• Bulletin of the Korean Chemical Society
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• 제31권8호
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• pp.2223-2227
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• 2010

Reaction of [(bpy)Pd]$(PF_6)_2$ (bpy = 2,2'-bipyridine) with racemic bis(isonicotinoyl)-1,1'-bi-2-naphtholate (L) in acetone, and followed by addition of chloroform and solvent evaporation allows to form amorphous micro-bowl morphology consisting of $[(bpy)PdL]_2(PF_6)_4$ without any template or additive. In contrast, the reaction and recrystallization in acetone for 1 week produce parallel-piped single crystals consisting of $[(bpy)_3Pd_3({\mu}_3-HPO_4)_2](PF_6)_2$. The formations of micro-bowl and parallel-piped single crystal morphologies appear to be primarily associated with the kinetic and thermodynamic control, respectively. The formation of micro-bowls may be attributed to eruption of organic solvents. Cosolvent effects and chemical properties on the formation of micro-bowl morphology have been observed.

• Bulletin of the Korean Chemical Society
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• 제24권10호
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• pp.1495-1500
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• 2003

Equilibria and applications of a synergistic extraction were studied for the determination of a trace lithium by using thenoyltrifluoroacetone (TTA) and trioctylphosphine oxide (TOPO) as ligands. Several equations were derived for the extraction of lithium into m-xylene as a phase of Li-TTA·mTOPO adduct. Distribution coefficients and extraction constant were determined together with a stability constant of the adduct. The adduct was quantitatively extracted from the basic solution of higher than pH 9 by shaking for 30 minutes. m-Xylene was selected as an optimum solvent by comparing the extraction efficiency among several kinds of organic solvents. The stability constant (${\Beta}_2$) for Li-TTA/2TOPO was 150 times higher than Li-TTA/TOPO. The distribution coefficient of Li-TTA/2TOPO into m-xylene was 9.12 and the logarithmic extraction constant (log $K_{ex}$) was 6.76. Trace lithium of sub-ppm level in seawater samples could be determined under modified conditions and a detection limit equivalent to 3 times standard deviation for background absorption was 0.42 ng/mL.

• BMB Reports
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• 제44권6호
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• pp.399-404
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• 2011

In this study, powder of Orostachys japonicus A. Berger (O. japonicus) was extracted with 95% ethyl alcohol and fractionated using a series of organic solvents, including n-hexane (hexane), dichloromethane (DCM), ethylacetate (EtOAc), n-butanol (BuOH), and water ($H_2O$). We investigated the anti-inflammatory effects of these O. japonicus extracts on lipopolysaccharide (LPS)-stimulated RAW 264.7 cells. Their effects on the expression of inflammatory mediators and transcription factors were analyzed by Western blotting. DCM fraction significantly inhibited formation of reactive oxygen species (ROS) as well as nitric oxide (NO) in LPS-stimulated RAW 264.7 cells. Phosphorylation of the pro-inflammatory transcription factor complex nuclear factor-kappa B (NF-${\kappa}$B) p65 and expression of inducible nitric oxide synthase (iNOS), one of its downstream proteins, were also suppressed by DCM fraction. These effects were regulated by upsteam proteins in the mitogen-activated protein kinase (MAPK) and phosphoinositide 3-kinase/Akt (PI3K/Akt) signaling pathways. Taken together, our data suggest that O. japonicus could be used as a potential source for anti-inflammatory agents.

• 대한방사성의약품학회지
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• 제2권1호
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• pp.17-21
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• 2016

Alkali metal fluoride sources (MFs) such as potassium fluoride (KF) have been widely used as a fluoride source in the nucleophilic displacement reaction. However, they have low solubility and nucleophilicity in most of the organic solvents. Bulky fluoride sources such as tetrabutylammonium fluoride (TBAF) were substituted for MFs to improve these properties. However, hygroscopic property of TBAF makes it less convenient for handling as well as its strong basic property can make the side-reaction occur. Recently, novel fluoride sources have been developed to solve these problems. In this paper, we would like to introduce coordinated fluoride sources as a new fluoride sources such as tetrabutylammonium tetra(t-butyl alcohol)-coordinated fluoride, crown ether metal complex fluoride, and various bulky alcohols coordinated fluoride complexes. In particular, bulky alcohol coordinated fluoride source could generated by the controlled hydrogen-bonded of fluoride with alcohols and these fluoride sources have better stability and reactivity with showing low hygroscopic property. The study of these fluoride sources will help to understand the characteristic of [$^{18}F$]fluoride for increasing the radiochemical yield in the [$^{18}F$]radiofluorination.

• 생명과학회지
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• 제33권5호
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• pp.383-390
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• 2023

본 연구는 기능성 식품의 개발을 위해 갈색거저리 유충 유래 추출물에서 새로운 생리활성 펩타이드를 확인하는 것이다. 동결건조된 T. molitor 유충에서 다양한 용매로 시간에 따라 추출하였다. T. molitor 유충 추출 결과 물 추출물에서 5시간과 10시간에서 총 단백질과 고형분 함량당 각각 가장 높은 2,2,1-diphenyl-1-picrylhydrazyl (DPPH) 활성을 보였다. 물 추출물을 메탄올 농도에 따라 분획하였을 때, 높은 메탄올 농도는 상등액 중에 고분자량 단백질의 수준을 감소시키는 반면, 상등액의 DPPH 활성 수준을 증가시켜 저분자량 펩타이드가 항산화 활성을 매개하는 것으로 나타났다. 유기용매 분배에서 부탄올을 제외한 유기 용매 분배에서 물층에서 유사한 활성을 보였다. 유기용매분획물을 열처리 후 활성이 28~44% 감소하여 열에 대한 불안정한 성분이 존재하는 것으로 추정되었다. 물 추출물에 프로테아제 K를 첨가하면 DPPH 활성이 10~20% 증가하여 전체 단백질에서 방출되는 펩타이드가 항산화 활성을 부분적으로 증가시켰음을 알 수 있다. 그러므로, T. molitor 유충 추출물은 항산화제로써 기능을 수행할 수 있는 물질이 존재하는 것으로 제의할 수 있다.

• 대한화학회지
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• 제34권5호
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• pp.438-444
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• 1990

촉매로서 Hg$^{2+}$을 사용한 수화반응에서 cis-[Co(en)$_2$(OH$_2$)Cl]$^{2+}$, [Co(NH$_3$)$_5$Cl]$^{2+}$, cis-[Co(NH$_3$)$_4$(OH$_2$)Cl]$^{2+}$ 및 [Co(NH$_2$CH$_3$)$_5$Cl]$^{2+}$착물들은 Hg$^{2+}$의 농도가 증가할수록 관측속도상수(k$_{obs}$)의 값이 증가하였다. Hg$^{2+}$에 의한 수화반응의 속도법칙은 Rate = k$_2$K[complex][Hg$^{2+}$]이었고, 그 메카니즘이 연구되었다. 또한 여러가지 유기용매-물 혼합용매에서 Co(Ⅲ)착물의 Hg$^{2+}$에 의한 수화반응이 연구되었다. 용매의 성질인 Y (solvent ionizing power)값에 대한 log k를 도시하여 그 기울기인 m값을 얻었다. 그 m값으로부터 수화반응의 메카니즘을 추정하였다. 속도론적인 자료로부터 Hg$^{2+}$에 의한 Co(Ⅲ)착물의 수화반응이 I$_{d^-}$메카니즘으로 제안되었다. 각 Co(Ⅲ)착물의 속도의 차이는 여러가지 리간드가 배위된 Co(Ⅲ)착물의 리간드장파라메타(${\Delta}$)값과 관계가 있었다.

• 대한화학회지
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• 제9권1호
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• pp.61-65
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• 1965

有機클로로酸, 또는 에스타와 各種金屬(亞鉛, 硅素, 마그네슘, 錫)과의 여러 溶媒存在下(아세트나이트라일, 디옥센 및 토루엔)의 反應에서 얻은 反應生成物, 또는 反應系中의 金屬分布狀態를 (n,${\gamma}$)反應으로 製造한 各種放射性 金屬트레이서를 使用하여 決定하였다. 有機클로로 金屬 콤푸렉스의 溶解度는 親水性溶媒에서는 顯著하게 增加하였으며, 無極性溶媒에는 減少하였다. 이 事實은 回收된 金屬, 또는 回收된 金屬混合物의 水洗液中의 金屬分布狀態의 增加로서 確認되었다. 카보닐化合物 存在下에서 反應시켰 때에도 같은 事實을 나타내었다. 親水性溶媒中의 金屬콤푸렉스의 溶解度는 亞鉛, 硅素, 錫 및 마그네슘이 順序로 減少되었으며 無極性溶媒下에서는 硅素, 錫, 마그네슘 및 亞鉛의 順으로 減少되었다. 有機할로겐化合物과 金屬과의 反應生成物로 普通 豫期되는 有機金屬化合物은 全反應을 通하여 거의 없었다. 反應結果를 論議하였으며, 本反應過程에서 觀察한 溶媒의 影響에 關하여 論及하였다.

• 한국환경보건학회지
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• 제43권4호
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• pp.324-333
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• 2017

Objectives: The purpose of this study was to assess the correlation relationship between personal exposure and urinary hippuric acid in biological monitoring for airborne toluene in an industrial complex and in general environments. Methods: Personal exposure to toluene and its metabolite, hippuric acid, in urine were simultaneously measured in occupational environments area near an industrial complex and in general environments. The study subjects were divided into three types: 137 workers who use organic solvents in the workplace, 210 residents living near a dyeing industrial complex, and 379 residents living in general environments. The toluene exposures of workers and residents were measured by a passive sampler for four days. The urine of participants was sampled when the passive samplers of personal exposure were collected. Results: The toluene and hippuric acid concentrations of workers were the highest, followed by the concentrations of residents living near a dyeing industrial complex and residents living in general environments. The coefficient of correlation between the concentrations of toluene and hippuric acid among workers was 0.749 (p<0.01) in the workplace. On the contrary, correlations between the concentrations of toluene and hippuric acid among residents living near a dyeing industrial complex and residents living in general environments were all not significant. The relationship between the concentrations of hippuric acid and toluene in three types could be described by the exponential growth model. Conclusions: This study analyzed the relationships between toluene exposure and the concentrations of hippuric acid in urine in high, middle, and low exposure environments, and could be described by the exponential growth model.

• 농약과학회지
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• 제16권2호
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• pp.121-130
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• 2012

농약의 잔류분석은 일반적으로 기존의 액액분배 추출법(liquid liquid extraction, LLE)이 적용되어 왔으나, 시료 전처리에 많은 유기용매와 분석기구가 사용되고, 분석시간이 길며, 복잡한 분석단계로 인하여 보다 신속하고 효율적인 방법의 개발이 요구되고 있다. 이에 따라 경제적이고 간편한 농약 잔류 분석법을 확립하고자, 기존 분석법과 고체상 분말을 시료에 직접 주입하여 농약성분을 추출, 정제하는 QuEChERS (quick, easy, cheap, effective, rugged and safe)시료 전처리법을 비교 실험하였다. 엽채소류 중 상추, 참나물 및 취나물을 대상으로 농가에서 많이 사용하고, LC로 분석 가능한 대표적인 농약 6종(boscalid, cyazofamid, dimethomorph, fludioxonil, imidacloprid, pyraclostrobin)을 선정하였다. 두 분석법 모두 검량선의 상관계수($R_2$)는 0.99 이상으로 양호하였고, 검출한계는 imidacloprid는 0.02 mg/kg, 나머지 농약성분들은 0.05 mg/kg 수준이었다. 실험 결과, 액액분배법의 회수율은 92.8-100.9%, RSD는 2.5%이하였고, QuEChERS법의 회수율은 92.2-101.6%, RSD는 1.9%이하였다. Paired t-test를 이용하여 두 분석법 간의 시간에 따른 농약 잔류량을 비교한 결과, p-value는 0.3148-0.9890으로 두 분석법 간의 유의한 차이가 발견되지 않았다. 이 결과들을 볼 때 QuEChERS법은 기존의 액액분배법를 이용한 분석과 비교하여 동등한 회수율 결과를 보였으며, 분석 시간은 기존보다 약 1/4 정도 단축되었다. 또한 추출 과정 중 dichloromethane 등의 유해 유기용매 사용을 배제하여 실험자의 건강보호 및 폐용매의 양을 현저하게 줄일수 있어 친환경적이면서 경제적인 분석법으로 판단되었다.

• 임산에너지
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• 제23권1호
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• pp.45-68
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• 2004

The word of lignin is derived from the Latin word 'ligum' meaning wood. Lignin is complex polymer consisting of coniferyl alcohol, sinapyl alcohol and p-coumaryl alcohol unit and has an amorphous, three dimensional network structure which is hard to be hydrolyzed by acid. Lignin is found in the cell wall of plants lignified. The mode of polymerization of these alcohols in the cell wall lead to a heterogeneous branched and cross-linked polymer in which phenyl propane units are linked by carbon-carbon and carbon-oxygen bonds. This polymerization of precursors, p-coumaryl alcohol, coniferyl alcohol and sinapyl alcohol to lignin is formed by enzymic dehydrolyzation. The reaction is initiated by an electron transfer which results in the formation of resonance-stabilized phenoxy radical. The combination of these radicals produces a variety of dimers, trimers and oligomers and so on. Lignin research has been divided into basic and practical application field. The basic studies contains biosynthesis, chemical structure, distribution in the cell wall and reactivity by reductants, oxidants and organic solvents. The application research will be approached the reaction of lignin in various pulp making involving pulp bleaching and its effect on pulp qualities. Lignin also will be studied for the production of fine chemicals, polymer products and the conservation into an energy source like petroleum oil because the amount of lignin produced in pulp making process is more than 51,000,000 tons per year in the world. Both basic and application research must lay emphasis on the development for the utilization of lignin and the pulping process. But these researches can not be completed without understanding lignin structure containing functional groups. Therefore, this paper was focused on the review of lignin formulation which has been studied since 1948 in chronological order. This review was based on monomers, dimers, trimers and tetramers of phenyl propane unit structures which were isolated and identified by different methods from various wood.ious wood.