• Title/Summary/Keyword: 8-Hydroxyquinoline

Search Result 204, Processing Time 0.027 seconds

Preparation and characterization of immobilized 8-hydroxyquinoline for chromatographic application (크로마토그래피용 고정화 8-hydroxyquinoline의 제조 및 특성분석)

  • Kim, Bum-Soo
    • Analytical Science and Technology
    • /
    • v.13 no.1
    • /
    • pp.49-54
    • /
    • 2000
  • The 8-hydroxyquinoline derivative of silica gel has been prepared through the 5 step reaction. We carried out infrared as well as nuclear magnetic resonance spectrometric characterization of products taken from each step of reaction. IR study of bare silica gel showed free and hydrogen bonded hydroxyl. From the 1st step reaction, we observed IR bands for N-H and C-H as well as NMR peaks for three methylene carbons in APTS group. From the 2nd step, we observed IR bands for carbonyl, nitro and aromatic carbon group with NMR peaks for aliphatic, aromatic and carbonyl carbons. The reduction of $NO_2$ group to $NH_2$ group is confirmed by IR and NMR from 3rd step reaction. In the last step, the immobilization of 8-quinolinol is confirmed by disappearance of $N{\equiv}N$ IR peak observed in 4th step.

  • PDF

Synthesis and Biological Activities of Carbamate Derivative (Carbamate 화합물의 합성 및 위생학적 연구)

  • 강회양
    • Journal of Environmental Health Sciences
    • /
    • v.22 no.2
    • /
    • pp.19-24
    • /
    • 1996
  • Carbamates are generally used as insecticide, thus 5.7-dichloro-8~hydroxyquinolinyl- N-ethylcarbamate was newly synthesized. Its physical properties were determined and chemical structure was identified by means of I.R., nmr in addition to elemental analysis. The yield of addition, using triethylamine as catalyst, 5.7-dichloro-8-hydroxyquinoline and isocyanate was better than that of condensation of 5.7-dichloro-8-hydroxyquinoline with carbamoylchloride. The effct of the compound on rabbit's ileum, and antibacterial activity against Staphylococcus aureus, Salmonella typhi, Echerichia coli, and Pseudomonas aeruginosa were examined. The present organic synthesized compound showed the bacteriostatic action on salmonella typhi, escherichia coli, and pseudomonas aeruginosa, but no otherwise effect of contraction of rabbit's ileum in the concentration of $250 \mu g/ml$.

  • PDF

Spectrophotometric Determination of Co (Ⅱ) with 7-Nitroso-8-Hydroxyquinoline-5-Sulfon (7-Nitroso-8-Hydroxyquinoline-5-Sulfonate 에 依한 Co (Ⅱ) 의 吸光光度定量)

  • Lee, Dong-Hyung
    • Journal of the Korean Chemical Society
    • /
    • v.9 no.2
    • /
    • pp.101-105
    • /
    • 1965
  • Spectrophotometric method for the determination of Co(Ⅱ) is developed based on the fact that Co(Ⅱ) forms a stable red complex with 7-nitroso-8-hydroxyquinoline-5-sulfonate at pH 4. 5. The absorbance is measured at 528$m{\mu}$, $25^{\circ}C$. Beer's law is followed in the concentration range of 0. 3 to 6. 0 p.p.m. of Co(Ⅱ) and molar extinction coefficient of the complex was $1.1{\times}10^4$. Of the diverse ions checked, Fe(Ⅱ), Fe(Ⅲ), Cu(Ⅱ), Mn(Ⅱ), Hg(Ⅰ), CN-, EDTA interfere. The composition of the complex is found to be 3:1 ligand to metal species by mole ratio and continuous variation methods.

  • PDF

Thermodynamics of Metal Chelate Formation of 8-Hydroxyquinoline-5-Sulfonic Acid (8-Hydroxyquinoline-5-Sulfonic Acid의 금속킬레이트 생성에 관한 열역학적 고찰)

  • Kun Moo LEE
    • Journal of the Korean Chemical Society
    • /
    • v.13 no.1
    • /
    • pp.5-8
    • /
    • 1969
  • Acid dissociation constants and chelate stability constants of 8-hydroxyquinoline-5-sulfonic acid have been determined for divalent metal ions. Co (Ⅱ), Ni (Ⅱ) and Zn (Ⅱ) by means of the Calvin-Bjerrum technique at the various temperatures. The standard free energy changes for the reactions at $20^{\circ}$, $30^{\circ}$, $40^{\circ}$and $50^{\circ}C$ were calculated, and the corresponding values of ${\Delta}H^{\circ}$ and ${\Delta}S^{\circ}$ applying over this temperature range are reported. The results are interpreted on the basis of current theories of metal chelate formation in aqueous solution.

  • PDF

Synthesis of 8-HQR and 8-HQRS Chelate Resins and It's Ion Exchange Properties (8-HQR 및 8-HQRS 킬레이트 수지의 합성과 그의 이온교환 성질)

  • Dong Won Kim;Kong Soo Kim;Hong Soo Kim
    • Journal of the Korean Chemical Society
    • /
    • v.30 no.1
    • /
    • pp.69-75
    • /
    • 1986
  • 8-Hydroxyquinoline-resorcinol(8-HQR) and 8-hydroxyquinoline-resorcinol-salicylic acid (8-HQRS) chelate resins were prepared by the condensation reaction of 8-hydroxyquinoline, or 8-hydroxyquinoline-salicylic acid, in the presence of resorcinol with formaldehyde. The ion exchange capacities of 8-HQR and 8-HQRS resins were 4.1 meq/g and 5.4 meq/g, respectively. The adsorption and distribution coefficient of metal ions, such as Fe(III), Cu(II), Pb(II), Co(II) and Ni(II) on these resins were discussed. The adsorption of metal ions on these chelate resins showed that the maximum adsorption condition is pH 7. And the distribution coefficient of metal ions on these resins was increased with decreasing of hydrochloric acid concentration.

  • PDF

Characterization of the Quinoline-Degrading Bacterium Pseudomonas sp. NFQ-1 Isolated from Dead Coal Pit Areas (폐광지역에서 분리한 quinoline 분해 세균인 Pseudomonas sp. NFQ-1의 특성연구)

  • 윤경하;황선영;권오성;오계헌
    • KSBB Journal
    • /
    • v.18 no.3
    • /
    • pp.174-179
    • /
    • 2003
  • The bacterium NFQ-1 capable of utilizing quinoline (2,3-benzopyridine) as the sole source of carbon, nitrogen and energy was enriched and isolated from soil samples of dead coal pit areas. Strain NFQ-1 was identified as Pseudomonas nitroreducens NFQ-1 by BIOLOG system, and assigned to Pseudomonas sp. NFO-1. Pseudomonas sp. NFQ-1 was used with the concentration range of 1 to 10 mM quinoline. Strain NFQ-1 could degrade 2.5 mM quinoline within 9 hours of incubation. Initial pH 8.0 in the culture was reduced to 6.8, and eventually 7.0 as the incubation was proceeding. 2-Hydroxyquinoline, the first intermediate of the degradative pathway, accumulated transiently in the growth medium. The highest concentration of quinoline (15 mM) in this work inhibited cell growth and quinoline degradation. Pseudomonas sp. NFQ-1 was able to utilize various quinoline derivatives and aromatic compounds including 2-hydroxyquinoline, p-comaric acid, benzoic acid, p-cresol, p-hydroxybenzoate, protocatechuic acid, and catechol. The specific activity of catechol oxygenases was determined to approximately 184.7 unit/㎎ for catechol 1.2-dioxygenase and 33.19 unit/㎎ for catechol 2,3-dioxygenase, respectively. As the result, it showed that strain NFQ-1 degraded quinoline via mainly orthp-cleavage pathway, and in partial meta-cleavage pathway.

Hg2+-Selective Chemosensor Derived from 8-Hydroxyquinoline Having Benzothiazole Function in Aqueous Environment

  • Youk, Jin-Soo;Kim, Young-Hee;Kim, Eun-Jin;Youn, Na-Jin;Chang, Suk-Kyu
    • Bulletin of the Korean Chemical Society
    • /
    • v.25 no.6
    • /
    • pp.869-872
    • /
    • 2004
  • Newly synthesized 8-hydroxyquinoline based benzothiazole derivative 2 showed a distinctive $Hg^{2+}$-selectivity over other transition metal ions in aqueous solution. The fluorescence emission at 455 nm of 2 was completely quenched upon interaction with $Hg^{2+}$ ions in dioxane-$H_2O$ system (9 : 1, v/v). The selectivity was decreased in the order of $Hg^{2+}\;>>\;Cu^{2+}\;>\;Cd^{2+}\;>\;Pb^{2+}\;{\thickapprox}\;Zn^{2+}\;{\thickapprox}\;Ni^{2+},\;and\;Hg^{2+}$ concentration dependent fluorescence quenching profile was observed in the presence of common interfering metal ions as background. The fluorescence behavior of 2 suggests that the prepared compound could be used as a fluorescent signaling subunit for the construction of new $Hg^{2+}$-sensitive ON-OFF type supramolecular switching systems.

Studies on the synthesis of phenylmercuric 8-oxyquinolinate and its fungicidal effect (Phenylmercuric 8-oxyquinolinate의 합성(合成)과 그 살균효과(殺菌效果)에 대하여)

  • Shu, Y.T.;Son, C.Y.;Lee, S.H.
    • Applied Biological Chemistry
    • /
    • v.6
    • /
    • pp.37-43
    • /
    • 1965
  • 8-Hydroxyquinoline, known to have the therapeutic effect to fusarium; and to diminish the amount of evaporation because of reducing the size of the stomata, and a new compound, phenylmercuric 8-oxyquinolinate, were synthesized. The fungicidal effect and diminishing effect of evaporation in phenylmercuric 8-oxyquinolinate were studied and the results are as follows. 1) 8-Hydroxyquinoline(m.p. $74{\sim}75^{\circ}C$, white needle crystalline) was synthesized by Skraup's method, 2) Phenylmercuric 8-oxyquinolinate(m.p. $159{\sim}160^{\circ}C$, yellowish brown needle crystalline) was synthesized by reacting phenylmercuricacetate to 8-hydroxyquinoline. 3) The orders of the fungicidal effects are; a) To Cochliobolus miyabeanus P.M.A.

  • PDF

Aluminum in rocks: Optimized microwave-assisted acid digestion and UV-Vis spectrophotometric measurement

  • Nguyen Thanh-Nho;Thai Huynh-Thuc;Le-Thi Anh-Dao;Do Minh-Huy;Le-Thi Huynh-Mai;Le Quang-Huy;Nguyen-Thi Kim-Sinh;Nguyen Cong-Hau
    • Analytical Science and Technology
    • /
    • v.36 no.5
    • /
    • pp.216-223
    • /
    • 2023
  • Aluminium (Al) is one of the major elements in rocks and its concentration can be varied, depending on different rock types as well as sources. The present study aimed to propose an analytical method based on the UV-Vis as a cheap, simple, and common instrument equipped in most laboratories for Al quantification in rocks after the microwave assisted acid digestion. The aluminone and 8-hydroxyquinoline were investigated for the colorimetric assay. The results show that the 8-hydroxyquinoline reagent was more favorable in terms of the minimized affects of the potential interferences present in the digested solutions, i.e., Fe3+, Si4+ and F-. The calibration curve was constructed from 0.10 mg/L to 3.00 mg/L with the goodness of linearity (R2 = 0.9996). The limits of detection and quantification (LOD and LOQ) were estimated, i.e., 0.029 mg/L and 0.087 mg/L, respectively. The 8-hydroxyquinoline was applied to real rock samples, demonstrating favorable precision (RSD = 0.34 %-1.8 %) and no remarkable differences were found compared to the inductively coupled plasma-mass spectrometry (ICP-MS) as a reference measurement approach.