• 약학회지
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• 제7권4호
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• pp.92-95
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• 1963

Magnesium Chlorophyllin 으로부터 상법에 의하여 제조한 Chlorin-e에 수용성 Cobalt 염을 작용시켜 Chlorophyllin에 Cobalt Complex 화합물을 제조하였다. Chlorin제법에 있어서 alcohol 용매를 사용해 온 방법은 Chlorin이 alcohol에 대한 용해도가 그히 적은 관계로 목적물을 양호한 수대율로 얻지 못할 뿐만 아니라 이에 따르는 조작도 복잡 불편하였으나 용매 를 빙초산으로 대치하므로써 좋은 성과를 얻을 수가 있었다.

• Bulletin of the Korean Chemical Society
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• 제23권3호
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• pp.500-502
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• 2002

• 대한화학회지
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• 제55권3호
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• pp.341-345
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• 2011

Schiff base 코발트(II) 착물, bis[4-chloro-2-((E)-(isopropylimino) methyl) phenol]cobalt(II), 을 합성하고 단결정 X-ray 회절 분석을 하였다. 코발트 (ii) 합성물의 현상학적, 속도론적 및 기계적 특성은 TG/DTG법으로 연구하였다. 실험 데이터에 기초하여, 활성화 에너지, 지수 앞자리인자, 활성화 엔트로피와 같은 속도론적 파라미터를 계산하였으며, 가장 가능성 있는 메카니즘 함수로는 $g({\alpha})={\alpha}^2$이 추정되었다. 따라서, 모든 분해 단계에서 속도 조절 단계는 1차원 확산 과정(Parabolic model) 이다.

• 전기화학회지
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• 제5권4호
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• pp.189-191
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• 2002

Reversible trans-cis isomerization of meta-bipyridylazobenzene coordinated to cobalt was achieved by a combination of photoirradiation with a single UV light source and a Co(II)/Co(III) redox reaction. The trans/cis conversion performance was significantly improved in the meta-form compared with the meta-form ligated to cobalt.

• Advances in materials Research
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• 제12권1호
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• pp.1-13
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• 2023

The combination of cobalt ferrite and natural rubber has a potential to enhance the functional properties of rubber ferrite composites available on the market. In this study, cobalt ferrite was synthesized by the sol-gel method with tapioca starch as a cheating agent and then incorporated into natural rubber using an internal mixer. The curing characteristics, magnetic hysteresis, complex permeability, and permittivity of the rubber ferrite composites were studied as a function of the loading from 0 to 25 phr. The cure time and scorch time tended to reduce with the addition of non-reinforced cobalt ferrite fillers. The remanent and saturation magnetizations were linearly proportional to the cobalt ferrite loading, consistent with the rule of mixture. On the other hand, the increase in cobalt ferrite loading from 5 to 25 phr slightly affected the coercive field and the complex permeability. Using the maximum loading of 25 phr, both real and imaginary parts of the permittivity were significantly raised and reduced with the frequency in the 10-300 MHz range.

• 대한화학회지
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• 제10권1호
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• pp.4-10
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• 1966

A new method of cobalt determination has been developed by employing ethylenediamine tetrabutyl acetate(EDTA-butyl ester) synthesized from EDTA and Butyl alcohol. The synthesized EDTA ester dissolved in butyl alcohol extracts various metal ions from aqueous solutions. Cobaltous ion extracted into organic phase containing EDTA ester to form Co (II)-EDTA butyl ester complex is back extracted into alkaline aqueous phase forming a stable pink colored complex of Co (III). The optimum condition for spectrophotometric determination of cobalt via the new complex has been established. The absorption peak occurs at 540$m{\mu}$ and Beer's law was obeyed over the concentration range of 0∼50 ${\mu}g/ml$ of cobalt.

• 대한화학회지
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• 제36권2호
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• pp.305-310
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• 1992

Cobalt 금속 중심으로 cyclopentadienyl을 ${\pi}$-착물로 결합하고, 또 oxime 화합물을 리간드로 하는 cobalt oxime sandwich형 착물을 합성하기 위하여 본 연구를 수행하였다. Cyclopentadienyl-cobalt 부분을 도입하기 위해, (${\eta}^5$-Cyclopentadienyl)bis(ethylene)cobalt (Jonas 시약), (η5-cyclopentadienyl)di(carbonyl)cobalt, 그리고 bis(${\eta}^5$-cyclopentadienyl)cobalt (cobaltocene)의 착물이 사용되었고, oxime을 각각 여러 가지 조건에서 반응시켰다. 그 중에서 Jonas 시약과 dienemonooxime인 2,4-hexadienealdoxime만이 반응되었으며, 그 생성물은 예상을 벗어난 (${\eta}^5$-cyclopentadienyl)(2,4-hexadienenitrile)cobalt [VII]로 밝혀졌다. 이 화합물의 구조는 NMR, mass spectrometer, IR 원소분석기를 통해 확인되었다.

• Bulletin of the Korean Chemical Society
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• 제12권6호
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• pp.629-632
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• 1991

The rate constants for the formation and dissociation of nickel(II) and cobalt(II) complexes with mandelate have been determined by the pressure-jump relaxation study. The forward and reverse rate constants for the mandelate complex formation reactions were obtained to be $k_f=3.60{\times}10^4\;M^{-1}s^{-1}$ and $k_r=1.73{\times}10^2\;s^{-1}$ for the nickel(II), and $k_f=1.75{\times}10^5\;M^{-1}s{-1}$ and $2.33{\times}10^3\;s^{-1}$ for the cobalt(II) in aqueous solution of zero ionic strength ($(\mu{\to}0)\;at\;25^{\circ}C$. The results were interpreted by the use of the multistep complex formation mechanism. The rate constants evaluated for each individual steps in the multistep mechanism draw a conclusion that the rate of the reaction would be controlled by the chelate ring closure step in concert with the solvent exchange step in the nickel(II) complexation, while solely by the chelate ring closure step for the cobalt(II) complex.

• Bulletin of the Korean Chemical Society
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• 제18권4호
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• pp.406-409
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• 1997

The various cobalt(Ⅱ) complexes were synthesized and characterized using tris-(2-benzimidazolylmethyl)amine (ntb) as a ligand where the ntb plays as a tripodal tetradentate ligand to form complexes with a trigonal pyramidal geometry. The complexes have 5 and 6 coordinate cobalt(Ⅱ) ions depending on the additional ligand used. In each complex the additional ligand, chloride anion, or acetate anion occupies the "open" site trans to the apical tertiary nitrogen atom of ntb ligand. Complex 1, [Co(Ⅱ)(ntb)Cl]Cl has a trigonal bipyramidal geometry. This geometry was easily constructed using ntb as a tetradentate ligand and chloride as a monodentate ligand. The complex is isostructural to the corresponding manganese(Ⅱ) complex. Crystal data are as follows: [Co(Ⅱ)(ntb)Cl]Cl·MeOH, 1. triclinic space group P1; a=13.524(2) Å, b=14.037(2) Å, c=17.275(1) Å; α=78.798(9), β=84.159(8)°, γ=65.504(9)°; V=2929.6(6) Å3; Z=4; R1=0.0715, wR2=0.1461 for reflections of I > 2σ(I). Six coordinate complex 2 [Co(ntb)(OAc)](OAc) was synthesized using ntb as a tetradentate ligand and acetate as a bidentate chelating ligand.

• Journal of Applied Biological Chemistry
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• 제53권2호
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• pp.108-111
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• 2010

New salens (3) and their Cobalt complexes (4) were prepared from meso-1,2-bis(ortho-hydroxyphenyl)-1,2-diaminoethane (1) and substituted salicylic aldehydes (2). In contrast to symmetric structure of salen ligand (3), salen-Co(III) complexes (4) showed dissymmetric molecular structure due to participation of three hydroxyl groups in complex formation. One of the salens (3b) revealed decrease in Cyclin D1 expression, which represents anti-cancer property.