• 대한화학회지
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• 제35권4호
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• pp.343-349
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• 1991

CHCl$_3$, CHCl$_3$ : CH$_2$Cl$_2$(1:1) 및 CH$_2$Cl$_2$ 용매 중에서 치환 aniline[aniline, N,N-dimethylaniline(N,N-DMA), 2,6-dimethylaniline(2,6-DMA) 및 2,4,6-trimethylaniline(2,4,6-TMA)]과 iodine간의 charge transfer complex 형성에 대하여 전도도법을 이용하여 속도론적으로 조사하였다. 초기에 일시적으로 생성된 outer charge transfer complex가 inner complex로 변환되는 과정에 있어서 치환 aniline의 electron donor 및 polar medium으로서의 작용에 대하여 고찰해 보았다. 또한 변환의 빠르기는 medium의 dielectric environment와 치환 aniline의 pK$_a$값에 의존하였으며 2,4,6-TMA, 2,6-DMA, aniline, N,N-DMA의 순서로 증가하였다. Chloroform 용매 중에서 2.5M 농도의 치환 aniline에 대해서 얻은 ${\Delta}H^{\neq}$값은 N,N-DMA, 3.47kcal/mol:aniline, 4.25kcal/mol:2,6-DMA, 7.79kcal/mol:2,4,6-TMA, 7.96kcal/mol:${\Delta}S^{\neq}$값은 모든 aniline에 있어서 -41~-55cal/mol${\cdot}$K의 큰 음의 값을 나타내었다.

• Bulletin of the Korean Chemical Society
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• 제19권12호
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• pp.1337-1341
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• 1998

The charge transfer (CT) complex dyes between electron donor phenothiazine and electron acceptors namely, 2, 3-dichloro-1,4-naphtoquinone and 2,3-dichloro-5-nitro-1,4-naphtoquinone, were formed in the dichloromethane solution and electrochromic properties were studied using Bu4NC1O4 as supporting electrolyte. A 1 : 1 correspondence between the donor and acceptor molecules in the CT complex was found.

• Applied Science and Convergence Technology
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• 제24권6호
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• pp.278-283
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• 2015

In this work, the electrical bistability of an organic CT complex is demonstrated and the possible switching mechanism is proposed. 2,9-Dimethyl-4,7-diphenyl-1,10-phenanthroline (BCP) and tetracyanoquinodimethane (TCNQ) are used as an organic donor and acceptor, respectively, and poly-methamethylacrylate (PMMA) is used as a polymeric matrix for spin-coating. A device with the Al/($Al_2O_3$)/PMMA:BCP:TCNQ[1:1:0.5 wt%]/Al configuration demonstrated bistable and switching characteristics similar to Ovshinsky switching with a low threshold voltage and a high ON/OFF ratio. An analysis of the current-voltage curves of the device suggested that electrical switching took place due to the charge transfer mechanism.

• 약학회지
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• 제33권3호
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• pp.141-148
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• 1989

The weak UV absorbing antihistaminics such as chlorpheniramine, triprolidine, tripelennamine and diphenhydramine were analyzed by charge-transfer spectrophotometric method. The results obtained are summarized as folows. It was possible to determine a weak UV absorbing antihistaminics using the intense charge-transfer UV bands in chloroform. Charge transfer complexes were formed in a 1:1 ratio between antihistaminics and iodine in chloroform. Linear relationship was found between absorbance and concentration in the range of $1.0\;{\times}\;10^{-5}M-5.0\;{\times}\;10^{-5}M$ for chlorpheniramine( ${\varepsilon}\;=\;2.082\;{\times}\;10^4$) and tripelennamine ( ${\varepsilon}\;=\;1.578\;{\times}\;10^4$), $1.0\;{\times}\;10^{-5}M-8.0\;{\times}\;10^{-5}M$ for triprolidine ( ${\varepsilon}\;=\;1.120\;{\times}\;10^4$) and $1.0\;{\times}\;10^{-5}M-1.0\;{\times}\;10^{-4}M$ for diphenhydramine ( ${\varepsilon}\;=\;9.900\;{\times}\;10^3$). Charge transfer complexes of chlorpheniramine, triprolidine and tripelennamine have absorption maxima at 293 nm and complex form of diphenhydramine has absorption maximum at 270 nm. By UV, IR spectra, it could be inferred that CT-complexes were formed by interaction between the basic nitrogen of antihistaminics as electron donor (non bonding electron) and iodine as electron acceptor (${\sigma}$ bonding electron).

• Bulletin of the Korean Chemical Society
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• 제31권12호
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• pp.3815-3817
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• 2010

• 대한화학회지
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• 제20권5호
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• pp.380-390
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• 1976

전자 공여체로서 할로겐으로 치환되어 있는 아니솔 유도체들(아니솔, 4-클로로아니솔, 2,3-디클로로 아니솔, 2-플루오로-4-클로로아니솔, 2-브로모-4-클로로아니솔, 2-요도드-4-클로로아니솔, 2-브로모 4,6-디클로로아니솔, 2-요오드-4,6-디클로로 아니솔, 2-요오드-2,4,6-드리클로로아니솔)을 쓰고 전자를 받아들이는 화합물로서는 요오드 또는 염화 요오드를 사용하여 그 사이에 생성되는 전하이동 착물에 관하여서 사염화탄소 또는 헥산을 용매계로 하여 연구하여 보았다. 연구한 결과로서 착물의 생성량이 벤젠고리의 2-치환 할로겐 원자의 Van der Waals 반경에 따라서 영향을 받음이 확인 되었으며 더 나아가서 전자 공여 화합물 분자의 입체적 배치 환경에 의하여서도 역시 영향을 받고 있음을 알 수 있었다. 이와 같은 경향은 클로로포름과의 착물 생성에서도 핵자기 공명분석법으로 확인될 수 있었다. 분광 분석법으로 얻은 착물 생성에 관한 데이터를 제시하였으며 벤젠고리에 치환된 2-할로겐 원자의 입체구조와의 상호관계를 논의하였다.

• 한국응용과학기술학회지
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• 제14권1호
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• pp.89-93
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• 1997

In this research, ultra-thin films of organic charge transfer complex were deposited on to ordinary microscope slide-glass subtrates with a Langmuir-Blodgett technique. ${\pi}$-A isotherm characteristics of these complex were studied in order to find optimum conditions of deposition by varying temperature of subphase, compression speed, and spreading amount. Transfer ratio of these films were studied during the process of deposition. The UV-visible absorbance spectra of LB films were measured to find state of deposition by varing layer number. The observed optimum conditions of surface, pressure, spreading amount, and dipping speed for depositing LB films(Y-type) were 38m/Nm, $150{\mu}l$ and 5mm/min, respectively. Since the tansfer ratio is close to 100%, the monolayer on the subphase seems to be well transferred to the solid substrate. The thickness of the film was well-controlled as the UV-vis absorbance of films were changed linear according to the number of layers.

• 대한화학회지
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• 제19권1호
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• pp.43-49
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• 1975

소량의 요오드 화합물이 윤활류에 함유될 때 금속표면사이의 마찰을 감소시키고 내마모성을 향상시키는데 이는 금속표면에 박층상구조의 이요오드화물이 형성되기 때문이라고 한다. 그러나 금속표면에서의 화학반응성, 마모와 극압실험 및 hot wire method에 의한 결과에 의하면 윤활기구는 이 요오드화물의 박층상 구조가 아니고 다른 기구에 의한 것임을 알았다. 유기 요오드화합물중에서 특히 N-iodopyridinium dichlorodate는 double charge transfer complex로써 다른 methyl iodide계의 화합물 보다 금속표면 사이의 마찰을 더욱 감소시키고 윤활기구는 interhalogen의 화학반응에 의한 것임을 알았다.

• Journal of Photoscience
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• 제10권1호
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• pp.105-119
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• 2003

Fullerenes, $C_{60}$ and $C_{70}$, display interesting physicochemical properties in solutions, especially due to their unique chemical structures and their good electron accepting abilities. Solubility of fullerenes in different organic solvents and their unusual solvatochromic behavior, the ability of the fullerenes to form aggregates in solutions, and their electron transfer and charge transfer interactions with variety of electron donors, are the subjects of extensive research activities for more than one decade. Many research groups including ours have contributed substantially in the understanding of the solvatochromism, aggregation behavior, and the photoinduced electron transfer and charge transfer chemistry of fullerenes, in condensed phase. Present article is aimed to summarize the important results reported on the above aspects of fullerenes, subsequent to the earlier report from our group (D.K. Palit and J.P. Mittal, Full. Sci. & Tech. 3, 1995, 643-659).)., 643-659)..

• 반도체디스플레이기술학회지
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• 제13권4호
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• pp.27-32
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• 2014

The cure properties of self-extinguishing epoxy resin systems with different charge transfer type latent catalysts were investigated, which are composed of YX4000H as a biphenyl epoxy resin, MEH-7800SS as a hardener, and charge transfer type latent catalysts. We designed and used five kinds of charge transfer type latent catalyst and compared to epoxy resin systems with Triphenylphosphine-Benzoquinone(TPP-BQ) as reference system. The cure kinetics of these systems were analyzed by differential scanning calorimetry with an isothermal approach, the kinetic parameters of all systems were reported in generalized kinetic equations with diffusion effects. The epoxy resin systems with Triphenylphosphine-Quinhydrone(TPP-QH), Triphenylphosphine-Benzanthrone(TPP-BT) and Triphenylphosphine-Anthrone(TPP-AT) as a charge transfer type latent catalyst showed a cure conversion rate of equal or higher rate than those with TPP-BQ. These systems with TPP-QH and Triphenylphosphine-Tetracyanoethylene(TPP-TCE) showed a critical cure reaction conversion of equal or higher conversion than those with TPP-BQ. The increases of cure conversion rates could be explained by the decrease of the activation energy of these epoxy resin systems. It can be considered that the increases of critical cure reaction conversion would be dependent on the crystallinity of the biphenyl epoxy resin systems.