• Journal of the Korean Chemical Society
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• v.54 no.6
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• pp.727-730
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• 2010

A tricyclic ring system bearing new stereogenic center namely 2,3-dihydro[1]benzothieno[3,2-b]pyrrole 4,4-dioxide was synthesized by asymmetric photoisomerization of 2,3-dihydropyrrolo[1,2-b]benzisothiazole 5,5-dioxide by irradiation with 245 nm emission of the low-pressure mercury lamp. The chemical structure and the purity of the photoproduct were delineated preliminarily by IR, NMR, and MS and finally confirmed by single crystal X-ray crystallography.

• Journal of the Korean Chemical Society
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• v.34 no.2
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• pp.117-122
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• 1990

The rate constants for the aquation of $trans-[CoETECl_2]^+ \;and \;cis-{\beta}-[CoTETCl_2]^+$ and the isomerization of $trans-[CoETEClOH_2]^{2+}$ were measured by spectrophotometric method under various temperature and pressure conditions. For the aquations of $trans-[CoETECl_2]^+ \;and\; cis-{\beta}-[CoTETCl_2]^+$, the activation entropies are 4.0 eu and 5.3 eu respectively and the activation volumes are $-5.8 cm^3mol-1\; and\; -6.6 cm^3mol^{-1}$ at 40$^{\circ}C$, respectively. From these data the dissociative mechanism involving trigonal bipyramid-type intermediate is proposed for the acquation reaction. For the isomerization of $trans-[CoETEClOH_2]^{2+}\; to\; cis-{\beta}-[CoETEClOH_2]^{2+}$ the activation entropy is 9.5 eu and the activation volume is $8.4 cm^3mol^{-1}(30^{\circ}C$. The mechanism of isomerization may be considered as the dissociative mechanism with $H_2O$-dissociation.

• Proceedings of the Korean Society of Dyers and Finishers Conference
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• 2011.03a
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• pp.32-32
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• 2011

염료의 포토크로미즘은 빛을 받았을 때, 염료의 분자구조가 변환되어 흡수파장이 달라지고 결과적으로 원래 색과 다른 색상을 나타내는 현상을 말한다. 대부분의 Golden yellow 색상을 나타내는 아조계 반응성염료는 Trans-Cis 간의 이성질체 전환을 통해 포토크로미즘 현상을 나타내며, 가역적으로 복색되기는 하지만 상업적으로 많은 문제와 불편을 초래한다. 한편 pyrazolone계 아조염료는 azo form 보다는 hydrazone form으로 더 많이 존재하는 것으로 알려져 있으며, 이로인해 상대적으로 Trans-Cis 이성질화가 잘 일어나지 않아 포토크로미즘 현상이 잘 일어나지 않을 것으로 기대된다. 이 연구에서는 3종의 pyrazolone계 golden yellow 반응성 염료를 합성하고, 합성한 염료를 면직물에 염색하여 염색성 및 견뢰도를 평가하였다. 또한 시판되고 있는 아조계 golden yellow 반응성 염료 4종을 선정하여 역시 염색성과 견뢰도 특성을 알아보았다. 그리고 7가지 염료의 광변색 특성을 조사하기 위해 포토크로미즘 평가방법인 ISO 105-B05법 및 이전 연구에서 제안된 광변색 평가방법을 사용하였다. ISO 105-B05법은 표준청색염포가 grey scale 4등급이 되는 시간을 구한 다음 이 시간의 1/4시간동안 조사한 후 포토크로미즘을 평가하는 것이며, 후자의 경우는 4시간동안 광조사된 시험편을 측색하고 시간에 따른 복색되는 정도를 평가한다. 합성한 pyrazolone계 염료들은 394-408nm의 최대흡수파장은 나타내었다. 7종의 yellow 반응성 염료들은 모두 면직물에 우수한 염색성 및 build-up성을 나타내었으며, 대체적으로 양호한 견뢰도를 얻었다. 또한 광변색 특성 평가결과 모든 염료들은 ISO 평가방법에 대하여 non-photochromic 특성으로 나타났으나, 다른 광변색 평가 결과 일부 염료들에 있어서 photochromic 특성이 있는 것으로 나타나 평가방법에 따라 차이를 보였다.

• Journal of the Korean Chemical Society
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• v.22 no.6
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• pp.417-422
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• 1978

Rather than undergo photooxygenation, the Z-configuration benzalpyrrolinones (Z-2, Z-4) photoisomerized to the E-configuration isomers under direct or sensitized irradiation. Rose bengal sensitized photochemical stereoisomerzation of benzalpyrrolinones (Z-2, Z-4 and E-2) with monochromatic light (at 557 nm, excitation of rose bengal only) showed that the triplet of benzalpyrrolinones was involved in the photoisomerization, since oxygen inhibited the photoisomerization.

• Horticultural Science & Technology
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• v.29 no.4
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• pp.374-381
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• 2011

Stilbenes are polyphenolic natural products, which have antioxidative and antifungal activities. In some plants, including grapevine, the stilbene compounds, as resveratrol derivatives, exist in very diverse forms. Experiments to identify the individual stilbene compounds were carried out first to quantify them in UV-irradiated grapevine leaves. For this, stilbene glycosides were extracted from grapevine leaves which irradiated intensively with UV light. The glycoside samples were hydrolyzed by ${\beta}$-glucosidase, before analyzed by HPLC-mass spectrometer at each m/z corresponding to the mass of specific stilbenes. As results, in chromatograms, the enzymatic hydrolysis resulted in decrease and increase of the peaks expected for glycosides and aglycones, respectively. The samples were also exposed to sunlight in order to photo-isomerize the stilbene compounds. The light exposure resulted in disappearance and appearance of peaks expected for trans- and cis-isomers of stilbenes, respectively. Such a change of the peaks in chromatograms provided information needed for the inference to peak components. In this way, it was possible to identify 16 kinds of stilbene compounds from grapevine leaves. The identified stilbenes were quantified from grapevine leaves irradiated mildly by UV light. The UV-irradiation increased markedly in the content of stilbene compounds, especially trans-resveratrol by several hundredfold. In addition, piceatannol, which is a mere minor component of stilbenes in control leaves and a more active radical scavenger than resveratrol, was also increased by several tenfold by the treatment. The increase in stilbene contents as influenced by UV irradiation seems to be one of the stress coping responses of grapevine as a hormesis phenomenon.

• Applied Chemistry for Engineering
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• v.30 no.2
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• pp.247-253
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• 2019

In this study, compounds with azo-mesogenic groups at 4-, 3,5-, or 3,4,5-positions of one phenyl ring were synthesized, and their liquid crystallinity and photochemistry were investigated. The compounds in the Azo1 and Azo2 series had linear and planar geometries, respectively, while those in the Azo3 series had relatively bulky structures. Compounds of BA-Azo2 and BA-Azo3 did not show any liquid crystallinity. Compounds of BE-Azo1 and BE-Azo2 exhibited a monotropic liquid crystallinity, while the other compounds showed an enantiotropic liquid crystallinity. The liquid crystalline behavior was imparted by the azo-mesogenic groups, and most of the liquid crystalline compounds formed a smectic phase. All the RM-AzoX compounds exhibited photoisomerism because of the presence of the azo groups in the molecule. The rate of photoisomerization followed the order of RM-Azo3 < RM-Azo1 < RM-Azo2 and was considered to depend on the steric hindrance around the azobenzene groups in the molecule. These results suggest that the liquid crystallinity and photochemical property of the compounds are affected by the position or the number of azo-mesogenic groups phenyl ring of the molecule.

• Journal of the Korean Chemical Society
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• v.22 no.1
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• pp.45-51
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• 1978

The luminescence of N-methyllutidone is studied in ethanol matrix at $77^{\circ}C$K. No fluorescence is observed but a strong phosphorescence with the quantum yield of 0.1 and the lifetime of 0.2 sec is recorded. An unusually high triplet energy of 85.1 kcal/mole is determined for the compound from the O-O band of phosphorescence. The cis ${\leftrightarrow}$ trans photoisomerization of high triplet energy olefins such as 2-hexene and trans-1,4-dichlorobutene-2 is efficiently sensitized by N-methyllutidone substantiating the high triplet energy of the compound. The negative polarization of O-O band reveals the emitting triplet state to be $({\pi},{\pi}^*)^3$ state. Alkaline metal salts such as lithium chloride enhances the phosphorescence intensity through cation-N-methyllutidone coordination widening the gap between $({\pi},{\pi}^*)^3$and $(n,{\pi}^*)^3$ states.