• 약학회지
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• 제35권5호
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• pp.353-359
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• 1991

Treatment of 1-ethyl-6-fluoro-1, 4-dihydro-4-oxo-7-(l-piperazinyl)-I, 8- naphthyridine-3-ca rboxylic acid (Enoxacin) with alkyl(or aryl) isothiocyanates which obtained from alkyl(or aryl) amines afforded six 1-ethyl-6-fluoro-1, 4-dihydro-4-oxo-7-(1-alkylthiocarbamylpiperazinyl)-1, 8- naphthyridine-3-carboxylic acids and five 1-ethyl-6-fluoro-1, 4-dihydro-4-oxo-7-(l-arylthiocarbamyl piperazinyl)-1, 8-naphthyridine-3-carboxylic acids. The compounds synthesized were evaluated for their antimicrobial activities, in vitro, against Escherichia coli 6-PE-4, Bacillus subtilis 74-51, Proteus vulgaris 78645, Klebsiella pneumoniae JYA-78314, Staphylococcus aureus 79110 and Pseudomonas aeruginosa 8765-1 P$_{2}$.

• 농약과학회지
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• 제12권2호
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• pp.103-110
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• 2008

제3 세대 cyclic imide(CyI)계 제초성 화합물을 탐색하기 위하여 새로운 1-(4-chloro-2-fluoro-5-propargyloxyphenyl)-3-thiourea 유도체(1-40)들을 합성하고 발아전(pre-emergence) 단계에서 벼(Orysa Sativa)와 논피(Echinochlor crus-galli)에 대한 제초활성($pI_{50}$)을 측정한 다음에 초종별 및 부위별 사이의 제초활성에 관련한 상관성을 검토하였다. Alkyl 보다는 aryl 유도체의 합성 수율(%)이 전반적으로 높았으며 특히, alkyl-유도체의 경우, alkyl amine의 구조적인 형태에 따라 합성수율에 큰 차이를 보였다. 두 초종 및 초종부위 사이의 제초활성에 관한 상관성을 검토한 결과, 논피에 대하여 가장 큰 제초활성을 나타내는 경우는 논피뿌리-논피줄기 사이의 상관성에서 화합물 8 및 24 이었고 논피에 대하여 선택성을 나타내는 화합물은 11 및 6이었다.

• 한국세라믹학회지
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• 제19권2호
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• pp.109-114
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• 1982

Fluoro-phlogopite crystals (Mica) were synthesized by two different methods; firstly the crystal was crystallized from the melts, and secondly mica crystalline was obtained from the direct solid state reaction. Addition of $CaF_2$ in the mica batch revealed the lowering the solid state reaction temperature. SEM and XRD were employed to observe mica crystalline flakes and solid solution forms. As a starting raw material Pyrophyllite was used resulting in the formation of mica crystals.

• 한국응용약물학회:학술대회논문집
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• 한국응용약물학회 2001년도 추계학술대회 및 정기총회
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• pp.81-81
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• 2001

The photoinducible DNA cleaving activities of bromofluoroacetophenones as a novel photonuclease were investigated. The photolytic behavior and DNA cleaving acitivity of fluorine derivative were compared with those of non-fluorine substituted compound, 4'-bromoacetophenones. Although the DNA cleaving activities of fluorine analogs were similar with those of 4'-bromoacetophenones, ο-bromo-$\rho$-fluoro derivatives gave the better DNA cleaving activities than $\rho$-bromo-ο-fluoro derivatives did.

• 한국정보디스플레이학회:학술대회논문집
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• 한국정보디스플레이학회 2002년도 International Meeting on Information Display
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• pp.483-486
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• 2002

Tree-ring types liquid crystalline compounds having fluoro and isothiocyanate substituent[1] were synthesized and their physical properties were measured to evaluate the applications to TFT-LCD TV. All synthesized compounds were showed remarkably high Tni point. Birefringence(${\triangle}n$) and dielectric anisotropy(${\triangle}{\varepsilon}$) were higher than fluoro analogues and isothiocyanate substituted bicyclohexyl-phenyl compounds.

• 대한화학회지
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• 제41권4호
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• pp.214-218
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• 1997

• Archives of Pharmacal Research
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• 제19권3호
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• pp.243-245
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• 1996

• Bulletin of the Korean Chemical Society
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• 제11권5호
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• pp.376-379
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• 1990

To find out a correlation between antibacterial activity and physical properties of 7-substituted 1-ethyl-6-fluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid, dipole moments, charge distributions, and hydrophobicities were calculated. The atomic charges and the dipole moments to not give any correlations with inhibition of DNA gyrase, but the calculated hydration free energies show some correlations.

• 대한약학회:학술대회논문집
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• 대한약학회 2002년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2
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• pp.366.2-366.2
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• 2002

In an effort to search for the chemically and enzymatically stable carbonucleoside. we designed ［1'-fluoro-2', 2'-bis-(hydroxymethyl) cyclopropyl methyl］ purines. The underlying concept for our design is to seek relatively conformationally-locked compound with minimal structural disturbance from acyclic carbonucleoside such as acyclovir or penciclovir. To meet such a requirement. we need to introduce cyclopropane and fluorine moiety. (omitted)

• 대한화학회지
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• 제54권6호
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• pp.711-716
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• 2010

비닐렌기에 플루오르 치환기를 도입한 새로운 전자발광 (EL) 고분자인 poly(m-silylphenyl-p-phenylene-difluorovinylene) (m-SiP-PPDFV)는 GILCH polymerization 방법에 의해 합성된다. 이들 고분자는 단층 구조 (ITO/PEDOT/polymer/Ca:Al)의 light-emitting diodes (LEDs)에서 EL 발광층으로 사용되었다. m-SiP-PPDFV는 $\lambda_{max}$ = 452 nm 주위에서 PL 발광파장을 나타내었고, $\lambda_{max}$ = 497 nm 주위에서 녹색의 EL 발광을 나타내었다. 고분자의 current-voltage-luminance (I-V-L) 특성에서는 4.0 V 정도에서부터 소자가 작동되기 시작하였다. 고분자의 전자 친화도를 증가시키는 m-SiP-PPDFV을 얻기 위해 m-SiP-PPV의 모든 비닐렌기에 두개의 플루오르기를 도입하였고, 이로 인하여 소자 구동에서 비닐렌기의 색 안정도를 나타냈었다. PPV 유도체들에서 일어나는 비닐렌기의 산화반응을 보호하는 플루오르기는 전자 끄는 효과를 가지고 있어 소자의 색 안정도를 유지시킨다. 이번 연구로, 보다 안정화된 PPV 유도체를 얻기 위해, 플루오르기가 비닐렌기에 도입될 수 있음을 보여주고 있다.