• 대한화학회지
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• 제9권1호
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• pp.1-7
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• 1965

토루엔, 디메틸폴움아마이드, 디메틸슬포옥사이드, 테트라하이드로퓨란, 아세토나이트라일 및 디옥센 等 溶媒存在下에서 모노클로로醋酸과 亞鉛을 反應시켜 본 結果, 溶媒효果를 나타내었다. 反應試藥의 反應度가 溶媒의 極性 및 親水性에 따라 增加하였다. 같은 溶媒系를 使用하여 에틸모노클로로醋酸을 反應시켜 본 結果, 溶媒효果를 나타냈으나 酸의 境遇보다 그 差가 크지 못하였다. 酸, 에스타, 亞鉛 및 카보닐化合物(벤즈알데히드 및 4-헤프타논)의 反應에 있어서는 알데하이드의 境遇에 있어서는 Reformatsky 反應生成物을 주었으나, 4-헤프타논과의 反應度는 없었다. 反應生成物의 收率은 試藥添加方法에 따라 變化되었다. 最高收率은 酸의 하이드로옥시酸(38.5%), 0.8g의 salt(아세트나이트라일溶媒)이며, 에스타의 境遇에는 에틸신나메이트(19.3%), 폴리머(21.6%)이였다. 카보닐化合物의 境遇에 있어서는 反應溫度에 따라 試藥의 反應度의 變化가 있었다. 硏究結果를 溶媒效果에 關聯시켜 論議하였으며, 硏究方法에 關하여 記述하였다.

• 대한화학회지
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• 제37권12호
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• pp.1047-1052
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• 1993

효소모델 코발트 화합물의 전자스펙트럼에서 축상의 이온성 리간드와 코발트사이의 전하전이에 해당하는 흡수띠의 위치가 극성도에 따라 변화하는 현상이 평면상의 거대고리 리간드의 공액도와 어떠한 상관관계가 있는가에 대하여 다음과 같은 여러가지의 공액도를 가진 거대고리 리간드의 유기코발트 착화합물을 사용하여 연구하였다. 완전히 공액인 $CH_3CoL,\;C_6H_5CoL,\;CNCoL,\;CH_3CoL',\;CNCoL'$부분적으로 공액인 $CH_3(py)Co(DH)_2, CH_3CoL＂$, 비공액의 이중결합을 포함하는 $[CH_3Co(1,4-CT)](ClO_4)_2$와 고리가 완전히 닫히지 않은 $CH_3Co(salen)$이 그들이다. 코발트와 탄소사이의 전하전이 흡수띠는 평면상의 거대고리 리간드가 완전히 공액일 때에만 용매의 극성도가 증가함에 따라 더욱 짧은 파장으로 이동하였고, 그에 해당하는 전이에너지$(E_T)$는 용매의 극성도(Z)와 직선의 상관관계에 있었으나, 거대고리 리간드가 불완전한 공액이거나 고리가 닫히지 않았을 때에는 전이 에너지와 용매의 극성도 사이에 상관관계를 발견할 수 없었다.

• 한국식품영양학회지
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• 제8권3호
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• pp.172-183
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• 1995

The nucleophilic substitution reactions of p-substituted benzyl bromide with l-substituted N,N-dimethylanilines in methanol and acetonitrile binary solvent mixture which is known to an isodielectric solvent system kinetically and the results are as follows. The positive charge is developed on the reaction center of the substrate and it means that the bond cleavage is preceded more than bond formation in the transition state on the analogy of Hammett px values. The bond form3tlon is not progressed in the case of electron donating substituent of substrate. However, the bond formation is much developed in the case of electron withdrawing substituent of substrate on the analogy of Hammett py values. The nucleophilic attacking ability is shown a highest at 80% (V/V) methanol content and the bond formation is well progressed at the same methanol composition on the result of a cross interaction coefficient, pxy. The result of transition state structure that is applicated to the potential energy surface model is in accord with the result that Is applicated to the reaction susceptibilities. The reaction Is subject to the polarity-polarizability term more than the hydrogen bond donor acidity term by application to the solvatochromic parameter eouation.

• 한국식품영양학회지
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• 제30권1호
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• pp.51-58
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• 2017

Antioxidant activities of 80% methanol, water, and 70% ethanol extracts of Lentinula edodes GNA01 were compared and estimated. The yield of Lentinula edodes GNA01 was identified to be in the following order: water>70% ethanol>80% methanol, but there was no significant difference between 80% methanol and 70% ethanol extracts. The highest total phenolic content (TPC) and total flavonoid content (TFC) were found in water extract, and TPC of 80% methanol extract was higher than that of 70% ethanol extract and TFC of 70% ethanol extract was higher than that of 80% methanol extract. Water extract exhibited the strongest DPPH, ABTS radicals, and nitrite scavenging activities, $Fe^{2+}$ chelating ability, and FRAP among the three extracts. In addition, antioxidant activity of 80% methanol extract was higher than that of 70% ethanol extract in most of the experiments. As a result, antioxidant activity of Lentinula edodes GNA01 showed a difference according to extraction solvent and concentration; nevertheless, water extract exhibiting high polarity had the strongest antioxidant effect. Consequently, water extract from Lentinula edodes GNA01 is anticipated to be useful for the development of a high value-added functional product.

• Ocean and Polar Research
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• 제36권3호
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• pp.247-254
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• 2014

In our continuing study on the antioxidant activity of Polysiphonia stricta, its crude extract was fractionated into n-hexane, 85% aqueous methanol (85% aq.MeOH), n-butanol (n-BuOH), and water fractions according to solvent polarity. The solvent fractions were evaluated for their potential to inhibit lipid peroxidation and reactive oxygen species (ROS) production in HT 1080 cells. The n-BuOH fraction most strongly inhibited both lipid peroxidation and ROS production in HT 1080 cells. The n-BuOH fraction was further separated by repeated silica gel column chromatography and RP-HPLC to give methyl aconitates (2 and 3). The chemical structure of isolated compounds was determinated by NMR spectral analysis.

• Food Science and Biotechnology
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• 제18권2호
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• pp.513-518
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• 2009

This study was carried out to investigate the changes of yield, total phenolics, saponin content and composition, antimicrobial, and antioxidant activities of various fractions of fine ginseng root (Panax ginseng C.A. Mayer) by maceration method in the order of increasing polarity (hexane, chloroform, ethyl acetate, butanol, and water). Butanol fraction showed the highest total saponin content compare to other fractions. Hexane fraction could harvest significantly high ginsenoside Rg2, Rg1, and Rf (p<0.05). And the contents of ginsenoside Rh1, Rg3, and Rg1 showed relatively higher in the fraction of ethyl acetate than other fractions. The system of hexane-chloroform-ethyl aceate-butanol showed relatively high content of ginsenoside Re, Rd, Rc, Rb3, and Rb1. However, the last fraction of water still remained lots of Rb2 content. The fraction of water was the highest phenolics. The 1,1-diphenyl-2-picryhydrazil, superoxide, and hydroxyl radical scavenging activity of water fraction was higher than the other fractions. In antimicrobial activity, the fraction of hexane showed relatively high antimicrobial activity against Pseudomonas aeruginosa, Salmonella typhimurium, Staphylococcus aureus, Bacillus cereus, and Escherichia coli. And the fractions of the chloroform and ethyl acetate showed higher antimicrobial activities than the other samples in against P. aeruginosa and S. typhimurium.

• Korean Chemical Engineering Research
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• 제53권6호
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• pp.717-722
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• 2015

감귤류의 과일 내에 포함된 것으로 알려진 d-limonene 성분은 정유 성분을 추출하여 분리하는 방법으로 얻을 수 있다. 연속 증류 추출법 중 하나인 Soxhlet 추출법을 사용하여 감귤 껍질의 정유 성분을 추출한 후, 역상 HPLC를 통해 정량분석을 하였다. 추출용매의 끓는점과 극성도가 수율에 주는 영향을 알아보기 위해 에탄올, n-헥산, 석유에테르 3가지 용매를 추출 용매로 사용하였다. $120^{\circ}C$에서 각각의 용매를 1, 2, 4시간 동안 추출했을 때의 시료를 얻어 총 9가지 시료를 분석하였다. 역상 HPLC에서 정량분석을 한 결과, 세 가지 용매 모두 2시간 동안 추출했을 때 d-limonene의 함유량이 가장 많았으며, 이 때 감귤 껍질 1 g당 함유량은 7.77 mg(에탄올), 0.49 mg(n-헥산), 0.28 mg(석유에테르)였다. 에탄올을 사용했을 때 수율이 가장 높은 것으로 보아 용매의 극성도가 끓는점보다 추출 효율에 더 큰 영향을 미치는 것을 알 수 있었다.

• 대한화학회지
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• 제24권4호
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• pp.288-294
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• 1980

$CH_3O(CO)Cl,\;CH_3S(CO)Cl\;및\;CH_3S(CS)Cl$/TEX>의 가메탄올 분해반응속도를 메탄올-아세토니트릴 혼합용매하에서 결정하였다. 반응속도는 주로 벌크한 용매성질에 의해서만 아니라 일부 친전자적 특수용매화에 의해서도 영향을 받는다는 것이 실험결과로 알려졌다. 용매의 극성은 반응속도에 영향을 미치는 중요인자는 아니지만, $S_N1$형의 천이상태 안정화에 기여함을 알았다. $CH_3S(CS)Cl$/TEX>의 가메탄올 분해반응은 메탄올에 의한 이탈기의 특수 용매효과 및 큰 유전상수를 가진 용매에 의한 천이상태 안정화가 중요한 $S_N1$형으로 진행됨을 알았다. $CH_3O(CO)Cl$의 가메탄올 분해반응은 위의 경우와는 반대로 $S_N2$형으로 진행됨을 알았다.

• Bulletin of the Korean Chemical Society
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• 제23권9호
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• pp.1315-1327
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• 2002

The model compounds, 8-methoxypsoralen-CH2O(CH2)n-adenine (MOPCH2OCnAd, n=2, 3, 5, 6, 8, and 10) in which 5 position of 8-methoxypsoralen (8-MOP) is linked by various lengths of polymethylene bridge to N9 of adenine. UV absorption spectra are identical with the sum of MOPCH2OC3 and adenine absorption spectra. Solvent effects on the UV absorption and fluorescence emission spectra indicate that the lowest excited singlet state is the $(\pi${\rightarrow}$\pi*)$ state. The spectral characteristics of the fluorescence of MOPCH2OCnAd are strongly dependent upon the nature of the solvents. The fluorescence emission spectra in aprotic solvents are broad and structureless due to the excimer formation through the folded conformation accelerated by hydrophobic ${\pi}-{\pi}$ stacking interaction. Increasing polarity of the protic solvents leads to higher population of unfolded conformation stabilized through favorable solvation and H-bonding, and consequently to an increase in the fluorescence intensity, fluorescence lifetime, and a shift of fluorescence maximum to longer wavelengths. The decay characteristics of the fluorescence in polar protic solvents shows two exponential decays with the lifetimes of 0.6-0.8 and 1.6-1.9 ns in 5% ethanol/water, while MOPCH2OC3 shows 0.5 and 1.7 ns fluorescence lifetimes. The long-lived component of fluorescence can be attributed to the relaxed species (i.e., the species for which the solvent reorientation (or relaxation) has occurred), while the short-lived components can be associated with the unrelaxed, or only partially relaxed, species.

• Bulletin of the Korean Chemical Society
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• 제31권9호
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• pp.2453-2458
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• 2010

Photochemical studies of N-[(trimethylsilyl)alkyl]saccharins were carried out to investigate their photochemical behavior. Depending on the nature of the substrate and the solvent system employed, reactions of these substances can take place by either SET-promoted silyl migration from carbon to either the amide carbonyl or sulfonyl oxygen or by a N-S homolysis route. The results of the current studies show that an azomethine ylide, arising from a SET-promoted silyl migration pathway, is generated in photoreactions of N-[(trimethylsilyl)methyl]saccharin and this intermediate reacts to give various photoproducts depending on the conditions employed. In addition, irradiation of N-[(trimethylsily)ethyl]saccharin produces an excited state that reacts through two pathways, the relative importance is governed by solvent polarity and protic nature. Finally, photoirradiation of N-[(trimethylsilyl)propyl]saccharin in a highly polar solvent system comprised of 35% aqueous MeOH gives rise to formation of a tricyclic pyrrolizidine and saccharin that generated via competitive SET-promoted silyl transfer and $\gamma$-hydrogen abstraction pathways.