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서백현 한라대학교 2007 論文集 Vol.10 No.-
전자내국신용장 이용과정에 대한 적정 모델과 보완해야할 과제를 고찰하였다. 요약하여 무역금융 취급세칙의 개정이 필요하다. 내국신용장거래는 사실상 무역금융 취급세칙이 사실상 신용장통일규칙을 상당부분 대체하고 있으므로 무역금융취급세칙은 eUCP의 주요 내용을 반영하여 개정하는 것이 바람직할 것이다. 다음으로 내국신용장거래의 형식을 양도가능, 선급내국신용장의 형태로 다양화하여 내국신용장의 효용을 제고시키는 것이 바람직하며, 전자내국신용장 유통시스템개발과정에서 이러한 점을 반영하여야할 것이다. 그리고 전체 거래과정을 완전 전자화하기 위해서 일치성 검토를 위한 엔진을 장착할 필요가 있으며 또한 중소기업의 이용을 촉진시키기 위해서 저비용으로 참여할 수 있는 전자내국신용장 유통시스템을 개발하고 교육지원과 같은 체계적인 프로그램이 필요하다고 하겠다.
Synthesis and Equilibria of Octahedral and Tetrahedral Complexes of Cobalt (II) 2,2'-Dipyridylamine
Paik Suh Myunghyun,Oh Young-Hee Korean Chemical Society 1982 Bulletin of the Korean Chemical Society Vol.3 No.1
Reactions of cobalt(II) chloride with 2,2'-dipyridylamine (dpa) in alcoholic solutions afford the complex of octahedral $Co(dpa)_2Cl_2{\cdot}CH_3OH$. The octahedral complex is converted to tetrahedral $Co(dpa)Cl_2$ in certain solvents or at the elevated temperature, and the tetrahedral complex is changed to the octahedral one with added dpa. The electronic spectra of the complexes in DMF, measured with various concentrations of 2,2'-dipyridylamine, establish the equilibrium; $td-Co(dpa)Cl_2+dpa_\rightleftarrows^Koh-Co(dpa)_2Cl_2$. The equilibrium constants determined by the analysis of the visible spectra are 6.4, 3.6 and 2.0 $M^{-1}$, respectively, at 25.5, 38.0 and $49.0^{\circ}C,\;with\;{\Delta}H^{\circ}\;and\;{\Delta}S^{\circ}$being -9.5 kcal/mole and -28 eu.
Paik, Young Ki,Suh, Jung Hun,Cho, Key Seung,Suh, Jeong Ihn,Paik, Bo Hyun,Oh, Se Zu 생화학분자생물학회 1977 BMB Reports Vol.28 No.2
A nicotinic acetylcholine receptor (nAchR) isolated from the electric tissues of Torpedo californica has been reconstituted into a vesicle comprising a bifunctional azo-ligand (Bae 1) compound, and a liposome containing phospholipids and cholesterol (1 : 1, w/w). The liposome-mediated reconstituted receptor showed a concentration-dependent response to cholinergic drugs in a lithium ion flux assay. This liposome-mediated reconstituted nAchR was immobilized onto an electrode using various synthetic polymers which were tested for their response to the cholinergic ligands. The immobilized nAchR not only exhibited a linear response to a wide range of cholinergic ligand concentrations but also retained an operational stability which lasted for longer than 6 days. Thus, this result provides a basis for application of the immobilized nAchR-based biosensor in detecting cholinergic ligands in vitro.
N-Alkylatin of Secondary Amines in Nickel(II) Complexes of Polyaza Macrotricyclic Ligands
Suh, Paik-Myunghyun,Kim, Myung-Jin,Kim, Hyun-Kyung,Oh, Kye-Young Korean Chemical Society 1992 Bulletin of the Korean Chemical Society Vol.13 No.1
The secondary nitrogen donors of the Ni(II) complexes of macrotricyclic ligands 8-methyl-1,3,6,8,10,13,15-heptaazatricyclo $[13.1.1.1^{13,15}]$octadecane (A) and 1,3,6,9,11,14-hexaazatricyclo $[12.2.1.1^{6,9}]$octadecane (B) are N-alkylated and the Ni(II) complexes of $N-Me_2A,\;N-Et_2A,\;and\;N-Me_2B$ are obtained. The Ni(II) complexes of $N-Me_2A\;and\;N-Et_2A$ are stable in acidic aqueous solutions while that of $N-Me_2B$ decomposes relatively rapidly. The N-alkylation leads to the decrease in the ligand field strength as well as an anodic shift in both of the oxidation and the reduction potentials of the Ni(II) complexes.
Suh, Myunghyun Paik,Cheon, Young Eun Commonwealth Scientific and Industrial Research Or 2006 Australian journal of chemistry Vol.59 No.9
<P> Single crystal to single crystal transformations have been the subject of growing interest in recent years. In this article, several examples of single crystal to single crystal transformations that occur in metal-organic open frameworks (MOFs) upon guest removal and rebinding, guest exchange, and chemical oxidation are introduced. Depending on the structures of the MOFs, host framework structures can be retained or altered upon guest removal. When host framework structures are altered, significant rearrangements of the molecular components, which involve sponge-like shrinkage/swelling, sliding, swing, bending, and/or rotational motions, occurs throughout the entire crystal to retain the single crystallinity. </P>
Myunghyun Paik Suh,Shin-Geol Kang,Teak-Mo Chung Korean Chemical Society 1990 Bulletin of the Korean Chemical Society Vol.11 No.3
Cu(II) hexaazamacrotricyclic complexes $[Cu(L)](ClO_4)_2$ and $[(Cu(L)Cl]ClO_4$, where L = 1,3,6,9,11,14-hexaazatricyclo$[12.2.1.1^{6,9}]octadecane(L_1)$ or 1,3,6,10,12,15-hexaazatricyclo$[13.3.1.1^{6,10}]eicosane(L_2)$, have been prepared by the simple template condensation reactions of triamines, diethylenetriamine for $L_1$, and N-(2-aminoethyl)-1,3-propanediamine for $L_2$, with formaldehyde in the presence of $Cu(OAc)_2\;or\;CuCl_2$. The Cu(II) complexes of $L_1$ contain two 1,3-diazacyclopentane ring moieties and those of $L_2$ contain two 1,3-diazacyclohexane ring moieties that are fused to the 14-membered macrocyclic framework. Spectra indicate that complexes $[Cu(L)](ClO_4)_2\;and\;[Cu(L)Cl]ClO_4$ have square-planar and square-pyramidal chromophores, respectively. square-planar $[Cu(L)](ClO_4)_2$ are remarkably stable against ligand dissociation in acidic aqueous solutions. Square-pyramidal $[Cu(L)Cl]ClO_4$ complexes dissociate their axial Cl-ligands easily in aqueous solutions to form $[Cu(L)H_2O]^{2+}$ species. Infrared and UV/vis absorption spectra of the Cu(II) complexes reveal that Cu-N interactions and the ligand field strengths are significantly weaker in the complexes of $L_2$ than in the complexes of $L_1$.
Myunghyun Paik Suh,Gee-Yeon Kong,Il-Soon Kim Korean Chemical Society 1993 Bulletin of the Korean Chemical Society Vol.14 No.4
The aerobic oxidation of the Fe(II) complex of 1,4,8,11-tetraazacyclotetradecane, [Fe(cyclam)$(CH_3CN)_2](ClO_4)_2$, in MeCN in the presence of a few drops of $HClO_4$ leads to low spin Fe(III) species [Fe(cyclam)$(CH_3CN)_2](ClO_4)_3$. The Fe(III) cyclam complex is further oxidized in the air in the presence of a trace of water to produce the deep green binuclear bismacrocyclic Fe(II) complex $[Fe_2(C_{20}H_{36}N_8)(CH_3CN)_4](ClO_4)_4{\cdot}2CH_3CN$. The Fe(II) ions of the complex are six-coordinated and the bismacrocyclic ligand is extensively unsaturated. $[Fe_2(C_{20}H_{36}N_8)(CH_3CN)_4](ClO_4)_4{\cdot}2CH_3CN$ crystallizes in the monoclinic space group $P2_1/n$ with a= 13.099 (1) ${\AA}$, b= 10.930 (1) ${\AA}$, c= 17.859 (1) ${\AA}$, ${\beta}$= 95.315 $(7)^{\circ}$, and Z= 2. The structure was solved by heavy atom methods and refined anisotropically to R values of R= 0.0633 and $R_w$= 0.0702 for 1819 observed reflections with F > $4{\sigma}$ (F) measured with Mo K${\alpha}$ radiation on a CAD-4 diffractometer. The two macrocyclic units are coupled through the bridgehead carbons of ${\beta}$-diimitie moieties by a double bond. The double bonds in each macrocycle unit are localized. The average bond distances of $Fe(II)-N_{imine}$, $Fe(II)-N_{amine}$, and $Fe(II)-N_{MeCN}$ are 1.890 (5), 2.001 (5), and 1.925 (6) ${\AA}$, respectively. The complex is diamagnetic, containing two low spin Fe(II) ions in the molecule. The complex shows extremely intense charge transfer band in the near infrared at 868 nm with ${\varepsilon}$= 25,000 $M^{-1}cm^{-1}$. The complex shows a one-electron oxidation wave at +0.83 volts and two one-electron reduction waves at -0.43 and-0.72 volts vs. Ag/AgCl reference electrode. The complex reacts with carbon monoxide in $MeNO_2$ to form carbonyl adducts, whose $v_{CO}$ value (2010 $cm^{-1}$) indicates the ${\pi}$-accepting property of the present bismacrocyclic ligand.