• 제목/요약/키워드: Coordination chemistry

검색결과 365건 처리시간 0.031초

바나듐 (v)-아미노폴리카르본산 착물의 탄소-13 및 바나듐-51 핵자기공명연구 (제1보) (Carbon-13 and Vanadium-51 Nuclear Magnetic Resonance Studies of Vanadium(v)-Aminopolycarboxylic Acids (Ⅰ))

  • 이만호;오대섭
    • 대한화학회지
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    • 제27권2호
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    • pp.117-126
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    • 1983
  • 탄소-13 및 바나듐-51 핵자기공명분광법을 이용하여 아미노폴리카르본산-바나듐(v) 착물의 용액 내에서의 구조에 대해 연구하였다. 이 때 사용한 리간드는 ethylenediaminetetraacetic acid (EDTA), trans-cyclohexanediaminetetraacetic acid (CDTA), 1,2-propylenediaminetetraacetic acid (PDTA), ethylenediaminediacetic acid (EDDA), 2-hydroxyethylethylenediaminetriacetic acid (HEDTA), diethylenetriaminepentacetic acid (DPTA), nitrilotriacetic acid (NTA) 등이었다. 모든 리간드는 바나듐(Ⅴ)과 시스-VO2핵을 함유하는 정8면체 구조의 1:1 착물을 생성하였다. 바나듐(V)과 시스-$VO_2$ 핵을 함유하는 정8면체 구조의 1:1 착물을 생성하였다. 바나듐(V)에 대한 히드록시에틸기의 배위는 아세테이트기의 배위에 비해 덜 바람직함을 알 수 있었다. 그리고 EDDA 및 PDTA는 각각 2가지의 이성체착물들을 생성함을 알 수 있었다.

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[1,2-Bis(diphenylphosphino)ethane](nitrato)(trifluoromethylsulfonato)platinum(II)의 합성 및 구조: [Pt(dppe)($NO_3$)($CF_3SO_3$)] (Preparation and Structure of [1,2-Bis(diphenylphosphino)ethane](nitrato)(trifluoromethylsulfonato)platinum(II): [Pt(dppe)($NO_3$)($CF_3SO_3$)])

  • 허현수;이순원
    • 한국결정학회지
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    • 제19권1호
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    • pp.21-24
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    • 2008
  • [[Pt(dppe)$Cl_2]$]와 1 당량 $AgNO_3$ 및 1 당량 AgOTf (OTf=$CF_3SO_3$)의 순차적 반응으로 표제 착물 [Pt(dppe)($NO_3$)($CF_3SO_3$)] (dppe=1,2-bis(diphenylphosphino)ethane, $Ph_2PCH_2CH_2PH_2$)이 합성되었다. Pt 금속은 dppe 리간드의 두 P 원자, nitrato ($NO^-_3$) 리간드의 O 원자, 그리고 triflato (trifluoromethylsulfonato, $OTf^-$) 리간드의 O 원자로 배위되어 있다. Pt 금속의 배위권은 일그러진 평면 사각형으로 기술될 수 있다.

NMR Studies of Ni-binding Luteinizing Hormone Releasing Hormone

  • Kim, Jin;Won, Ho-Shik
    • 한국자기공명학회논문지
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    • 제13권2호
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    • pp.143-153
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    • 2009
  • Luteinizing Hormone Releasing Hormone (LHRH) is composed of 10 amino acids, and is best known as a neurotransmitter. Because of the 80% homology in animals, much more concerns have focused on the substances that have similar functions or can control LHRH. Ni, Cu-LHRH complexes were synthesized. The degree of complexation was monitored by $^1H,\;^{13}C$-NMR chemical shifts, and final products were identified by ESI-Mass spectrum. Solution-state structure determination of Ni-LHRH complex was accomplished by using NMR results and NMR-based distance geometry (DG). Interproton distances from nuclear Overhauser effect spectroscopy (NOESY) were utilized for the molecular structure determination. Results were compared with previous structures obtained from energy minimization and other spectroscopic methods. Structure obtained in this study has a cyclic conformation which is similar to that of energy minimized, and exhibits a specific a-helical turn with residue numbers (2~7) out of 10 amino acids. Comparison of chemical shifts and EPR studies of Ni, Cu-LHRH complexes exhibit that Ni-LHRH complex has same binding sites with the 4-coordination mode as in Zn-LHRH complex.

Crystallographic Evidence for the Reduction of CO in Partially Dehydrated Silver Zeolite A

  • Kim, Yang;Song, Seong-Hwan;Seff, Karl
    • Bulletin of the Korean Chemical Society
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    • 제10권3호
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    • pp.230-234
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    • 1989
  • The crystal structure of $Ag^+$-exchanged zeolite A vacuum-dehydrated at $370^{\circ}C$ and then treated with carbon monoxide at $$23^{\circ}C$ has been determined by single crystal x-ray diffraction methods in the cubic space group Pm3m at $23^(1){\circ}C$ ; a = 12.116 (2)${\AA}$. The structure was refined to the final error indices $R_1\;=\;0.061\;and\;R_2$(weighted) = 0.068 using 349 independent reflections for which I > 3${\sigma}(I).\;3.6\;Ag_+-CO$ complexes, where -CO may represent -CHO or -$CH_2OH$, were found in each large cavity. By coordination to silver atoms followed by reaction with $Ag^{\circ}and\;H^+$ within the zeolite, carbon monoxide has been partially reduced. In about 28% of the sodalite units, a $Ag_6(Ag^+)_2$ cluster may be present. In about 37% of the sodalite units, three $Ag^+$ ions are found on threefold axes where they may be bridged by three water molecules. The remaining 35% of the sodalite units are empty of silver species. Two $Ag^+$ ions per unit cell are associated with 8-ring oxygens. The remaining ca $$3Ag^+$ ions per unit cell have been reduced during the synthesis and have migrated to form small silver crystallities on the surface of the zeolite single crystal.

Two Crystal Structures of Dehydrated Fully $Ca^{2+}$-Exchanged Zeolte A Reacting with Rubidium Vapor

  • Song, Seong-Hwan;Kim, Yang
    • Bulletin of the Korean Chemical Society
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    • 제14권2호
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    • pp.258-262
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    • 1993
  • Two single crystals of fully dehydrated $Rb^+$ -exchanged zeolite A have been prepared by the reduction of all $Ca^{2+}$ ions in dehydrated $Ca_6$-A by rubidium vapor. Their structures were determined by single crystal X-ray diffraction methods in the cubic space group Pm3m (a=12.160(2) $^{\AA}$ and 12.166(2) $^{\AA}$) at 22(1)$^{\circ}$C. In these structures, 12.4(2) to 13.3(2) Rb species are found per unit cell, more than 12 Rb$^+$ ions needed to balance the anionic charge of the zeolite framework, indicating that the sorption $Rb^0$ has occurred. In each structure, three $Rb^+$ ions per unit cell are located at the centers of the 8-rings. Six to eight $Rb^+$ ions are found opposite the 6-rings on threefold axes, and three $Rb^+$ ions are found in a sodalite unit. About 0.5 $Rb^+$ ion lies opposite a 4-ring. The structural analysis indicates the presence of a triangular rubidium cluster in the sodalite cavities. The triangular rubidium clusters may be stabilized by the coordination to two and/or three rubidium ions in the large cavity. Therefore, this cluster may be viewed as $(Rb_5)^{4+}$ and/or $(Rb_6)^{4+}$.

Effect of different types of biochar on the growth of Chinese cabbage (Brassica chinensis)

  • Lee, Jae-Han;Seong, Chang-Jun;Kang, Seong-Soo;Lee, Ho-Cheol;Kim, Soo-Hun;Lim, Ji-Sun;Kim, Jae-Hong;Yoo, Joun-Hyuk;Park, Jung-Hyun;Oh, Taek-Keun
    • 농업과학연구
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    • 제45권2호
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    • pp.197-203
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    • 2018
  • Biochar is the carbon solid produced through the pyrolysis of a biomass from organic sources such as agricultural waste, animal manure, and sludge under limited or anaerobic conditions. Biochar has the effect of reducing greenhouse gases through the carbon sequestration method; additionally, biochar is known to function as a soil amendment. This experiment was conducted to evaluate the application of biochar on the growth characteristics of Chinese cabbage at Chungnam National University in Daejeon, Korea. The Chinese cabbage was grown for 50 days in a glasshouse in pots. A pruning branch was used to produce the bead and pellet forms of biochar through pyrolysis. The biochar was added to the soil at 0, 2, and 5% by weight. The Chinese cabbage with the 2% treatment of the bead form of biochar had the highest fresh weight ($149.43{\pm}15.92g\;plant^{-1}$) which was increased by 10% compared to the control ($136.91{\pm}31.46g\;plant^{-1}$). Moreover, for the 5% treatment of the bead form of biochar ($60.91{\pm}9.82g\;plant^{-1}$), the growth decreased by 57% compared to the control. As the content of the bead form of biochar increased, the shoot dry weight, leaf number, leaf length and lead width that appeared decreased. An increase in the total organic matter, Avail. $P_2O_5$, Ex. cation and EC was observed when the biochar content was increased. Our results support the application of 2% biochar in the bead form for increased growth of Chinese cabbage.

The Radial Distribution Functions of the Scaled OSS2 Water

  • Lee, Song Hi
    • 대한화학회지
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    • 제56권6호
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    • pp.669-672
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    • 2012
  • Classical molecular dynamics (MD) simulations using a scaled OSS2 potential originally derived from ab initio calculations are used to study the radial distribution functions of water. The original OSS2 water potential is shown to represent a glassy or an ice at ambient temperature, but the diffusion coefficient increases on increasing the temperature of the system or decreasing the density. This suggests scaling the OSS2 potential. The O-O, O-H, and H-H radial distribution functions and the corresponding coordination numbers for the scaled OSS2 potential, obtained by MD simulation, are in good agreement with the experiment results and calculations for the SPC/E water potential over a range of temperatures.

NMR Studies of Metal-binding Luteinizing Hormone Releasing Hormone

  • Won, Ho-Shik
    • Bulletin of the Korean Chemical Society
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    • 제32권11호
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    • pp.4021-4026
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    • 2011
  • Functions of the luteinizing hormone releasing hormone (LHRH) and its induced release by divalent metal ions have received great attention because this neurotransmitter subsequently regulates the secretion of luteinizing hormone (LH). Metal-LHRH complexes were synthesized by addition of various Cu(II),Ni(II),Zn(II) ions into LHRH in order to understand how the induced release of LHRH is possible. The degree of complexation was monitored by $^1H$, $^{13}C$-NMR chemical shifts, and final products were identified by Mass spectrometry. Solutionstate structure determination of Zn(II)-LHRH out of metal-complexes was accomplished by using NMR and NMR-based distance geometry (DG). Interproton distance information from nuclear Overhauser effect spectroscopy was utilized for structure determination. Structure obtained in this study has a cyclic conformation exhibiting a specific ${\alpha}$-helical turn with residue numbers His[2]-Leu[7] out of 10 amino acids. Comparison of chemical shifts and EPR studies of Ni(II),Cu(II)-LHRH complexes exhibit that these metal complexes have 4-coordination geometry.

알카리성 분위기에서 소석고의 수화에 미치는 카르복실산의 영향 (Effect of Carboxylic Acid on the Hydration of Plaster of Paris under Alkalinity)

  • 이승헌
    • 한국세라믹학회지
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    • 제31권10호
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    • pp.1107-1114
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    • 1994
  • Although various theories have been presented on the mechanism of setting retardation of plaster in addition to organic admixtures. The purpose of this paper is that Hydration studies of plaster of paris in the presence of carboxylic acids under alkalinity are examined in the coordination chemistry. Setting of plaster of paris is retarded by the addition of carboxylic acids except oxalic acid. And setting of plaster of paris contained 5 wt% of Ca(OH)2 is also retarded by the addition of above-mentioned carboxylic acids. The degree of retarding effect under alkalinity is found to be a function of the number of the functional group and the length of carbon chain of carboxyl acids. These reasons are attributed to the soluble complex formation, that is calcium complex formation between calcium ion and carboxylic acids. The author's proposal was confirmed by the results of electrical conductivity measurement. The formation of calcium complex was surpported by IR spectra.

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Coordination of Basic and Development Researches on Vitamins

  • Mitsuda, Hisateru
    • 한국식품과학회지
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    • 제3권3호
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    • pp.193-210
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    • 1971
  • Reviewed biosynthetic pathways in green leaves of thiamine, riboflavin and folate as disclosed by the authors, and the regulatory systems operating on their biosynthesis and biodegradation as revealed since a potent inhibitory activity of ATP was found for the phosphatase reactions in 1965. Physiological roles of ascorbic acid in plant were evidenced by its higher content in green and flower leaves; the content in persimmon leaves for example was found ten or more times of that in citrus fruits. A close relationship existing between basic and development researches was illustrated by examples chosen from the author's researches. Examples cited were as follows; basic researches on vitamins were extended to the creation of thiamine enriched rice, to the growth promotion of rice plant by foliar application of thiamine, and to the use of ascorbic acid to prevent the appearance of beer cloudness; histological and biochemical studies on protein bodies in rice endosperm turned out amino acid enriched rice; techniques acquired in the studies on catalase were successfully employed for the utilization of single cell protein (MIPRON) for human food; conception of hybernation was led up to under-water or under-ground storage of cereal grains.

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