Chain conformation of aliphatic α,ω-diamines in aqueous solutions

Shinichi Yamazaki, Takahiro Yoshida, Yoshio Muroga, Ichiro Noda

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Abstract

Potentiometric titration of aliphatic α,ω-diamines such as 1.3-, 1,4-, and 1,6-diamines was carried out in aqueous solutions with and without added salt to study the effect of electrostatic interactions on the chain conformations. The ratios of first to second association constants of proton K1/K2 were larger than 4 indicating the effects of electrostatic interactions on the second association constant in a similar manner as α,ω-diacids. These data were analyzed by the theories of Bjerrum and Kirkwood-Westheimer, and the resulting charge distances were compared with the end-to-end distances of various chain models.

Original languageEnglish
Pages (from-to)1237-1242
Number of pages6
JournalPolymer Journal
Volume31
Issue number12
Publication statusPublished - 1999
Externally publishedYes

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ASJC Scopus subject areas

  • Materials Chemistry
  • Polymers and Plastics

Cite this

Yamazaki, S., Yoshida, T., Muroga, Y., & Noda, I. (1999). Chain conformation of aliphatic α,ω-diamines in aqueous solutions. Polymer Journal, 31(12), 1237-1242.