• 대한화학회지
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• 제37권10호
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• pp.888-894
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• 1993

아세토니트릴 용액 중에서 copper-1-(2-pyridylazo)-2-naphthol(Cu-PAN) 착물의 전기화학적 성질을 순환 전압전류법, 직류 폴라로그래프법, 정전위 전기분해법 및 UV-Vis 분광광도법으로 조사하였다. 아세토니트릴 용액 중에서 Cu-PAN 착물은 3개의 환원파를 보였다. 환원파의 환원전위는 각각 -1.27 V, -1.64 V 와 -2.08 V vs. Ag/AgNO$_3$(AN)였다. 각 환원단계에 관여하는 전자수는 일정전위 전기분해법으로 구하였으며, 전기분해한 전해 생성물의 UV-Vis Spectrum으로부터 전해 생성물을 확인하였다. 이상의 실험 결과로부터 아세토니트릴 용액 중에서 Cu-PAN 착물의 환원 반응기구를 제안하였다.

• 분석과학
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• 제20권5호
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• pp.406-412
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• 2007

분광 광도법을 이용하여 ${\beta}$-CD와 $[Cu(dien)(sub-py)]^{2+}$ 이온 간의 복합체 형성에 관한 연구를 하였다. ${\beta}$-CD와 $Cu^{2+}$ 착물이 복합체를 형성 할 때 ${\gamma}_{max}$은 리간드에 전자 주는기($CH_3$)가 치환 된 경우는 $^2T_2{\rightarrow}^2E$로 한 곳에서, 전자 끄는기(Cl)가 치환된 경우는 $^2T_2{\rightarrow}^2E$와 MLCT에 의하여 두 곳에서 나타났다. 형성상수는 온도가 올라가면 결합에너지의 감소로 작아졌다. 모든 반응은 엔트로피의 감소를 보였으나 큰 발열반응으로 자발적 반응이었다. 치환기 상수(${\sigma}_x$)에 따른 Hammett plot 결과 좋은 직선성(${\gamma}=0.996$)을 보여 형성상수를 정량적으로 설명할 수 있었다.

• Bulletin of the Korean Chemical Society
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• 제16권3호
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• pp.202-204
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• 1995

The ultraviolet photochemistry of N,N'-bis(salicylidene)ethylenediamine copper(II), Cu(sal)2en, was investigated with low pressure mercury lamp. Redution of Cu(Ⅱ) and formation of Cl- were shown on 254 nm irradiation both for aerated and deaerated chlorinated hydrocarbon solvent such as CH2Cl2, chloroform, and 1,2-dichloroethane. Relatively long lived $({\tau}=100{\mu}sec)$ intermediate was detected by flash photolysis. Overall photo-process can be described as the formation of Cl- and new copper complex, product(1) by chlorohydrocarbon mediation, photoinduced reduction by abstraction of halogen from solvent, followed by redox induced substitution of axial ligand with chlorine. Product(1) is possibly Cu(III) chlorosalicylaldeimido complex and cyclic -CH2CH2- moiety is absent in the structure. 247nm band of Cu(sal)2en should contain ligand to metal charge transfer character.

• 공업화학
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• 제8권1호
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• pp.23-28
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• 1997

활성탄에 의한 암모니아 구리착물의 흡착 특성에 대하여 연구하였다. 활성탄 비표면적을 BET 흡착장치에서 측정하였고, 암모니아수용액에서 암모니아 착물을 이용하여 Cu(II)이온 제거 특성과 활성탄에 의한 착물흡착에서 암모니아착물 형태에 대하여 연구하였다. 실험 결과 비표면적 크기는 mesh No.가 감소할 수록 증가하였고, 활성탄에 의한 Cu(II)이온 흡착은 pH 6 범위가 적합함을 알았다. 또한 암모니아수용액에서 암모니아 구리착물이 활성탄에 흡착되는 형태는 $[Cu(NH_3){_2}]^{2+}$와 $[Cu(NH_3){_3}]^{2+}$로 흡착됨을 알았으며, 암모니아 농도는 $2.25{\times}10^{-4}{\sim}2.25{\times}10^{-3}(mol/{\ell})$ 범위에서 검토하였다.

• 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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• 제17권9호
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• pp.836-839
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• 1996

A new copper complex containing 2,2'-dipyridylbenzamide(dpba), Cu(dpba)(NO3)2(CH3CN), has been synthesized and characterized. The crystal structure has been determined. Crystal data: space group P212121, Z=8, a=13.911(3) Å, b=16.813(3) Å, c=18.932(3) Å, V=4427.9(1) Å3 and R=0.0674 for 1716 reflections. The copper environment is square pyramidal containing acetonitrile in axial site. Spectroscopic properties has been characterized in solution state. The redox property of the Cu(dpba)(NO3)2 complex is different from that of corresponding copper-dpa complex.

• 약학회지
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• 제9권1_2호
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• pp.18-22
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• 1965

A new organic reagent, 1-isonicotinoyl-2-furfurylidene hydrazine was synthesized from isonicotinic acid hydrazide and furfural, gives precipitate with copper(II), mercury(II) and argent(I), whereas, it gives a water soluble yellow complex with iron(III). Copper complex of the reagent is soluble in EtOH MtOH, pyridine, dioxane and dimethylformamide with green yellow coloration. The complex has a maximum absorption at 385 m.$\mu$ and molar ratio of copper; reagent was estimated as 1:1 by continuous variation method, slop method and chelate titration method. Molar extinction coefficient (9600) and apparant formation constant of this complex was spectrophotometrically determined. K=1.7 * $10^{7}$ (Babko's method) K=2.1 * $10^{7}$ (Anderson's method). This reagent reacted with copper so sensitive that it would be available for determination of Cu (II).

• Bulletin of the Korean Chemical Society
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• 제16권5호
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• pp.406-409
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• 1995

The complex formation from Cu(Ⅱ) ion and 2,2-bis(hydroxymethyl)-2,2',2"-nitrilotriethanol (Bistris) in aqueous solution has been studied potentiometrically and spectrophotometrically. Bistris (L) coordinates to Cu(Ⅱ) as tridentate. The complex CuL2+ undergoes deprotonation in neutral and basic media. The deprotonated complexes involve metal-alcoholate coordinate bond in stable chelate structures.

• Bulletin of the Korean Chemical Society
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• 제10권6호
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• pp.551-554
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• 1989

Quadrupole coupling constants of $^{63}$CU in the high $T_c$ superconductor $YBa_2Cu_3O_7_{-x}$, as determined by NQR or NMR studies, are compared with the values for representative Cu(Ⅱ) complexes determined by analyzing the forbidden lines in their EPR spectra. It is shown that the two NQR lines at 22 and 31 MHz correpsond to the quadrupole coupling constants of a square planar Cu(Ⅱ) complex and a square pyramidal Cu(Ⅱ) complex, respectively.t This result is in agreement with the assignment of these lines to Cu(1) and Cu(2) sites in YBCO based on the NMR spectra of oriented single crystals.

• Bulletin of the Korean Chemical Society
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• 제19권2호
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• pp.197-201
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• 1998

The complex formation from Cu(Ⅱ) ion and 1,3-bis(tris(hydroxymethyl)methylamino)propane (bistrispropane) in aqueous solution has been studied potentiometrically and spectrophotometrically. Bistrispropane (btp) coordinates to Cu(Ⅱ) as multidentate. In the btp (L) complex CuL2+, two of the hydroxyl oxygen atoms as well as the amine nitrogens of the ligand are coordinated. In neutral and weakly acidic media, one of the coordinated hydroxyl groups is deprotonated. In basic media, an additional hydroxyl group undergoes deprotonation. The equilibrium constants for the formation of CuL2+, CuLH-1+, and CuLH-2 have been determined. The nature of the coordinate bonds has been deduced from the potentiometric data and the spectra of these complexes.