• 대한화학회지
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• 제37권7호
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• pp.655-661
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• 1993

$[{Mo(NO)_2Cl_2}_n]$ 및 $[{W(NO)_2Cl_2}_n]$의 다핵착물과 킬레이트 리간드인 1,10-phenanthroline을 반응시켜 중성화합물인 $[Mo(NO)_2Cl_2(phen)]$ 과 $[W(NO)_2Cl_2(phen)]$을 각각 합성하였다. 아세톤 용매에서 이 cis-디니트로실 화합물과 과염소산 은(I)을 1:1로 반응시켜 $[Mo(NO)_2(phen)(S)Cl][ClO_4]$ 및 $[W(NO)_2(phen)(S)Cl] [ClO_4]$ (S = acetone)의 양이온 화합물을 얻었다. 이 1가 양이온 화합물과 피라진을 2:1의 양론으로 각각 반응시켜 $[Cl(phen)(NO)_2M(pyz)M'(NO)_2(phen)Cl][C1O_4]_2$(M = Mo, M' = W) 및 $[Cl(phen)(NO)_2M(pyz)M'(NO)2(phen)Cl][C1O4]2$(M = Mo, M' = W)형의 호모 및 헤테로 이핵착물을 합성하였다. 합성한 착물의 특성은 원소분석과, $^1H-,\;^{13}C-$핵자기 공명 및 자외선, 전자흡수스펙트럼을 이용해서 조사하였으며 이들 분광학적 결과로부터 디니트로실 이핵착물의 기하학적 구조가 피라진 다리 리간드를 중심으로 한 $C_{2v}$ 대칭구조임을 확인할 수 있었다.

• 한국정보디스플레이학회:학술대회논문집
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• 한국정보디스플레이학회 2005년도 International Meeting on Information Displayvol.II
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• pp.1280-1283
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• 2005

A novel zinc complex, Zn(phen)q, was synthesized from 1,10-phenanthroline (phen) and 8-hydroxyquinoline (q) as organic ligands and its electroluminescent (EL) properties were characterized. The structure of Zn(phen)q was elucidated by FT-IR, UV-Vis and XPS. The complex Zn(phen)q showed thermal stability up to $300^{\circ}C$ under nitrogen flow, which was measured by TGA and DSC. The photoluminescence (PL) of the Zn(phen)q was measured from the THF solution and the solid film on quartz substrate. The PL emission of Zn(phen)q exhibited green light centered at about 505nm. The EL devices were fabricated by the vacuum deposition. The EL devices having the structure of ITO/a-NPD/Zn(phen)q/Li:Al were studied, where 4,4'-bis[N-(1-naphthyl)-N-phenylamino]biphenyl(a-NPD) used as a hole transport layer(HTL). a-NPD has high Tg of $96^{\circ}C$ and thus makes the device thermally stable. The EL emission of Zn(phen)q exhibited also green light centered at 532nm.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2005년도 추계학술대회 논문집 Vol.18
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• pp.313-314
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• 2005

Organic light emitting diodes(OLEDs) are widely used as one of the information display techniques. We synthesized (1,10-phenanthroline)- (8-hydroxyquinoline) [Zn(Phen)q]. We studied the improvement of OLEDs properties using Zn(phen)q. The Ionization Potential(IP) and the Electron Affinity(EA) of Zn(phen)q investigated using cyclic voltammetry(CV). The IP, EA and Eg were 7.leV, 3.4eV and 3.7eV, respectively. The PL spectrum of Zn(phen)q was yellowish green as the wavelength of 535nm. In this study, we used Zn(phen)q as electron transporting layer(ETL) inserted between emitting layer(EML) and cathode. As a result, Zn(phen)q is useful as electron transporting layer to enhance the performance of OLEDs.

• 대한화학회지
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• 제23권2호
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• pp.75-79
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• 1979

Benzolgous pyridine계 리간드에 대한 전자상태와 반응성을 조사하기 위하여 단순 Huckel 분자궤도법을 이용하여 프론티어궤도함수의 에너지상태 및 superdelocalizability와 전하밀도를 계산하였다. 리간드의 최고 점유궤도함수와 최저비점유궤도함수사이에 에너지차인 ${\Delta}E_{\pi}$ 값에 대한 계산결과로부터 착물을 형성하는 리간드의 안정도 순위는 1,10-Phen > 4,5-Phen > 1,5-Phen > 8-Hox > Hox-azolinato순으로 나타났으며, 리간드의 superdelocalizability와 전하밀도로서 친적자적, 친핵적 및 라디칼반응에 대한 반응성과 결합강도를 각각 조사하였다.

• Bulletin of the Korean Chemical Society
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• 제23권3호
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• pp.399-403
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• 2002

The complex of iron(II) tris(3-Br-phen) (3-Br-phen; 3-bromo-1,10-phenanthroline) was prepared as a precursor of electropolymerization and the crystal structure of [Fe(3-Br-phen)3]($PF_6$)2${\cdot}$CH3CN with a distorted octahedral geometry has been investigated. The reductive electropolymerization of $>[Fe(3-Br-phen)3]^{2+}$ complex onto the surface of a glassy carbon electrode and indium tin oxide (ITO) optically transparent electrode were performed in acetonitrile at room temperature. Thin film of poly-$>[Fe(3-Br-phen)3]^{2+}$ formed was adherent, electroactive and stably deposited on a glassy carbon disk electrode. The thin metallopolymeric film formed was also confirmed by absorption spectroscopy.

• Bulletin of the Korean Chemical Society
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• 제27권10호
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• pp.1655-1658
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• 2006

The solution of $[Ru(phen)_2(dppz)]^{2+}$ and SDS has high Resonance Light Scattering (RLS) signals due to $[Ru(phen)_2(dppz)]^{2+}$ assemble on the surface of the SDS micelle. Because of the high affinity ($KB\geq10^6\;L\;mol^{-1}$) between $[Ru(phen)_2(dppz)]^{2+}$ and DNA, the adding of DNA in the solution of $[Ru(phen)_2(dppz)]^{2+}$-SDS makes the dissociation of $[Ru(phen)_2(dppz)]^{2+}$-SDS, and results in decreasing of the RLS signals and increasing of the absorbance. Based on this, a novel method is proposed for DNA assay. Under optimum condition, good linear relationship was obtained within the concentration range of 0.018-1.26 $\mu g\;mL^{-1}$, the linear equation is $I_{RLS}$ = 504.8-348.8 c (c: $\mu g\;mL^{-1}$) and the correlation coefficient (r) is 0.9992. The detect limit for calf thymus DNA is 8.6 ng $mL^{-1}$. The proposed method was successful applied to determine the extracted colibacillus plasmid DNA.

• 한국전기전자재료학회논문지
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• 제11권10호
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• pp.871-877
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• 1998

Electroluminescent(EL) devices based on organic materials have been of great interest due to their possible applications for large-area flat-panel displays, where they are attractive because of their capability of multicolor emission, and low operation voltage. In this study, glass substrate/ITO/Eu(TTA)$_3$(phen)/Al, glass substrate/ITO/Eu(TTA)$_3$(phen)/Al and glass substrate/ITO/Eu(TTA)$_3$(phen)/AlQ$_3$/Al 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) aluminu-m(AlQ$_3$) as an electron transporting layer. Electrolumescent(EL) and I-V characteristics of Eu(TTA)$_3$-(-phen) were investigated. These structures show the red EL spectra, which are almost the same at the PL spectrum of Eu(TTA)$_3$(phen). I-V characteristics of this structure show that turn-on voltage was 9V and current density was 0.01A/㎤ at a operation voltage of 9V. Electrical transporting phenomena of these structures were explained using the trapped-charge-limited current model with I-V characteristics.

• 대한화학회지
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• 제51권6호
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• pp.595-599
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• 2007

• 대한화학회지
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• 제39권4호
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• pp.318-322
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• 1995

• 대한화학회지
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• 제32권3호
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• pp.203-210
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• 1988

물-아세톤, 물-아세토니트릴 및 물-디메틸포름아미드의 2성분 혼합용매중에서 한개의 산소다리로 된 이핵몰리브텐(V)착물, $[Mo_2O_3(Phen)_2(NCS)_4]$은 두개의 산소다리로 된 이핵 몰리브텐(V)착물, $[Mo_2O_4(Phen)_2(NCS)_2]$을 생성한다. $[Mo_2O_3(Phen)_2(NCS)_4]$가 $[Mo_2O_4(Phen)_2(NCS)_2]$로 바뀌는 속도는 분광광도법으로 측정하였다. 이 때 온도는 $10^{\circ}C$에서 $40^{\circ}C$, 압력은 1bar에서 1500bar로 변화시켰다. 속도상수는 물의 농도 증가에 따라 증가하였다. 수소이온농도의 증가에 따라서는 감소하였다. 여러가지 공용매에서 산소고리화 반응속도는 유전상수$({\varepsilon}/{\varepsilon}_0)$의 증가와 같이 ACT < AN < DMF의 순으로 증가하였다. 관찰된 음의 활성화엔트로피($[\Delta}S^{\neq}$), 활성화부피($[\Delta}V^{\neq}$) 및 활성화 압축율(${\Delta}{\beta}^{\neq}$) 값은 착물이 전이상태에서 용매 물분자를 강하게 당기는 회합성메카니즘임을 알게 한다.