• 천문학회지
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• 제11권1호
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• pp.31-36
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• 1978

Although Serkowski used a single value K=1.15 in representing all the observed interstellar linear polarization curves by his empirical relation $p({\lambda})/P_{max}$=exp (-K $1n^2({\lambda}_{max}/{\lambda})$), where $p_{max}$ is the maximum polarization at wavelength ${\lambda}_{max}$, we have noticed a meaningful variation in K from observations of 72 stars. By comparing K's with $P_{max}/E_{B-V}\;and\;with\;{\lambda}_{max}$, we have examined how the shape of the polarization curve is related with the degree of grain alignment on one hand, and with grain sizes on the other. We have shown that correlations between K, $P_{max}/E_{B-V}\;and\;with\;{\lambda}_{max}$, are consistent with the idea of Davis-Greenstein mechanism for grain alignment.

• Applied Biological Chemistry
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• 제41권5호
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• pp.399-404
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• 1998

우리 나라에서 오랫동안 식용 및 황색 색소원으로 이용되어 온 치자(Gardenia jasminoides)열매로부터 iridoid glycoside인 geniposide를 분리, 정제한 후 ${\beta}-glucosidase$로 가수분해하여 얻은 genipin을 glycine, alanine, histidine, lysine, phenylalanine, glutamate 등 여섯 종류의 아미노산과 반응시켜 수용성 치자청색소로 전환되는 과정을 규명하였다. Genipin이 아미노산과 반응하여 청색소가 되는 과정에서 pH의 영향을 알아보기 위하여 여러 pH에서 반응을 시켜본 결과 청색소 생성의 최적조건은 pH 7.0 이었고, pH 3.0 조건에서는 청색소가 전혀 생성되지 않았으며, pH 12.0 조건에서는 미량의 청색소만 생성되었다. 아미노산의 종류에 따라서도 청색소 생성량 및 색감에 차이가 있었는데 $Iysine({\lambda}_{max}=573\;nm),\;glycine({\lambda}_{max}=595 \;nm),\;phenylalanine({\lambda}_{max}=602\;nm),\;alanine({\lambda}_{max}=595\;nm)$에 비해 $histidine({\lambda}_{max}=601\;nm)$과 $glutamate({\lambda}_{max}=601\;nm)$의 경우에는 비교적 적은 양의 청색소가 생성되었다. 청색소 생성 속도상수를 여러 온도$(60,\;70,\;80,\;90^{\circ}C,\;pH\;7.0\;phosphate$ 완충용액)에서 구하였는데, 염기성 아미노산이 중성 및 산성 아미노산에 비해 생성속도가 빨랐다. 이들 값으로부터 Arrhenius 활성화에너지를 계산한 결과 $glycine(E_A=9.8\;kcal/mol)$이 다른 아미노산$(E_A=13.3{\sim}15.4\;kcal/mol)$에 비해 특히 작은 값의 활성화에너지를 나타내었다.

• 한국수산과학회지
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• 제24권6호
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• pp.397-404
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• 1991

남조류와 crytomonads를 포함한 식물플랑크톤의 일차적 형광특성을 in vivo 상태에서 조사하였다. 형광과 exciatation 스펙트럼을 측정한 견과, 약 580-640 nm 영역에 걸친 형광 스펙트럼이, 조사된 모든 식물플랑크톤으로부터 얻어졌다. 관찰된 형광 스펙트럼의 $\lambda_{max}$ 값은, Synechofoccus sp.(SYN)을 제외하고 모두 유사한 것으로 나타났다 $(\pm3nm)$. 관찰된 형광 스펙트럼의 형광소(fluorophore)를 밝히기 위하여, 식물플랑크톤의 형광 스펙트럼의 세기와 모양, $\lambda_{max}$를 식물플랑크톤에 존재하는 유기화합물의 표준용액의 것과 비교하였다. 식물플랑크톤의 fluorescence $lifetime(\lambda)$과 fluorescence decay curve를 식물플랑크톤에 존재하는 유기화합물의 표준용액의 $\lambda$값과 비교하였다. 580 nm의 형광 파장을 사용하여 얻은 식물플랑크톤의 fluorescence decay는 menoex-ponential과 biexponential decay를 보였으며, 식물플랑크톤의 $\lambda(1.39-1.95ns)$ b-phycoerythrin의 표준용액의 $\lambda(3.23ns)$값보다 현저히 작게 나타났다. 이는 이미 알려진 광합성 능력을 가진 intact cell 내부에서 엽록소 a와 biliprotein간의 효율적인 에너지 전달 체계에 의한 $\lambda$값의 단축으로 여겨지며, 580nm의 형광특성이 biliprotein에 의한 것임을 보여준다.

• 천문학회지
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• 제28권2호
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• pp.245-253
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• 1995

We have analyzed the time series of Ca II H,K and ${\lambda}8498$ line profiles taken for a sunspot (SPO 5007) with the Echelle spectrograph attached to Vacuum Tower Telescope at Sacramento Peak Solar Observatory. Each set of spectra was taken simultaneously for 20 minutes at a time interval of 30 seconds. A total of 40 photographic films for each line was scanned by a PDS at Korea Astronomy Observatory. The central peak intensity of Ca II H ($I_{max}$), the intensity measured at ${\Delta}{\lambda}=-0.1{\AA}$ from the line center of ${\lambda}8498(I_{{\lambda}8489})$, the radial velocity ($V_r$) and the Doppler width (${\Delta}{\lambda}_D$) estimated from Ca II H have been measured to study the dynamical behaviors of the sunspot chromosphere. Fourier analysis has been carried out for these measured quantities. Our main results are as follows: (1) We have confirmed the 3-minute oscillation being dominant throughout the umbra. The period of oscillations jumps from 180 sec in the umbra to 500 to 1000 sec in the penumbra. (2) The nonlinear character of the umbral oscillation is noted from the observed sawtooth shaped radial velocity fluctuations with amplitudes reaching up to $5{\sim}6\;km/sec$. (3) The spatial distribution of the maximum powers shows that the power of oscillations is stronger in the umbra than in the penumbra. (4) The spatial distributions of the time averaged < $I_{max}$ > and < $V_r$ > across the spot are found to be nearly axially symmetric, implying that the physical quantities derived from the line profiles of Ca II H and ${\lambda}8498$ are inherently associated with the geometry of the magnetic field distribution of the spot. (5) The central peaks of the CaII H emission core lead the upward motions of the umbral atmosphere by $90^{\circ}$, while no phase delay is found in intensities between $I_{max}$ and $I_{{\lambda}8498}$, suggesting that the umbral oscillation is of standing waves.

• 대한화학회지
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• 제6권2호
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• pp.170-175
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• 1962

The ultraviolet and visable absorption spectra of trans, cis-azoxybenzene, substituted azoxybenzenes and their conjugate acids have been studied. The 320-350$m{\mu}$ main bands of free-base of azoxybenzenes are due to ${\pi}{\to}{\pi}^{\ast}$ transition. These bands of their conjugate acids shown bathochromic shift into visible range. The following emperical relationship between absorption maxima of the main bands was found. ${\lambda}_{max}={\lambda}^{\circ}_{max}+{\Delta}{\lambda}_x+{\Delta}{\lambda}_y$ This relationship in terms of wave number is also hold in good agreement. ${\nu}={\nu}_{\circ}-({\Delta}{\nu}_x+{\Delta}{\nu}_y)$

• 대한수학회지
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• 제56권4호
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• pp.985-1000
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• 2019

Let k be an integer with $k{\geq}3$. Define $h(k)=[{\frac{k+1}{2}}]$, ${\sigma}(k)={\min}\(2^{h(k)-1},\;{\frac{1}{2}}h(k)(h(k)+1)\)$. Suppose that ${\lambda}_1,{\ldots},{\lambda}_5$ are non-zero real numbers, not all of the same sign, satisfying that ${\frac{{\lambda}_1}{{\lambda}_2}}$ is irrational. Then for any given real number ${\eta}$ and ${\varepsilon}>0$, the inequality $${\mid}{\lambda}_1p^2_1+{\lambda}_2p^2_2+{\lambda}_3p^2_3+{\lambda}_4p^2_4+{\lambda}_5p^k_5+{\eta}{\mid}<({\max_{1{\leq}j{\leq}5}}p_j)^{-{\frac{3}{20{\sigma}(k)}}+{\varepsilon}}$$ has infinitely many solutions in prime variables $p_1,{\ldots},p_5$. This gives an improvement of the recent results.

• 대한화학회지
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• 제54권6호
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• pp.711-716
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• 2010

비닐렌기에 플루오르 치환기를 도입한 새로운 전자발광 (EL) 고분자인 poly(m-silylphenyl-p-phenylene-difluorovinylene) (m-SiP-PPDFV)는 GILCH polymerization 방법에 의해 합성된다. 이들 고분자는 단층 구조 (ITO/PEDOT/polymer/Ca:Al)의 light-emitting diodes (LEDs)에서 EL 발광층으로 사용되었다. m-SiP-PPDFV는 $\lambda_{max}$ = 452 nm 주위에서 PL 발광파장을 나타내었고, $\lambda_{max}$ = 497 nm 주위에서 녹색의 EL 발광을 나타내었다. 고분자의 current-voltage-luminance (I-V-L) 특성에서는 4.0 V 정도에서부터 소자가 작동되기 시작하였다. 고분자의 전자 친화도를 증가시키는 m-SiP-PPDFV을 얻기 위해 m-SiP-PPV의 모든 비닐렌기에 두개의 플루오르기를 도입하였고, 이로 인하여 소자 구동에서 비닐렌기의 색 안정도를 나타냈었다. PPV 유도체들에서 일어나는 비닐렌기의 산화반응을 보호하는 플루오르기는 전자 끄는 효과를 가지고 있어 소자의 색 안정도를 유지시킨다. 이번 연구로, 보다 안정화된 PPV 유도체를 얻기 위해, 플루오르기가 비닐렌기에 도입될 수 있음을 보여주고 있다.

• 폴리머
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• 제30권5호
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• pp.426-431
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• 2006

Azacrown ether를 포함하는 청색발광 형광체, 9,10-bis [p-(1-aza-18-crown-6)methyl phenyl] anthracene (3)과 N,N-bis [9-(p-methylphenyl)anthracenylmethyl] -1,5-diaza-18-crown-6 (4)를 안트라센 유도체 1과 2를 mono- 및 diaza-18-crown-6와 반응시켜 합성하였다. 역시 azacrown ether를 포함하는 형광체 공중합체(5)를 1,6-diaza-18-crown-6와 1을 반응시켜 합성하였다. 제 1족, 2족 그리고 여러 가지금속 양이온을 결합시킴으로써 형광 발광세기 변화에 대한 연구를 진행하였다. 형광체는 ${\lambda}_{max}$=372nm에서 최대흡수를 그리고 ${\lambda}_{max}$=430 nm에서 최대 발광을 보여주었다. 형광체들의 최적 PH 조건을 조사하기 위해 형광 발광 세기의 pH 의존성도 측정하여 하였다.

• 한국염색가공학회지
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• 제9권3호
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• pp.42-49
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• 1997

In order to study the dyeability of reactive dyes fixable at neutral pH, three reactive dyes(DYE-NC, DYE-PC, and DYE-LC) were prepared by the reaction of Cibacron Brilliant Red 3B-A with nicotinic acid, pyridine, and lutidine, respectively. FT-IR and UV/Vis spectrophometry were used to identify the dyes prepared. While the maximum absorption wavelength (&{\lambda}_{max}&) of Cibacron Brilliant Red 3B-A was 515nm, the &{\lambda}_{max}& of DYE-NC, DYE-PC, and DYE-LC were 522nm, 525nm, and 536nm, respectively. The &{\lambda}_{max}& was shifted to the longer wavelength by introducing the electron donating groups to the pyridine ring of Cibacron Brilliant Red 3B-A. All of the reactive dyes synthesized showed good exhaustion and fixation property to cotton fabric at higher temperature and neutral pH condition. It was regarded that the quaternary pyridinium ion functionated as the leaving group instead of the chloride ion. Among them, DYE-NC showed the best dyeability at the above condition. It was considered that the electron withdrawing carboxylic acid group in nicotinic acid enhanced the cationic property of nitrogn in pyridine ring, resulting the good reactivity with OH group in cellulose.

• Bulletin of the Korean Chemical Society
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• 제25권6호
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• pp.889-894
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• 2004

Polyaddition reactions of 1,1-diethynyl-3-triethylsilyl-1-silacyclopent-3-ene with several organoborane derivatives have afforded the oligomeric materials containing organosilacyclic group and organoboron moiety along the oligomer main chains. All of these materials are soluble in THF as well as chloroform, and their molecular weights are in the range of 1,990/1,190-21,950/7,050 ($M_w/M_n$) with the polydispersity indexes of 1.67-3.43. The prepared oligomers are characterized by several spectroscopic methods such as $^1H,\;^{13}C, \;^{29}Si,\;^{11}B$ NMR and FTIR spectra along with elemental analysis. FTIR spectra of all the oligomers show that the new strong C=C stretching frequencies appear at 1599-1712 $cm^{-1}$, in particular. The UV-vis absorption spectra of the materials in THF solution exhibit the strong absorption bands at the ${\lambda}_{max}$ of 268-275 nm. The oligomeric materials show that the strong excitation peaks appear at the ${\lambda}_{max}$ of 255-279 nm and the strong fluorescence emission bands at the ${\lambda}_{max}$ of 306-370 nm. All the spectroscopic data suggest that the obtained materials contain both the organoboron ${\pi}$-conjugation moiety of C=C-B-C=C and the organosilacyclic group of 3-triethylsilyl-1-silacyclopent-3-ene along the oligomer main chains. The oligomers are thermally stable up to 162-200 $^{\circ}C$ under nitrogen.