• Bulletin of the Korean Chemical Society
• /
• 제5권5호
• /
• pp.194-198
• /
• 1984

The UV action spectra and quantum yields for photodestruction of tryptophan (Trp) in peptide such as N-acetylphenylalanyl-L-tryptophan (NAPT) and 3-methyl indole (scatole) were determined in aerated aqueous and organic solvents. The photodestruction of aqueous NAPT was shown to be initiated by photoionization without requirement of threshold energy, as demonstrated by the similarity of fluence effect curves obtained for the action at various wavelengths and the wavelength dependence of quantum yield comparable to that reported for the photoionization of L-Trp. N-formylkynurenine (NFK)-type photoproduct, which is a photodynamic sensitizer, was not found to be involved in the photodestruction of Trp in NAPT in aqueous solution. In contrast, the action spectra of NAPT and scatole in organic solvents have revealed evidences for the significant role of internal photosensitization by NFK-type photoproduct in photolysis of Trp in peptide.

• 생약학회지
• /
• 제6권3호
• /
• pp.149-150
• /
• 1975

Silicagel colum chromatography of the ether extract of the fruits of Angelica decursiva $F_R$. et SAV. gave four crystalline products of coumarins and one steroid. The following furocoumarins and ${\beta}-sitosterol$ were identifed by UV, IR, NMR spectra and physicochemical tests: ${\beta}-sitosterol$, iso-imperatorin, imperatorin, bergapten, umbelliferone.

• 대한화학회지
• /
• 제34권3호
• /
• pp.310-312
• /
• 1990

• 한국원자력학회:학술대회논문집
• /
• 한국원자력학회 2005년도 춘계학술발표회
• /
• pp.327-328
• /
• 2005

• Bulletin of the Korean Chemical Society
• /
• 제22권2호
• /
• pp.141-144
• /
• 2001

6- and 7-Benzylpteridine derivatives have been converted to the corresponding 6- and 7-benzoylpteridines by the oxidation reaction with KMnO4. The newly synthesized compounds have been characterized by pKa determinations, UV, and 1H-NMR spectra.

• 한국방사성폐기물학회:학술대회논문집
• /
• 한국방사성폐기물학회 2011년도 추계학술논문요약집
• /
• pp.109-110
• /
• 2011

• 한국물환경학회지
• /
• 제32권1호
• /
• pp.98-107
• /
• 2016

This study examined the effects of environmental conditions and the presence of refractory organic matter on oxidation rates of total organic carbon (TOC) measurements based on high temperature combustion and ultraviolet-sulfate methods. Spectroscopic indices for prediction of oxidation rates were also explored using the UV spectra and fluorescence excitation-emission matrix (EEM) of humic acids. Furthermore, optimum TOC instrument conditions were suggested by comparing oxidation rates of a standard TOC material under various conditions. Environmental conditions included salts, reduced ions, and suspended solids. Salts had the greatest influence on oxidation rates in the UV-sulfate method. However, no effect was detected in the high temperature combustion method. The UV-sulfate method showed lower humic substance oxidation rates, refractory natural organic matter, compared to the other methods. TOC oxidation rates for the UV-sulfate method were negatively correlated with higher specific-UV absorbance, humification index, and humic-like EEM peak intensities, suggesting that these spectroscopic indices could be used to predict TOC oxidation rates. TOC signals from instruments using the UV-sulfate method increased with increasing chamber temperature and increasing UV exposure durations. Signals were more sensitive to the former condition, suggesting that chamber temperature is important for improving the TOC oxidation rates of refractory organic matter.

• 천문학회보
• /
• 제37권1호
• /
• pp.48.1-48.1
• /
• 2012

We present the ultraviolet (UV) color-color relation of early-type galaxies (ETGs) in the nearby universe (0.05 < z < 0.12) to investigate the properties of hot stellar populations responsible for the UV excess (UVX). The initial sample of ETGs is selected by the spectroscopic redshift and the morphology parameter from the SDSS DR 7, and then cross-matched with the GALEX far-UV (FUV) and near-UV (NUV) GR6 data. The cross-matched ETG sample is further classified by their emission line characteristics in the optical spectra into quiescent, star-forming, and active galactic nucleus categories. Contaminations from early-type spiral galaxies, mergers, and morphologically disturbed galaxies are removed by visual inspection. By drawing the FUV-NUV (as a measure of UV spectral shape) versus FUV-r (as a measure of UVX strength) diagram for the final sample of -3700 quiescent ETGs, we find that the "old and dead" ETGs consist of a well-defined sequence in UV colors, the "UV red sequence," so that the stronger UVX galaxies should have a harder UV spectral shape systematically. However, the observed UV spectral slope is too steep to be reproduced by the canonical stellar population models in which the UV flux is mainly controlled by age or metallicity parameters. Moreover, 2 mag of color spreads both in FUV-NUV and FUV-r appear to be ubiquitous among any subsets in distance or luminosity. This implies that the UVX in ETGs could be driven by yet another parameter which might be even more influential than age or metallicity.

• 한국안광학회지
• /
• 제13권3호
• /
• pp.7-12
• /
• 2008

목적: 투명과 착색 안경렌즈의 자외선 차단 특성을 평가하고자 하였다. 방법: 안경렌즈의 투과 스펙트럼은 ANSI Z80.1에 제시된 방법으로 측정하였고, UV(200~380 nm; UVA, UVB, UVC) 및 청색광 영역(380~400 nm)에 대하여 각 렌즈의 투과율을 계산하였다. 결과: 중굴절률, 고굴절률의 투명 플라스틱 렌즈 및 착색 플라스틱 렌즈는 UV에서 우수한 자외선 차단 특성을 보였으나, 자외선 차단제를 처리하지 않은 크라운 유리나 CR39는 그렇지 않았다. 고굴절률 렌즈와 눈부심 방지 야간용 렌즈를 제외한 모든 렌즈는 청색광을 효과적으로 차단하지 않았다. 결론: 크라운 유리와 CR39 렌즈는 UV로부터 눈을 보호하기 위해서 자외선 차단제가 필요하다. 또한 고굴절률 렌즈와 눈부심 방지 야간용 렌즈를 제외한 모든 렌즈는 청색광으로부터 눈을 보호하기 위해서 청색광 차단제가 필요하다.

• 약학회지
• /
• 제33권3호
• /
• pp.141-148
• /
• 1989

The weak UV absorbing antihistaminics such as chlorpheniramine, triprolidine, tripelennamine and diphenhydramine were analyzed by charge-transfer spectrophotometric method. The results obtained are summarized as folows. It was possible to determine a weak UV absorbing antihistaminics using the intense charge-transfer UV bands in chloroform. Charge transfer complexes were formed in a 1:1 ratio between antihistaminics and iodine in chloroform. Linear relationship was found between absorbance and concentration in the range of $1.0\;{\times}\;10^{-5}M-5.0\;{\times}\;10^{-5}M$ for chlorpheniramine( ${\varepsilon}\;=\;2.082\;{\times}\;10^4$) and tripelennamine ( ${\varepsilon}\;=\;1.578\;{\times}\;10^4$), $1.0\;{\times}\;10^{-5}M-8.0\;{\times}\;10^{-5}M$ for triprolidine ( ${\varepsilon}\;=\;1.120\;{\times}\;10^4$) and $1.0\;{\times}\;10^{-5}M-1.0\;{\times}\;10^{-4}M$ for diphenhydramine ( ${\varepsilon}\;=\;9.900\;{\times}\;10^3$). Charge transfer complexes of chlorpheniramine, triprolidine and tripelennamine have absorption maxima at 293 nm and complex form of diphenhydramine has absorption maximum at 270 nm. By UV, IR spectra, it could be inferred that CT-complexes were formed by interaction between the basic nitrogen of antihistaminics as electron donor (non bonding electron) and iodine as electron acceptor (${\sigma}$ bonding electron).