Alder reaction took place at first on heating I.The active centres were produced above 275℃.then the chain growth reaction was followed.The trasformation of confi-guration.rearrangement and different paths of chain growth reactiOIlS occurred during the polymerization.The chain termination was caused mainly by disproportion reactions.