• Journal of the Korean Chemical Society
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• v.39 no.5
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• pp.356-363
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• 1995

The chemical behavior of the transition metal (Nb4+ and Mo4+) complexes with organoligand (dichloro-bis(η-cyclopentadienyl) has been investigated by the UV/vis-spectrophotometric, magnetic, and electrochemical method. The two or three energy absorption bands are observed by the spectra of these complexes. The magnitude of crystal field splitting energy, the spin pairing energy and bond strength was obtained from the spectra of the complexes. These are found to be delocalization, low-spin state, and strong bonding strength. The magnetic dipolemoment are found to be paramagnetic and diamagnetic complexes. The redox reaction processes of complexes were investigated by cyclic voltammetry in aprotic media. As a result the redox reaction proceses of Nb-C complex was couple-single reaction with diffusion and reaction current one electron process, and also Mo-C complex was couple-single reaction with reaction current of one electron process.

• Applied Chemistry for Engineering
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• v.7 no.1
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• pp.145-152
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• 1996

A fine oil-in-water (O/W) emulsion using nonaqueous emulsification technique was developed and the behaviors of POE(25)octyldodecyl ether in nonaqueous solvent/oil systems were studied by observing the surface tension, interfacial tension, turbidity and transition temperature. It was found that POE(25)octyldodecyl ether existed soluble in nonaqueous solvent while, in aqueous system, it formed micelles. So, when a solvent, like glycerine in which POE(25)octyldodecyl ether has poor solubility, was added, POE(25)octyldodecyl ether moved to the surface. After saturated at surface, POE(25) octyldodecyl ether began to precitate. The mean particle size of the final emulsion was 230nm. Also, the emulsion system was stable at 0, 25, 40, $50^{\circ}C$ and cycling test for a month, while the conventional emulsion system showed unstability. It is concluded that, by pertinent combination of solvents, the adsorption efficiency of surfactant could be improved.

• Journal of the Korean Chemical Society
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• v.40 no.10
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• pp.649-655
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• 1996

The chemical behaviour of Pt(Ⅱ) and Pd(Ⅱ) complexes with the organic ligand tetramethylenesulfoxide(TMSO) has been investigated by UV/vis-spectrophotometric, magnetic, and electrochemical methods. Two energy absorption bands are observed in the spectra of these complexes. The crystal field splitting energy, spin pairing energy, and bond strength were obtained from the spectra of the complexes. The electronic properties of the complexes are found to be delocalized, and low-spin state. The correlation between ligand and metals were strong bonding strength. These complexes are diamagnetics. The redox reaction processes of the complexes were investigated by cyclic voltammetry in an aprotic solvent. The redox processes of complexes turned out to be respect to one-electrton one step. These complexes were considerably diffusion and reaction controlled.

• Journal of Physiology & Pathology in Korean Medicine
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• v.21 no.6
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• pp.1619-1623
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• 2007

This study was desiged to investigate the Obesity and Right-left(region) of Patients with Bell's palsy. We measured the sex, age, BMI and pulse diagnosis of 149 patients who were diagnosed as Bell's palsy. The results were as follows : In distribution of sex, the ratio of male was 52.35%(78 cases), female 47.65%(71 cases). The distribution of age revealed that 40s was the most in 50 cases(33.6%). The distribution of region in facial palsy was left 73 cases, right 76 cases(1:1.04). In distribution of region in facial palsy patients with obesity, the ratio of left was 32.86%(49 cases), right 34.23%(51 cases). But facial palsy patients with obesity was the most in 100 cases(67.11%), low weght was 3 cases(2.01%). In distribution of pulse diagnosis in facial palsy patients with obesity, the ratio of huh-mac(虛脈) was 63.64%(42 case), sil-mac(實脈) 36.36%(24 cases). The huh-mac(虛脈) was simlliar to gi-huh(氣虛). So we found that the facial palsy patients with obesity was more gi-huh(氣虛) than with low weght. In distribution of region in facial palsy patients with obesity-huh-mac(虛脈), the ratio of left was 41.38%(12 cases), right 58.62%(17 cases).

• Analytical Science and Technology
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• v.15 no.2
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• pp.97-101
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• 2002

Co(II) complexes with tridentate Schiff base-NOIPH and tetradentate Schiff base-$NOTDH_2$ and $TNBPH_4$ were synthesized. The redox process of the complexes in DMF solution containing 0.1M TBAP was investigated at glassy carbon electrode by cyclic voltammetry and differential pulse voltammetry techniques. Reduction step of [Co(II)$(NOIP)_2$] and [Co(II)$(H_2O)_2$] complexes were observed in two step as one electron process of irreversible or quasi-reversible and diffusion-controlled reaction. [$Co(II)_2$(TNBP)] complex was observed in one step as one electron process of quasi-reversible and diffusion-controlled reaction.

• The Journal of Internal Korean Medicine
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• v.28 no.3
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• pp.615-623
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• 2007

We made a comparative study, A patient who had suffered dizziness and ataxia took Hyungbangsabaek-san(荊防瀉白散) at first and next took Hyungbangdojeock-san(荊防導赤散). He was diagnosed as a Soyangin suffering chest knotting syndrome(結胸證) by Sasang constitutional medicine(四象醫學) and took two kinds of herbs in a row. We observed his phase of dizziness and ataxia with the conditions of stool and urine excavation, pink eye, sweating, and tongue color and tongue coating. When he took Hyungbangdojeock-san these conditions improved more than when he took the other one and his dizziness and ataxia also improved. Hyungbangdojeock-san was more useful when the severity of the disease was shallower and he had more exterior syndromes than Hyungbangsabaek-san.

• Journal of the Korean Chemical Society
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• v.38 no.8
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• pp.590-597
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• 1994

The chemical behavior of the trivalent lanthanide$(Pr^{3+}, Eu^{3+}, Gd^{3+} 그리고 Yb^{3+})$complexes with organo-ligand (2,2,6,6-tetramethyl-3,5-heptanedione) has been investigated by the use of UV/Vis-spectrophotometric, magnetics, and electrochemical method. The two or three energy absorption bands are observed by the spectra of these complexes. The magnetitude of crystal field splitting energy, the spin pairing energy and bond stength was obtained from the spectra of the complexes. These are found to be localization, low-spin (or high-spin state, and strong bonding strength. The magnetic dipole moment are found to be diamagnetic complexes (or paramagnetic). The electrochemical behavior of complexes was observed by the use of cyclic voltammetry in aprotic media. These reduction peaks were irreversible two and three step reduction processes by electron transfer.

• Journal of the Korean Chemical Society
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• v.50 no.4
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• pp.307-314
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• 2006

The redox characteristics of 2-ketohydrazono-3-phenyl-5-substituted-2,3-dihydro-1,3,4-thiadiazoles and its derivatives (1a-h) has been investigated in nonaqueous solvents such as 1,2-dichloroethane (DCE), dichloromethane (DCM), acetonitrile (AN), tetrahydrofuran (THF), and dimethylsulfoxide (DMSO) containing 0.1 mol.dm-3 tetra n-butylammonium perchlorate (TBAP) as supporting electrolyte at platinum ectrode. Through controlled potential electrolysis, the oxidation and reduction products of the investigated compounds can be separated and indentified. The redox mechanism is suggested and proved. It was found that all the investigated compounds are oxidized in two irreversible one-electron processes following the well known pattern of EC-mechanism. On the other hand, these compounds are reduced in a single two electron or in a successive two one electron processes following the well known pattern of EEC-mechanism according to the nature of the substituent

• Journal of the Korean Chemical Society
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• v.47 no.6
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• pp.585-590
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• 2003

Cobalt oxygen carrier complex N,N'-ethylenebis(3-methoxysalycylideneiminato)cobalt(II), Co(3MeOsalen) was prepared at $25{\circ}C$. UV and visible absorption spectra of the complex and hydrazobenzene were studied in non-aqueous solvent methanol in the range of wavelength 200-600 nm. The oxidation of hydrazobenzene by oxygen in non-aqueous solvent is catalysed by Co(3MeOsalen). In the presence of triphenylphosphine($PPh_3$), the rate decreases in methanol. This is presumably attributable to the coordination of $PPh_3$ to the Co(3MeOsalen), resulting in the catallytically inactive compound. The initial rates of the oxidation of hydrazobenzene with the ligand triphenylphosphine were measured by the theoretical values of the rates, Rate=$k_1+k_2K_1[P]/1+K_1[P]+K_1K_2[P]^2$. This fact would be a poorer σ-donor ligand than methanol.

• Journal of the Korean Chemical Society
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• v.39 no.1
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• pp.47-56
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• 1995

Tridentate Schiff base molybdenum(V) complexes such as [Mo(Ⅴ)2O(SOHB)4], [Mo(Ⅴ)2O3(SOIP)2(NCS)2] and [Mo(Ⅴ)2O3(SOTB)2(H20)2](SOHB: Salicylidene-o-imino hydroxybenzene, SOIP; Salicylidene-o-imino pyridine, SOTB; Salicylidene-o-imino thiolbenzene) were synthesized and identified by elemental analysis, spectroscopy, and thermogravimetric analysis (TGA). It was found that the mole ratio of Schiff base ligand to the metal in these complexes is 1 : 1 or 1 : 2. The redox processes of the complexes were investigated by cyclic voltammetric and differential pulse polarographic techniques in nonaquous solvent containing 0.1 M tetraethylammonium perchlorate (TEAP) as supporting electrolyte at glassy carbon electrode. It was found that diffusion controlled reduction processes with one electron were Mo(Ⅴ)Mo(Ⅴ)e-→ Mo(Ⅴ)Mo(Ⅳ)e-→Mo(Ⅳ)Mo(Ⅳ)e-→Mo(Ⅳ)Mo(Ⅲ).