• 제목/요약/키워드: Crown Ether

검색결과 175건 처리시간 0.021초

PET Fabric Supported Fixed Site Carrier Membrane for Selective Metal ion Transport

  • Jin, Long Yi;Mah, Soukil
    • Fibers and Polymers
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    • 제3권1호
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    • pp.14-17
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    • 2002
  • Development of a novel fixed site carrier membrane (FCM), supported by PET fabric for metal ion separation is reported. The membranes were prepared by dipping PET fabric into the methylene chloride solution of Poly(5-vinyl-m-phe-nylene-m'-phenylene-32-crown-10) (P(VCE)), a polymeric metal ion carrier. It was found that the flux of mono-valent metal ion transported across the membrane is signif=cantly differed from each other and the flux decreases in the order $Cs^+$>$Rb^+$>$K^+$>$Na^+$>$Li^+$ irrespective to the anion except perchlorate anion. It was explained in terms of the stability of the complex, formed by crown ether unit of the P(VCE) and the various metal ions, meanwhile, the lower rate of transport in the presence of perchlorate anion was ascribed to its low hydrophilicity.

Dibenzo-16-crown-5 Lariat Ether와 금속이온과의 착물형성에 관한 연구 (Thermodynamic Studies on Complexes for Dibenzo-16-crown-5 Sulfur Lariat Ether with Metal Ions)

  • 조문환;이상철;조재훈;김응태;이창환;최영섭;이종찬
    • 대한화학회지
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    • 제42권4호
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    • pp.443-448
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    • 1998
  • 용액열량계를 이용하여, 25$^{\circ}C$ 메탄올 용액에서 dibenzo-16-crown-5(DB16C5)의 유도체들과 금속이온과의 착물형성에 관한 열역학적인 파라미터인 log K, ${\Delta}H$, $T{\Delta}S$를 결정하고, dibenzo-16-crown-5의 유도체들을 운반체로 사용하여 벌크액체막과(bulk liquid membrane, BLM) 지지액체막(supported liquid membrane, SLM) 실험을 통하여 금속이온의 이동현상을 관찰하였다. BLM과 SLM에서 운반체로 DB16C5유도체를 사용했을 때 $Ag^+$ 이온이 많이 이동되었고 다른 금속이온들은 약간 이동된 것으로 관찰되었다. 액체막을 통한 그속이온의 이동에서 중요한 파라미터로 작용하는 인자는 리간드의 구조, 곁가지의 길이, 주개원자의 수와 종류, 안정도상수, 리간드의 농도 등을 들 수 있다.

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고성능 액체 크로마토그래피에서 키랄 크라운 에테르로부터 유도된 키랄 고정상을 이용한 광학분리의 비교 (Comparative Enantiomer Separation on Chiral Stationary Phases Derived from Chiral Crown Ether by HPLC)

  • 황호;전소희;김지연;이원재
    • KSBB Journal
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    • 제27권4호
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    • pp.232-236
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    • 2012
  • Comparative liquid chromatographic enantiomer separation of ${\alpha}$-amino acids, their esters and primary amino compounds was performed using two chiral stationary phases (CSPs) prepared by covalently bonding (+)-(18-crown-6)-2,3,11,12-tetracarboxylic acid (18-C-6-TA) of the same chiral selector. In general, the separation factors and resolution factors for these analytes on CSP 1 were greater than on CSP 2, while these capacity factors on CSP 2 were quite greater than on CSP 1. Except for leucine methyl ester and phenylalanine methyl ester, the elution orders of all analytes including ${\alpha}$-amino ${\alpha}$-alkyl acids and phenylglycine alkyl esters on CSP 1 are identical to those on CSP 2. This study showed that different connecting structures for these two CSPs might influence their ability to resolve the analytes depending on their structures related to the chiral recognition mechanism.

Ammonium Ion Binding Property of Naphtho-Crown Ethers Containing Thiazole as Sub-Cyclic Unit

  • Kim, Hong-Seok;Do, Kyung-Soon;Kim, Ki-Soo;Shim, Jun-Ho;Cha, Geun-Sig;Nam, Hak-Hyun
    • Bulletin of the Korean Chemical Society
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    • 제25권10호
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    • pp.1465-1470
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    • 2004
  • A short and efficient synthesis, solvent extraction and potentiometric measurements of new thiazole-containing naphtho-crown ethers are reported. The naphthalene moiety enhances the ammonium ion selectivity over potassium ion. The selectivity of ${NH_4}^+/K^+$ follows the trend $3\;{\approx}\;2\;>\;1$, indicating that the differences in conformational changes of 2 and 3 in forming ammonium complexes affect little on the resulting ammonium/potassium extraction selectivity ratio. The ammonium ion-selective electrodes were prepared with noctylphenyl ether plasticized poly(vinyl chloride) membranes containing 1-4 the effect of one naphthalene unit introduced on either right (2) or left (3) side of thiazolo-crown ether on their potentiometric properties (e.g., ammonium ion selectivity over other cations, response slopes, and detection limits) were not apparent. However, the ammonium ion selectivity of 1, 2 and 3 over other alkali metal and alkaline earth metal cations is 10-100 times higher than that of nonactin.

Investigation of Enantiomer Separation Using Chiral Crown Ethers as Chiral Selectors

  • Lee, Wonjae
    • 통합자연과학논문집
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    • 제9권1호
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    • pp.28-34
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    • 2016
  • A number of chiral selectors have been developed and applied for enantiomer separation of a variety of chiral compounds. Among these chiral selectors are chiral crown ethers, a class of synthetic host polyether molecules that bind protonated chiral primary amines with high selectivity and affinity. In this paper, two important chiral crown ethers as chiral selectors of bis-(1,1'-binaphthyl)-22-crown-6 and (18-crown-6)-2,3,11,12-tetracarboxylic acid (18-C-6-TA) are focused. They have been widely used to resolve the enantiomers of chiral compounds containing a primary amino moiety using chiral stationary phases (CSPs) or chiral selectors by high-performance liquid chromatography (HPLC), capillary electrophoresis (CE) and so on in chirotechnology. Also, it was described that the commercially available covalent type HPLC CSPs derived from (+)- and (-)-18-C-6-TA have been developed and successfully applied for the resolution of various primary amino compounds including amino acids.

Sodium Ion-Selective Membrane Electrode Based on Dibenzopyridino-18-Crown-6

  • Tavakkoli, Nahid
    • Bulletin of the Korean Chemical Society
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    • 제25권10호
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    • pp.1474-1476
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    • 2004
  • A sodium ion- selective electrode based on dibenzopyridino-18-crown-6 as membrane carrier was successfully prepared. The electrode exhibits a Nernstian response for $Na^+$ ions within the concentration range of $1.0\;{\times}\;10^{-4}-1.0\;{\times}\;10^{-1}$ M. The response time of the sensor is 20 s. The sodium ion-selective electrode exhibited comparatively good selectivities with respect to alkali, alkaline earth and some transition metal ions.

크라온에테르를 이용한 탈륨(I) 이온 선택성 전극 (Tallium(I) Ion-Selective Electrodes Based on Crown Ethers)

  • 김성민;정성욱;김진은;김재상
    • 대한화학회지
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    • 제37권8호
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    • pp.773-778
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    • 1993
  • Tl$^+$이온 센서로서 크라운 에테르 B15C5와 DB18C6를 중성운반체로 한 PVC 액체막 이온 선택성 전극을 제작하였다. 막용매로는 DOA, NPPE 및 NPOE를 사용하였으며 친유성 염, KTClPB의 농도를 변화시킨 여러가지 조성의 막을 시험하였다. B15C5와 DB18C6 막 전극의 감응전위는 농도범위, 10$^{-1}$∼10$^{-5}$M에서 직선으로 나타났으며 최대 기울기는 전극에 따라서 40∼55 mV/decade였다. 선택계수는 분리용액법으로 결정하였으며 알카리금속 이온, 알칼리토금속 이온 및 일부 전이금속 이온에 대하여 좋은 선택성을 나타냈다. 제작된 액체막 전극은 Ph > 3 에서 안정한 감응전위를 보였다.

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모노아자크라운에테르 기능기를 가진 생리활성 포스피네이트 유도체의 합성 (Syntheses of Biologically Active Phosphinate Derivatives with a Pendant Monoazacrown Ether)

  • 남종우;정영진;양일우
    • 대한화학회지
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    • 제37권1호
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    • pp.154-161
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    • 1993
  • 모노아자크라운에테르 기능기를 분자내에 갖는 4종의 새로운 포스피네이트 유도체들을 합성하고 그들의 생리활성을 조사하였다. 생리활성 포스피네이트 유도체들의 합성은 페닐포스피네이트를 알데이드 및 모노아자크라운에테르와 한 단계로 반응시켜 61~72%의 비교적 높은 수율로 이루어질 수 있었다. 합성된 화합물들의 생리활성은 수컷의 생쥐에 대한 복강주사로 검사하였으며, $LD_{50}$ 값이 65~90mg/kg으로서 크라운에테르 기능기가 부착되면 단순한 페닐포스피네이트에서 보다 독성이 현저히 증가됨을 나타내었다. 모노아자-15-크라운-5를 부착한 화합물과 모노아자-18-크라운-6을 부착한 화합물의 고리 크기에 의한 독성차는 현저하지 않았으나, 에스테르기의 종류에는 다소 영향을 받아 올틸 또는 프로필 포스피네이트 유도체들이 에틸 포스피네이트 유도체에 비해 독성이 높게 나타났다.

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