• Journal of the Korean Chemical Society
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• v.44 no.3
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• pp.243-248
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• 2000

Oganic electroluminescent devices (OELD) with multilayer structures have been studied actively for the application to a flat-panel display. Netal-chelate complexes hrboxylate. These complexes were characterized by FT-IR, MS/FAB, $^1$H-NMR, UV-vis and photoluminescence (PL). More importantly, the electrochemical gap (Eg), electron affinity(EA) and ionization potential (IP) of these complex films were investigated. Data from cyclic voltammetry(CV) were compared with the bandgap obtained from UV-vis and discussed. Further studies on the EL of these new materials are now in progress.

• Journal of the Korean Chemical Society
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• v.34 no.4
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• pp.345-351
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• 1990

Optical isomers of DABS-amino acids have been separated in a reversed phae high performance liquid chromatography by adding Cu (Ⅱ)-L-Proline chelate to the mobile phase. The retention behaviors for the DABS-amino acids are discussed in terms of pH of the mobile phase and the concentrations of acetonitrile, Cu (Ⅱ) complex, and buffer. The selectivity of the optical isomers of DABS-amino acids increases with the pH of the mobile, and the concentration of the chelate, but decreases with concentration of the oganic modifier. The concentration of buffer does not affect the optical separation selectivity. A separation mechanism is illustrated by cis and trans formation based on the steric effect of the ligand exchange reaction between DABS-amino acids and the copper chelate.

• Journal of the Korean Chemical Society
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• v.34 no.2
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• pp.165-170
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• 1990

The reactivity and structural change of optical active $[Co(edta)]^- and [Co(Hedta)Cl]^- complexes has been investigated in the presence of several catalyst (H^+, OH^-, and Cd^{2+}). When Δ-[Co(edta)]- complex was reacted with H^+ or OH^- as the catalyst, G-ring opening of ligand in the complex was accompanied, and then, optically active, [Co(Hedta)OH_2], and racemic mixture, [Co(edta)OH]_2- were produced. When (-)546-[Co(Hedta)Cl]- complex was reacted with Cd^{2+}$ as the catalyst, the Ring-close was accompanied, and Δ-[Co(edta)]- complex was produced, which the absolute configuration was retained.

• Journal of the Korean Chemical Society
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• v.21 no.3
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• pp.161-170
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• 1977

Several Pt(II) complexes containing glycine (or glycino anion) and styrene have been prepared, and their structures have been confirmed by infrared spectroscopy. The results confirm the structure of chloro(glycino)(styrene)platinum(II) in which the nitrogen atom of the chelated glycino anion is coordinated to the platinum in the trans position to styrene (N-trans isomer).

• Clean Technology
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• v.20 no.4
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• pp.367-374
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• 2014

Several experiments have been done to investigate the removal of hydrogen sulfide ($H_2S$) synthetic gas from biogas streams by means of chemical absorption and chemical reaction with 0.1-1 M Fe/EDTA solution. The roles of Fe/EDTA were studied to enhance the removal efficiency of hydrogen sulfide because of oxidizing by chelate. The motivation of this investigation is first to explore the feasibility of enhancing the toxic gas treatment in the biogas facility. The biogas purification strategy affords many advantages. For instance, the process can be performed under mild environmental conditions and at low temperature, and it removes hydrogen sulfide selectively. The end product of separation is elemental sulfur, which is a stable material that can be easily disposed with minor potential for further pollution. As the Fe-EDTA concentration increased, the conversion rate of hydrogen sulfide increased because of the high stability of Fe-EDTA complex. pH as an important environmental factor was 9.0 for the stability of chemical complex in the oxidation of hydrogen sulfide.

• Proceedings of the Korean Environmental Sciences Society Conference
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• 1997.04a
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• pp.48-50
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• 1997

• Journal of the Korean Chemical Society
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• v.24 no.2
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• pp.121-128
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• 1980

Isonitrosobenzoylacetone is particularly interesting, as the isonitroso group has two potentially coordinating sites which can compete with the cabonyl groups in forming bonds with the metal ions. In this paper tris(isonitrosobenzoylacetonato)cobalt(III) and bis(isonitrosobenzoylacetonato)palladium(II) have been prepared, and their structures have been investigated. Spectroscopic studies lead to the conclusion that the both complexes do not contain an OH group in the chelated five-membered ring structure in which the ligand coordinates to metal through oxygen of the acetyl group and nitrogen of the isonitroso group. The coordination manner of this ligand is similar to that of isonitrosobenzoylacetone obtained by Patel and Haldar.

• Journal of the Korean Chemical Society
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• v.35 no.5
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• pp.527-533
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• 1991

Template condensation reactions of formaldehyde with appropriate tetramines and diamines in the presence of N(II) or Cu(II) ion produce square planar complexes of hexaaza macrotricyclic and macrotetracyclic ligands $[M(L)]^{2+}$(M = Ni(II) or Cu(II); L = 4-methyl-1,3,6,8,11,14-hexaazatricyclo[12,2,1,$1^{8,11}$]octadecane(C), 1,3,10,12,15,18-hexaazatetracyclo[16,2,1,$1^{12,15},0^{4,9}]$docosane(D) 4-methyl-1,3,6,8,12,15-hexaazatricyclo[13,3,1,$1^{8,12}$]eicosane(F), or 1,3,10,12,16,19-hexaazatetracyclo[l7,3,1,$1^{12,16},0^{4,9}]$tetracosane(G). These complexes contain two 1,3-diazacyclopentane or 1,3-diazacyclohexane rings in the six-membered chelate rings. The complexes of C and F contain one methyl group and those of D and G one cyclohexane ring in the five-membered chelate ring. Synthesis and characterization of the Ni(II) and Cu(II) complexes are presented. The effects of the ligand structure on the equilibrium $[Ni(L)]^{2+}2H_2O{\rightleftharpoons}[Ni(L)(H_2O)_2]^{2+}$ in aqueous solutions are described.

• Journal of the Korean Chemical Society
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• v.31 no.5
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• pp.434-443
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• 1987

The formation constants of the complexes between Ln-EDTA 1 : 1 complex and IMDA have been investigated by a potentiometric titration method at 20.0${\pm}$0.2 degree C and ${\mu}$ = 0.1 (KNO$_3$). Unusually large stability in Ln(EDTA) mixed ligand complexes was found. Trends in the formation constants vs. atomic number of the lanthanide metals were discussed on the basis of coordination number and ionic radius of the metals.

• Journal of the Korean Chemical Society
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• v.39 no.5
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• pp.379-383
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• 1995

The elution behaviors of stannous ion by PSA(phenol sulfonic acid) as an eluent on chelating resin, Amberlite IRC-718 have been investigated. When 0.10 M stannous solution was adsorbed on the resin and eluted with various concentrations of PSA, the two peaks of stannous ion were appeared in the elution curve. These two peak areas were changed according to the PSA concentration. Using these results, the stability constant of the complex formation between Sn2+ and PSA was calculated. This value is 2.0 ${\times}$ 10-1.