Premium
Ionic polymers with expanded π‐conjugation systems derived from through‐space interaction in piperazinium and homopiperazinium rings
Author(s) -
Yamaguchi Isao,
Matsuda Yukari,
Sato Moriyuki
Publication year - 2011
Publication title -
polymer international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.592
H-Index - 105
eISSN - 1097-0126
pISSN - 0959-8103
DOI - 10.1002/pi.2913
Subject(s) - pyridinium , chemistry , ring (chemistry) , polymer , ionic bonding , piperazine , chloride , delocalized electron , crystallography , polymer chemistry , medicinal chemistry , ion , organic chemistry
Reactions of N ‐(2,4‐dinitrophenyl)‐4‐arylpyridinium chlorides (aryl (Ar) = phenyl and 4‐biphenyl) with piperazine or homopiperazine caused opening of the pyridinium ring and yielded polymers that consisted of 5‐piperazinium‐3‐arylpenta‐2,4‐dienylideneammonium chloride (N(CH 2 CH 2 ) 2 N + (Cl − )CHCHC(Ar)CHCH) or 5‐homopiperazinium‐3‐arylpenta‐2,4‐dienylideneammonium chloride (N(CH 2 CH 2 CH 2 )(CH 2 CH 2 )N + (Cl − )CHCHC(Ar)CHCH) units. 1 H NMR spectral analysis suggested that the π‐electrons of the penta‐2,4‐dienylideneammonium group of the polymers were delocalized. UV‐visible spectral measurements revealed that the π‐conjugation system expanded along the polymer chains because of the orbital interaction between electrons of the two nitrogen atoms of the piperazinium and homopiperazinium rings. However, the π‐conjugation length depended on the distance between the two nitrogen atoms; that is, the polymers containing the piperazinium ring had a longer π‐conjugation length than those containing the homopiperazinium ring. Conversion of the piperazinium and homopiperazinium rings from the boat to the chair form led to a decrease in the π‐conjugation length. The surface of pellets that were molded from the polymers exhibited metallic luster, and these polymers underwent electrochemical oxidation in solution. Copyright © 2010 Society of Chemical Industry