• 제목/요약/키워드: Macrocyclic ligand

검색결과 94건 처리시간 0.024초

The Stability Constant of 1, 7, 10, 16-Tetraoxa-4, 13-Diazacyclooctadecane-Uranium (Ⅵ) Complex in Aqueous Solution

  • Suh, Moo-Yul;Eom, Tae-Yoon;Kim, Si-Joong
    • Bulletin of the Korean Chemical Society
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    • 제4권5호
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    • pp.231-234
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    • 1983
  • The stability constant for the complex of $UO_2^{2+}$ with a macrocyclic aminoether ligand, 1,7,10,16-tetraoxa-4,13-diazacyclooctadecane, has determined in aqueous solution. The conductivity and pH metric measurements suggest that the ligand forms a stable 1:1 complex with $UO_2^{2+}$ ion, and the complex is an ionic form, $UO_2L^{2+}$, in aqueous solution. The fact that the ligand does not form a complex with lanthanides, such as $Ce^{3+}$, $Sm^{3+}$, and $Nd^{3+}$ ions, in aqueous solution suggests a possibility of separation of the lanthanide elements from uranium matrix using the macrocyclic aminoether ligand.

이가철 거대고리 리간드의 착화합물과 산소 분자간의 반응 : 이가철 거대고리 리간드 착화합물의 산화성 탈수소 반응에 의한 새로운 불포화 고리계의 합성 (Reaction of the Fe(II) Macrocyclic Complexes with Dioxygen : Preparation of New Unsaturated Ring Systems by Oxidative Dehydrogenation Reactions of Fe(II) Macrocyclic Ligands)

  • 백명현;강신걸;우규환
    • 대한화학회지
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    • 제28권6호
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    • pp.384-392
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    • 1984
  • 완전히 포화된 거대고리 리간드의 Fe(II) 착화합물 [Fe([14]aneN$_4)(CH_3CN)_2]^{2+}$과 ([14]ane$N_4$:1,4,8,11-tetraazacyclotetradecane) 산소분자간의 반응을 아세토니트릴 용액중에서 연구하였다. [Fe([14]aneTEX>$_4)(CH_3CN)_2]^{2+}$는 산소와 쉽게 반응하여 낮은 스핀 Fe(III) 착화합물 [Fe([14]aneN$_4)(CH_3CN)_2]^{3+}$을 생성하고 이는 다시 산화성 탈수소 반응에 의해 낮은 스핀 Fe(II) 착화합물 [Fe([14]tetraeneN$_4)(CH_3CN)_2]^{2+}$을 형성한다. [Fe([14]tetraeneN$_4)(CH_3CN)_2]^{2+}$의 리간드는 불포화도가 매우 높고 이중결합이 컨쥬게이션 되어 있다. 또한 반응의 중간체로서 [Fe([14]dieneN$_4)(CH_3CN)_2]^{2+}$ 및 [Fe([14]dieneN$_4)(CH_3CN)_2]^{3+}$도 분리되었다. 이 반응과 관련된 Fe(II) 착화합물들은 일산화탄소와 반응하여 [FeL(CH$_3CN)(CO)]^{2+}$ (L = 거대고리 리간드) 형태의 착화합물을 이룬다. [FeL(CH$_3CN)(CO)]^{2+}$$v_{CO}$ 값과 [FeL(CH$_3CN_2)^{2+}$의 Fe(II) ${\to}$ Fe(III)의 전기화학적 산화포텐셜 및 산소에 대한 정성적인 안전성은 거대고리 리간드의 불포화도가 높아질수록 증가한다.

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Spectroscopic characterization of N,N'-bis(salicylidene)pentane-1,3-diamine nickel(II) complex

  • Kim, Gilhoon;Won, Hoshik
    • 한국자기공명학회논문지
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    • 제18권2호
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    • pp.74-81
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    • 2014
  • The $N_2O_2$ tetradentate Schiff base ligand, N,N'-bis(salicylidene)pentane-1,3-diamine (Salpn), coupled with 1:2 concentration ratio of 1,3-diaminopentane and salicylaldehyde was used to produce a series of macrocyclic Nikel(II) complexes. In the metal complexation, it was observed that Salpn macrocyclic ligand can adopt more than a metal ion giving an unique multinuclear metal complexes including Ni(II)Salpn and $Ni(II)_3(Salpn)_2$. Characteristic IR ${\upsilon}(M-O)$ peaks for Ni(II)Salpn and $Ni(II)_3(Salpn)_2$ were observed to be $1028cm^{-1}$ and $1024cm^{-1}$, respectively. Characteristic UV-Vis absorption ${\lambda}_{max}$ peaks for $Ni(II)_3(Salpn)_2$ were observed to be 241nm and 401 nm. Structural characterization of $Ni(II)_3(Salpn)_2$ by NMR exhibits that the salicylidene ring moiety has two different resonance signals originated from the magnetically asymmetric diligand and trinuclear bis complex. Complete NMR signal assignments and characterizations elucidating structural features of $Ni(II)_3(Salpn)_2$ were described in detail.

OenNtn 합성수지를 이용한 금속이온들의 흡착에 관한 연구 (A Study on the Adsorption of Metal Ions Utilizing OenNtn Synthetic Resin)

  • 김준태;노기환
    • 환경위생공학
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    • 제14권3호
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    • pp.80-89
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    • 1999
  • The ion exchange resins have been synthesized from chlormethyl styrene-1,4-divinyl benzene(DVB) with 1%, 5%, and 10%-crosslinking and macrocyclic ligand of cryptand type by copolymerization method and the adsorption characteristics of uranium(VI), lead(II) and holmium(III) ions have been investigated in various experimental conditions. The correlation between the adsorption characteristics of rare earths and transition metal on the resins and stability constants of complexes with macrocyclic ligand have been examined. The $UO_2^{2+}$ aqueous solutions are not adsorbed on the resins below pH 3.0, but the power of adsorption of $UO_2^{2+}$ increased rapidly above pH 4.0. The adsorption power was in the order of 1%, 10%, and 5%-crosslinked resin, but adsorptive characteristics of resins decreased in proportion to the order of dielectric constants of solvents.

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Adsorption Characteristics of U ranium (VI) Ion on Cryptand Synthetic Resin Adsorbent

  • Kim, Hae-Jin
    • 통합자연과학논문집
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    • 제10권4호
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    • pp.225-231
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    • 2017
  • Cryptand resins were synthesized by mixing 1-aza-18-crown-6 macrocyclic ligand with styrene divinylbenzene copolymer having 1%, 2%, 5%, and 10% crosslink by a substitution reaction. These synthetic resins were confirmed by chlorine content, elementary analysis, SEM, surface area, and IR-spectrum. As the results of the effects of pH, crosslink of synthetic resin, and dielectric constant of a solvent on uranium ion adsorption for resin adsorbent, the uranium ion showed high adsorption at pH 3 or over. Adsorption selectivity for the resin in methanol solvent was the order of uranium ($UO_2{^{2+}}$) > calcium ($Ca^{2+}$) > neodymium ($Nd^{3+}$) ion, adsorbability of the uranium ion was the crosslink in order of 1%, 2%, 5%, and 10% and it was increased with the lower dielectric constant.

Manganese Metallamacrocycles with Various Coordination Solvents

  • Song, Ji-Heh;Moon, Doh-Yun;Lah, Myoung-Soo
    • Bulletin of the Korean Chemical Society
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    • 제23권5호
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    • pp.708-714
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    • 2002
  • The hexanuclear metallamacrocycles were observed repeatedly in various conditions including the presence of several different tricationic metal ions in the macrocyclic ring system and of the linear alkyl chains at the acyl site of N-acylsalicylhydrazide ligand, which contrasts to the formation of the decanuclear metallamacrocycle with bulkier side chains such as phenyl group at the acyl site of the ligand. We synthesized a series of metallamacrocycles in various solvents to find the relationship between the solvents and the nuclearity of the metallamacrocycles. Whether the solvents are sterically more demanding or not, the complexes formed kept the hexanuclear metallamacrocycle system.