• Bulletin of the Korean Chemical Society
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• 제30권7호
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• pp.1661-1664
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• 2009

• Bulletin of the Korean Chemical Society
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• 제6권2호
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• pp.119-120
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• 1985

Stereospecific coordination of racemic 2,3-diaminobutane has been observed in the reaction with platinum(Ⅱ) complexes of optically active 6,6'-dimethyl-2,2'-diaminobiphenyl. The reaction between [Pt (R-dmdabp) Cl$_{2}$] (R-dmdabp is R-6,6'-dimethyl-2,2'-diaminobiphenyl) and unresolved bn (bn is 2,3-diaminobutane) has yielded [Pt(R-dmdabp)-(R-bn)] Cl$_{2}$ only, while the reaction of [Pt(S-dmdabp)Cl$_{2}$] with unresolvd bn has yielded [Pt(S-dmdabp) (S-bn)]Cl$_{2}$ only. On the other hand, the standard [Pt(R-dmdabp) (R-bn)] Cl$_{2}$ complex has been independently prepared from the reaction of [Pt(R-dmdabp)Cl$_{2}$] with R-bn, and the standard [Pt(S-dmdabp) (S-bn)] Cl$_{2}$ from the reaction of [Pt(S-dmdabp)Cl$_{2}$] with S-bn. The stereospecific behavior of the racemic 2,3-diamino-butane is thus confirmed from the comparison of these Pt(Ⅱ) complexes prepared using racemic bn with the standard Pt(Ⅱ) complexes prepared using R-bn or S-bn.

• 대한화학회지
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• 제28권2호
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• pp.135-142
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• 1984

초과산화이온$(O_2^-)$의 발생원으로서 $KNO_2$를 사용하여 새로운 형태의 산착화합물가교팔라듐착화합물을 합성했다. 이 방법은 구핵치환과 전자 이동에 의한 반응으로서, 저원자가전이금속착화합물에 산소분자를 산화적으로 부가시켜 합성한 종전의 방법과는 완전히 다르다. $O_2^-$에 의하여 {\pi}$-알릴리간드를 갖는 새로운 형태의 5가지 산소가교팔라듐착화합물을 합성했다

• Bulletin of the Korean Chemical Society
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• 제23권3호
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• pp.404-412
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• 2002

Nine copper(Ⅱ) oxyanion, and mixed oxyanion complexes that have four- or five-coordinate geometries around copper(Ⅱ) centers were derived from sparteine copper(Ⅱ) dinitrate precursor [Cu($C_{15}$$H_{26}$N2)(NO3)2]. The precursor complex undergoes an anion exchange with various oxyanions, and an interchange reaction with other sparteine copper(Ⅱ) complexes. The [Cu($C_{15}$$H_{26}$N2)(CH3CO2)2] also undergoes "halogen atom abstraction" reaction with CCl4 to produce the mixed anion complex [Cu($C_{15}$$H_{26}$N2)(CH3CO2)Cl]. The whole set of prepared complexes has been used for the comparative electrochemical and spectroscopic studies.

• Bulletin of the Korean Chemical Society
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• 제12권3호
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• pp.276-281
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• 1991

Electrochemical behaviors of optically active sparteine-Cu(II) dihalide complexes were investigated by polarography and cyclic voltammetry (CV). These Cu(II) complexes are rather easier to be reduced to Cu(I) states when comparison is made with other nonplaner copper complexes, We have assigned the CV peaks and polarographic waves related to the redox processes for these complexes. We could also observe the exchange reaction of Cu(II) ion in the complex with mercury metal in the cell having mercury pool. The redox mechanism of these complelxes is as follows; The 1st wave appeared at +0.47 V/+0.65 V corresponds to the reaction of $SpCuX_2+ e{\rightleftarrow}SpCuX_{2^-}$ and the 2nd one at +0.26 V/+0.21 V does the reaction of $SpCuX_{2 ^-} +e{\rightleftarrow}SpCuX_2^{2-}$. The 3rd one at -0.35 V/-0.27 V is dueto the reduction of mercury complex formed via exchange reaction. Where, X is chloride ion.

• Bulletin of the Korean Chemical Society
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• 제12권3호
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• pp.286-289
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• 1991

The changed isotropic absolute Raman intensities of the phosphate residue in the complexes of positive charge oligopeptides, lys-lys, arg-arg, lys-aromat-lys, negative charge diethyl phosphoric acid (DEP) and polyriboadenylic acid{poly(rA)} were reported and discussed. Our measurements showed that the absolute intensities of phosphate stretch vibration in complexes were different according to the reaction partners. Due to the partial electrical charge and molecular structure of oligopeptides for the complex formation lysine can interact more strongly than arginine when the reaction partners have short chain and no steric hindrance. Owing to these reasons the intensity of phosphate stretching vibration is very sensitive according to the circumstance of reaction. From our results we could suggest that we can discriminate any one of the the lysine and arginine in the complicated biological molecule during interaction between nucleotides and proteins. The activity of reaction of two basical oligopeptides is not quite similar for complex formation in aqueous solution. The activity of dipeptides depends upon the structure of molecule and environment for complex formation. Aromatic ring contributes to electrostatic interaction in complexes. The amount of the absolute intensity for pure stacking interaction is smaller than electrostatic interaction in macromolecular complexes.

• Bulletin of the Korean Chemical Society
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• 제28권8호
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• pp.1299-1304
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• 2007

New sulfur functionalized cyclopentadiene ligands, 1-[2-(thioanisole)]-2,5-dimethylcyclopentadiene (3), 1-[2- (thioanisole)]-2,3,5-trimethylcyclopentadiene (4), and 1-[2-(thioanisole)]-2,3,4,5-tetramethylcyclopentadiene (5), were prepared. In these ligands, the S-donor atom is connected to a cyclopentadiene ring by a rigid phenylene spacer. CpCo(III)-diiodo half-sandwich complexes (6-8) were obtained from reaction the ligands (3- 5) with Co2(CO)8, followed by treatment of I2. Substitution reaction of CpCo(III)-diiodo complexes with MeLi yielded the corresponding CpCo(III)-dimethyl complexes (9-11). Further transformation to the corresponding cationic cobalt complexes (12-14) were achieved by reaction of the CpCo(III)-dimethyl complexes with HB(ArF)4·2Et2O and trapping with CD3CN. The new sulfur functionalized cyclopentadiene ligands having a rigid phenylene spacer and the corresponding cobalt complexes were characterized by 1H, 13C and 19F NMR spectroscopy. The diiodo Complex 6 was also characterized by a single crystal X-ray diffraction method.

• 대한화학회지
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• 제39권5호
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• pp.356-363
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• 1995

유기 리간드(디크로로 비스[η-싸이크로 펜타디엔닐])을 가지고 전이금속 4가$(Nb^{4+}와\;Mo^{4+}$와의 착물들에 대한 거동을 UV-vis 분광학적, 자기적, 그리고 전기화학적 방법에 의해 조사하였다. 2 또는 3개의 에너지 흡수띠가 이들 착물들의 스펙트라에 의해 관찰되었다. 결정장 갈라짐 에너지 크기와 스핀 짝지움 에너지 그리고 결합 세기는 착물들의 스펙트라로부터 얻어졌다. 이들은 비편재화이고, 낮은 스핀 상태이며 그리고 강한 결합 세기임을 알았다. 자기쌍극자 모멘트는 상자기성과 반자기성 착물이었다. 착물들의 산화환원 과정은 비수용매속에서 순환 전압전류법에 의해서 조사되었다. Nb-C 착물의 산화환원 반응과정은 일전자의 확산과 반응 전류에 의한 짝-단일 반응이었고 또한 Mo-C 착물에서는 일전자의 반응전류에 의한 짝-단일 반응이었다.

• 공업화학
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• 제3권1호
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• pp.64-71
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• 1992

초과산화이온($O_2{^-}$)의 발생원으로서 $KO_2$를 사용하여 새로운 형태의 산소가교 팔라듐 착화합물을 합성했다. 이 방법은 구핵치환반응과 전자이동에 의한 반응으로서 원자가가 낮은 전이금속 착화합물에 산소분자를 산화적으로 부가시켜 합성한 종전의 방법과는 완전히 다르다. 초과산화이온($O_2{^-}$)에 의하여 아민을 리간드로 갖는 새로운 형태의 3종류의 산소가교 팔라듐 착화합물을 합성했다.

• 대한화학회지
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• 제40권1호
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• pp.65-71
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• 1996

유기 리간드(tris[3-(trifluoromethylhydroxymethymelene-camphorato])와 tris[3-(heptafluoropropylhydroxymethymelene-camphorato])을 Eu(Ⅲ)와의 착물들에 대한 거동을 UV-vis 분광학적, 자기적, 그리고 전기화학적 방법에 의해 조사하였다. 둘 또는 세개의 에너지 흡수 띠가 이들 착물들의 스펙트라에 의해 관찰되었다. 결정장 갈라짐 에너지 크기와 스핀 짝지움 에너지 그리고 결합 세기는 착물들의 스펙트라로부터 얻어졌다. 이들 착물은 전자 배열이 비 편재화이고, 낮은 스핀 상태이며 그리고 강한 결합 세기임을 알았다. 자기 쌍극자 모멘트는 반 자기성 착물로 나타났다. 착물들의 산화.환원 과정은 반 양성자성 용매속에서 순환 전압 전류법에 의해서 조사하였다. 착물들의 산화.환원 과정은 일전자의 확산전류에 의한 단일-짝 반응이었다.