• Journal of Microbiology and Biotechnology
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• 제18권2호
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• pp.314-321
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• 2008

Acaricidal effects of materials derived from Diospyros kaki roots against Dermatophagoides farinae and D. pteronyssinus were assessed using impregnated fabric disk bioassay and compared with that of the commercial benzyl benzoate. The observed responses varied according to dosage and mite species. The $LD_{50}$ values of the chloroform extract of Diospyros kaki roots were 1.66 and $0.96{\mu}g/cm^2$ against D. farinae and D. pteronyssinus. The chloroform extract of Diospyros kaki roots was approximately 15.2 more toxic than benzyl benzoate against D. farinae, and 7.6 times more toxic against D. pteronyssinus. Purification of the biologically active constituent from D. kaki roots was done by using silica gel chromatography and high-performance liquid chromatography. The structure of the acaricidal component was analyzed by GC-MS, $^1H-NMR,\;^{13}C-NMR,\;^1H-^{13}C$ COSY-NMR, and DEPT-NMR spectra, and identified as plumbagin. The acaricidal activity of plumbagin and its derivatives (naphthazarin, dichlon, 2,3-dibromo-1,4-naphthoquinone, and 2-bromo-1,4-naphthoquinone) was examined. On the basis of $LD_{50}$ values, the most toxic compound against D. farinae was naphthazarin $(0.011{\mu}g/cm^2)$ followed by plumbagin $(0.019{\mu}g/cm^2),$ 2-bromo-1,4-naphthoquinone $(0.079{\mu}g/cm^2)$, dichlon $(0.422{\mu}g/cm^2)$, and benzyl benzoate $(9.14{\mu}g/cm^2)$. Additionally, the skin color of the dust mites was changed from colorless-transparent to dark brown-black by the treatment of plumbagin. Similar results have been exhibited in its derivatives (naphthazarin, dichlon, and 2-bromo-1,4-naphthoquinone). In contrast, little or no discoloration was observed for benzyl benzoate. From this point of view, plumbagin and its derivatives can be very useful for the potential control agents, lead compounds, and indicator of house dust mites.

• 대한화학회지
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• 제47권1호
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• pp.38-42
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• 2003

신농약 개발을 목적으로 isosterism 이론을 근거로 하여 선도화합물, 2-imino-1,3-thiazoline의 분자 수정을 통하여 분자내에 1,3-thiazole과 urea기가 포함된 새로운 화합물 2를 디자인하였다. N-Methylthiourea 5와 bromoacetonitrile을 에탄올 용액 중에서 반응시켜 위치 선택적으로 생성된 2,4-diimino-1,3-thiazole 4를 phenylisocyanate 유도체와 반응하여 화합물 2의 tautomer인 7을 얻었고 이것의 구조를 여러 가지 스펙트럼($^1H$ NMR, $^{13}C$ NMR, FT-IR, HRMS)과 X-ray 결정 데이터로부터 확인하였다. 화합물 7의 구조이성질체 8은 열역학적으로 불안정한 중간체 2,4-diimino-1,3-thiazole 6을 통하여 생성되었다.

• 공업화학
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• 제17권6호
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• pp.609-613
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• 2006

본 연구는 유기발광다이오드(OLED)용 적색형광 물질인 4-(Dicyanomethylene)-2-methyl-6-(4-dimethylaminostyryl)-4H-pyran (DCM)유도체들의 합성에 관한 것으로서, 유도체들은 Knoevenagel 축합반응에 의하여 합성되었다. 이들은 전자공여성의 아미노스티릴기와 전자흡인성의 시아노(니트릴)기의 공액구조를 가지고 있다. 합성한 물질은 각각 FT-IR, $^1H-NMR$ 등을 통하여 그 구조적 특성을 확인하였고, 융점, 수득율 등을 통하여 열적 안정성, 반응성 등을 확인하였으며, UV-visible과 PL분석으로부터 이 형광재료들의 광학적 특성을 확인하였다.

• 한국초전도저온공학회지:초전도와저온공학
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• 제20권2호
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• pp.15-22
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• 2018

The present article briefly overviews the plan for a new project on joint technology for HTS wires/cables and describes the development plan for the world's highest field NMR magnet, which is a major development item in the project. For full-fledged social implementation of superconducting devices, high temperature superconducting (HTS) wire is a key technology since they can be cooled by liquid nitrogen and they can generate a super-high magnetic field of >>24 T at liquid helium temperatures. However, one of the major drawbacks of the HTS wires is their availability only in short lengths of a single piece of wire. This necessitates a number of joints being installed in superconducting devices, resulting in a difficult manufacturing process and a large joint resistance. In Japan, a large-scale project has commenced, including two technical demonstration items: (i) Development of superconducting joints between HTS wires, which are used in the world's highest field 1.3 GHz (30.5 T) NMR magnet in persistent current mode; the joints performance is evaluated based on NMR spectra for proteins. (ii) Development of ultra-low resistive joints between DC superconducting feeder cables for railway systems. The project starts a new initiative of next generation super-high field NMR development as well as that of realization of better superconducting power cables.

• 한국자기공명학회논문지
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• 제15권1호
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• pp.69-79
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• 2011

HP0827 has two RNP motif which is a very common protein domain involved in recognition of a wide range of ssRNA/DNA.We acquired 3D NMR spectra of HP0827 which shows well dispersed and homogeneous signals which allows us to assign 98% of all $^1H_N$, $^{15}N$, $^{13}C_{\alpha}$, $^{13}C_{\beta}$ and $^{13}C$=O resonances and 90% of all sidechain resonances. The sequence-specific backbone resonance assignment of HP0827 can be used to gain deeper insights into the nucleic acids binding specificity of HP0827 in the future study. Here, we report secondary structure prediction of HP0827 derived from NMR data. Additionally, ssRNA/DNA binding assay studies was also conducted. This study might provide a clue for exact function of HP0827 based on structure and sequence.

• 대한화학회지
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• 제39권3호
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• pp.191-197
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• 1995

본 실험의 중성 화합물인 $[Mo(NO)_2L_2Cl_2]$는 $CH_2Cl_2$ 용매하에서 $[{Mo(NO)_2Cl_2}_n]$과 한자리 리간드를 반응시켜 얻었다. $[Mo(NO)_2L_4](ClO_4)_2$은 아세톤 용매하에서 중성$[Mo(NO)_2L_2Cl_2]$와 한자리 리간드의 반응으로 얻어진다. 합성에 이용된 리간드는 4-dimethylaminopyridine(dmap), pyridine(py) 그리고 isoquinoline(isoq)을 사용하였다. 합성한 cis-dinitrosylmolybdenum 착물은 elemental analysis, infrared, UV-Visible spectroscopy 그리고 $^1H\;NMR$ 등을 이용하여 그 특성을 조사하였다. 적외선 스펙트럼은 모든 착물이 팔면체 구조로서 두 개의 NO기가 cis 위치로 배위되어 있음을 나타낸다.

• 대한화학회지
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• 제54권4호
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• pp.402-410
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• 2010

새로운 착물인 cis-[$Mo_2O_3(Hapdhba)_2$], trans-[$UO_2(Hapdhba)_2$], [Pd(Hapdhba)Cl($H_2O$)], [Pd(bpy)(Hapdhba)]Cl, [Ag(bpy) (Hapdhba)], [$Ru(Hapdhba)_2(H_2O)_2$], [$Rh(Hapdhba)_2Cl(H_2O)$] 및 [Au(Hapdhba)$Cl_2$]를 보고한다. 여기서 $H_2$apdhba는 2-aminopyrimidine 및 2,4-dihydoxybenzaldehyde에서 비롯된 Schiff-염기이다. 이들 착물은 IR, UV-Vis 그리고 질량 스펙트럼을 비롯하여 전기전도도, 자기 및 열 분석을 통해 특성을 조사하였다. 구리의 부식에 대한 $H_2$apdhba의 방해효과는 0.5 M HCl에서 potiodynamic polarization 측정을 통해 조사하였다.

• Natural Product Sciences
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• 제21권4호
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• pp.278-281
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• 2015

Chemical investigation on a colonial marine tunicate, Didemnum sp. led to the isolation of a series of indole alkaloids including a new (1) and two known metabolites (2-3). Based on the spectroscopic analysis including 1D and 2D NMR along with MS spectra, the structure of 1 (16-epi-18-acetyl herdmanine D) was elucidated as a new amino acid derivative. The absolute configuration of 1 was determined by comparison of specific rotation with the known compound. The structures of compounds 2 and 3 were also identified as bromoindole containing compounds N-(6-bromo-1H-indole-3-carbonyl)-L-arginine and (6-bromo-^1H-indol-3-yl) oxoacetamide, respectively, based on $^1H$ and $^{13}C$ NMR data, MS data and specific rotation value. Their pharmacological potentials as antibacterial agents and FXR antagonists were investigated, but no significant activity was found. However, the structural similarity of compound 1 to compound 4 suggested the anti-inflammatory potential of compound 1.

• 대한화학회지
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• 제51권2호
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• pp.115-124
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• 2007

α, β-불포화 케톤 유도체를 실리카-황산 촉매 하에서 비용매 교차 알돌 응축 반응법을 이용하여 합성하였다. 합성 수율은 90% 이상이었으며, 사용된 촉매는 회수 가능하였다. 합성돤 화합물들의 물리화학적인 특성은 IR, NMR, Mass 등의 분광학적 분석 방법을 이용하여 결정하였다. 케톤 생성물에 미치는 치환기 효과는 측정된 분광 데이터와 Hammet 치환기 상수간의 상관관계로 표현되는 다중 상관계수 방정식에 의하여 잘 설명될 수 있었다.

• 대한화학회지
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• 제38권7호
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• pp.485-495
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• 1994

$[M(NO)_2Cl_2]_n(M = Mo, W)$을 출발물질로 사용하여 3단계 합성과정을 거쳐 $[Cl(dppp)(NO)_2M({\mu}-pyz)M'(NO)_2(dppp)Cl][ClO_4]_2$와 $[Cl(phen)(NO)_2M({\mu}-pyz)M'(NO)_2(dppp)Cl][ClO_4]_2$(M,M'= Mo or W; phen = 1,10-phenanthroline; dppp = 1,3-bis(diphenylphosphino)propane; pyz = 1,4-pyrazine) 형의 새로운 대칭 및 비대칭 이핵 착물을 합성하였다. 최종 생성물은 실리카겔 칼럼($2{\times}20$ cm)을 통해 아세톤으로 용리시켜 분리하였다. 합성한 착물은 원소분석과 적외선, 핵사기 공명 및 전자 흡수스펙트럼 등을 이용해서 그 특성을 조사하였다. 적외선 스펙트럼은 모든 착물이 팔면체 구조로서 두 개의 NO기가 cis 위치로 배위되어 있음을 나타냈으며, $^1H$ 및 $^{13}C$ 핵자기 공명 스펙트럼은 이들 착물이 pyz가 다리결합하고 있는 이핵 착물임을 나타내었다.