• 제목/요약/키워드: Photoreactivity

검색결과 24건 처리시간 0.027초

Photoreactivity and Thermogravimetry of Copper(II) Complexes of N-Salicylideneaniline and Its Derivatives

  • Osman, Ahmed H.;Aly, Aref A.M.;El-Mottaleb, Mohamed Abd;Gouda, Gamal A.H.
    • Bulletin of the Korean Chemical Society
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    • 제25권1호
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    • pp.45-50
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    • 2004
  • $Cu^{II}$-complexes of N-salicylideneaniline and its derivatives were not light sensitive in most solvents such as acetonitrile. A photo-decomposition occurred upon irradiation in halocarbon solvents such as $CHCl_3$. It has been suggested that such photoreactivity is attributed to the reactivity of charge-transfer to solvent (CTTS) excited state attained upon irradiation. A mechanism has been proposed to account for the results obtained. The complexes have been thermally analysed in nitrogen and static air using thermogravimetry (TG) and derivative thermogravimetry (DTG). The thermal degradation of the complexes proceeds in two or three stages. The kinetic parameters obtained from the Coats-Redfern and Horowitz-Metzger equations show the kinetic compensation effect.

Photoreactivity of Anthraquinones for the Analysis of Ginsenosides Using Photoreduction Fluorescence Detection-HPLC

  • Park, Man-Ki;Kim, Bak-Kwang;Park, Jeong-Hill;Shin, Young-Geun;Cho, Kyung-Hee;Do, Young-Mi
    • Archives of Pharmacal Research
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    • 제19권6호
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    • pp.562-565
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    • 1996
  • The photoreactivity of twelve anthraquinone derivatives was examined to evaluate its usefulness as a photo-reagent for the analysis of ginsenosides using photoreduction fluorescence (PRF) detection method. Among the tested compounds, 2-tert-butylandthraquinone (TBAQ), 2-chloroanthraquinone (CAQ) and anthraquinone (AQ) showed good characteristics as photoreagents. The detection limits of ginsenoside $Rg_{1}$PRF-HPLC method using TBAQ, CAQ or AQ as a photo-reagent were found to be ca. 35 ng, 50 ng and 50 ng, respectively.

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극지 식물플랑크톤의 유색 용존 유기물의 생산과 광반응성에 대한 자외선 영향 (UV Effects on Production and Photoreactivity of Chromophoric Dissolved Organic Matter in Media of Polar Marine Phytoplanktons)

  • 박미옥;하선용
    • 해양환경안전학회지
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    • 제28권5호
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    • pp.712-720
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    • 2022
  • 본 연구는 극지 식물플랑크톤의 자외선 영향을 파악하기 위해, Phaeocystis antarctica와 Phaeocystis pouchetii를 대상으로 유색 용존 유기물의 생산과 광반응성을 평가하였다. 강한 자외선에 노출 배양 시, 가시광선 파장대에서 유색 용존 유기물의 흡광도는 두 식물플랑크톤 모두 배양 초기에 비해 48시간 동안 감소하였다. 반면, 자외선 파장에서는 P. antarctica는 48시간 배양 후, 유색 용존 유기물의 흡광도는 초기 농도에 비해 약 30% 감소하였지만, P. pouchetii의 흡광도는 오히려 10% 증가한 경향을 보였다. 이 결과들은 강한 자외선에 노출될 경우, P. antarctica이 생산한 유색 용존 유기물은 광분해에 의한 감소로 인해 해수 중 수중 생태계에 자외선 차단 효과는 감소하는 반면, P. pouchetii가 생산한 유색 용존 유기물에 의한 광보호 효과가 더 효율적임을 알 수 있었다. 또한, 자외선 영향 하에서 배양된 P. pouchetii의 배양액에서 시간에 따라 증가한 유색 용존 유기물의 형광 특성이 지구 거대물질로 알려진 humic-like (C-peak)와 일치하여, 이는 자외선 차단 물질로 알려진 MAAs 생물 생산에 의한 것임을 확인하였다. 이는 기후변화에 의한 성층화가 강화되는 극지 해양환경에서, 광반응성이 낮은 P. pouchetti가 용존 유기물의 증가에 기여할 수 있을 것으로 기대된다.

Synthesis and High Photocatalytic Activity of Zn-doped TiO2 Nanoparticles by Sol-gel and Ammonia-Evaporation Method

  • Nguyen, Thanh Binh;Hwang, Moon-Jin;Ryu, Kwang-Sun
    • Bulletin of the Korean Chemical Society
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    • 제33권1호
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    • pp.243-247
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    • 2012
  • Photocatalysis has been applied to decompose the waste and toxic materials produced in daily life and in the global environment. Pure $TiO_2$ (Zn-$TiO_2$-0) and Zn-doped $TiO_2$ (Zn-$TiO_2$-x, x = 3-10 mol %) samples were synthesized using a novel sol-gel and ammonia-evaporation method. The Zn-doped $TiO_2$ samples showed high photocatalytic activity for the degradation of methylene blue (MB). The physicochemical properties of the samples were investigated using XRD, SEM, ICP, DLS and BET methods. In addition, the most important measurement of photocatalytic ability was investigated by a UV-vis spectrophotometer. The effects of the mol % of zinc ion doping in $TiO_2$ on photocatalytic activity were studied. Among the mol % Zn ions investigated, the Zn-$TiO_2$-9 sample showed the highest photoreactivity. This sample removed 91.4% of the MB after 4 h, while the pure $TiO_2$ only removed 46.4% of the MB.

New Soluble and Intrinsically Photosensitive Polyimide: Synthesis and Properties of Poly(amide-co-imide) Containing p-Phenylenediacryloyl Moiety

  • Lee, Myong-Hoon;Cheong, Yun-Sang;Gong, Myoung-Seon
    • Macromolecular Research
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    • 제9권6호
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    • pp.327-331
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    • 2001
  • A new soluble photosensitive poly(amide-co-imide) containing p-phenylenediacryloyl moiety was synthesized and its photoreactivity was characterized. The copolymer was synthesized fromp-phenylenediacryloyl chloride, 4,4-(hexafluoroisopropylidene)diphthalic anhydride and two equivalents of bis(4-aminophenyl) ether in NMP with a subsequent chemical imidization of the resulting poly[amide$\xi$ο-(amic acid)] by acetic anhydride and pyridine. The structure and thermal properties of the polymer were characterized by spectroscopic methods and thermal analyses. The polymer was stable up to 350$\^{C}$, showed good solubility in polar aprotic solvents, and became insoluble after UV irradiation due to the[2+2] cycloaddition of phenylenediacryloyl moiety. Photoreactivity of the polymer was investigated in solution or as a film with respect to the various exposure conditions by UV/Vis spectroscopy. The photosensitivity was noticeably increased with the irradiation temperature, especially in the presense of photosensitizer. The reason for the increased sensitivity was speculated based on the flexibilization of main chain at elevated temperature. Exposure characteristic curves were obtained from the gel fraction experiments after UV irradiation. The sensitivity and contrast at 160$\^{C}$ were measured to be 293 mJ/㎠ and 1.64, respectively.

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Phototoxicity Evaluation of Pharmaceutical Substances with a Reactive Oxygen Species Assay Using Ultraviolet A

  • Lee, Yong Sun;Yi, Jung-Sun;Lim, Hye Rim;Kim, Tae Sung;Ahn, Il Young;Ko, Kyungyuk;Kim, JooHwan;Park, Hye-Kyung;Sohn, Soo Jung;Lee, Jong Kwon
    • Toxicological Research
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    • 제33권1호
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    • pp.43-48
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    • 2017
  • With ultraviolet and visible light exposure, some pharmaceutical substances applied systemically or topically may cause phototoxic skin irritation. The major factor in phototoxicity is the generation of reactive oxygen species (ROS) such as singlet oxygen and superoxide anion that cause oxidative damage to DNA, lipids and proteins. Thus, measuring the generation of ROS can predict the phototoxic potential of a given substance indirectly. For this reason, a standard ROS assay (ROS assay) was developed and validated and provides an alternative method for phototoxicity evaluation. However, negative substances are over-predicted by the assay. Except for ultraviolet A (UVA), other UV ranges are not a major factor in causing phototoxicity and may lead to incorrect labeling of some non-phototoxic substances as being phototoxic in the ROS assay when using a solar simulator. A UVA stimulator is also widely used to evaluate phototoxicity in various test substances. Consequently, we identified the applicability of a UVA simulator to the ROS assay for photoreactivity. In this study, we tested 60 pharmaceutical substances including 50 phototoxins and 10 non-phototoxins to predict their phototoxic potential via the ROS assay with a UVA simulator. Following the ROS protocol, all test substances were dissolved in dimethyl sulfoxide or sodium phosphate buffer. The final concentration of the test solutions in the reaction mixture was 20 to $200{\mu}M$. The exposure was with $2.0{\sim}2.2mW/cm^2$ irradiance and optimization for a relevant dose of UVA was performed. The generation of ROS was compared before and after UVA exposure and was measured by a microplate spectrophotometer. Sensitivity and specificity values were 85.7% and 100.0% respectively, and the accuracy was 88.1%. From this analysis, the ROS assay with a UVA simulator is suitable for testing the photoreactivity and estimating the phototoxic potential of various test pharmaceutical substances.

Substituent Effect on Diastereoselectivity in Photochemistry of Valerophenone

  • Park, Bong-Ser;Cho, Sung-Su;Chong, Sang-Hyuk
    • Bulletin of the Korean Chemical Society
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    • 제28권7호
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    • pp.1156-1158
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    • 2007
  • Valerophenone shows a dramatic shift of photoreactivity by a cyclopropyl group at alpha position to the carbonyl group. By the minor change of structure, the diastereoselectivity of the Yang photocyclization is reversed and the ratio of cyclization to elimination products increases significantly.

Photocyclodimerization of Maleimide

  • Shim, Sang-Chul;Bong, Pill-Hoon
    • Bulletin of the Korean Chemical Society
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    • 제3권3호
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    • pp.115-119
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    • 1982
  • The photoreaction of maleimide, one of the best model compounds of DNA molecules for psoralen-DNA photoreactions, is studied in order to investigate the photoreactivity and the mechanism of the maleimide-psoralen photoreaction. The (2+2) photocyclodimer of maleimide was obtained in solution state by direct or sensitized irradiation. The rate constant of dimerization is determined by quenching studies and found to be of the order of $10^9 M^{-1}sec^{-1}$. The direct dimerization of maleimide is found to undergo through the triplet excited state. The quantum yields of dimerization are dependent on the maleimide concentration.