• Title/Summary/Keyword: 치환체

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Electrochemical Behaviors for Cathodic Reaction of N'-aryl-N-alkyl-N-nitrosourea Drivatives (N'-aryl-N-alkyl-N-nitrosourea 유도체의 환원반응에 대한 전기화학적 거동)

  • Won, Mi Sook;Kim, Jack C.;Jeong, Euh Duck;Shim, Yoon-Bo
    • Journal of the Korean Chemical Society
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    • v.39 no.11
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    • pp.842-847
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    • 1995
  • The electrochemical reduction reactions of N '-aryl-N-alkyl-N-nitrosourea derivatives with a glassy carbon electrode were diffusion controlled and irreversible. The exchange kinetic constant ko values for reduction reaction of the N '-aryl-N-alkyl-N-nitrosoureas were at the range of $1.48{\times}10^{-6}{\sim}5.32{\times}10^{-7}\;cm/sec.$ The $k_0$ values for phenyl substituted on the aryl position were about 1.3∼2.8 times higher than that of other substituents. The same substituent for aryl groups on the both of N '-aryl-N-alkyl-N-nitrosourea and N '-aryl-N-(2-chloroethyl)-N-nitrosourea exhibited same value. The $E_p$ value was shifted to the negative direction as pH increased. The number of protons participated to the reduction was 4∼5, respectively. The substituent effect of aryl group on the reduction potential was not observed in this case.

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Electrical Conductivity of Sr-doped $ErCrO_3$Solid Solutions (Sr이 치환된 $ErCrO_3$고용체의 전기전도도)

  • 형경우;권태윤
    • Journal of the Korean Ceramic Society
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    • v.37 no.12
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    • pp.1159-1164
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    • 2000
  • 페롭스카이트 구조를 갖는 E $r_{1-x}$S $r_{x}$Cr $O_{3-y}$ 계에서 x=0.0, 0.05, 0.1, 0.2인 비화학양론적 화합물 고용체를 1573 K 대기압 하에서 제조하였다. X-선 회절분석을 통하여 제조된 모든 계들이 등방정계 단일상을 형성하였고, 또한 반지름이 큰 S $r^{2+}$를 doping 시켜줌에 따라 격자상수 및 환산부피가 증가됨을 알 수 있었으며, 단위 세포의 부피는 직선성을 보이며 증가하였다. TG-DTA에 따른 열분석 결과 Sr이 치환되지 않은 계에서는 상전이가 발생하는 반면, x값이 0.05 이상인 계들은 고온영역에 이르기까지 등방정계에서 마름모정계로의 상전이가 억제되었다. 전자현미경을 통하여 치환된 Sr의 몰비에 따른 시료들이 미세구조를 관찰하였고, d.c 전도도 측정을 통하여 다결정성 시료계들이 가지는 전도도의 온도 의존성으로부터 구한 활성화 에너지는 0.17 eV였다.다.

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Synthesis and biological activities of Chloronicotinyl derivatives (Chloronicotinyl 유도체의 합성 및 생물활성 검정)

  • Park, Su-Jin;Kim, In-Hae;Choi, In-Young;Kim, Song-Mun;Han, Dae-Sung;Hur, Jang-Hyun
    • The Korean Journal of Pesticide Science
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    • v.3 no.1
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    • pp.20-28
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    • 1999
  • Chloronicotinyl derivatives were synthesized by substitution of amino in 3-pyridylmethylamine with phosphite groups and their insecticidal and fungicidal activities were determined. At 500 ppm, compound 4 with methyl and butyl group in phosphonate and compound 5, 6, 7, and 8 with two butyl, 2,2,2-trifluorotehtyl, 2-ethylhexyl, phenyl, respectively, in phosphonate showed 90% insecticidal activities against brown plant-hopper (Nilaparvate lugens). These compounds showed, however, poor insecticidal activities against diamond-back moth (Plutella xylostella) and two-spotted spider mite (Tetranychus urticae) (<65%), suggesting that insecticidal activity of chloronicotinyl derivatives containing phosphorus moieties are species-dependent. Newly synthesized chloronicotinyl derivatives with halogen and/or heterocycle (compound $10{\sim}21$) did not show insecticidal activities. We also determined fungicidal activity of the synthesized chloronicotinyl derivatives against rice sheath blight (Pyricularia grisea), cucumber gray mold (Bortytis cinerea), tomato late blight (Phytophthora infestans), wheat leaf rust (Puccinia recondita), and barley powdery mildew (Erysiphe graminis). Compound 10 with butyl and 4-nitrophenyl in phosphonate at 10 ppm showed 85% fungicidal activity against rice blast, suggesting that chloronicotinyl derivatives containing phosphorus moieties could be developed as a fungicidal agent of a novel chemical structure.

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안트라싸이클린계 항암한생제의 유사제제의 합성에 관한 연구

  • 장영동
    • Proceedings of the Korean Society of Applied Pharmacology
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    • 1994.04a
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    • pp.216-216
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    • 1994
  • 안트라싸이클린계 항암항생제의 부작용 발생기전으로는 C-고리의 퀴논 부위에 전자가 전달되어 퀴논고리가 환원되는 과정이 제시되고 있으며 그중 하나의 전자가 전달되어 생성되는 활성산소(activated oxygen)가 심장독성과 관련이 있는 것으로 알려져 있다. 이 때 퀴논고리의 환원력(전자흡수능력)이 C-고리 자체의 변환, 또는 인접 B-고리에 도입된 치환체의 영향으로 억제될 수 있다는 보고를 이론적 근거로 하여 안트라싸이클리논 골격을 전자흡수능력을 가진 acridone 골격으로 치환한 9-ethynyl-6,9-trihydroxy-7,8,9,10-tetrahydro-benzo〔b〕acridone을 합성하였으며 이를 daunosamine과 축합하기 위하여 $C_{7}$위치에 OH기를 도입한 화합물로 변환하였다.

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Adamantyl-based N-arylamide as a Novel Series of Androgen Receptor Antagonists (아다만틸을 기반한 N-아릴아미드 신규 안드로겐 수용체 길항제)

  • Woo, Byoung Young;Shin, Song Seok;Hong, Yong Deog;Joo, Yung Hyup;Jeong, Yeonsu;Lee, Beom-Jin;Kim, Soo-Dong
    • Journal of the Society of Cosmetic Scientists of Korea
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    • v.46 no.1
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    • pp.43-47
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    • 2020
  • A novel series of adamantyl derivatives of N-aryl amides as androgen receptor antagonists were synthesized and their anti-androgenic activities were evaluated. The N-aryl amides containing adamantyl derivatives had more activity than those lacking adamantyl substitutions. The synergistic effect of bulkiness of the adamantyl group and modulation of electron density on the aromatic ring by pendant groups was crucial to the potent antagonism. Molecular modeling studies were performed to elucidate the interactions between ligands and receptors.

Synthesis of 2,3-Dihydrobenzofuran Derivatives over HMCM-41 Catalysts (HMCM-41 촉매에서 2,3-Dihydrobenzofuran 유도체의 합성)

  • Kim, Hyung Jin;Seo, Gon;Kim, Jung-Nyun;Choi, Kyung Ho
    • Korean Chemical Engineering Research
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    • v.43 no.6
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    • pp.662-667
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    • 2005
  • 2,3-Dihydrobenzofuran derivatives, important intermediates of medicines and agricultural chemicals, were prepared from aryl methallyl ethers over MCM-41 mesoporous material catalysts. Two mesoporous materials with Si/Al mole ratios of 40 and 50 were prepared to investigate the effect of acid site concentration on their catalytic activities. Aryl methallyl ethers with various substituents on their benzene rings were used to investigate the effect of electron density on benzene ring on the conversion of the ethers and the yield of 2,3-dihydorbenzofuran derivatives. The catalyst with a high acid site concentration showed high conversions, but it is difficult to correlate the yield of the derivatives with the acid site concentration. The increase in the electron density of the benzene ring by introducing electron-donating groups accelerated Claisen rearrangement reaction, resulting in the enhanced yield of the derivatives. On the other hand, the decrease in the electron density by introducing electron-attracting groups accelerated the cracking reaction of aryl methallyl ether by acid catalysts, producing phenol derivatives rather than 2,3-dihydrobenzofuran derivatives.

Improvement of Structural Performance of RC Beams retrofitted Hybrid Fiber using Recycled Coarse Aggregate and Ground Granulated Blast Furnace Slag (순환굵은골재 및 고로슬래그 미분말을 사용한 하이브리드섬유보강 철근콘크리트 보의 구조성능 개선)

  • Yi, Dong-Ryul;Ha, Gee-Joo
    • Journal of the Korea institute for structural maintenance and inspection
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    • v.18 no.6
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    • pp.1-10
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    • 2014
  • In this study, thirteen reinforced concrete beams, ground granulated blast furnace slag, replacing recycled coarse aggregate with PVA fiber (BSPG series) and recycled coarse aggregate with hybrid fiber ($BSPGR_1$, $BSPGR_2$ series), and standard specimen (BSS) were constructed and tested under monotonic loading. Experimental programs were carried out to improve and evaluate the Structural performance of such test specimens, such as the load-displacement, the failure mode, and the maximum load carrying capacity. All the specimens were modeled in 1/2 scale-down size. Test results showed that test specimens ($BSPGR_1$, $BSPGR_2$ series) was increased the compressive strength by 13%, the maximum load carrying capacity by 4~21% and the ductility capacity by 4~28% in comparison with the standard specimen (BSS). And the specimens ($BSPGR_1$, $BSPGR_2$ series) showed enough ductile behavior and stable flexural failure.

Thermal and UV Curing of Vacuum Deposited Film of Acetylene Substituted Fluorenes (아세틸렌기가 치환된 플루오렌 증착박막의 열 및 자외선 경화)

  • 정상현;김정수;강영구;이창진
    • Polymer(Korea)
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    • v.25 no.3
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    • pp.327-333
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    • 2001
  • Acetylene substituted fluorenes such as 2-ethynylfluorene and 2,7-diethynyl-fluorene were synthesized and thin films were prepared by the vacuum deposition. Curing of these fluorene derivatives could be achieved by heat treatment and UV irradiation. The curing temperature of 2-ethynylfluorene and 2,7-diethynylfluorene were found to be 231 and $198^{\circ}C$, respectively. The cured poly(2-ethynylfluorene) and poly(2,7-diethynylfluorene) started to decompose at 280 and $ 385^{\circ}C$, respectively. Fluorescent characteristics of the cured films were similar to those of monomers, but fluorescent efficiency of the film was decreased about 3 to 10 fold.

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