• Title/Summary/Keyword: 트리에틸렌디아민

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Structure and Chemical Reactivity of the Transition Metal Complexes (I). Synthesis and Geometrical Isomerism of the Ethylenediamine-triacetatocobalt (III) Complexes with Ammine or Diamines (전이금속착물의 구조와 그 반응성 (I). 암민류를 포함하는 Ethylenediamine-triacetatocobalt (III) 착물의 합성과 기하이성질현상)

  • Dong-Jin Lee;Bong-Gon Kim;Myung-Ki Doh
    • Journal of the Korean Chemical Society
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    • v.29 no.5
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    • pp.516-521
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    • 1985
  • Ethylenediamine-triacetatocobalt (III) complexes with an ammine, an ethylene-diamine, and a trimethylenediamine as the unidentate ligand were prepared, and were isolated as only one isomer for each case by the Dowex 50W-X8, cation exchange resin in $H^+$ form. The geometrical isomer of these complexes have been assigned cis-equatorial form in the three possible geometrical isomers from the elemental analysis, pH titration, IR, NMR, and electronic absorption spectrum. It was found that $[CoN_3O_3]$ system of the meridional form with multidentate ligand have the first absorption band of the largely splitting pattern, and that the diamines (ethylenediamine, trimethylenediamine) have coordinated to the central cobalt (III) ion as a unidentate ligand.

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Cobalt(III) Complexes Containing Ethylenediamine-Triacetate and Aliphatic Diamine (I). The Reaction of Etylenediamine-tetraacetatocobaltate(Ⅲ) with Trimethylenediamine in Aqueous Solution (지방족디아민과 에틸렌디아민-트리아세테이트를 포함하는 코발트 (Ⅲ) 錯物에 관한 연구 (제1보). 수용액 중에서 [Co(EDTA)]- 錯物에 트리메틸렌디아민의 반응)

  • Myung-Ki Doh;Dong-Soo Kim
    • Journal of the Korean Chemical Society
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    • v.22 no.1
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    • pp.25-29
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    • 1978
  • Cobalt(III) complex containing ethylenediamine-triacetate and trimethylenediamine has been isolated from the reaction of ethylenediamine-tetraacetatocobaltate(III) with trimethylene-diamine in aqueous solution by Dowex 50W-X8, cation exchange resin in $H^+$ form. The ethylenediamine-triacetate($EDTRA^{3-}$) ligand coordinates to the cobalt(III) ion as a quadridentate with a free acetate branch. It has been observed that the complex has trans(O-O) (1) structure via the elemental analysis, UV, IR and NMR data.

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The Effects of Solvent Composition and Pressure on the Rate of Solvolysis of trans-$[Co(en)_2Cl_2]^+$, trans-$[Co(N-eten)_2Cl-2]^+$, trans-$[Co(N-meen)_2Cl-2]^+$ and trans-$[Co(tn)_2Cl-2]^+$ in Aceton-Water Mixture. Excess Free Energy & Free Energy Cycle and Reaction Mechanism (아세톤-물 혼합용매에서 trans-$[Co(en)_2Cl-2]^+$, trans-$[Co(N-eten)_2Cl-2]^+$, trans-$[Co(N-meen)_2Cl_2]^+$, trans-$[Co(tn)_2Cl_2]^+$ 착이온의 가용매 분해반응에 대한 압력과 용매조성의 영향. 반응메카니즘과 자유에너지 변화사이클 및 Excess 자유에너지)

  • Yu-Chul Park;Young-Je Cho
    • Journal of the Korean Chemical Society
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    • v.29 no.6
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    • pp.629-636
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    • 1985
  • The rates of solvolysis of trans-$[Co(AA)_2Cl_2]^+$ in which AA indicates ethylenediamine(en), N-ethylethylenediamine (N-eten), N-methylethylenediamino (N-meen) and trimethylenediamine(tn) respectively have been investigated using conductometric and spectrophotometric methods at various pressure up to 2,000 bar in acetone-water mixture. The activation volumes (${\Delta}V^{\neq}) obtained from the pressure effect on rate constants were -0.2∼0.9 $cm^3mole^{-1}$ for en, -0.2∼0.6 $cm^3mole^{-1}$ for N-eten, -0.8∼6.0 $cm^3mole^{-1}$ for N-meen and 0.7∼7.0$cm^3mole^{-1}$ for tn. The rates of solvolysis of these complexes were analyzed by comparing with the results obtained from excess free energy ($G^E$) and free energy cycle. It was found that $S_N1$ character was increased with decreasing the pressure and increasing the content of acetone in the mixture solvent. In addition to that, the effect of charge separation on the mechanism of solvolysis was discussed.

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Radon Removal Efficiency of Activated Carbon Filter from Coconut (코코넛 기반 활성탄 필터의 라돈 제거 효율)

  • Yun-Jin Ahn;Gi-Sub Kim;Tae-Hwan Kim;Sang-Rok Kim
    • Journal of radiological science and technology
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    • v.46 no.2
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    • pp.141-149
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    • 2023
  • The Korea Institute of Radiological and Medical Sciences plans to produce 225Ac, a therapeutic radio-pharmaceutical for precision oncology, such as prostate cancer. Radon, a radioactive gas, is generated by radium, the target material for producing 225Ac. The radon concentration is expected to be about 2000 Bq·m-3. High-concentration radon-generating facilities must meet radioactive isotope emission standards by lowering the radon concentration. However, most existing studies concerning radon removal using activated carbon filters measured radon levels at concentrations lower than 1000 Bq·m-3. This study measured 222Rn removal of coconut-based activated carbon filter under a high radon concentration of about 2000 Bq·m-3. The 222Rn removal efficiency of activated carbon impregnated with triethylenediamine was also measured. As a result, the 222Rn removal amount of the activated carbon filter showed sufficient removal efficiency in a 222Rn concentration environment of about 2000 Bq·m-3. In addition, despite an expectation of low radon reduction efficiency of Triethylenediamine-impregnated activated carbon, it was difficult to confirm a significant difference in the results. Therefore, it is considered that activated carbon can be used as a radioisotope exhaust filter regardless of whether or not Triethylenediamine is impregnated. The results of this study are expected to be used as primary data when building an air purification system for radiation safety management in facilities with radon concentrations of about 2000 Bq·m-3.