• Bulletin of the Korean Chemical Society
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• 제32권4호
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• pp.1228-1230
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• 2011

A new amine receptor 2 utilizing anthracene and nitrophenyl group as signaling group was designed and synthesized. The receptor 2 only utilizes four amine N-H's and 9-anthracenyl hydrogen to bind anions. The receptor 2 can bind anions through hydrogen bonds with a selectivity of $CH_3CO_2^-$ > $H_2PO_4^-$ > $F^-$ > $C_6H_5CO_2^-$ > $Cl^-$ in highly polar solvent such as DMSO without protonation of amine.

• 한국동물학회지
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• 제4권1호
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• pp.7-12
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• 1961

1) Respiratory metabolism patterns and its enzyme systems in the gill tissue of the fresh water mussels, Cristaria plicata were investigated through the examination on the effects of respiratory enzyme inhibitors, (KCN, NAF) and succinoxidase assay, while studying the effects of neutral salts (NaCL, KCL, CaCl2) and pH on oxygen consumption of the gill tissue. 2) In the limited concentration of KCL (0.3mM) and NaCl (0.4mM) solutions, oxygen consumption of the intact gill tissue was accelerated, but in CaCl2(0.5mM) solution, it showed no significant effect. The oxygen consumption was gradually decreased at the above concentrations of these limitations. The optimum pH for the respiration of the gill was 7.3. 3)Cyanide in 10-8M solution inhibited 88.8% of the respiration of the intact gill tissue. Methylene blue accelerated the respiration of the noral gill tissue, and slightly but significantly reversed the cyaniide poisoned respiration. 4)Oxygen consumption of the gill homogenate was apparently increased by the mixed addition of succinate, cytochrome c and activators (AlCl3 and CaCl2). This results suggested that succinoxidase system acts on the respiratory pattern of the gil tissue. 5) It was able to recognize that the enolase, which acts on the anaerobic glycolytic system, participated in the tissue respiration of the gill for NaF in 5$\times$10-2 M solution inhibited 55.5% of the respiration of the same intact tissue.

• Bulletin of the Korean Chemical Society
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• 제27권5호
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• pp.759-761
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• 2006

The compound B(C6F5)3 and its variations have been widely employed as alkyl carbanion abstracting reagents to produce metallocene cations for olefin polymerization.1-3 Weakly coordinating anions containing boron can greatly improve the activity of metallocene catalysts used in industrial olefin polymerization4 and thus group IV and V metallocene complexes of the organohydroborate anions have been intensively investigated.5 Recently, many organohydroborate metallocene complexes have been reported by Shore and co-workers.6-8 A common structural feature of those complexes is the three-center two electron M-H-B bond, like that observed in transition metal tetrahydroborate complexes but the reactivity and fluxional behavior of organohydroborate complexes are unlike those of the tetrahydroborate analogues.6 Although many of those metallocenes have been synthesized, few complexes could be used in the olefin polymerization and then this laboratory has been involved in the chemistry of the cyclic organohydroborate anions, and their group IV metallocene derivatives for the catalyst.9 Described here is recent work that led to the preparation of a novel cyclic organohydroborate hafnocene complex (h5-C5H5)2Hf ？(μ-H)2BC8H14 ,Cl. The hafnocene complex contains the three-center two electron bond Hf-H-B10 in which the hydride abstraction for olefin polymerization may occur.

• 대한전기학회:학술대회논문집
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• 대한전기학회 1999년도 추계학술대회 논문집 학회본부 C
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• pp.848-850
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• 1999

In this study, PZT etching was performed using planar inductively coupled Ar(20)/$Cl_2/BCl_3$ plasma, The etch rate of PZT film was 2450 $\AA/min$ at Ar(20)/$BCl_3$(80) gas mixing ratio and substrate temperature of $80^{\circ}C$. X-ray photoelectron spectroscopy (XPS) analysis for film composition was utilized. The chemical bond of PbO is broken by ion bombardment, and the peak of metal Pb in a Pb 4f peak begins to appear upon etching, decreasing Pb content faster than Zr and Ti. As increase content of additive $BCl_3$, the relative content of oxygen decreases rapidly. We thought that abundant Band BCl radicals made volatile oxy-compound such as $B_{x}O_{y}$ and/or $BClO_x$ bond. To understand etching mechanism, Langmuir probe and optical emission spectroscopy (OES) analysis were utilized for plasma diagnostic.

• Bulletin of the Korean Chemical Society
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• 제34권12호
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• pp.3690-3694
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• 2013

The $H_2Ge=Ge:$ and its derivatives ($X_2Ge=Ge:$, X = H, Me, F, Cl, Br, Ph, Ar${\ldots}{\ldots}$) is a new species. Its cycloaddition reactions is a new area for the study of germylene chemistry. The mechanism of the cycloaddition reaction between singlet state Cl2Ge=Ge: and formaldehyde has been investigated with CCSD(T)//MP2/$6-31G^*$ method. From the potential energy profile, it could be predicted that the reaction has only one dominant reaction pathway. The reaction rule presented is that the two reactants first form a fourmembered Ge-heterocyclic ring germylene through the [2+2] cycloaddition reaction. Because of the 4p unoccupied orbital of Ge: atom in the four-membered Ge-heterocyclic ring germylene and the ${\pi}$ orbital of formaldehyde forming a ${\pi}{\rightarrow}p$ donor-acceptor bond, the four-membered Ge-heterocyclic ring germylene further combines with formaldehyde to form an intermediate. Because the Ge: atom in intermediate hybridizes to an $sp^3$ hybrid orbital after transition state, then, intermediate isomerizes to a spiro-Ge-heterocyclic ring compound via a transition state. The research result indicates the laws of cycloaddition reaction between $H_2Ge=Ge:$ and formaldehyde, and laid the theory foundation of the cycloaddition reaction between $H_2Ge=Ge:$ and its derivatives ($X_2Ge=Ge:$, X = H, Me, F, Cl, Br, Ph, Ar${\ldots}{\ldots}$) and asymmetric ${\pi}$-bonded compounds, which is significant for the synthesis of small-ring and spiro-Ge-heterocyclic compounds. The study extends research area and enriches the research content of germylene chemistry.

• 한국육종학회지
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• 제41권3호
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• pp.236-243
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• 2009

벼멸구 저항성 유전자의 mapping, 벼멸구 저항성 관련 QTL 분석, 주요 농업형질과 벼멸구 저항성과의 관계 분석 등에 관한 연구를 수행 하여 얻은 결과는 다음과 같다. 벼멸구 저항성을 가진 통일형 벼인 '삼강'과 자포니카형 벼인 '낙동'을 교배하여 양성된 $F_1$의 약을 배양하여 육성된 120 DH 계통을 유전자 지도 작성을 위한 mapping 재료로 이용 하였다. Maker 검정에서 양친에 다양성을 나타낸 SSR 73, STS 89개 등 총 162개의 marker를 이용하여 전체 길이가 1,884 cM이고 평균 marker간 거리가 11.6 cM인 연관지도를 작성하였다. 유전자지도 작성에 이용된 120 DH 계통에 대한 벼멸구 저항성 정도를 조사하여 저항성 관련 QTL을 분석한 바, 3번, 6번, 7번, 8번 그리고 12번 염색체에서 1개씩 총 5개의 QTL을 확인하고 이들을 qBPR3, qBPR6, qBPR7, qBPR8, qBPR12로 명명하였다. 간장, 수장, 수수 및 출수일수에 대한 QTL을 분석하여, 총8개의 QTL이 7개의 염색체에 위치하는 것으로 확인되었다. 벼멸구 저항성과 주요 농업형질관련 QTL과의 연관관계를 분석한 바, 3번 염색체 상의 벼멸구 저항성 QTL(qBPR3)이 간장 및 수수 관련 QTL(qCL3, qNP6)과 연관되어 있었으며, 7번 염색체 상의 qBPR7은 분상질립 관련 QTL qPGC7.1과 qPWBP7.2과 그리고 8번 염색체상의 벼멸구 저항성 QTL 역시 간장관련 QTL(qCL8)과 연관되어 있는 것으로 나타났다.

• 한국식품영양과학회지
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• 제42권9호
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• pp.1518-1523
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• 2013

적양배추싹의 저장온도에 따른 미생물학적 유통기한을 예측하기 위해서, 적양배추싹을 polyolefin film과 PA/PA/PE film에 각각 포장 후 4와 $10^{\circ}C$에 저장하여 저장기간 중 총호기성균 수를 측정하였다. 측정된 data를 Gompertz's model 식을 이용하여 최대성장속도와 유도기를 구하였고, shelf life 예측모델 식으로부터 계산된 적양배추싹의 shelf life는 polyolefin film과 PA/PA/PE film에 포장 후 $10^{\circ}C$에 저장된 시료가 각각 19.7과 22.6시간인 반면, $4^{\circ}C$에 저장된 시료는 49.4와 52.3시간으로 나타났다. 성장예측모델 식의 적합성 평가를 위해 $A_f$, $B_f$, MSE 값을 산출한 결과, 예측모델 식의 적합성이 뛰어났다. 한편, aqueous $10^{\circ}C$/fumaric acid와 UV-C 병합처리 된 적양배추싹 시료의 shlef life는 7일 이상으로 예측되었다. 따라서 aqueous $10^{\circ}C$/fumaric acid와 UV-C 병합처리 후 저온저장은 적양배추싹의 shelf life 연장에 효과적인 것으로 판단된다.

• 열처리공학회지
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• 제13권4호
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• pp.217-223
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• 2000

The boronizing effects of STD 61 steel have been studied on the micro structure and hardness. The STD 61 Steel was soaked in molten salt, consisted of KCl, $BaCl_2$, NaF, $B_2O_3$, FeB, and Ce, at various temperatures and times. The boronizing conditions for the peak hardness were the temperature range of $900^{\circ}C$ to $950^{\circ}C$ for 5 hr and that of $1000^{\circ}C$ for 3 hr, respectively. Four boride layers such as FeB, $Fe_2B$, ${\alpha}$ and matrix layer surface were observed from the microscopic surface examination. The thickness of boride layer was increased by increasing the boronizing time and the temperature. The structure of boride layer was tooth shape.

• 대한화학회지
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• 제30권5호
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• pp.441-448
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• 1986

몰리브덴산암모늄 수용액에서 적절한 살리실알데히드의 메탄올 혼합용액으로부터 디옥소비스(치환-살리실알데히다토) 몰리브덴늄(VI), $MoO_2(X-sal)_2(X=H,\;5-CH_3)$착물을 합성하고, 이들 각각의 화합물과 다양한 일차아민의 반응에 의하여 디옥소비스(치환-살리실알디미나토) 몰리브덴늄(VI)착물, $MoO_2(X-sal-N-R)_2,\;(R=C_6H_5,\;p-F-C_6H_4,\;m-Cl-C_6H_4,\;p-I-C_6H_4$ 및 $p-C_2H_5-C_6H_4)$을 합성하였다. 이들 착물은 모두 $900{\sim}940cm^{-1}$ 부근에서 ${\upsilon}_{Mo}=0$에 기인한 두 개의 강한 흡수띠가 관찰되었고, 핵자기공명스펙트럼에서 N=CH양성자에 대한 한 개의 시그날이 8.9ppm부근에서 나타났다. 이는 이들 착물이 $cis-MoO_2$기를 가진 6배위팔면체 착물임을 나타낸다. 질량분석의 결과로부터, $MoO_2$ : ligand의 결합비가 1:2임을 확인하였고, $MoO_2(5-CH_3-sal-N-R)_2$착물에 대한 분해과정을 조사하였다. 전자흡수스펙트럼에서 $N{\to}Mo$와 $O{\to}Mo$에 해당하는 전하이동전이는 $29,000cm^{-1}$과 $32,000cm^[-1}$부근에서 각각 일어났다. 한편, 디메틸포름아미드에서 측정한 이들 착물에 대한 몰전도도로부터 이들 착물이 비이온성 물질임을 확인하였다.

• Corrosion Science and Technology
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• 제2권5호
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• pp.212-218
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• 2003

Electronic properties of passive films formed on Ti at film formation potentials $(E_f)V_{SCE}$ in pH 8.5 buffer solution and in an artificial seawater were examined through the photocurrent measurement and Mott-Schottky analysis. The passive films formed on Ti in pH 8.5 buffer solution exhibited a n-type semiconductor with a band gap energys $(E_g);E_g^{n=2}=3.4$ eV for nondirect electron transition, and $E_g^{n=0.5}=3.7$ eV for direct electron transition. These band gap values were almost same as those for the passive films formed in artificial seawater, indicating that chloride ion ($Cl^-$ in solution did not affect the electronic structure of the passive film on Ti. $E_g$ for passive films formed on Ti were found to be greater than those ($E_g^{n=0.5}=3.1$ eV, $E_g^{n=2}=3.4$) for a thermal oxide film formed on Ti in air at $400^{\circ}C$. The disorder energy of passive film, determined from the absorption tail of photocurrent spectrum, was much greater than that for the thermal oxide film farmed on Ti in air at $400^{\circ}C$. The greater $E_g$ and the higher disorder energy for the passive film compared with those for the thermal oxide fIlm suggest that the passive film on Ti exhibited more disorded structure than the thermal oxide film. The donor density (about $2.4{\times}10^{20}cm^{-3}$) for the passive film formed in artificial seawater was greater than that (about $20{\times}10^{20}cm^{-3}$) formed in pH 8.5 buffer solution, indicating that $Cl^-$ increased the donor density for the passive film on Ti.