• 한국결정성장학회지
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• 제12권2호
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• pp.110-114
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• 2002

HBPCA를 유기질 공해물질의 모델로서 선정하고 $TiO_2$에 흡착시켜서 흡착된 분자의 배향성과 광분해 생성물의 관계에 대하여 조사하였다. 용액의 pH를 변화시켜서 UV광을 조사한 뒤 생성된 광분해 생성물을 UIF와 Raman 분광기로 스펙트럼을 얻어 분석 비교하였다. 용액의 pH는 흡착된 분자의 배향에 영향을 미쳐서 광분해 생성물이 달라지며, 흡착된 분자의 배향과 광분해 생성물과의 관계는 아주 밀접하게 관련되어 있음을 확인하였다.

• BMB Reports
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• 제32권6호
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• pp.554-560
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• 1999

TTD1BI cells are non-hypersensitive to UV irradiation and perform normal genome repair of pyrimidine dimers but fail to excise 6-4 photoproducts and, concomitantly, are unable to restore RNA synthesis levels following UV irradiation. This pointed to a detect in gene-specific repair and this study was undertaken to examine repair of 6-4 photoproducts at the gene-level. The results indicated a defect in gene-specific repair of 6-4 photoproducts in active genes, although strand-specificity of 6-4 photoproduct removal was essentially similar to that of normal cells. These findings indicate that the near normal UV resistance of TTD1BI cells may be due to the inability of these cells to remove DNA lesions preferentially, as well as to the cells opting out of the cell cycle to repair damage before resuming replication.

• Bulletin of the Korean Chemical Society
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• 제27권9호
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• pp.1305-1309
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• 2006

Photolysis of (2-hydroxymethylphenyl)pentamethyldisilane 1 in methanol provides a novel intramolecular photoproduct 4 via silene intermediate 2 but the photoreaction of (2-acetoxymethyl- or allyloxymethylphenyl) pentamethyldisilanes 5 or 10 in methanol affords unexpected photoproducts 8 or 13, respectively, instead of expected intramolecular photoproducts.

• Journal of Photoscience
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• 제10권1호
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• pp.81-87
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• 2003

Based on structural information provided by recently reported crystal structures of rhodopsin, we present rationales for the regiospecific protein perturbation on the previously reported $\^$19/F chemical shifts of the vinyl and trifluoromethylrhodopsins and their photoproducts. The crystal structures also suggest that H-bonding is a likely cause for the earlier reported regiospecific photoisomerization of the 10-fluororhodopsins. Photoisomerization was revealed by chemical shift of the photoproducts. Additionally, possible use of 3-bond F,F coupling constants for following photoisomerization of retinal-binding proteins is discussed.

• Environmental Analysis Health and Toxicology
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• 제11권3_4호
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• pp.33-44
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• 1996

Photolysis of TCBs in aqueous solutions of sodium nitrite and triethylamine (TEA) at neutral pH has been investigated. TCBs yielded trichloronitrobenzenes(TCNBs) as primary photoproducts, and their corresponding trichlorophenols (TCPs) via two types of reaction, one, nitration, and the other, by direct hydroxylation with OH radical. Isomerized products and TCBs were also identified. Photosensitization with TEA resulted in the formation of small yields of dichlorobenzenes(DCBs) by reductive dechlorination of TCBs.

• 한국자기공명학회:학술대회논문집
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• 한국자기공명학회 2001년도 제18회 학술발표회
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• pp.14-14
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• 2001

• Bulletin of the Korean Chemical Society
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• 제29권5호
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• pp.1018-1024
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• 2008

Photolysis of 2-(pentamethyldisilanyloxy)phenylpentamethyldisilane 1 in methanol provides five photoproducts 3, 4, 5, 6, and 7. Compounds 3 and 4 were probably formed from the methanol addition reactions of silene intermediate 2 and the formation of 5, 6, and 7 can best be explained by the nucleophilic attack of methanol to silicon atom in pentamethyldisilanyloxy or pentamethyldisilanyl group of the photoexcited state of 1. Irradiation of 1 in n-hexane gives a photoproduct 6 via silyl radical intermediate 8 and a novel intramolecular cyclization photoproduct 11 via silene 9 and silyl radical intermediate 10. Irradiation of 1 in deaerated methylene chloride in the presence of acetone affords a novel photoproduct 11 and phenol 7 but the expected photoproducts from the reaction of the silene intermediate with acetone were not obtained.

• Bulletin of the Korean Chemical Society
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• 제30권6호
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• pp.1331-1336
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• 2009

Photolysis of (2-hydroxyethoxyphenyl)pentamethyldisilane 2 in benzene provides a novel intramolecular cyclization photoproduct 9 which was probably formed from the intramolecular reaction to form a seven-membered ring in silatriene intermediate 7 and then the photochemical disrotatory ring closure of 1,3-butadiene moiety to cyclobutene. Irradiation of 2 in methanol afforded photoproducts 5 and 6 which were formed by the nucleophilic attack of methanol to $\beta$ or $\alpha$ silicon atom in pentamethyldisilanyl group of the photoexcited state of 2. Compounds 10 and 11 were also formed by the same way as in the formation of the photoproducts 5 and 6 in the photolysis of (2-allyloxyethoxyphenyl)pentamethyldisilane 3 in methanol solvent. Photoreaction of (2-acetoxyethoxyphenyl) pentamethyldisilane 4 in methanol gave a photoproduct 12 which was formed via the elimination of dimethylsilylene species in the photoexcited state of 4.

• Journal of Photoscience
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• 제9권2호
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• pp.482-484
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• 2002

UV irradiation activates various intracellular signaling pathways causing cell death in a DNA damage-dependent and an independent manner. As DNA photoproducts, major forms of DNA damage, are maximally formed by UV light at 260-nm, short wavelength UV (UVC) is more harmful than middle wavelength UV (UVB). However, the differences or similarities in responses of DNA damage-independent intracellular signaling molecules to UVB and UVC are not elucidated. We examined activation of signaling molecules towards apoptosis in normal human fibroblastic cells after irradiation with UVB or UVC at a dose generating the equal amount of DNA photoproducts. Both UVB and UVC induced transient phosphorylation of ERK and sustained phosphorylation of p38. Phosphorylation of p53 at Ser15 and at Ser392 residues were also observed, which were inhibited by a phosphoinositide 3-kinase inhibitor, wortmannin. In contrast, an antioxidant N-acetyl-cysteine and a p38 inhibitor SB203580 suppressed only Ser392 phosphorylation, suggesting that UV-induced oxidative stress and p38 activation were involved in the phosphorylation of this site. The apoptic signals such as mitochondrial cytochrome C release and annexin V binding were then observed. Overall, no difference was found in chronological responses of p53, MAPK, and apoptosis between UVB-irradiated and UVC-irradiated cells. These results suggested that DNA damage-independent intracellular signaling molecules similarly responded to UVB and UVC when the equal level of DNA photoproducts were generated.

• 농약과학회지
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• 제4권4호
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• pp.12-18
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• 2000

제초제 quinclorac의 수중 및 토양중 잔류량을 인위적으로 감소시키기 위하여 광분해를 촉진시킬 수 있는 6종의 감광제를 선발하여 수중 및 모래에서의 광분해 시험을 수행하였다. 자연광 조건하에서 증류수중 quinclorac의 분해는 암조건과 비교할 때 차이가 없어 직접적인 광분해는 용이하지 않음을 알 수 있었다. Methanol 용액에서 quinclorac의 광분해율은 40.3%였으나, 감광제 PS-1 (방향족 ketone), PS-3 (quinone), 그리고 PS-6 (반도체 광촉매)가 함유되어 있는 용액 및 현탁액에서 quinclorac의 광분해율은 각각 96.6%, 72.7%, 그리고 95.7%로서 가장 양호한 광분해 촉진효과를 보였다. 한편 모래에서는 감광제 PS-1, PS-3 그리고 PS-6중에서 PS-3가 64.1%로 가장 양호한 광분해 촉진효과를 보였다. Methanol중 quinclorac의 광분해산물로 5종의 화합물이 그리고 감광제 PS-1에서는 3종의 분해산물이 GC-MS로 구명되었고 aldehyde기를 보유한 광분해산물은 sodium 3,5-dinitrosalicylate의 환원반응에 의하여 확인되었다. 토양에 처리된 quinclorac은 30 ppm 이상의 감광제 PS-3 처리로 광분해되어 남아있는 quinclorac 잔류물은 강피를 방제하지 못했다. 이와 같은 결과들은 감광제 PS-1, PS-3, PS-6가 수용액 및 토양중 quinclorac 잔류물을 효과적으로 광분해시킬 수 있음을 시사한다.