• Bulletin of the Korean Chemical Society
• /
• 제29권7호
• /
• pp.1327-1331
• /
• 2008

Novel $CO_2$-soluble 8-hydroxyquinoline (8-HQ) chelating agents were synthesized and evaluated for solubility and metal ion extraction ability in supercritical $CO_2\;(Sc-CO_2)$. Among them, secondary amide-containing 8- HQ derivatives cannot be dispersed well into Sc-$CO_2$, but tertiary amide-containing derivatives can dissolve completely in Sc-$CO_2$ even at low CO2 pressures, perhaps owing to the predominant intermolecular interaction between the chelating agent and the $CO_2$ molecule. Based on 8-HQ chelating agent solubility data, we investigated the extraction of metal ions ($Co^{2+}$, $Cu^{2+}$, $Sr^{2+}$, $Cd^{2+}$, and $Zn^{2+}$) using two highly $CO_2$-soluble 8-HQ derivatives (4d, 4e) in Sc-$CO_2$. The extraction efficiency of tertiary amide-containing 8-HQ ligands, both fluorinated and non-fluorinated forms, was dramatically increased in the presence of diethyl amine (organic base). We suggest that diethyl amine could play an important synergistic role in the stronger metal binding ability of 8-HQ through an in situ deprotonation reaction in Sc-$CO_2$ medium.

• Journal of Pharmaceutical Investigation
• /
• 제34권6호
• /
• pp.453-457
• /
• 2004

Atenolol and related compounds found in raw materials and commercial products were analyzed by reversed-phase high-performance liquid chromatography. A mixed solution of phosphate buffer (3.4 g/l, pH 3.0), tetrahydrofurane and methanol (800:20:180, v/v/v) including sodium octanesulfonate (1 g/l) and tetrabutylammonium-hydrogensulfate (0.4 g/l) was used as mobile phase at the flow rate of 0.25 ml/min. Detection was carried out at UV 226 nm. Atenolol related compounds, such as bis ether, tertiary amine and blocker acid were identified by comparing the retention time of the standard. The within-day and between-day precisions of the separated compounds were less than 1.2% and 3.4%, respectively. The contents of related compounds of the tested samples were under the limit prescribed in the European Pharmacopoeia. The pattern of the related compounds showed that atenolol raw materials and products could be classified in three different groups, indicating that the materials originated from different source or treated in different way.

• 한국환경농학회지
• /
• 제14권1호
• /
• pp.55-71
• /
• 1995

소맥 종자의 발아 과정중 strontium의 생리적 작용을 규명하기 위해 초엽, 종근 및 배유에서의 free amine의 함량변화가 측정되었다. $GA_3$를 포함한 배양액에 strontium 농도의 증가는 종근에서의 putrescine과 초엽에서의 spermidine의 축적을 현저히 유발하였다. $10\;{\mu}M$ 정도의 저농도에서도 strontium에 의한 putrescine 증가는 뚜렷한 반면, spermidine 증가는 10 mM의 고농도 처리에서 현저했다. 종근 생장을 억제하는 1mM 내지 10mM의 strontium 농도에서, g 생체중당 putrescine 수준은 동일농도 calcium 처리에서 보다 각각 22.4배와 15.3배 높았다. 특히 putrescine과 spermidine 증가에 의한 총 free amine 수준의 중가는 생체중 대비 뿐만이 아닌 RNA 함량 대비에서도 중요한 생리적 반응으로 보여졌다. Strontium과 대조적으로 고농도 calcium (10 mM) 처리는 초엽과 종근에서의 agmatine과 cadaverine 함량의 증가를 유발했다. Cadaverine은 calcium을 처리했을 경우에만 검출되었다. 그러나 $1\;{\mu}M$ 에서 1 mM 수준의 calcium 처리는 총 free amine 함량의 감소를 가져왔다. Strontium과 calcium 존재하에서의 발아과정중 축적되는 amine 종류의 차이와 총 free amine 중 diaminine 비율과 총 free amine 중 Polyamine 비율의 변화는 strontium과 calcium 간의 생리적 대사반응의 차이중 하나로 판단되었다.

• 대한화학회지
• /
• 제19권5호
• /
• pp.343-350
• /
• 1975

염산수용액중에 존재하는 이리듐을 그 분자량 아민(Alamine 336)의 벤젠용액으로 추출한 바 20${\sim}$100${\mu}g$의 이리듐을 정량적으로 추출할 수 있음을 알았고 이때 이리듐 추출의 가능성에 관하여는 방사성 추적자(Ir-192)를 써서 확인하였다. 유기층에 추출된 화학종의 흡광도를 파장 322.5nm에서 측정한 결과 본 방법은 이리듐의 정량을 위한 미량분석법으로 사용할수 있음을 알았다. 이리듐이 아민층에 추출되는 메카니즘에 대한 설명을 시도하였다.

• 대한화학회지
• /
• 제43권3호
• /
• pp.294-301
• /
• 1999

제미널 비스포스폰에이트기를 포함하는 화합물들은 칼슘과 관련된 다양한 질병들 즉 Paget's disease, 악성칼슘과다증, 골다공증등에 약효가 있는 것으로 잘 알려져 있다. 이러한 화합물을 합성하기 위하여 먼저 methylvhyl ketone과 triethylphosphite를 가지고 5배 위된 옥사포스포린 화합물을 합성하였다. 이렇게 합성된 5배위 결합된 옥사포스프린을 bromination, 응용된 Westheimer반응, 그리고 가수분해를 통해서 Y-keto-bisphosphonates를 얻을 수 있었다. 그리고 이 Y-ketobisphosphonates 화합물들은 환원성아민화를 이용해서 N-알킬화된 Y-aminobisphosphonates로 전환하였다. 이렇게 합성된 2차아민 형태의 N-알킬화된 Y-aminobisphosphonates는 N-알킬화반응으로 3차아민을 만든 후 N,N디알킬화된Y-aminobisphosphonates 화합물로 합성할 수 있었다.

• KSBB Journal
• /
• 제9권4호
• /
• pp.406-411
• /
• 1994

용매추출에 의한 구연산발효를 시도하였다. 발효 배지내 구연산 농도와 추출용매의 독성이 구연산의 생산성을 결정하는 주 인자였다. 특히 이온화되지 않은 구연산은 강력한 발효억제효과를 가져 구연산 농도가 $5g/\ell$ 이상이면 구연산 생산은 거의 중지되었다. 구연산 추출효율을 높이기 위해 3차 아민과 oleyl alcohol의 혼합액을 용매로 사용하였다. 구연산의 추출발효에 척함한 용매조성은 30% 아민 70 % oleyl alcohol로 밝혀졌다. 이 조건에서 추출발효시 구연산농도는 $15.2g/\ell$ 로 동임한 조건에셔 용매 를 첨가하지 않고 발효하여 얻은 구연산농도 $5g/\ell$에 비해 3배 이상 높았다. 아빈 농도가 30%를 념으 면 추출능은 향상되나 용매의 독성효과로 생산성은 오히려 감소하였다. 균체에 대한 용매의 독성효과는 균체를 polyure-thane foam에 고정화함으로써 현저하게 줄일 수 있었다.

• 약학회지
• /
• 제35권3호
• /
• pp.182-189
• /
• 1991

Systematic study on the extraction of ion pair by the use of picric acid (PCA) as an ion pair forming reagent to the aliphatic amines has not be done by spectrophotometric method. The extraction of ion pair by the use of PCA and 23 kinds of the aliphatic amines was examined. The procedure is as follows; Elving's buffer solution (pH 1.3~10, ionic strength 0.5) each amine solution, and PCA solution were taken into a test tube. The mixture was shaken mechanically with chlorform. The organic phase was filtered through a filter paper to remove water droplets. The absorbance was examined at $\lambda_{max}$ against a reagent blank. Primary and secondary whose carbon number were more than 7 or 6, respectively, are extractable as ion pairs with PCA, while tertiary amines and quaternary ammonium salts are also extractable without the correlation of carbon number. It was considered that the ion pair extraction of primary and secondary amines was affected by the number of carbon of amines, but its extraction of tertiary amines or quaternary ammonium salts was affected by kind of aliphatic amines rather than pKa values or carbon number of amines.

• Bulletin of the Korean Chemical Society
• /
• 제18권8호
• /
• pp.890-895
• /
• 1997

The approximate rates and stoichiometry of the reaction of excess lithium tripiperidinoaluminum hydride (LTPDA), an alicyclic aminoaluminum hydride, with selected organic compounds containing representative functional groups under the standardized conditions (tetrahydrofuran, 25°) were examined in order to define the reducing characteristics of the reagent for selective reductions. The reducing ability of LTPDA was also compared with those of the parent lithium aluminum hydride (LAH) and lithium tris(diethylamino)aluminum hydride (LTDEA), a representative aliphatic aminoaluminum hydride. In general, the reactivity of LTPDA toward organic functionalities is weaker than LTDEA and much weaker than LAH. LTPDA shows a unique reducing characteristics. Thus, benzyl alcohol, phenol and thiols evolve a quantitative amount of hydrogen rapidly. The rate of hydrogen evolution of primary, secondary and tertiary alcohols is distinctive. LTPDA reduces aldehydes, ketones, esters, acid chlorides and epoxides readily to the corresponding alcohols. Quinones, such as p-benzoquinone and anthraquinone, are reduced to the corresponding diols without hydrogen evolution. Tertiary amides and nitriles are also reduced readily to the corresponding amines. The reagent reduces nitro compounds and azobenzene to the amine stages. Disulfides are reduced to thiols, and sulfoxides and sulfones are converted to sulfides. Additionally, the reagent appears to be a good partial reducing agent to convert primary carboxamides into the corresponding aldehydes.

• Bulletin of the Korean Chemical Society
• /
• 제15권10호
• /
• pp.881-888
• /
• 1994

The approximate rates and stoichiometry of the reaction of excess sodium tris(diethylamino)aluminum hydride (ST-DEA) with selected organic compounds containing representative functional groups under standardized conditions(tetrahydrofuran, $0{\circ}$) were studied in order to characterize the reducing characteristics of the reagent for selective reductions. The reducing ability of STDEA was also compared with those of the parent sodium aluminum hydride (SAH) and lithium tris(diethylamino)aluminum hydride (LTDEA). The reagent appears to be milder than LTDEA. Nevertheless, the reducing action of STDEA is very similar to that observed previously for LTDEA, as is the case of the corresponding parent sodium and lithium aluminum hydrides. STDEA shows a unique reducing characteristics. Thus, benzyl alcohol, phenol and 1-hexanol evolved hydrogen slowly, whereas 3-hexanol and 3-ethyl-3-pentanol, secondary and tertiary alcohols, were essentially inert to STDEA. Primary amine, such as n-hexylamine, evolved only 1 equivalent of hydrogen slowly. On the other hand, thiols examined were absolutely stable. STDEA reduced aidehydes and ketones rapidly to the corresponding alcohols. The stereoselectivity in the reduction of cyclic ketones by STDEA was similar to that by LTDEA. Quinones, such as p-benzoquinone and anthraquinone, were reduced to the corresponding 1,4-dihydroxycyclohexadienes without evolution of hydrogen. Carboxylic acids and anhydrides were reduced very slowly, whereas acid chlorides were reduced to the corresponding alcohols readily. Esters and epoxides were also reduced readily. Primary carboxamides consumed hydrides for reduction slowly with concurrent hydrogen evolution, but tertiary amides were readily reduced to the corresponding tertiary amines. The rate of reduction of aromatic nitriles was much faster than that of aliphatic nitriles. Nitrogen compounds examined were also reduced slowly. Finally, disulfide, sulfoxide, sulfone, and cyclohexyl tosylate were readily reduced without evolution of hydrogen. In addition to that, the reagent appears to be an excellent partial reducing agent: like LTDEA, STDEA converted ester and primary carboxamides to the corresponding aldehydes in good yields. Furthermore, the reagent reduced aromatic nitriles to the corresponding aldehydes chemoselectively in the presence of aliphatic nitriles. Consequently, STDEA can replace LTDEA effectively, with a higher selectivity, in most organic reductions.

• 대한전기학회:학술대회논문집
• /
• 대한전기학회 1988년도 추계학술대회 논문집 학회본부
• /
• pp.246-248
• /
• 1988

The electrical insulation characteristics of the Epoxy resin is generally depended upon the cross-Link. Therefore, when the Epoxy is cured the full cross-Link must be gotten to obtain the best electrical insulation property. This paper alms at examining the cure condition to get the best cross-link. The Epoxy used in this experiment is DGEBA, the curing materiel is MNA, and the accellator is tertiary amine. In this study, the best curing condition of cross-link is suggested by analysing the each Epoxy resin which is differenty cured according Lo the variable temperatures and curing times.