논문 상세보기

CTABr 미셀 용액속에서 2-Alkylbenzimidazole 음이온에 의해 추진되는 Isopropyl phenyl-4-nitrophenyl phosphinate(IPNPIN)의 탈인산화반응 KCI 등재

Dephosphorylation of Isopropyl phenyl-4-nitrophenylphosphinate (IPNPIN) onto 2-Alkylbenzimidazolide Anion in CTABr Micellar Solution

  • 언어KOR
  • URLhttps://db.koreascholar.com/Article/Detail/366222
서비스가 종료되어 열람이 제한될 수 있습니다.
한국환경과학회지 (Journal of Environmental Science International)
한국환경과학회 (The Korean Environmental Sciences Society)
초록

This study is mainly focused on micellar effect of cetyltrimethyl ammonium bromide(CTABr) solution including alkylbenzimidazole(R-BI) on dephosphorylation of isopropyl-4-nitrophenylphosphinate(IPNPIN) in carbonate buffer(pH 10.7). The reactions of IPNPIN with R-BI⊖ are strongly catalyzed by the micelles of CTABr. Dephosphorylation of IPNPIN is accelerated by BI⊖ ion in 10-2 M carbonate buffer(pH 10.7) of 4×10-3 M CTABr solution up to 89 times as compared with the reaction in carbonate buffer by no benzimidazole(BI) solution of 4×10-3 M CTABr. The value of pseudo first order rate constant(kψ) of the reaction in CTABr solution reached a maximum rate constant increasing micelle concentration. Such rate maxima are typical of micellar catalyzed bimolecular reactions. The reaction mediated by R-BI⊖ in micellar solutions are obviously slower than those by BI⊖, and the reaction rate were decreased with increase of lengths of alkyl groups. It seems due to steric effect of alkyl groups of R-BI⊖ in Stern layer of micellar solution. The surfactant reagent, CTABr, strongly catalyzes the reaction of IPNPIN with R-BI and its anion(R-BI⊖) in carbonate buffer(pH 10.7). For example, 4×10-3 M CTABr in 1×10-4 M BI solution increase the rate constant(kψ=98.5×10-3 sec-1) of the dephosphorylation by a factor ca.25, when compared with reaction(kψ=3.9×10-4 sec-1) in 1×10-4 M BI solution(without CTABr). And no CTABr solution, in 1×10-4 M BI solution increase the rate constant(kψ=3.9×10-4 sec-1) of the dephosphorylation by a factor ca.39, when compared with reaction (kψ=1.0×10-5 sec-1) in water solution(without BI). This predicts that the reactivities of R-BI⊖ in the micellar pseudophase are much smaller than that of BI⊖. Due to the hydrophobicity and steric effect of alkyl group substituents, these groups would penetrate into the core of the micelle for stabilization by van der Waals interaction with long alkyl groups of CTABr.

목차
Abstract
 1. 서 론
 2. 재료 및 방법
  2.1. 시약 및 기기
  2.2. Alkylbenzimidazole(R-BI)의 해리상수(Ka)값과 CTABr과의 결합상수(Ks)의 측정
  2.3. CTABr 용액속에서 alkylbenzimidazole에 의해 추진되는 IPNPIN의 탈인산화반응의 속도상수(kψ)결정
 3. 결과 및 고찰
  3.1. CTABr 미셀 수용액에서의 alkylbenzimidazole의 Ka 값과 결합상수(Ks) 값
  3.2. CTABr 미셀 유사층 내에서의 R-BI⊖의 농도
  3.3. CTABr 미셀 용액내에서 R-BI⊖에 의한 탈인산화반응의 유사일차속도상수, kΨ (sec-1)
  3.4. 문제해결을 위한 가정
  3.5. 반응속도에 미치는 농도의 영향과 “닻줄효과(anchor effect)”
 4. 결 론
 참 고 문 헌
저자
  • 김정배(계명대학교 환경대학 지구환경학과) | Jeung-Bea Kim (Faculty of Environmental Studies, Keimyung University) Corresponding author