• 제목/요약/키워드: ethers

검색결과 307건 처리시간 0.028초

Single Electron Transfer Induced Photoaddition Reactions of Silyl Enol Ether to N-Methylphthalimide

  • Oh, Sun-Wha;Kim, Jin-Young;Cho, Dae-Won;Choi, Jung-Hei;Yoon, Ung-Chan
    • Bulletin of the Korean Chemical Society
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    • 제28권4호
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    • pp.629-634
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    • 2007
  • Photochemical reactions of N-methylphthalimide with silyl enol ethers have been explored. Irradiations of phthalimide (1) and cyclic silyl enol ethers (5a-b) are observed to promote formation of photoreduced phthalimides and photoaddition products by sequential SET-desilylation pathways. The photoreaction of phthalimide (1) and acyclic silyl enol ethers (5c-d) leads to produce oxetanes which arise by competitive single electron transfer (SET) and classical 2+2 photocycloaddition (Parteno-Buchi reaction) pathways.

광학분리를 위한 키랄 크라운 에테르를 이용한 키랄공학의 개발과 응용 (The Development and Application of Chirotechnology Using Chiral Crown Ethers for Enantiomer Separation)

  • 백만정;윤원남;이원재
    • KSBB Journal
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    • 제27권4호
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    • pp.199-206
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    • 2012
  • Chiral crown ethers are synthetic macrocyclic polyethers that bind protonated chiral primary amines with high selectivity and affinity. They have been widely used to separate or distinguish the enantiomers of chiral compounds containing a primary amino moiety by high-performance liquid chromatography, capillary electrophoresis, and NMR spectroscopy. In this paper, two important chiral crown ethers including chiral binaphthyl unit and (18-crown-6)-2,3,11,12-tetracarboxylic acid as chiral selectors are focused. And several chiral resolution techniques and their applications in chirotechnology using these chiral crown ethers with related chiral recognition mechanism studies are reviewed. Especially, it was shown that the commercially available HPLC columns based on (18-crown-6)-2,3,11,12-tetracarboxylic acid have been developed and successfully applied for the resolution of various primary amino compounds including amino acids.

Cesium separation from radioactive waste by extraction and adsorption based on crown ethers and calixarenes

  • Wang, Jianlong;Zhuang, Shuting
    • Nuclear Engineering and Technology
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    • 제52권2호
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    • pp.328-336
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    • 2020
  • Cesium is a major product of uranium fission, which is the most commonly existed radionuclide in radioactive wastes. Various technologies have been applied to separate radioactive cesium from radioactive wastes, such as chemical precipitation, solvent extraction, membrane separation and adsorption. Crown ethers and calixarenes derivatives can selectively coordinate with cesium ions by ion-dipole interaction or cation-π interaction, which are promising extractants for cesium ions due to their promising coordinating structure. This review systematically summarized and analyzed the recent advances in the crown ethers and calixarenes derivatives for cesium separation, especially focusing on the adsorbents based on extractants for cesium removal from aqueous solution, such as the grafting coordinating groups (e.g. crown ether and calixarenes) and coordinating polymers (e.g. MOFs) due to their unique coordination ability and selectivity for cesium ions. These adsorbents combined the advantages of extraction and adsorption methods and showed high adsorption capacity for cesium ions, which are promising for cesium separation The key restraints for cesium separation, as well as the newest progress of the adsorbents for cesium separation were also discussed. Finally, some concluding remarks and suggestions for future researches were proposed.

촉매량의 Piperidine-1-oxyl과 NaOCl계에서 벤질 에테르 유도체들의 산화 반응 (Oxidation of Benzyl Ethers in Sodium Hypochlorite Mediated Piperidine-1-oxyl System)

  • 조남숙;박찬헌
    • 대한화학회지
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    • 제39권8호
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    • pp.657-665
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    • 1995
  • 여러가지 비대칭 벤질 에테르들과 벤질 알킬 에테르들을 $CH_3CO_2Et$-NaOCI수용액(6.6 mol eq.)의 2상 용매계에서 4-methoxy-2, 2, 6, 6,-tetramethylpiperidine-1-oxyl(0.03 mol eq., 4-methoxy-TEMPO)을 이용하여 산화시키면 벤조에이트로 산화가 일어난다. 4-methoxy-TEMPO는 2차 산화제인 NaOCI에 의하여 본반응의 산화제인 N-oxo-4-2, 2, 6, 6, -tetramethyl-piperidium 염(N-oxoammonium 염)으로 변환된다. N-oxoammonium 염은 에테르를 산화시키고 N-hydroxy-4-methoxy-2, 2, 6, 6,-tetramethylpiperidine(hydroxyamine)으로 환원된다. Hydroxy-amine은 NaOCI에 의하여 N-oxoammonium 염으로 순환 재생되므로 4-methoxy-TEMPO는 촉매량 사용하였다. 이 반응은 또한 조촉매인 KBr(0.03 mol eq.)가 필수적이고 반응 중 pH는 8.0 이하로 유지되어야 한다. 0 - 5$^{\circ}C$의 반응 온도로 2.5시간 반응시키면 대부분 벤조에이트로 산화 되었다. 벤질 알킬 에테르들의 선택성 산화는 수소의 산도와 알킬기의 입체효과에 영향을 받음이 고찰되었다.

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