• Journal of the Korean Chemical Society
• /
• v.32 no.3
• /
• pp.243-248
• /
• 1988

The hypersensitive $f{\rightarrow}f$ transitions of Nd(III), Ho(III), and Er(III) have been studied for some lanthanide complexes in aqueous solution. Based on the linear correlation between the oscillator strength of the transition and the basicity$(pK_a)$ of the ligand, the covalency in the metal-ligand bonding is discussed for lanthanide anthranilate, pyrazine-2-carboxylate, and pyruvate.

• Journal of the Korean Chemical Society
• /
• v.28 no.6
• /
• pp.384-392
• /
• 1984

Reaction of the Fe(II) complex of a fully saturated tetradentate macrocyclic ligand [Fe([14]aneN$_4)(CH_3CN)_2]^{2+}$, where [14]ane$N_4$ represents 1,4,8,11-tetraazacyclotetradecane, with $O_2$ has been investigated in acetonitrile solutions. [Fe([14]aneN$_4)(CH_3CN)_2]^{2+}$ reacts with oxygen to yield low spin Fe(III) species, [Fe([14]aneN$_4)(CH_3CN)_2]^{3+}$, which undergoes metal ion assisted oxidative dehydrogenation of the macrocyclic ligand to produce low spin Fe(II) complex, [Fe([14]tetraeneN$_4)(CH_3CN)_2]^{2+}$. The macrocyclic ligand in [Fe([14]tetraeneN$_4)(CH_3CN)_2]^{2+}$ is highly unsaturated and its double bonds are conjugated. [Fe([14]dieneN$_4)(CH_3CN)_2]^{2+}$ and [Fe([14]dieneN$_4)(CH_3CN)_2]^{3+}$ are isolated as the intermediates of the reaction. The Fe(II) complexes involved in this oxidative dehydrogenation reaction react with carbon monoxide to give respective carbon monoxide derivatives, [FeL$(CH_3CN)(CO)]^{2+}$ (where L = macrocyclic ligand). The values of $v_{CO}$ of [FeL$(CH_3CN)(CO)]^{2+}$, and the electrochemical oxidation potentials of Fe(II) ${\to}$ Fe(III) and the qualitative stability toward air-oxidation for [FeL(CH$_3CN_2)^{2+}$ increase as the degree of unsaturation of the macrocyclic ligands increase.

• Journal of the Korean Chemical Society
• /
• v.47 no.3
• /
• pp.199-205
• /
• 2003

Complexes of uranyl ion $UO^{+2}_2$with Schiff-bases obtained by condensing glycylglycine with salicylaldehyde; 2-hydroxy-1-naphthaldehyde, 2,3-dihydroxybenzaldehyde, and 2,4-dihydroxybenzaldehyde have been synthesized and characterized through elemental analysis, conductivity measurements, magnetic susceptibility determinations, u.v., i.r. and $^1H$ nmr spectra as well as d.t.a., t.g. and d.s.c. techniques. Structures and mechanisms of thermal decomposition are proposed.

• Journal of the Korean Chemical Society
• /
• v.13 no.1
• /
• pp.16-24
• /
• 1969

Ni, Co, Zn, Cd, Mn, Mg, Ca, Sr, Ba 등의2가 금속과 U(VI) 및 V(IV)의 이온이 만드는 $MCup_2$ 조성의 cupferrates 착화합물에 관하여, 그 용해도가 좋은 dioxane-$H_2O$, methanol-$H_2O$, ethanol-$H_2O$ 및 2-propanol-$H_2O$의 혼합용매를 사용하여, 그들의 몰분율을 변화시키면서 제 1, 제 2 및 전체의 열역학적인 안정도상수를 전위차적정법에 의하여 측정하고, 안정도 상수와 유기용매의 몰분율에 관한 실험식을 얻었다. 한편 분광광전법에 의하여 가능한 cupferrates의 전체 안정도 상수를 측적하여 이들과 비교하였다. 2가 금속 cupferrates의 안정도상수는 위에 적은 금속의 순서로 감소하고, 이들의 log $K_1$은 log $K_2$보다 크지만, U(VI)과 V(IV)의 cupferrates는 log $K_1$$K_2$여서 1:1과 1:2 착화합물 사이에 구조 변화가 있는듯하다. 몰분율이 영인 점에서의 안정도상수는 금속 cupferrates의 수용액에서의 용해반응의 평형상수에 해당하며, 금속의 착화합물의 안정도상수와 용해도와는 무관하고, K<$10^5$인 cupferrates에 관해서는 분광전법을 적용하기 어렵다.

• Korean Journal of Soil Science and Fertilizer
• /
• v.19 no.4
• /
• pp.307-314
• /
• 1986

Cu(II) binding mechanisms with water soluble organic fractions (WSOF) extracted from an agricultural soil (W), a soil treated with sludge for 6 years ($WS_6$), a sludge-soil mixture incubated for one week ($WS_1$), and sewage sludge (SS) were studied by electron spin resonance (ESR) spectroscopy and potentiometric titrations. Cu(II)-WSOF complexes produced $g_{11}$ values which were larger than $g_{\perp}$ values, indicating that the coordination of Cu(II) complex was an elongated octahedron. At liquid $N_2$ temperature (77K), the Cu(II)-W complex showed an anisotropic ESR spectrum while the Cu(II)-SS complex showed an isotropic spectrum. These spectral results suggest that the oxygen donor ligands of W may form relatively strong bonds with $Cu^{2+}$ due to extensive chelation while ligands of SS may form little or no chelate bonds with $Cu^{2+}$. The ESR spectra of Cu(II)-SS complex also suggest that each of four in-plane ligands (e.g., $COO^-$, $H_2O$, $Cl^-$, etc.) may act independently as monodentate ligands. Oxygen donor ligands such as aromatic carboxyl groups were probably the major Cu(II) binding sites in W. Sulfonate, aliphatic carboxyl group, and N-containing ligands were probably the major binding sites in SS at pH 5. The Cu(II) complexation with N-containing groups increased as sludge was added to the soil. Much higher (6x) pyridine concentrations were required to displace W from Cu(II)-W complex as compared to the Cu(II)-SS complex.

• YAKHAK HOEJI
• /
• v.13 no.1
• /
• pp.38-42
• /
• 1969

Chloropentammine chromium(III) chloride를 출발물질로 하여 여러가지의 thiocyanatoammine계 착화합물을 합성하는 실험에 있어서 그 수득량이 예상보다 매우 적고 그 염의 모액이 농적자색이라는 점으로 보아 그 모액중에 어떠한 다른 착화합물이 다량 형성되어 있으리라고 추측하여 그 분리를 시도하였다든바 미려한 적자색의 결정을 얻었다. 그리고 분석에 의하여 이 물질이 potassium hexathiocyanatochromate(III) 임을 증명하였다. Cr$^{+++}$ 의 thiocyanate 착화합물형성에 관하여는 Niel Bjerrm$^{(8)}$에 의한 보고문이 있고 또 이들의 제법으로서는 Roesler$^{(9)}$들에 의하여 Potassium chromium alum에서부터 이 물질을 만드는 방법만이 보고되어 있을뿐이다. 따라서 Chloropentammine chromium(III) chloride에서 부터 이 물질을 만드는 이 새로운 방법이 이러한 화합물들의 제법으로서 앞으로 이용될 수 있는것으로 사료한다. 제조 방법: Chloropentammine chromium(III) chloride 3g을 KSCN 24g, 빙초산 24ml및 물 48ml의 혼합수용액에 현탁시킨 혼합물을 처음에는 잘 교반하면서 가온하고 다음 완전히 용해될때까지 끊인다. 냉각시킨 다음 생성된 증황색의 침반 Thiocyanatopentammine chromium(III) thiocyanate를 여과하고 여액 65ml에 KSCN 50g을 추가하여 완전용해시킨다. 이 용액을 방냉시키면 적자색의 미려한 결정이 석출되므로 이 결정을 여과하여 ethanol로 세척하고 진공 desiccator중에서 건조시켰다. 수득량 1.2~1.3g.

• Journal of the Korean Chemical Society
• /
• v.26 no.3
• /
• pp.142-147
• /
• 1982

Substituent effects on the fluorescence of 2-(substituted anilino) nicotinic acids and their aluminum chelate compounds were examined, and satisfactory linear relationships between Hammett substituent constant, ${\sigma}$, and the lowest excited singlet energy levels were obtained. Effects of solvent on the native and aluminum chelate compounds were also investigated.

• Journal of the Korean Chemical Society
• /
• v.26 no.3
• /
• pp.148-154
• /
• 1982

The effects of the various ligands on the oscillator strengths of the hypersensitive transitions of Nd(III) and Ho(III) have been studied in aqueous solution. The ligands used in the study are furoate, anthranilate, and squarate. The covalent character of the metal-ligand bond in the complex is discussed on the basis of the correlation diagram between pKa of the ligands and the oscillator strengths of the complexes previously reported.

• Proceedings of the Korean Environmental Sciences Society Conference
• /
• 2004.05a
• /
• pp.265-267
• /
• 2004

• Journal of the Korean Electrochemical Society
• /
• v.10 no.2
• /
• pp.150-154
• /
• 2007

Redox complexes to transport electrodes from biomaterial to electrodes are very important part in commercial biosensor industry. A novel osmium redox complex was synthesized by the coordinating pyridine group with osmium metal. A novel osmium complex is described as $[Os(dme-bpy)_2(ap-im)Cl]^{+/2+}$. We have been studied the electrochemical characteristics of this osmium complex with electrochemical techniques such as cyclic voltammetry and chronoamperommetry. In order to immobilize osmium redox complexes on the electrode, we deposited gold nano-particles on screen printed carbon electrode(SPE). The electrical signal converts the osmium redox films into an electrocatalyst for glucose oxidation. The catalytic currents were monitored that the catalytic currents were linearly increased from 1 mM to 5 mM concentrations of glucose.