Polymerizations by 1,3-Dipolar Cycloaddition Reactions. V. The 1,3-Dipolar Polycycloadditions of Dinitrile N -Oxides with Diolefins

  • Iwakura Y
  • Shiraishi S
  • Akiyama M
  • et al.
N/ACitations
Citations of this article
5Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Terephthalonitrile di-N-oxide and isophthalonitrile di-N-oxide were synthesized from the corresponding hydroxamic chlorides by dehydrochlorination with triethylamine. Their chemical properties and the polycycloadditions with diolefins were examined. The polymers obtained were amorphous and their molecular weights were not so high. The thermal gravimetric analyses of them showed that the polymers were stable up to 300–350°C in air.

Cite

CITATION STYLE

APA

Iwakura, Y., Shiraishi, S., Akiyama, M., & Yuyama, M. (1968). Polymerizations by 1,3-Dipolar Cycloaddition Reactions. V. The 1,3-Dipolar Polycycloadditions of Dinitrile N -Oxides with Diolefins. Bulletin of the Chemical Society of Japan, 41(7), 1648–1653. https://doi.org/10.1246/bcsj.41.1648

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free