• Bulletin of the Korean Chemical Society
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• 제18권6호
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• pp.579-584
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• 1997

A series of ferrocene-containing chelating bidentate nitrogen ligands (1 & 2) and polyazamacrocycles (3 & 4) were prepared in high yields from the reaction of ferrocenecarboxaldehydes with corresponding diamines under various catalytic and stoichiometric reaction conditions. The stoichiometric condensation to form Schiff bases required the presence of MgSO₄in the reaction mixture as a water-absorbent. Employment of cyclic diamines such as 1,2-diaminocyclohexane and p-phenylenediamine in the reaction with 1,1'-ferrocenedicarboxaldehyde resulted in the formation of polymers in stead of the expected macrocycles. All these compounds were characterized by microanalytical and spectroscopic techniques. In one case, the structure of 3a was confirmed by X-ray crystallography.

• Journal of Electrochemical Science and Technology
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• 제10권2호
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• pp.170-176
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• 2019

Alkanethiol self-assembled monolayers (SAMs) and partially ferrocene (Fc) modifications were applied to the Au ultramicroelectrode (UME) rather than to standard sized electrodes with dimension of millimeters. The electron transfer mediation of the SAMs and Fc modified Au UME was investigated by using a p-aminophenol (p-AP) oxidation reaction via cyclic voltammetry. The electrocatalytic p-AP oxidation at the SAMs and Fc modified Au UME showed a much larger electrocatalytic current density than that at the standard sized electrode due to the fast mass transfer rate at the UME.

• Bulletin of the Korean Chemical Society
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• 제10권3호
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• pp.279-282
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• 1989

Two rhodium(I) complexes of the types [Rh(BPPF)(NBD)]$ClO_4$ (10) and [Rh(BPPF)$Cl]_2$ (11) (BPPF = 1,1'-bis(diphenylphosphino)-ferrocene) have been prepared and investigated as catalysts for the regioselective hydrogenation of polynuclear heteroaromatic nitrogen and sulfur compounds such as quinoline (1), acridine (2), phenanthridine (3), 7,8-benzoquinoline (4), benzothiophene (5), isoquinoline (6), indole (7), pyridine (8), and thiophene (9). Both complexes 10 and 11, except for the cases of indole (7) and mononuclear heteroaromatics 8-9, are very efficient in the selective reduction under quite mild hydrogenation conditions to give the corresponding saturated nitrogen and sulfur heterocyclic analogues of 1-6 in fast conversion rates and in excellent yields. Relative rate studies revealed that the reduction depends significantly on the steric and electronic effects of the substrates. Of the two complexes 10-11, the dimeric species 11 gives faster reaction rates in all cases studied.

• 한국응용과학기술학회지
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• 제21권3호
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• pp.214-224
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• 2004

Although the structure of carbon nanotubes is important factor characterizing its properties, it is very difficult to control the structure of carbon nanotubes (MWNTs) and to predict the range of their diameter, which is the primary factor of MWNTs' physical properties. We tried to control the diameter of MWNTsby governing the feed injection temperature of floating catalyst method. The structure of MWNTs was influenced by the phase change of ferrocene fed as the catalyst,. The carbon nanotubes were very narrow at injection temperatures close to the sublimation pt. of ferrocene, in which most MWNTs had diameters in the range of 20$^{\sim}$30 nm. At injection temperatures between the boiling pt. and melting pt. of ferrocene, the diameters became larger and had broad distribution. However, at injection temperatures higher than the boiling pt., the diameters became narrow again and had very uniform distribution.

• 한국진공학회지
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• 제19권5호
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• pp.377-384
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• 2010

본 연구에서는 수직 가열로(vertical furnace)를 이용하여 $1150^{\circ}C$의 온도에서 섬유형태의 고순도 단일벽 탄소나노튜브(singlewalled carbon nanotubes)를 합성하였다. 탄소나노튜브의 구조에 영향을 미치는 실험 변수인 페로센(ferrocene)의 농도, 혼합용액의 주입 속도, 싸이오펜(thiophene)의 농도, 수소($H_2$)의 주입 양을 조절하여 고순도의 단일벽 탄소나노튜브 섬유의 최적화 된 대량 합성 조건을 확립하였다. 또한 각 요인들이 탄소나노튜브의 생성에 미치는 영향에 대해 논의하였다. 분석 결과, 최적화 된 조건에서 1.16~1.64 nm의 직경을 가진 고순도의 단일벽 탄소나노튜브가 다발(bundle) 구조로 정렬되어 있음을 확인할 수 있었다.

• Bulletin of the Korean Chemical Society
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• 제33권8호
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• pp.2773-2776
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• 2012

• 한국진공학회:학술대회논문집
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• 한국진공학회 2002년도 제22회 학술발표회 초록집
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• pp.146-146
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• 2002

• Bulletin of the Korean Chemical Society
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• 제23권8호
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• pp.1177-1180
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• 2002

• 한국진공학회:학술대회논문집
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• 한국진공학회 2001년도 제21회 학술발표회 초록집
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• pp.45-45
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• 2001

• 분석과학
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• 제13권3호
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• pp.315-322
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• 2000

시금치의 뿌리 조직과 ferrocene을 탄소반죽 전극에 고정하여 과산화수소를 정량할 수 있는 전극을 만들었다. Ag/AgCl 전극에 대하여 -0.3~0.0V의 전위의 범위에서 전극의 감도를 관찰하였으며 전극의 감응시간은 11.8sec로 나타났다. 전극의 검출한계는 $2.25{\times}10^{-6}M$ 이었으며, $1.0{\times}10^{-3}M$ 과산화수소를 이용해 15회 반복 측정한 결과, 상대표준편차는 1.87% 이었다. 효소전극의 감도는 19일 사용 후 40%로 감소하였다.