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The Catalytic Effect of Alkali Metal Ions on Reactions of 8-(5-Nitroquinolyl) 2-Furoate with Alkali Metal Ethoxides in Anhydrous Ethanol
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  • The Catalytic Effect of Alkali Metal Ions on Reactions of 8-(5-Nitroquinolyl) 2-Furoate with Alkali Metal Ethoxides in Anhydrous Ethanol
  • The Catalytic Effect of Alkali Metal Ions on Reactions of 8-(5-Nitroquinolyl) 2-Furoate with Alkali Metal Ethoxides in Anhydrous Ethanol
저자명
음익환,이성은,민지숙,Eum. Ik Hwan,Lee. Seong Eun,Min. Ji Suk
간행물명
Bulletin of the Korean Chemical Society
권/호정보
2001년|22권 7호|pp.669-672 (4 pages)
발행정보
대한화학회
파일정보
정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
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기타언어초록

Pseudo-first-order rate constants have been measured spectrophotometrically for the title reactions. The plot of kobs vs the concentration of alkali metal ethoxides is linear for the reactions performed in the presence of complexing age nt, 18-crown-6 ether, but curved upwardly for the corresponding reactions performed in the absence of the complexing agent, indicating that the alkali metal ions studied in this study behave as a catalyst. The catalytic effect was found to increase in the order Li+ << K+ ${leq}$ Na+. Second-order rate constants were determined for the reactions with dissociated free ethoxide (kEtO-) and with ion paired alkali metal ethoxides (kEtO-M+ ) from ion pairing treatments. The magnitude of catalytic effect (kEtO-M+/kEtO-) was found to be 2.3, 9.5 and 8.7 for the reaction of 8-(5-nitroquinolyl) 2-furoate, while 1.4, 3.6 and 4.2 for that of 4-nitrophenyl 2-furoate, indicating that the catalytic effect is larger in the reaction of the former substrate than in that of the latter one. The larger catalytic effect was attributed to two possible complexing sites with alkali metal ions in the former substrate.