• 한국식물병리학회지
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• 제14권6호
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• pp.682-688
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• 1998

Fungicide resistance of 48 isolates of Botrytis cinerea collected from citrus in Cheju was investigated and genetic diversity was analyzed with random amplified polymorphic DNA(RAPD). High levels of resistance to benzimidazole fungicides benomyl and thiophanate-methyl and N-phenylcarbamate fungicide diethofencarb were observed. Negative cross resistance was clear between benzimidazole and N-phenylcarbamate fungicides, and multiple resistance to the fungicides was also observed. There was cross resistance among the dicarboximide fungicides procymidione, vinclozolin and iprodione as it was observed between the benzimidazole fungicides benomyl and thiophanate-methyl. The lowest levels of resistance were to the dicarboximide fungicides, but no sensitive isolate to polyoxin B was observed. The isolates showed genetically diverse RAPD profiles according to the geographic origin collected, but there was no significant correaltion between RAPD profiles of genomic DNA and the levels of fungicide resistance of the isolates. The isolates showed genetically diverse RAPD profiles, indicating that genetic differentiation had already occurred in the populations of B. cinerea distributed in Cheju.

• 농업과학연구
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• 제22권2호
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• pp.127-133
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• 1995

일련의 phenyl N-methylcarbamate 유도체들을 합성하고 ACh.E에 대한 carbamylation 과정으로 일어나는 살충활성 반응의 중심인 carbonvl group의 분자궤도(MO) 함수량과 살충활성($pI_{50}$) 값에 대한 치환기의 영향을 검토한 바, phenyl group에 결합된 치환기(X) 변화에 따른 carbonyl group의 알짜전하와 적외선 진동수($cm^{-1}$) 및 bond population에 미치는 치환기 효과(${\rho}=0$)는 관측되지 않았다. 전체 에너지(${\Delta}Et$)와 ipso $C_1-O_7$결합을 회전축으로 한 각도(${\theta}$)와의 관계로 부터 가장 안정한 형태는 평면인 phenyl group에 대하여 carbamyl group이 수직(${\theta}=90^{\circ}$ )인 (Z)-N-methyl-(Z}-O-phenylcarbamate 형태이었다. Carbamylation 과정의 1단계 평형($k_1/k_{-1}$) 반응은 thermodynamically control 반응이기 때문에 carronyl oxygene에 대한 acidic group(ACh.E)의 양성자화 반응과 Serine hydroxyl group의 친핵성 첨가반응 그리고 m-methyl group의 hyperconjugation effect에 의하여 anionic site(ACh.E)와의 상호작용으로 설명되는 일련의 새로운 carbamylation 메카니즘을 가정하여 제안하였다.

• Journal of Photoscience
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• 제6권3호
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• pp.145-151
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• 1999

The use of O-carbamoyloximes as photobase generators was investigated. $\alpha$-Meth-ylbenzilydeneamino phenylcarbamate(2a) and $\alpha$-methyl benzilydeneamino cyclohexylcarbamate(2b) were prepared by the reaction of phenyl or cyclohexyl isocyanates with acetophenone oxime , respectively. Aniline, phenylhydrazine and N, N'-diphenylhydrazine were detected in thephotolysis of 2a and cyclohexylamine and cyclohexylhydrazine in the photolysis of 2b. A monomer having pendant carbamoyloxyimino groups (BGM) was prepared by the reaction fo methancryloyloxyethyl iocyanate with acetophenone oxime, and copolymerized with styrene. The BGM copolymer films turned insoluble on UV irradiation, and the degree of insolubilizationwas increased by post-baking. The photocrosslinking was thought to be due to coupling of resulting pendant aminyl radicals, and the thermal crosslinking was due to association of resulting amino and hydrazino groups by hydrogen bonding. The introduction of epoxy groups into polymer increased the degree of thermal crosslinking by post-baking.

• Korean Chemical Engineering Research
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• 제56권1호
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• pp.119-124
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• 2018

아닐린과메탄올의산화 카르보닐화방법에의한 Methyl N-phenyl carbamate 제조는 기존의포스겐을사용하는폴리머의 단량체 생산공정을 대체할 수 있는 환경 친화적인 공정으로 많은 관심을 가지고 있다. 본 연구에서는 담지체로 Y-zeolite, $SiO_2$, $Al_2O_3$를 사용하여 불균일화 촉매를 제조하였고, 제조 된 불균일화 촉매를 이용하여 아닐린과 메탄올로부터 산화카르보닐화 연속운전을 시도하였다. 회분식반응기를 이용하여 담지체를 결정하였으며, 담지된 palladium 촉매를 이용하여 조촉매의 영향과 반응온도, 반응압력 등 여러 반응최적조건을 확립하였다. 최적의 반응조건 MPC의 수율은 98.6% 였으며, 반응속도론적 연구를 수행하였다. 각 반응온도의 반응속도상수로부터 얻어진 활성화 에너지는 각각 E=82.38 kJ/mol, E=66.20 kJ/mol 이었다. 또한 확립된 반응조건에서 장시간 연속운전을 수행하여 카바메이트 공정 개발을 위한 기초자료를 구하였다.