• 대한화학회지
• /
• 제68권1호
• /
• pp.12-14
• /
• 2024

• Bulletin of the Korean Chemical Society
• /
• 제23권3호
• /
• pp.399-403
• /
• 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
• /
• 제34권11호
• /
• pp.3481-3484
• /
• 2013

• 대한화학회지
• /
• 제37권7호
• /
• pp.655-661
• /
• 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.

• 분석과학
• /
• 제8권4호
• /
• pp.643-648
• /
• 1995

Cyclic voltammetric method is used to survey microscopic environments which take place at the surfactant-modified carbon electrode when the hydrophobic and hydrophilic environments of $Ru(ph){_3}^{2+}$(tris 1,10-phenanthroline ruthenium(II) chloride) is created by the addition of anionic surfactant, sodium dodecyl sulfate(SDS). Critical micelle concentration(CMC) of SDS in $Ru(ph){_3}^{2+}$ measured by cyclic voltammetry(CV) is in aggrement with that by surface tensiometry. Influence of the concentration of supporting electrolyte at surfactant-modified carbon electrode is investigated.

• Bulletin of the Korean Chemical Society
• /
• 제21권10호
• /
• pp.1052-1054
• /
• 2000

Binding geometries of $[Ru(II)(110-phenanthroline)_2L]^2+$, complexes (where L = dipyrido [3,2-a:2',3'-c]phena-zine (DPPZ) or benzodipyrido[3,2-a:2',3'-c] phenazine (BDPPZ)) to poly(dG)${\cdot}$poly(dC)${\cdot}$poly(dC) + triplex DNA (CGC + triplex) has been investigated by linear dichroism and normal absorption spectroscopy. Analysis of the linear dichroism for the CGC+ triplex and $[Ru(II)(phen)_2BDPPZ]^2+$ complex indicates that the extended ligand of the metal complex lie perpendicular to the polynucleotide helix axis. Together with strong hypochromism and red shift in the interligand absorption region, we concluded that the extended BDPPZ or DPPZ ligand in-tercalated between the bases of polynucleotide. The spectral properties of the metal complexes bound to CGC+ triplex are similar to those bound to $poly(dA)[poly(dT)]^2$ triplex (Choi et al., Biochemistry 1997, 36, 214), sug-gesting that the metal complex is located in the minor groove of the CGC+ triplex.

• Bulletin of the Korean Chemical Society
• /
• 제33권5호
• /
• pp.1769-1772
• /
• 2012

• 한국정보디스플레이학회:학술대회논문집
• /
• 한국정보디스플레이학회 2007년도 7th International Meeting on Information Display 제7권2호
• /
• pp.1103-1107
• /
• 2007

Highly efficient organic electroluminescent devices (OLEDs) based on 4,7- diphenyl-1, 10- phenanthroline (BPhen) as the electron transport layer (ETL), tris (8-hydroxyquinoline) aluminum ($Alq_3$) as the emission layer (EML) and N,$\acute{N}$-bis-[1-naphthy(-N,$\acute{N}$diphenyl-1,1´-biphenyl-4,4´-diamine)] (NPB) as the hole transport layer (HTL) were developed. The typical device structure was glass substrate/ ITO/ NPB/$Alq_3$/ BPhen/ LiF/ Al. Since BPhen possesses a considerable high electron mobility of $5\;{\times}\;10^{-4}\;cm^2\;V^{-1}\;s^{-1}$, devices with BPhen as ETL can realize an extremely high luminous efficiency. By optimizing the thickness of both HTL and ETL, we obtained a highly efficient OLED with a current efficiency of 6.80 cd/A and luminance of $1361\;cd/m^2$ at a current density of $20\;mA/cm^2$. This dramatic improvement in the current efficiency has been explained on the principle of charge balance.

• Bulletin of the Korean Chemical Society
• /
• 제26권4호
• /
• pp.537-542
• /
• 2005

It was proposed that Ru(II)[(1,10-phenanthroline)$_2$dipyrido[3,2-a:2',3'-c]phenazine ([Ru(phen)$_2$DPPZ]$^{2+}$)complexes and 4',6-diamidino-2-phenylindole (DAPI) simultaneously bind to poly[d(A-T)$_2$] (Biophysics. J. 2003, 85, 3865). Förster type resonance energy transfer from excited DAPI to [Ru(phen)2DPPZ]$^{2+}$ complexes was observed. In this study, we synthesized $\Delta$- and $\wedge$-[Ru(phenanthroline)$_2$dipyrido[3,2-a:2’3’c]6-azaphenazine] ([Ru(phen)$_2$DPAPZ]$^{2+}$) at which the DNA intercalating ligand DPPZ was replaced and we studied its binding properties to poly[d(A-T)$_2$] in the presence and absence of DAPI using polarized spectroscopy and fluorescence techniques. All the spectroscopic properties of the [Ru(phen)$_2$DPAPZ]$^{2+}$-poly[d(A-T)$_2$] complex were the same in the presence and absence of DAPI that blocks the minor groove of polynucleotide, suggesting both $\Delta$- and $\wedge$-[Ru(phen)$_2$DPAPZ]$^{2+}$ complexes are located at the major groove of poly[d(A-T)2]. On the other hand, in contrast with [Ru(phen)$_2$DPPZ]$^{2+}$, both $\Delta$- and $\wedge$-[Ru(phen)$_2$DPAPZ]$^{2+}$ exhibited almost twice the efficiency in the fluorescence quenching of DAPI that binds at the minor groove of poly[d(A-T)$_2$]. This observation indicates that the efficiency of the Förster type resonance energy transfer can be controlled by a small change in the chemical structure of the intercalated ligand.

• 생명과학회지
• /
• 제10권2호
• /
• pp.218-227
• /
• 2000

Bone morphogenetic protein 1 (BMP-1) is part of a complex capable of inducing ectopic bone formation in mammals. Studies on TGF-β1 processing and Drosophila dorsal-ventral patterning have focused attention on BMP-1 as important in mediating the biological activity of this bone inducing complex. Herein, the bacterial expression, refolding, purification, and initial characterization of the BMP-1 proteolytic domain (BPD) are described. A semi-quantitative fluorescence-based thin layer chromatography assay was developed to assist in rapidly screening for optimal renaturation conditions. According to a preliminary screen for optimal conditions for the refolding of BPD , a detectable proteolytic activity against a high turnover substrate for astacin, a homologous protease from crayfish was observed. The conditions identified have allowed the expression of sufficient amounts of BPD for the characterization of the protein. Its proteolytic activity exhibits the same cleavage specificity as astacin against seven substrates that were previously synthesized for studying astacin. Furthermore, this activity is inhibited by the metal chelator 1,10-phenanthroline but not by its analogue 1,7-phenanthroline. The collagenase inhibitor Pro-Leu-Gly hydroxamate was found to inhibit both astacin and BPD activity. The results presented in this paper argue that BMP-1 does in fact possess an intrinsic proteolytic activity.