• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2006년도 하계학술대회 논문집 Vol.7
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• pp.358-359
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• 2006

In the Langmuir-Blodgett (LB) technique, a monolayer on the water surface is transferred onto a substrate, which is raised and dipped through the surface. From this, multilayers can be obtained in which constituent molecules are periodically arranged. The LB technique has attracted considerable interest in the fabrication of electrical and electronic devices. Many researchers have investigated the electrical properties of monolayer and multiplayer films. Dendrimers represent a new class of synthetic macromolecules characterized by a regularly branched treelike structure. Multiple branching yields a large number of chain ends that distinguish dendrimers from conventional star-like polymers and microgels. The azobenzene dendrimer is one of the dendritic macromolecules that include the azo-group exhibiting a photochromic character. Due to the presence of the charge transfer element of the azo-group and its rod-shaped structure, these compounds are expected to have potential interest in electronics and ptoelectronics, especially in nonlinear optics. In the present paper, we give pressure stimulation to organic thin films and detect the induced displacement current.

• 대한화학회지
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• 제53권5호
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• pp.485-490
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• 2009

0.1 M 중탄산소듐 용액에서 납전극부식에 대한 로소니아, 감초뿌리 및 카로브 추출물수용액의 부식방지작용에 대한것을 정전류극성방법을 사용해 연구하였다. 이들 물질들의 부식방지작용을 지적해주는 것으로 이들 물질들이 존재할 때 부식속도가 감소하는 것이 발견되었다. 부식방지효율은 추출물농도가 증가하면 증가한다. 이들 추출물의 부식방지작용은 납표면에 이들 추출물이 흡착되어 물질 및 하전이동의 장벽을 만들어 나타내는 것으로 설명되었다. 이들 추출물의 납표면에 흡착은 자발적으로 일어나며, Freundlich 등온흡착을 따르는 것으로 발견되었다. 또한, 변전위양극분극법을 사용해 이들 추출물은 염소를 포함한 용액에서 납의 움푹패이게 하는 부식으로부터 잘 보호해주는 것이 발견되었다.

• 대한화학회지
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• 제45권5호
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• pp.442-447
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• 2001

Octamethylenethiafulvalene(OMTTF)와 $HAuCl_4{\cdot}3H_2O$를 THF 용액 내에서 직접 반응시켜 $(OMTTF)AuCl_4$를 합성하였다. $(OMTTF)_2PtCl_4,\; (OMTTF)_2\;IrCl6{\cdot}2H_2O,\; (OMTTF)OsCl5{\cdot}THF$ 등은 각각 $H_2PtCl_6{\cdot}xH_2O,\;H_2IrCl_6{\cdot}xH_2O$ 및 $H_2OsCl_6$를 사용하여 유사한 방법으로 합성하였다. 합성된 화합물들은 자기적(EPR, 자화율 측정), 분광학적(IR, UV-Vis), 전기화학적(CV) 특성과 전기전도도를 측정하였다. 상온에서의 분말 전기전도도는 모두 ~$10^{-7}\; S{\cdot}cm^{-1}$ 이하의 낮은 전기전도도를 나타내었다. 합성 과정에서 OMTTF로부터 Au, Pt, Ir, Os 금속 화합물로 전하 이동이 이루어져 OMTTF는 완전히 이온화된 $OMTTF^+$ 양이온 라디칼로 존재하였다. $OMTTF^+$ 양이온 라디칼의 안정성은 산화·환원 전위 값에서 확인하였다. 자화율 결과로부터 $(OMTTF)_2IrCl_6{\cdot}2H_2O$ 및 $(OMTTF)OsCl5{\cdot}THF$에서는 $OMTTF^+$ 이온에 존재하는 홀전자와 중심 금속(Ir 및 Os)에 편재화된 홀전자들 사이에는 강한 반강자성 상호작용이 존재함을 알 수 있었다.

• 대한화학회지
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• 제22권2호
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• pp.86-94
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• 1978

Theophylline 鹽酸鹽의 結晶 및 分子 構造를 3次元的인 X-線 回折 data로부터 Patterson法에 의하여 決定하였고, Block-diagonal least square와 Fourier法으로서座標를 精密化하였다. 이化合物은 a = 14.01, b = 11.49, c = 6.77${\AA}$의 單位格子를 가지는 斜方晶系에 屬하는 結晶 이며 空間群은 $P_{na21}$ 이다. 743개의 觀測된 data에 대한 최종 R값은 12.2%이다. Theophylline 分子內 原子間 距離는 유사化合物에서 얻은 값과 거의 일치한다. 이들 原子는 同一平面을 이루고 있으며 HCl의 鹽素原子는 theophylline의 N(1) 原子와 3.06${\AA}$ 距離의 Cl${\cdot}{\cdot}{\cdot}$N(1), 水素結合을 이루고 있다. 모든 分子 는 대략 (001)과 (002)面上에 배열되어 있고 各分子間은 van derWaals force에 의해 三次元的 構造를 이루고 있다.

• 분석과학
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• 제8권3호
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• pp.249-258
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• 1995

Polyazine, polyazomethine ( I ) 및 ( II )는 각각 p-benzoquinone과 hydrazine hydrate, p-phenylenediamine, 그리고 diaminomaleonitrile을 dimethylsulfoxide(DMSO)하에서 중합하여 얻었다. Polyazine, polyazomethine ( I ) 및 ( II )의 IR spectra 분석결과 $1600cm^{-1}$ 부근에서 Schiff base의 특성 peak인 -C=N-를 확인하였다. 또한 각 polyazine, polyazomethine ( I ) 및 ( II )를 conc. $H_2SO_4$에 용해시켜 UV/VIS spectrum 측정결과 protonate (>$C\limits^{\small\oplus}=NH-$)에 해당되는 것으로 생각되는 흡수 band가 300nm 부근에서 나타났으며 350~415nm 부근에서 전하이동전이와 같은 흡수로 생각되는 흡수 band가 나타났다. Polyazine, Polyazomethine ( I ) 및 ( II )의 자체 전기전도도는 약 $10^{-14}{\sim}10^{-11}{\Omega}^{-1}cm^{-1}$로 나타났으며 $I_2$를 도핑한 후 최고 전기전도도가 $10^{-2}{\Omega}^{-1}cm^{-1}$ 정도로 약 $10^{12}{\sim}10^9$배 향상되었다.

• Bulletin of the Korean Chemical Society
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• 제30권5호
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• pp.1157-1163
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• 2009

Complexes of Pd(btnbmtp)$Cl_2$ and Pt(btnbmptp)$Cl_2$ (btnbmtp = 2,5-bis(thiophen)-1-nonyl-3,4-bis(methylthio)- pyrrole) were prepared and their crystal structures were determined at room temperature. In the structures, the two thiophene moieties lie in cis form with an average dihedral angle of $55.26^{\circ}$ to the pyrrole frame. The luminescence properties of the free ligand and the complexes were investigated in solution and solid states. The luminescence of the compounds were not favored by substituting thiophene moieties to the pyrrole frame, compared to the unsubstituted nbmptp (nbmptp = 1-nonyl-3,4-bis(methylthio)pyrrole). In particular, thiophene substitution quenched the emission from the complexes dissolved in ,$CH_2Cl_2$ and reduced the charge transfer transitions from S atoms of the thio moieties to Pt in crystalline state, which was very characteristic of Pt(nbmptp)$Cl_2$.

• 센서학회지
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• 제30권4호
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• pp.191-195
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• 2021

Pure ZnFe₂O₄ and Fe₂O₃-ZnFe₂O₄ hetero-composite spheres were prepared by ultrasonic spray pyrolysis of a solution containing Zn- and Fe-nitrates. Additionally, the sensing characteristics of these spheres in the presence of 5 ppm ethanol, benzene, p-xylene, toluene, and CO (within the temperature range of 275-350 ℃) were investigated. The Fe₂O₃-ZnFe₂O₄ hetero-composite sensor with a cation ratio of [Zn]:[Fe]=1:3 exhibited a high response (resistance ratio = 140.2) and selectivity (response to p-xylene/response to ethanol = 3.4) to 5 ppm p-xylene at 300 ℃, whereas the pure ZnFe₂O₄ sensor showed a comparatively lower gas response and selectivity. The reasons for the superior response and selectivity to p-xylene in Fe₂O₃-ZnFe₂O₄ hetero-composite sensor were discussed in relation to the electronic sensitization due to charge transfer at Fe₂O₃-ZnFe₂O₄ interface and Fe₂O₃-induced catalytic promotion of gas sensing reaction. The sensor can be used to monitor harmful volatile organic compounds and indoor air pollutants.

• Bulletin of the Korean Chemical Society
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• 제26권12호
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• pp.1946-1952
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• 2005

New group 15 organometallic compounds, M$(phenanthrenyl)_3$ (M = P (1), Sb (2), Bi (3)) have been prepared from the reactions of 9-phenanthrenyllithium with $MCl_3$. A reaction of 9-(diphenylphosphino)phenanthrene with 2,6-diisopropylphenyl azide led to the formation of (phenanthrenyl)${(Ph)}_2P$=N-(2,6-$^iPr_2C_6H_3$) (4). The crystal structures of 2 and 4 have been determined by single-crystal X-ray diffractions, both of which crystallize with two independent molecules in the asymmetric unit. Compound 2 shows a trigonal pyramidal geometry around the Sb atom with three phenanthrenyl groups being located in a screw-like fashion with an approximately $C_3$ symmetry. A significant amount of CH- -$\pi$ interaction exists between two independent molecules of 4. The phosphorus center possesses a distorted tetrahedral environment with P-N bond lengths of 1.557(3)$\AA$ (P(1) N) and 1.532(3)$\AA$ (P(2)-N), respectively, which are short enough to support a double bond character. One of the most intriguing structural features of 4 is an unusually diminished bond angle of C-N-P, attributable to the hydrogen bonding of N(1)-H(5A) [ca. 2.49$\AA$ between two adjacent molecules in crystal packing. The compounds 1-3 show purple emission both in solution and as films at room temperature with emission maxima ($\lambda_{max}$) at 349, 366, and 386 nm, respectively, attributable to the ligand centered $\pi$ $\rightarrow$ $\pi^\ast$ transition in phenanthrene contributed by the lone pair electrons of the Gp 15 elements. Yet the nature of luminescence observed with 4 differs in that it originates from $\pi$ (diisopropylbenzene)-$\pi^\ast$ (phenanthrene) transitions with the $\rho\pi$contribution from the nitrogen atom. The emission maximum of 4 is red-shifted ranging 350-450 nm due to the internal charge transfer from the phenanthrenyl ring to the N-arylamine group as deduced from the ab initio calculations.

• 한국결정성장학회지
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• 제19권1호
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• pp.15-18
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• 2009

본 연구에서는 근 자외선 및 가시광 영역에서 우수한 발광 강도를 가지는 적색 형광체를 얻기 위하여 고상 반응법으로 합성하여 $EU^{3+}$와 $Bi^{3+}$가 도핑 된 ${Y_2}{SiO_5}$의 발광 특성을 관찰하였다. 근자외선 영역인 ${\lambda}_{ex}=395nm$ 기준으로 측정하였고, $^5D_0-^7F_2$의 에너지 천이에 의해 612 nm 영역에서 강한 peak가 발생하였다. CST가 $Eu^{3+}-O^{2-}$에 의해 258 nm 영역 대에서 생성되었고, $Bi^{3+}$가 함께 도핑 된 것은 $Eu^{3+}-Bi^{3+}-O^{2-}$에 상호작용에 의해 282 nm 영역대의 장파장 쪽으로 이동하였다. $350\;nm{\sim}480\;nm$ 영역 대에 '$^7F_0{\to}^5L_9$ (364 nm), $^7F_0{\to}^5G_3$(381 nm), $^7F_0{\to}^5L_6$(395nm), $^7F_0{\to}^5D_3$(415 mn) and $^7F_0{\to}^5D_2$(466 nm)는 $Bi^{3+}$와 $EU^{3+}$ f-f 천이에 의해 발생하였다. $Bi^{3+}$의 도핑농도가 증가할수록 발광 강도가 증가함을 보이다가 0.125 mol 일 때 발광강도가 가장 우수하였고, $Bi^{3+}$의 도핑 농도가 0.125 mol 이상 되면 발광강도가 현저히 감소하는 것을 확인하였다.

• 대한전기학회논문지:전기물성ㆍ응용부문C
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• 제48권5호
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• pp.285-295
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• 1999

Electroluminescent(EL) devices based on organic materials have been of great interest due to their possible applications for large-area flat-panel displays. They are attractive because of their capability of multi-color emission, and low operation voltage. An approach to realize such device characteristics is to use active layers of lanthanide complexes with their inherent extremely sharp emission bands in stead of commonly known organic dyes. In general, organic molecular compounds show emission due to their $\pi$-$\pi*$ transitions resulting in luminescence bandwidths of about 80 to 100nm. Spin statistic estimations lead to an internal quantum efficiency of dye-based EL devices limited to 25%. On the contrary, the fluorescence of lanthanide complexes is based on an intramolecular energy transfer from the triplet of the organic ligand to the 4f energy states of the ion. Therefore, theoretical internal quantum efficiency is principally not limited. In this study, Powders of TPD, $Eu(TTA)_3(phen) and AlQ_3$ in a boat were subsequently heated to their sublimation temperatures to obtain the growth rates of 0.2~0.3nm/s. Organic electrolumnescent devices(OELD) with a structure of $glass substrate/ITO/Eu(TTA)_3(phen)/AI, glass substrate/ITO/TPD/Eu(TTA)_3(phen)/AI and glass substrate/ITO/TPD/Eu(TTA)_3(phen)/AIQ_3AI$ structures were fabricated by vacuum evaporation method, where aromatic diamine(TPD) was used as a hole transporting material, $Eu(TTA)_3(phen)$ as an emitting material, and Tris(8-hydroxyquinoline)Aluminum$(AlQ_3)$ as an electron transporting layer. Electroluminescent(EL) and current density-voltage(J-V) characteristics of these OELDs with various thickness of $Eu(TTA)_3(phen)$ layer were investigated. The triple-layer structure devices show the red EL spectrum at the wavelength of 613nm, which is almost the same as the photoluminescent(PL) spectrum of $Eu(TTA)_3(phen)$.It was found from the J-V characteristics of these devices that the current density is not dependent on the applied field, but on the electric field.