• Journal of the Korean Chemical Society
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• v.38 no.8
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• pp.552-561
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• 1994

The cis → trans thermal isomerization of azobenzene derivatives has been studied. A sizable solvent effect on the rates for thermal isomerization of push-pull azobenzenes are observed. It is suggested that the isomerization proceeds via a rotational mechanism. For non push-pull azobenzenes, the lack of solvent effects on the rate of isomerization was observed. This suggests that the isomerization proceeds via an inversional mechanism for non push-pull azobenzenes.

• Journal of the Korean Chemical Society
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• v.20 no.4
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• pp.290-294
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• 1976

Radiation-induced cis-trans isomerization of ${\beta}$-styrylnaphthalene is studied by determination of G values and the radiostationary states. The results are compared with data obtained in direct and sensitized photoisomerization of the compound. Both the excited singlet and triplet states are involved in the isomerization of ${\beta}$-styrylnaphthalene in the radiolysis of benzene solution.

• Korean Journal of Food Science and Technology
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• v.31 no.6
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• pp.1453-1457
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• 1999

The optimal conditions of alkali isomerization to obtain conjugated linoleic acid (CLA) concentrate from vegetable oils which have antioxidant and anticarcinogenic properties were studied. The result of alkali isomerization of various vegetable oils indicated that CLA content of safflower oil which contains more linoleic acid than any other vegetable oils was the highest of all experimental vegetable oils. During alkali isomerization, the amount of cis-9, trans-11 CLA and total CLA content in safflower oil was the highest at $8{\sim}11%$ KOH concentration and $180{\sim}185^{\circ}C$. But heating time had no effect on CLA formation after $20{\sim}40$ minutes. As a result of alkali isomerization of neutral lipid, glycolipid and phospholipid in safflower oil, CLA content of neutral lipid class was higher than any other lipid classes. By urea treatment and HPLC fractionation, total CLA content in alkali-isomerized safflower oil increased to 95.4% from 78.9%.

• Proceedings of the KAIS Fall Conference
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• 2012.05a
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• pp.239-242
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• 2012

효모 (Saccharomyces Cervisiae)는 단일 세포의 형태로 존재하는 진핵 세포로써 동물세포와 유사한 기작으로 분비성 단백질을 생성한다. 따라서 박테리아와 달리 효모를 이용하면 당단백질이나 이황결합을 포함하는 분비성 단백질을 경제적으로 대량 합성할 수 있다. 효모의 필수 단백질 중 하나인 단백질 이황이성질화 효소는 소포체에 위치하며 분비성 단백질에 구조적으로 안정한 이황결합을 제공하는 효소이다. 본 연구는 단백질 이황이성질화 효소 (protein disulfide isomerase)가 지니고 있는 두 개의 활성도메인 중 분비성 단백질들의 합성 효율에 직접적으로 관여하는 부위를 찾는 연구이다. 효모 유전체로부터 단백질 이황이성질화 효소의 유전자 (PDI1)을 제거하고 효소의 변이 유전자를 주입한 후 효모의 성장 속도를 측정하였다. 또한 효모의 대표적 분비성 단백질을 각 변이 효소를 지니는 효모에 과발현시켜 합성 및 이황결합 형성 효율을 측정하였다. 단백질 이황이성질화 효소내 두 개의 활성 부위 중 아미노 말단쪽에 위치한 a 도메인에 있는 활성 부위가 분비성 단백질의 활성에 중요한 역할을 한다는 것을 알 수 있었다. 이 결과는 이황결합이나 당을 포함하는 외래 단백질의 고효율 합성을 위한 새로운 효모종 개발에 중요한 정보를 제공할 것으로 기대 된다.

• Journal of the Korean Chemical Society
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• v.25 no.3
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• pp.166-171
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• 1981

The reactions of trimethylbenzenes were investigated over dealuminated, cation-exchanged mordenite catalysts. Higher reaction temperature favored the formation of disproportionation products. In the reaction of 1,2,4-trimethylbenzene, the formation of 1,3,5-trimethylbenzene and the disproportionation products decreased sharply with reaction time. The product distribution, especially the distribution of trimethylbenzenes, suggests that the effective pore diameter of Ba-exchanged dealuminated mordenite catalysts lies somewhere between 8.1 and 8.6${\AA}$.

• Journal of the Korean Chemical Society
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• v.32 no.4
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• pp.390-405
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• 1988

The chlorination of $C_7H_16,\;C_8H_18,\;C_10H_22,\;and\;(Me_2CH)_2$ with N-Chlorosuccinimide, tert-BuOCl, $CCl_3SO_2Cl,\;CCl_4,\;CCl_3SCl,\; PCl_5,\;and\;Cl_2\;in\;C_6H_6\;or\;CS_2$ which both form loose complexes with $Cl_2$ atoms yielded mixtures of isomeric monochloroalkanes which were analyzed quantitatively. An isomer ratio differing from that known for the substitution of paraffinic hydrocarbons was observed. The isomer distribution observed is the result of the combined effects of the differing C-H dissociation energies of the different types of H atoms of the alkane and of the free energy of the attacking radical with polar effects of the attacking radical as well as of the hydrocarbon.

• Proceedings of the Materials Research Society of Korea Conference
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• 1994.11a
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• pp.113-113
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• 1994

• Proceedings of the Korean Fiber Society Conference
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• 1999.10a
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• pp.433-437
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• 1999

• Ceramist
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• v.14 no.4
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• pp.18-25
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• 2011

• 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.