• 대한수학회지
• /
• 제46권4호
• /
• pp.675-689
• /
• 2009

As a sequel to the papers [2, 3], we will complete our identification of the groups of units of the finite local rings $\mathbb{Z}_4$[X]/($X^k$ + 2t(X), $2X^{\gamma}$) which is the most general type of finite local rings with a single nilpotent generator over $\mathbb{Z}_4$.

• 대한수학회지
• /
• 제46권2호
• /
• pp.313-325
• /
• 2009

We consider zero-divisor graphs with respect to primal, nonprimal, weakly prime and weakly primal ideals of a commutative ring R with non-zero identity. We investigate the interplay between the ringtheoretic properties of R and the graph-theoretic properties of ${\Gamma}_I(R)$ for some ideal I of R. Also we show that the zero-divisor graph with respect to primal ideals commutes by localization.

• 대한약학회:학술대회논문집
• /
• 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2-2
• /
• pp.158.1-158.1
• /
• 2003

We report here the results on N-acetyl-N"-methylamide of oxazolidine (Ac-Oxa-NHMe) calculated using the ab initio molecular orbital method with the self-consistent reaction field (SCRF) theory at the HF level of theory with the 6-31 +G(d) basis set. The displacement of the $\gamma$-$CH_2$ group in proline ring by oxygen atom has affected the structure of proline, cis-trans equilibrium, and rotational barrier. The up-puckered structure is found to be prevalent for the trans conformers of the Oxa amide. (omitted)

• Journal of Radiation Protection and Research
• /
• 제17권1호
• /
• pp.21-30
• /
• 1992

KCCH cyclotron neutron(30cCy/min) 및 $^{60}Co\;{\gamma}-ray(210cGy/min)$를 시험관내의 정상인체 말초혈액임파구에 조사하여 염색체이상(dicentric 및 centric ring)을 관찰하고 이의 선량-반응관계식을 linear model$(Y=K_1D+a)$, power-law model$(Y=K_2D^n)$, quadratic model$(Y=K_3D^2)$ 및 linear-quadratic model$(Y={\alpha}D+{\beta}D^2)$을 사용하여 구하고 이들 model중 염색체이상의 측정치와 가장 일치하는 관계식을 근거로 하여 ${\gamma}-ray$에 대한 neutron의 relative biological effectiveness (RBE)를 산출하였다. 염색체 이상(dicentric plus centric ring)의 발생분포는 ${\gamma}-ray$의 경우 linear model(P=0.067)을 제외한 power-law model$[Y=(5.81{\pm}1.96){\times}10^6D^{1.93+0.06},\;P=0.931]$, quadratic model$[Y=(3.91{\pm}0.09){\times}10^{-6}D^2,\;P=0.972]$ 및 linear-quadratic model $[Y=(6.55{\pm}6.83){\times}10^{-5}D+(3.72{\pm}0.22){\times}10^{-6}D^2$ P=0.922]에 적합하였다 neutron의 경우 linear model $(Y=(6.12{\pm}0.17){\times}10^{-3}\;D-0.22,\;P=0.987]$에 가장 일치하였고 quadratic model (P<0.005)을 제외한 power-law model $[Y=(5.36{\pm}3.02) {\times}10^{-4}D^{1.42+0.11},\;P=0.601]$ 및 linear-quadratic model $[Y=(2.43{\pm}0.70){\times}10^{-3}D+(1.21{\pm}0.39){\times}10^{-7}D^2,\;P=0.415]$에 비교적 적합하였다. 세포당 0.1-1.5개의 염색체이상을 나타내는 neutron의 ${\gamma}-ray$에 대한 RBE는 $2.714{\pm}0.408$이었다.

• Journal of Photoscience
• /
• 제10권1호
• /
• pp.9-20
• /
• 2003

Recent studies on the photoreactivity of l,4-unsaturated systems have changed some ideas that were firmly established in this area of research for many years. Thus, we have described the first examples of 2-aza-di-$\pi$-methane (2-ADPM) rearrangements promoted by triplet-sensitization and by single electron transfer (SET) using electron-acceptor sensitizers. These reactions afford N-vinylaziridine and cyclopropylimine photoproducts in the first examples of di-$\pi$-methane processes that yield three-membered ring heterocycles. l-Aza-1,4-dienes also undergo SET-promoted l-aza-di-$\pi$-methane (l-ADPM) rearrangements via radical-cation intermediates using electron acceptor sensitizers. In some cases, alternative cyclizations yielding different carbocycles and heterocycles have been observed. The l-ADPM and di-$\pi$-methane (DPM) reactions also occur via radical-anion intermediates on irradiation using electron donor sensitizers. On the other hand, the photoreactivity reported for $\beta$,${\gamma}$-unsaturated aldehydes for many years was decarbonylation to the corresponding alkenes. However, our studies demonstrate that these compounds undergo the oxa-di-$\pi$-methane (ODPM) rearrangement with high chemical and quantum efficiency. A comparison of the photochemical reactivity of $\beta$,${\gamma}$-unsaturated aldehydes and corresponding methyl ketones has shown that the ketones do not undergo the ODPM rearrangement while the corresponding aldehydes are reactive by this pathway. Monosubstituted $\beta$,${\gamma}$-unsaturated aldehydes at C-2 undergo the ODPM rearrangement yielding the corresponding cyclopropane carbaldehydes diastereoselectively. Finally, we have described the first examples of reactions, similar to the well know Norrish Type I process, which take place in the triplet excited state of $\beta$,${\gamma}$-unsaturated carbonyl compounds by excitation of the C-C double bond instead of the carbonyl group.

• 한국작물학회지
• /
• 제53권spc호
• /
• pp.115-120
• /
• 2008

비타민 vitamin E 구성 성분으로 항산화, 항암, 고지혈증 개선 등 다양한 생리활성을 나타내는 tocotrienol이 국내산 차조기에서 보고된 바, 존재 여부 확인을 위하여 국내수집 6종, 일본수집 8종 등 총 14종의 차조기 유전자원과 들깨 종실을 대상으로 HPLC 및 GC, GC/MS 비교 분석을 수행 하였으며 그 결과는 다음과 같다. 1. 순상의 HPLC 이용시 차조기에서 4종의 tocopherol 및 ${\beta}-tocotrienol$, ${\gamma}-tocotrienol$과 매우 유사한 머무름 시간의 발견되었다. 2. 그러나 동일 시료를 GC로 재분석한 결과 13개 차조기 유전자원에서 모두 4종의 tocotrienol과 일치하는 물질은 발견되지 않았다. 3. GC 이용시 ${\delta}-tocotrienol$ 및 ${\gamma}-tocotrienol$과 유사한 머무름 시간의 peak가 검출되었으나 GC/MS를 이용하여 확인한 결과 tocotrienol이 아닌 것으로 확인되었다. 4. 이상의 HPLC 및 GC 비교분석결과에 기초할 때, 차조기에는 tocotrienol류의 vitamin E는 존재하지 않는 것으로 추정되었으며 GC를 이용한 vitamin E isomer 분석이 HPLC 이용시 발생가능한 유사 머무름시간대 물질을 tocotrienol로 판단하는 오류 방지에 효과적임을 알 수 있었다.

• 천문학회지
• /
• 제50권6호
• /
• pp.167-178
• /
• 2017

We present a study of the inexplicit connection between radio jet activity and ${\gamma}$-ray emission of BL Lacertae (BL Lac; 2200+420). We analyze the long-term millimeter activity of BL Lac via interferometric observations with the Korean VLBI Network (KVN) obtained at 22, 43, 86, and 129 GHz simultaneously over three years (from January 2013 to March 2016); during this time, two ${\gamma}$-ray outbursts (in November 2013 and March 2015) can be seen in ${\gamma}$-ray light curves obtained from Fermi observations. The KVN radio core is optically thick at least up to 86 GHz; there is indication that it might be optically thin at higher frequencies. To first order, the radio light curves decay exponentially over the time span covered by our observations, with decay timescales of $411{\pm}85$ days, $352{\pm}79$ days, $310{\pm}57$ days, and $283{\pm}55$ days at 22, 43, 86, and 129 GHz, respectively. Assuming synchrotron cooling, a cooling time of around one year is consistent with magnetic field strengths $B{\sim}2{\mu}T$ and electron Lorentz factors ${\gamma}$ ~ 10 000. Taking into account that our formal measurement errors include intrinsic variability and thus over-estimate the statistical uncertainties, we find that the decay timescale ${\tau}$ scales with frequency ${\nu}$ like ${\tau}{\propto}{\nu}^{-0.2}$. This relation is much shallower than the one expected from opacity effects (core shift), but in agreement with the (sub-)mm radio core being a standing recollimation shock. We do not find convincing radio flux counterparts to the ${\gamma}$-ray outbursts. The spectral evolution is consistent with the 'generalized shock model' of Valtaoja et al. (1992). A temporary increase in the core opacity and the emergence of a knot around the time of the second ${\gamma}$-ray event indicate that this ${\gamma}$-ray outburst might be an 'orphan' flare powered by the 'ring of fire' mechanism.

• Asian Journal of Atmospheric Environment
• /
• 제4권2호
• /
• pp.63-71
• /
• 2010

The removal characteristics for aromatic and aliphatic VOCs by electron beam (EB) were discussed in terms of several removal variables such as initial VOC concentration, absorbed dose, background gas, moisture content, reactor material and inlet temperature. It was reviewed that only reactor material was an independent variable among the potential control factors concerned. It was also suggested that main mechanism by EB should be radical reaction for the VOC removal rather than that by primary electrons. It was discussed that the removal efficiency of benzene was lower than that of hexane due to a closed benzene ring. In the case of aromatic VOCs, it was observed that the decomposition of the VOCs with more functional groups attached on the benzene ring was much easier than those with less ones. As for aliphatic VOCs, it was also implied that the longer carbon chain was, the higher the removal efficiency became. An EB-catalyst hybrid system was discussed as an alternative way to remove VOCs more effectively than EB-only system due to much less by-products. This hybrid included supporting materials such as cordierite, Y-zeolite, and $\gamma$-alumina.

• 통합자연과학논문집
• /
• 제8권3호
• /
• pp.192-203
• /
• 2015

In view of the growing medicinal importance of pyrazole and its derivatives, the single crystal X-ray diffraction study was carried out for the potential active 2-Benzyl-3-[3-(4-bromo-phenyl)-1-phenyl-1H-pyrazol-4yl]-4,6-dioxo-5-phenyl-octahydro-pyrrolo[3,4-C]pyrrole-1-carboxylic acid ethyl ester ($C_{37}H_{31}BrN_4O_4$, H2O). In the title compound are two molecules exist in the asymmetric unit. It crystallizes in the monoclinic space group $P{\hat{i}}$ with unit cell dimension $a=13.361(18){\AA}$, $b=13.424(17){\AA}$ and $c=21.649(2){\AA}$ [${\alpha}=80.745(9)^{\circ}$, ${\beta}=79.770(10)^{\circ}$ and ${\gamma}=60.788(6)^{\circ}$]. The pyrazole ring adopts planar conformation. The sum of the bond angles at nitrogen atom of the pyrazole ring indicates the $Sp^2$ hybridized state. The crystal structure is stabilized by intramolecular C-H...O hydrogen bond interaction.

• Bulletin of the Korean Chemical Society
• /
• 제23권11호
• /
• pp.1527-1530
• /
• 2002

1,12-diazacyclodocosane-2,11-dione was first isolated from a plant Phyllanthus niruri Linn. Its structure has been determined by means of spectroscopy methods and X-ray crystallography. Two peptide groups in the big ring (lactam) are the main factors influencing intermolecular contacts. The hydrogen-bond interaction of these hydrophilic groups is observed in the crystal structure. Meanwhile, C-H···O hydrogen bonds in molecules contribute to the formation of the whole crystal. These two kinds of hydrogen-bond form six- member rings among molecules. This compound crystallizes in the triclinic space group P-1 with a= 9.588(1) $\AA$, b= $9.850(1)\AA$, c = $11.810(1)\AA$, $\alpha=$ 68.18(1)$^{\circ}C$ , $\beta=$ 84.98(1), $\gamma$ = 86.03(1)$^{\circ}C$ , V = $1030.66(17)\AA3$ , Z = 2. A disorder of five-member carbon chain in the whole ring is observed in the title compound. The bond angle 105.8(4) is determined for a extreme configuration C(14)-C(15)-C(16), and 117.7(10) for another extreme configuration C(14')-C(15')-C(16'). In this crystal, two molecules are tied each other by short intermolecular hydrogen bonds, the oxygen atom being tied by hydrogen bond to nitrogen atom of another two molecules. The NMR and IR spectral data coincides to the structure of the compound.