Multifunctional Hydrolytic Catalyses. 7. Cooperative Catalysis of the Hydrolysis of Phenyl Esters by a Copolymer of N-Methylacrylohydroxamic Acid and 4-Vinylimidazole

Toyoki Kunitake, Yoshio Okahata

研究成果: Contribution to journalArticle査読

46 被引用数 (Scopus)

抄録

A bifunctional polymer catalyst was prepared by radical polymerization of benzyl N-methylacrylohydroxamate and 4-vinylimidazole, followed by the removal of the benzyl group, and the hydrolysis of four phenyl ester substrates was examined in 28.9 vol/vol % EtOH-H2O at 30 °C. The Michaelis-Menten kinetics were observed only for a long-chain, anionic substrate. The major course of catalysis was acylation and deacylation at the hydroxamate group. The acylation process consisted of the simple nucleophilic attack of the hydroxamate anion (kA- ) and the general base (imidazole) catalyzed nucleophilic attack of the hydroxamic acid (kHA)· In the case of p-nitrophenyl acetate (PNPA), KHA and kA-were 0.50 and 36 M-1 s-1, respectively, and the difference was much smaller for other substrates. The deacylation reaction proceeded efficiently due to the general-base catalysis of the imidazole group. Thus, the imidazole group acts as a general base in both the acylation and deacylation process, in close resemblance to the charge relay system of serine proteases.

本文言語英語
ページ(範囲)7793-7799
ページ数7
ジャーナルJournal of the American Chemical Society
98
24
DOI
出版ステータス出版済み - 11 1 1976

All Science Journal Classification (ASJC) codes

  • 触媒
  • 化学 (全般)
  • 生化学
  • コロイド化学および表面化学

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