• Bulletin of the Korean Chemical Society
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• 제21권3호
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• pp.351-352
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• 2000

• Bulletin of the Korean Chemical Society
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• 제25권1호
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• pp.42-44
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• 2004

Valerophenones containing a substituent at alpha position to the carbonyl group show the remarkable substituent effects on their photochemical reactions. ${\alpha}$-Bromovalerophenone gives only the C-Br bond cleavage products, but the ${\alpha}$-chlorovalerophenone follows the classical Norrish/Yang reaction pathway predominantly.

• Bulletin of the Korean Chemical Society
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• 제18권12호
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• pp.1264-1268
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• 1997

The poly(methylsilene) (1) was modified with the group 4 metallocene Cp2MCl2/Red-Al (M = Ti, Zr, Hf) combination catalyst and with the group 6 metal carbonyl M(CO)6 (M = Cr, Mo, W) catalyst, producing the highly cross-linked isoluble polymer and the lowly cross-linked soluble polymer, respectively. An interrelationship between molecular weight and percent ceramic residue yield with metal within the respective group was not found. The polymers modified with the group 4 metallocene combination catalysts have higher molecular weight and lower percent ceramic residue yield than the polymers modified with the group 6 metal carbonyl catalysts do. The catalytic activity of group 4 metallocene combinations appears to be higher at ∼100 ℃, but to be lower at very high temperature than those of group 6 metal carbonyls. The pyrolysis of the modified 1 yielded SiC ceramic.

• Bulletin of the Korean Chemical Society
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• 제19권12호
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• pp.1310-1314
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• 1998

The oligo(methylsilene) (1) was treated with the group 4 metallocene Cp2MCl2/Red-Al (M = Ti, Zr, Hf) combination catalysts and with the group 6 metal carbonyl M(CO)6 (M = Cr, W) catalysts, producing the modified, cross-linked polymers. The average molecular weights and percent ceramic residue yields of modified polymers increase as the catalyst goes down from Ti to Hf and similarly as the catalyst goes down from Cr to W. An interrelationship between average molecular weights and percent ceramic residue yield is found within the respective group of catalysts, but is not observed as the catalyst goes down from Ti to W. The polymers modified with the group 4 metallocene combination catalysts have higher molecular weights and similar percent ceramic residue yields as compared to the polymers modified with the group 6 metal carbonyl catalysts. The catalytic activities of group 4 metallocene combinations appear to be higher -100 ℃, but to be lower at very high temperature than those of group 6 metal carbonyls.

• 한국염색가공학회지
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• 제15권4호
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• pp.17-23
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• 2003

Fourier transform infrared spectroscopy(FT-IR) was used to characterize the intermolecular ester crosslinkages in cotton cellulose. The FT-IR data show that the band of the ester carbonyl group can be separated from overlapping carboxyl/carbonyl band by converting carboxyl group to carboxylate. When esterification occurs between a polycarboxylic acid and cotton cellulose, the carbonyl groups retained in the cotton exist in three forms; ester, carboxyl, and carboxylate anion. The FT-IR data were also correlated to the durable press rating result obtained. The appearance of BTCA-finished durable press silk/cotton fabrics were improved.

• Nuclear Engineering and Technology
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• 제4권4호
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• pp.294-300
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• 1972

메틸 클로로 및 플로로 훼메이트의 각종 구조에 대한 CNDO/2 및 INDO 계산을 실시하였다. 결과로 가장 안정한 구조는 할로겐 원자와 메틸기가 trans인 형 임을 알았다. 원자의 전하와 결합전자밀도를 볼 때 에텔 산소의 비공유 전자쌍의 공액과 칼보닐 산소와 메틸기 간의 정전기적인 상호작용으로 분자가 안정화되어 있음을 알 수 있었다. 쌍극자 모멘트는 trans의 값이 실험간에 가까우며 결합모멘트로 계산된 쌍극자 모멘트로 부터 일반적인 결론을 내리기 어려움을 밝혔다.

• Bulletin of the Korean Chemical Society
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• 제8권3호
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• pp.162-165
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• 1987

The reduction rate of borohydride exchange resin (BER) was greatly enhanced in the presence of lithium salts. Thus 2-heptanone was reduced completely with BER-LiCl in 1 h at room temperature. However, no reduction was observed with BER alone under the same conditions. With this system, organic compounds containing various fuctional groups were examined in ethanol at room temperature. This study revealed that BER-LiCl system exhibits an excellent chemoselectivity for carbonyl group in the presence of other functional groups. Keto esters and epoxy ketones were reduced with BER-LiCl to give the corresponding hydroxy esters and epoxy alcohols with excellent yields. Selective reductions of carbonyl groups were also possible in the presence of other organic compounds containing functional groups such as 1-idooctane, 1-bromooctane, caproamide, hexanenitrile, nitrobenzene, n-butyl disulfide, dimethyl sulfoxide and 1-dodecene.

• Bulletin of the Korean Chemical Society
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• 제13권2호
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• pp.166-172
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• 1992

Studies have been conducted to explore single electron transfer (SET) induced photocyclization reactions of N-(trimethylsilylmethoxyalkyl)phthalimides(alkyl=E thyl, n-propyl, n-butyl, n-pentyl, and n-octyl). Photocyclizations occur in methanol in high yields to produce cyclized products in which phthalimide carbonyl carbon is bonded to the carbon of side chain in place of the trimethylsilyl group. Mechanism for these photocyclizations involving intramolecular SET from oxygen in the $\alpha-silylmethoxy$ groups to the singlet excited state phthalimide moieties followed by desilylation of the intermediate $\alpha-silylmethoxy$ cation radicals and cyclization by radical coupling are proposed. In contrast, photoreaction of N-(trimethylsilylmethoxyethyl) phthalimide in acetone follows different reaction routes to produce two cyclized products in which carbon-carbon bond formation takes place between the phthalimide carbonyl carbon and the carbon $\alpha$ to silicon and oxygen atoms via triplet carbonyl hydrogen abstraction triplet carbonyl silyl group abstraction pathways. The normal singlet SET pathway dominates these triplet processes for photoreaction of this substance in methanol. The efficient and regioselective cyclization reactions observed for photolysis in methanol represent synthetically useful processes for construction of medium and large ring heterocyclic compounds.

• 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.

• Nuclear Engineering and Technology
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• 제4권1호
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• pp.35-38
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• 1972

고체전분이 방사선에 조사될때 생성되는 carbonyl 물질이 gas chromatograph에 의하여 검파되었는데 2,4-dinitrophenylhydrazine으로 침전시켜 얻은 hydrazones을 분석하였다. Carbonyl groups의 생성은 선량이 2$\times$$10^{21}$ eV/g될때까지 직선으로 증가하며 form-aldehyde와 acetaldehyde가 검파되었다. 이외에 최소한 미상의 3개의 peak가 발견되었다.