• 제목/요약/키워드: $C_{14}H_{14}O_4N_2$

검색결과 246건 처리시간 0.033초

Di-N-hydroxyethylated Tetraaza 거대고리 Copper(II) 착물 (Copper(II) Complex of a Di-N-hydroxyethylated Tetraaza Macrocycle)

  • 최기영;김용선;류해일;서일환;추금홍
    • 한국결정학회지
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    • 제11권3호
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    • pp.147-150
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    • 2000
  • The complex [CuL}Cl₂·3H₂O(1)(L=2,13-bis(2-hydroxyethyl)-5,16-dimethyl-2,6,13,17-tetraazatricyclo[14,4,0/sup 1.18/,0/sup 7.12/] docosane) has been synthesized and characterized by X-ray crystallography. 1. crystallized in the monoclinic, space group C2/c, with a=21.647(6)Å, b=8.549(1)Å, c=18.132(5)Å, β=118.58(2)°, V=2946.8(12)ų, Z=4, R₁(wR₂) for 2374observed reflections of [I>2σ(I)] was 0.052(0.187). The centrosymmetric complex 1 has an axially elongated octahedral geometry with four secondary and tertially amines of the macrocycle and tow oxygen atoms of the pendant hydroxyethyl groups.

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토양내 Phenanthrene의 생물학적분해에 미치는 계면활성제와 환경변수의 영향 (Effect of surfactants and Environmental Factors on the Bioremediation of Phenanthrene)

  • 류두현;최상일;김광수
    • 한국토양환경학회지
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    • 제3권2호
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    • pp.115-125
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    • 1998
  • 오염된 토양 중 phenanthrene의 분해에 미치는 비이온계 계면활성제와 생물계면활성제의 영향을 살펴보았다. 비이온계 합성 계면활성제로 polyoxyethylene oreyl esterC$^{17}$ H$^{33}$ COO($C_2$$H_4$O)nH) 와 생물계면활성제인 sophorolipid를 적용하였다. 계면활성제의 농도, 수분함량, 접종균 처리 방법 및 종류, pH, 온도, 부가영양분 등의 변수들이 phenanthrene의 생분해에 미치는 영향을 비교실험 하였다. 계면활성제 농도가 CMC이하의 경우 계면활성제는 phenanthrene의 생분해성을 촉진하였으나, CMC 값 이상의 영역에서는 계면활성제가 미생물의 phenanthrene분해작용을 저해하였다. 30%의 수분함량과 pH 7, $30^{\circ}C$에서, 부가영양분으로 glucose를 10g/L수준으로 첨가하였을 때 좋은 분해도를 나타내었다. 충진제로 짚이 첨가되는 경우 토양 : 짚의 중량비가 5:2이고, 수분함량이 50%인 경우 phenanthrene의 분해가 촉진되었다.

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Novel Sulfonated Poly(arylene ether ketone) Containing Benzoxazole Membranes for Proton Exchange Membrane Fuel Cell

  • Li Jin-Huan;Lee Chang-Hyun;Park Ho-Bum;Lee Young-Moo
    • Macromolecular Research
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    • 제14권4호
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    • pp.438-442
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    • 2006
  • Novel sulfonated poly(aryl ether ketones) containing benzoxazole were directly synthesized by aromatic nucleophilic polycondensation using various ratios of 2,2'-bi[2-( 4-flurophenyl)benzoxazol-6-yl]hexafluoropropane to sodium 5,5'-carbonylbis(2-fluorobenzenesulfonate). The copolymers were soluble in polar aprotic solvents such as N-methyl-2-pyrrolidone, N,N-dimethylacetamide, and N,N-dimethylformamide at a relatively high solid composition (>15 wt%) and formed tough, flexible and transparent membranes. The membranes exhibited a degradation temperature of above $290^{\circ}C$. The exact dissolution times of these membranes at $80^{\circ}C$ in Fenton's reagent (3 wt% $H_2O_2$ containing 2 ppm $FeSO_4$) were undetectable, confirming their excellent chemical stability in fuel cell application. The membranes showed a moderate increase in water uptake with respect to increasing temperature. The proton conductivities of the membranes were dependent on the composition and ranged from $1.10{\times}10^{-2}$ to $5.50{\times}10^{-2}Scm^{-1}$ at $80^{\circ}C$ and 95% relative humidity (RH). At $120^{\circ}C$ without externally humidified conditions, the conductivities increased above $10^{-2}Scm^{-1}$ with respect to increasing benzoxazole content, which suggested that the benzoxazole moieties contributed to the proton conduction.

Phenolic Glycosides from Cercidiphyllum japonicum Leaves

  • Lee, Tae-Seong;Min, Hee-Jeong;Bae, Young-Soo
    • Journal of the Korean Wood Science and Technology
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    • 제43권5호
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    • pp.591-599
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    • 2015
  • Cercidiphyllum japonicum leaves were collected, air-dried and extracted with 70% aqueous acetone, then concentrated and sequentially fractionated using n-hexane, methylene chloride ($CH_2Cl_2$), ethylacetate (EtOAc), and $H_2O$. A portion of EtOAc fraction (10 g) was chromatographed on a Sephadex LH-20 column, by the successively elution with various aqueous $MeOH-H_2O$ (1:9, fraction $1-2{\rightarrow}3:7$, fraction $3-5{\rightarrow}1:1$, fraction $6-9{\rightarrow}7:3$, fraction $10-13{\rightarrow}9:1$, fraction 14-16). Compound 2 was isolated from fraction 6 and compound 1 was separated from fraction 11 and 12. Compound 3 and 4 were purified from fraction 13. The isolated compounds were elucidated as quercetin-3-O-${\alpha}$-L-rhamnopyranoside (1), chlorogenic acid (2), quercetin-3-O-${\alpha}$-L-arabinofuranoside (3) and quercetin-3-O-${\beta}$-D-xylopyranoside (4) by the spectral and literature data, and by comparison with the authentic samples. These compounds were reported, for the first time, from the extracts of C. japonicum leaves. Also chlorogenic acid (2) has never been reported before in domestic tree species and can be used as an index compound for C. japonicum.

음이온 교환크로마토그래피법에 의한 여러가지 산에서 우라늄과 바나듐의 용리현상에 관한연구 (Study on the Elution Behaviors of Uranium and Vanadium in the Various Acids by Anion Exchange Chromatography)

  • 차기원;김종훈
    • 대한화학회지
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    • 제28권5호
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    • pp.309-314
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    • 1984
  • 과염소산, 염산 그리고 황산의 농도 변화에 따른 우라늄과 바나듐 이온의 음이온수지에 대한 용리곡선으로부터 이들 이온의 화학종의 변화와 평형관계를 음이온교환크로마토그래피법으로 연구하였다. 우라늄은 $0.01\;{\sim}\;0.5M$ 과염소산용액에서는 $UO_2^{2+}$의 화학종으로만 존재하며 염산용액에서는 0.5M 까지는 $UO_2^{2+}$ 상태로 존재하나 염산의 농도가 증가함에 따라 여러가지 $Cl^-$의 착물이 형성되는 용리현상을 보였고 황산용액에서는 묽은 황산의 농도에서 우라늄이 상당히 늦게 용리되어 나오는 것으로 보아 $SO_4$=과의 $UO_2(SO_4)_2$= 같은 음이온성 착물이 생성되는 것 같다. 바나듐은 $0.01\;{\sim}\;0.5M$ 과염소산용액에서 바나듐의 용리현상으로부터 $H_2V_{10}O_{28}^{4-}$$VO_2^+$간에 다음과 같은 평형이 존재함을 알았다. $H_2V_{10}O_{28}^{4-} + 14H^+ = 10VO_2^+ + 8H_2O$ 염산 및 황산용액에서도 이런 농도범위에서는 위와같은 평형이 존재하나 $VO_2$+과 $Cl^-$$SO_4^{2-}간의 착이온이 형성되는 것 같다. 위 식의 평형상수값은 $1.9{\times}108$이었다.

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石村湖의 營養鹽類 및 수질의 動態에 관한 조사연구 (A Study on the Variation of Nutrients and Water Quality in Suk Chon Lake)

  • Choi, Han-Young;Kim, Tai-Jeon;Park, Sung-Bae
    • 한국환경보건학회지
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    • 제14권1호
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    • pp.47-53
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    • 1988
  • This study was performed to investigate a seasonal and vertical variation of the nutrients, water temperature, pH, DO, BOD, COD in Sukchon lake from May 1985 to Jan. 1986. The results were as follows. 1. Vertical descent of water temperature was the remarkable situation on Jul. and difference between surface layer and bottom layer was 3.5$\circ$C. 2. The value of pH was average 8.0 in both lake. The value of pH in the winter was average 7.6, and Summer was average 8.3. 3. The contents of dissolved oxygen was the highest value (13.0mg/l in surface layer on Jan. and the lowest value (8.1mg/l in bottom layer on Ul. 4. The contents of PO$_4$-P, NH$_3$-N, NO$_3$-N and T-N were 0.03~O.17mg/l 0.12~0.34mg/l 0.36~0.91mg/l and 0.76~1.37mg/l respectively.

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Structural Characterization of the (TEX)$Sr_2Co_0.5Nb(Ta)_0.5O_4$(/TEX) and (TEX)$Sr_3CoNb(Ta)O_7$(/TEX)

  • 조한상;;류광현;유철현
    • Bulletin of the Korean Chemical Society
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    • 제21권7호
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    • pp.679-684
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    • 2000
  • The Sr2Co0.5Nb(Ta)0.5O4 and Sr3CoNb(Ta)O7 compounds, both with Ruddlesden-Popper structures, have been synthesized by the ceramic method at $1150^{\circ}C$ under atmospheric pressure. The crystallographic structure of the compounds was assigned to the tetr agonal system with space group 14/mmm by X-ray diffraction(XRD) Rietveld refinement. The reduced lattice volume and lattice parameters increased as the Ta with 5d substitutes for the Nb with 4d in the compounds. The Co/Nb(Ta)O bond length has been determined by X-ray absorption spectroscopic(EXAFS/XANES) analysis and the XRD refinement. The CoO6,octahedra were tetragonally distorted by elongation of Co-O bond along the c-axis. The magnetic measurement shows the compounds Sr2Co0.5Nb(Ta)0.5O4 and Sr3CoNb(Ta)O7 have paramagnetic properties and the Co ions with intermediate spin sates between high and low spins in D4h symmetry. All the compounds showed semiconducting behavior whose electrical conductivity increased with temperature up to 1000 K. The electrical conductiviy increased and the activation energy for the conduction decreased as the number of perovskite layers increased in the compounds with chemical formula An+1BnO3n+1.

N-아실-α-아미노숙신이미드와 N-아실-α-아미노글루탈이미드의 합성 (Synthesis of N-acyl-α-aminosuccinimides and N-acyl-α-aminoglutarimides)

  • 정대일;김문주;송현애;김윤영;이용균;박유미;최순규;한정태;박민수
    • 생명과학회지
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    • 제14권1호
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    • pp.91-97
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    • 2004
  • 앞선 연구의 구조적 특성을 근거로 하여, 한 분자내에 MES 유발경련에 작용하는 cyclicimide의 구조를 포함하면, 그들의 구조가 경련 유발 수용체들에 상호 보완적으로 작용, MES및 PTZ유발 경련에 모두 작용할 수 있는 적용 범위가 넓은 항경련성 화합물이 될 수 있을 것으로 생각하여 N-acyl-$\alpha$-aminosuccinimide 1과 N-acyl-$\alpha$-aminoglutar- imide 2 유도체를 합성하였다. 먼저 (R)-2-benzyloxy carbonylamino-succinic acid 3을 출발 물질로 하여 N-acyl-a-aminosuccinimide 1 유도체인 (R)-Benzoic acid 4-benzyloxycarbonyl-amino-2-oxo-pyrrolidin-l-yl ester 6a, (R)4-nitro-benzoic acid 4-benzyloxycarbon-ylamino-2-oxo-pyrrolidin-1-yl ester 6b, (R)-4-nitro-benzoic acid 4-benzyloxycarbonylamino-2-oxo-pyrrolidin-1-yl ester 6c, 그리고 (R)-propionic acid 4-benzyloxycarbonylamino-2-oxo-pyrrolidin-1-yl ester 64를 합성하였다 또한 (R)-3-car-bobenzyloxy-aminoglutarrnic acid 7를 출발물질로 하여 N-acyl-$\alpha$-aminoglutarimide 2유도체인 (R)-(3-Benzyloxycarbonyl-amino-2,6-dioxo-piperidin-1-yloxy)-acetic acid methyl ester 10a, (R)-(3-benzyloxyarbonylamino-2,6-dioxo-piperidin-1-yloxy)-acetic acid ethyl ester l0b, 그리고 (R)-2-(3-benzylox-ycarbonylanino-2,6-dioxo-piperidin-1-yloxy)-propionic acid methyl ester l0c를 합성하였다. 합성된 화합물 6a, 6b, 6c, 6d, 10a, lOb, l0c에 대한 활성평가는 각 단계별 MES test와 PTZ test의 항경련 활성 시험 방법을 가지고 실험할 예정이다.

$LiMn_{2-y}M_yO_4$ 정극 활물질의 전기화학적 특성 - II. $LiMn_{2-y}M_yO_4$ (M=Zn, Mg)의 충방전 및 순환전위전류 특성 (The Electrochemical Characterization of$LiMn_{2-y}M_yO_4$ Cathode Material - II. Charge and Discharge Property and Cyclic Voltametry of $LiMn_{2-y}M_yO_4$ (M=Zn, Mg))

  • 정인성;김종욱;구할본;김형곤;손명모;박복기
    • 한국전기전자재료학회논문지
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    • 제14권4호
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    • pp.316-322
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    • 2001
  • Cathode materials $LiMn_{2-y}$$M_{y}$ $O_4$(M=Zn and Mg) were obtained by reacting the mixture of LiOH.$H_2O$, Mn $O_2$ and MgO ar ZnO at 80$0^{\circ}C$ for 36h in an air atmosphere. These materials showed an extended cycle life in lithium-anode cells working at room temperatue in a 3.0 to 4.3V potential window. Among these materials, LiM $n_{1.9}$M $g_{0.1}$ $O_4$ showed the best cycle performance in terms of the capacity and cycle life. The discharge capacities of the cathode for the Li/LiM $n_{1.9}$ $M_{0.1}$ $O_4$ cell at the 1st cycle and at the 70th cycle were about 120 and 105mAh/g, respectively. This cell capacity is retained by 88% after 70th cycle. In cyclic voltammetry measurement, all cells revealed tow oxidation peaks and reduction peaks. However, Li/$LiMn_{2-y}$$M_{y}$ $O_4$ cell substituted with Zn and Mg showed new reaction peak during reduction reaction.eaction.ion.ion.

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CA저장 사과를 이용한 Fresh-cut Apple의 제조 및 MAP저장 (Processing and MAP(modified atmosphere packaging) Storage of Fresh-cut Apples using CA Stored Apples)

  • 정헌식;문광덕;최종욱
    • 한국식품저장유통학회지
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    • 제6권4호
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    • pp.351-356
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    • 1999
  • CA 저장 사과로 제조한 신선절단 사과의 비타민 C 강화와 품질유지기간을 연장하기 위한 방법을 개발하기 위한 일환으로 신선절단 사과를 10% L-ascorbic acid 용액에 침지처리하고 0.03 mm LDPE, 0.04 mm PP 및 0.08 mm Nylon/PE(질소치환) 필름으로 포장하여 1$0^{\circ}C$에서 저장하면서 포장내 기체농도와 품질변화를 조사하였다. 저장 중 포장내 산소는 Nylon/PE 포장구에서 가장 낮게 l~3%로 유지되었고 다음으로 PP, LDPE 포장구 순이었다. 저장초기 포장내 에틸렌 농도의 증가속도는 Nylon/PE 포장구에서 가장 낮았다. 신선절단 사과의 비타민 C 함량은 241mg/100g으로 강화되었으며, 저장 중에는 저산소 조성 포장조건일수록 ascorbic acid 산화를 억제시켜서 Nylon/PE 포장구에서 가장 높게 유지되었다. 절단사과에서 갈변은 저산소 조성 포장조건일수록 억제하는 경향이었으며 LDPE, PP 및 무포장 절단사과는 저장 6일 후부터 발생되었으나 Nylon/PE 포장 절단사과는 저장 14일 후까지도 발생되지 않았다. 절단사과에서 부패와 이취는 LDPE, PP 및 무포장에서는 저장 9일 후에 인지되었으나 Nylon/PE 포장에서는 저장 14일 후까지도 인지되지 않았다. 이상의 결과에서 볼 때 장기간 CA 저장한 사과로 비타민 C 함량이 강화된 신선절단 사과의 제조가 가능하였고 이의 품질유지에 적합한 포장조건은 산소투과도가 낮은 포장재와 산소 제거 후 밀봉하는 것으로 나타났다.

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