• 대한화학회지
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• 제9권1호
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• pp.33-36
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• 1965

5-Acetyl-8-hydroxyquinoline 의 酸解離定數를 $25^{\circ}C({\mu}$=0.1)에서 分光光度法과 pH滴定法에 依하여 測定하였다. 두 方法에 의하여 얻은 $pK_1$은 近似하게 一致하였으며 pK값은 8-hydroxyquinoline의 該當 pK값보다 작다. 그것은 acetyl group의 芳香族環에 대한 電子吸引性에 基因한 結果라고 생각한다.

• 대한화학회지
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• 제9권1호
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• pp.37-40
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• 1965

8-Hydroxyquinoline-5-sulfonic acid 를 alkali 媒質에서 $10^{\circ}C$以下로 維持하여 nitroso 化시켜 7-nitroso-8-hydroxy-quinoline-5-sulfonate (NHQS)를 合成하였으며 그 酸解離定數를 分光光度法과 pH滴定法에 依하여 測定하였다. 두 方法에 依하여 近似하게 같은 값은 얻어졌고 이것들은 8-hydorxyquinoline의 該當 pK값에 比해 작다. 8-hydroxyquinoline에 比해 NHQS의 낮은 鹽基性은 導入된 電子吸引性基들의 影響으로 생각되며 特히 nitroso 基는 ortho位의 phenol性 OH基의 酸性度의 增加에 많은 影響을 주는 것으로 생각된다.

• 대한화학회지
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• 제9권1호
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• pp.41-44
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• 1965

7-Nitroso-8-hydroxyquinoline-5-sulfonate의 Fe(II)錯鹽의 性質을 700$m{\mu}$, $26^{\circ}C$에서 分光光度法으로 調査하였다. 이 錯鹽은 pH6.0에서 가장 큰 吸光度를 나타내며 熱安定度도 대단히 좋다. Ligand나 Fe(III)의 還元에 使用한 hydroxylamine이 過剩으로 存在할때 에도 錯鹽의 生成에 影響을 주지 않는다. 錯鹽의 組成을 몰比法과 連續變化法으로 調査한 結果, 金屬과 ligand의 몰比는 1:3이였다. 檢量線은 實驗한 濃度範圍內에서 Beer의 法則에 따른다.

• Molecular & Cellular Toxicology
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• 제3권2호
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• pp.90-97
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• 2007

8-Hydroxyquinoline is used as antibacterial agent and antioxidant based on its function inducing the chelation of ferrous ion present in host resulting in production of chelated complex. This complex being transported to cell membrane of bacteria and fungi exerts antibacterial and antifungal action. In this study, we have carried out in vitro genetic toxicity tests and microarray analysis to understand the underlying mechanisms and the mode of action of toxicity of 8-hydroxyquinoline. TA1535 and TA98 cells were treated with 8-hydroxyquinoline to test its toxicity by basic genetic toxicity test, Ames and two new in vitro micronucleus and COMET assays were applied using CHO cells and L5178Y cells, respectively. In addition, microarray analysis of differentially expressed genes in L5178Y cells in response to 8-hydroxyquinoline were analyzed using Affymatrix genechip. The result of Ames test was that 8-hydroxyquinoline treatment increased the mutations in base substitution strain TA1535 and likewise, 8-hydroxyquinoline also increased mutations in frame shift TA98. 8-Hydroxyquinoline increased micronuclei in CHO cells and DNA damage in L5178Y. 8-Hdroxyquinoline resulted in positive response in all three tests showing its ability to induce not only mutation but also DNA damage. 783 Genes were initially selected as differentially expressed genes in response to 8-hydroxyquinoline by microarray analysis and 34 genes among them were over 4 times of log fold changed. These 34 genes could be candidate biomarkers of genetic toxic action of 8-hydroxyquinoline related to induction of mutation and/or induction of micronuclei and DNA damage. Further confirmation of these candidate markers related to their biological function will be useful to understand the detailed mode of action of 8-hydroxyquinoline.

• Bulletin of the Korean Chemical Society
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• 제17권4호
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• pp.338-342
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• 1996

A sensitive method for the determination of trace cadmium after the preconcentration by extracting its 8-hydroxyquinoline complex into a molten benzophenone was developed. Several experimental conditions such as the pH of solution, the amounts of 8-hydroxyquinoline and benzophenone, stirring time, and standing time were optimized. Trace cadmium in 100 mL water sample was chelated with 2.5 mL of 0.001 M 8-hydroxyquinoline at pH 8.0. After 0.07 g benzophenone was added, the solution was heated to about 70 ℃ and stirred vigorously for 1 minute to dissolve the complex quantitatively in a molten benzophenone, and stood for 30 minutes to reproduce the microcrystalline benzophenone. The benzophenone containing Cd-8-hydroxyquinoline complex was filtered and dissolved in acetone. Cadmium was determined by a flame atomic absorption spectrophotometry. The interfering effects of diverse concomitant ions were investigated and eliminated. This method could be applied to natural water samples and the recovery of more than 90% was obtained in the real samples.

• 분석과학
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• 제20권3호
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• pp.246-250
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• 2007

The quantitative determination of chromium(VI) by separation from chromium(III) complex of 8-hydroxyquinoline using solvent extraction has been studied. The reaction conditions for chromium(III) complex of 8-hydroxyquinoline and the solvent extraction of complex were investigated in detail. The chromium(III) complex was extracted with organic solvent (n-hexane) and residual chromium(VI) was determined by ICP-AES in aqueous layer. This technique is quantitative in the pH range of 8-9 and the limitations such as interfering ions were discussed.

• 대한화학회지
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• 제12권3호
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• pp.81-84
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• 1968

Stabilities of chelates of 7-nitroso-8-hydroxyquinoline-5-sulfonate have been determined for divalent transition metal ions, Mn(Ⅱ), Fe(Ⅱ), Co(Ⅱ), Ni(Ⅱ), Cu(Ⅱ), and Zn(Ⅱ) by means of the Calvin-Bjerrum technique. Comparison of these stability constants with those obtained for 8-hydroxyquinoline, and 8-hydroxyquinoline-5-sulfonate shows that the observed differences are essentially the results of the lower basicity of the sulfonated group and different metal-ligand bond. The divalent metal chelate stability sequence is not in agreement with the reported metal orders for other chelating agents. The stabilities were found to follow the order Mn(Ⅱ) < Fe(Ⅱ) ${\approx}$ Co(Ⅱ) > Ni(Ⅱ) < Cu(Ⅱ) > Zn(Ⅱ).

• 한국산학기술학회논문지
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• 제18권12호
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• pp.100-105
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• 2017

수질환경에서 구리이온을 검출하기 위하여 광섬유 센서의 구리 이온 감지 물질로 8-Hydroxyquinolin-2carboxaldehyde와 4-Aminoantipyrine으로 합성된 8-Hydroxyquinoline 합성유도체에 대해 광학적 반응 특성을 조사하였다. 실험은 광섬유를 이용한 측정시스템을 이용하여 수용액에 용해된 구리 이온의 농도에 대해 합성유도체에 의한 흡광도와 관계를 평가하기 위하여 수행되었다. 8-Hydroxyquinoline 합성유도체는 수질 환경에서 다양한 금속 이온들 중에서 구리 이온에 대해 노란색에서 붉은색으로 변화되는 높은 발색 현상을 나타냈으며 530 nm의 고유 흡광 파장을 보였다. 제작된 합성유도체의 Cu 이온에 대한 선택성을 평가하기 위하여 Hg 이온의 영향을 조사하였다. Cu와 Hg 이온의 다양한 농도 비 (Cu:Hg ratio 0.05부터 20까지)에서 흡광도를 측정한 결과, Cu 이온의 농도 증가에 따라 530nm에서 흡광도가 증가하는 경향을 보였다. 구리 이온의 고유 흡광 파장인 530 nm에서 합성 유도체에 의한 흡광도 세기는 구리 이온의 로그 농도에 선형으로 비례하였다. 따라서 8-Hydroxyquinoline합성유도체는 광섬유 센서의 구리 이온 감지 물질로 우수한 특성을 보임을 실험적으로 확인할 수 있었다.

• Journal of Applied Biological Chemistry
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• 제58권1호
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• pp.1-3
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• 2015

This study investigated the inhibitory activities of 2-hydroxyquinoline and its analogs against ${\alpha}$-glucosidase and ${\alpha}$-amylase. Based on the $IC_{50}$ values of 2-hydroxyquinoline analogs tested against ${\alpha}$-glucosidase and ${\alpha}$-amylase, 2-hydroxyquinoline had potent inhibitory activity (64.4 and $130.5{\mu}g/mL$, respectively), while 2-methyl-8-hydroxyquinoline showed weakly inhibitory activity (90.7 and $215.4{\mu}g/mL$, respectively). 2-Methylquinoline demonstrated no activity against ${\alpha}$-glucosidase and ${\alpha}$-amylase. In conclusion, 2-hydroxyquinoline analogs, with the existence of a methyl group and hydroxyl on quinoline, can be useful as a new diabetes treatment.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 1999년도 춘계학술대회 논문집
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• pp.193-196
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• 1999

Organic electroluminescent devices have attracted a great deal of attention due to thier potential application to full-color flat-panel displays. The 8-hydroxyquinollne Zinc(Znq$_2$) were synthesized successfully from zinc chloride(ZnCl$_2$) and zinc acetate(Zn(C$_2$H$_3$O$_3$)$_2$) as green omitting material. A double-layer ELD consist of an emitting layer of B-hydroxyquinoline Zinc(Znq$_2$) and a hole-transport layer of tai-phenylene diamine(TPD) derivatives sandwiched between an Aluminium(Al) and Indium-Tin-Oxide(ITO) electrodes omitted green light resulting from Znq$_2$. The electroluminescent devices (ELD) exhibited a maximum luminance of 1000cd/$\textrm{cm}^2$ at a driving voltage of 8V and a driving current density of 0.4mA/$\textrm{cm}^2$.