Poly(1-vinyl-2-pyrrolidone)- and dextran-bound protoheme mono[N-[3-(imidazol-1-yl)propyl]amide] and mono[N-[5-(2-methylimidazol-1-yl)pentyl]amide] and their reversible oxygen binding in an aqueous medium

Hiroyuki Nishide, Makoto Yuasa, Etsuo Hasegawa, Eishun Tsuchida

Research output: Contribution to journalArticle

13 Citations (Scopus)

Abstract

Protoheme mono[N-[3-(imidazol-1-yl)propyl]amide] and mono[N-[5-(2-methylimidazol-1-yl)pentyl]amide] were covalently bound with poly(1-vinyl-2-pyrrolidone) (1) and dextran (2). The polymer-bound hemes formed oxygen adducts with lifetimes of ca. 1 h for 1 and a few minutes for 2 in an aqueous ethylene glycol (1/1) solution cooled to -30°C, whereas nonbound heme analogues did not form under the same conditions. It is considered that the water-soluble but hydrophobic poly(vinylpyrrolidone) protects the heme-oxygen adduct from its proton-driven irreversible oxidation. Oxygen binding rate constant of 1 was reduced by the surrounding polymer, and oxygen binding affinity was close to that of hemoglobin. Mössbauer parameters of the iron-57-labeled 1 were also measured.

Original languageEnglish
Pages (from-to)1913-1917
Number of pages5
JournalMacromolecules
Volume20
Issue number8
Publication statusPublished - 1987

ASJC Scopus subject areas

  • Materials Chemistry

Fingerprint Dive into the research topics of 'Poly(1-vinyl-2-pyrrolidone)- and dextran-bound protoheme mono[N-[3-(imidazol-1-yl)propyl]amide] and mono[N-[5-(2-methylimidazol-1-yl)pentyl]amide] and their reversible oxygen binding in an aqueous medium'. Together they form a unique fingerprint.

  • Cite this