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1,1-dichloro-2,3,4,5-tetraphenyl-1-silacyclopentadiene의 합성과 이에 대한 Mass Spectroscopic Study
주완철,이동석 成均館大學校 科學技術硏究所 1984 論文集 Vol.35 No.2
1, 1-Dichloro-2, 3, 4, 5-tetraphenyl-l-silacyclopentadiene is synthesized from the reaction of diphenylacetylene with metal and tetrachlorosilane, where the optimal reaction conditions are also studied. From-the mass spectroscopic study of this 1,1-dichloro-2, 3, 4, 5-tetraphenyl-l-silacyclopentadiene the elimination of meta-stable dichlorosilylene species is confirmed.
6개 원소로 이루어진 짝이중결합화합물과 R_2AsCI와의 반응
주완철,이용암,유응철 성균관대학교 기초과학연구소 1986 論文集 Vol.37 No.2
From the reactions of orthohydroxy-6-membered conjugated system, benzil-mono-orthohydroxyanil, with Me_2AsCl and chloro [Toluene-(2, 3)-dithiolato(2)] arsenic (Ⅲ), reaction products was isolated. From the IR and NMR-spectroscopic analysis for these reaction products, it is confirmed that reaction products are charge-transfer complexes of As. From these results, we found that the chemical behaviour of trivalent As is not analogous to trivalent P.
새로운 방법에 의한 1,1-R,R'-2,3,4,5-테트라페닐-1-실라사이크로펜타디엔의 합성
주완철,흥장환,최석봉 성균관대학교 기초과학연구소 1988 論文集 Vol.39 No.1
A new synthesis of 1,1-R, R',-2, 3, 4, 5-tetraphenyl-1-silacyclopentadiene was described. It was synthesized from one-pot reaction of 1,4-dilithio-1, 2, 3, 4-tetraphenylbutadiene with R_nSiCl_4-n (n=0, 1, 2), where 1, 4-dilithio-1, 2, 3, 4-tetraphenyl butadiene was prepared from the reaction of diphenyl acetylene and lithium metal in ether solution with good yield (80∼85%).
주완철,박경래 成均館大學校 1979 論文集 Vol.26 No.-
Previous investigators have prepared carbamates by the Hoffmann-like rearrangement of amides using lead tetraacetate as an oxidation agent. Almost of these investigations are concerned mainly with the procedures of the carbamate preparations. For the formation of carbamates by the Hoffmann-like rearrangement of amides it seems very important to know the influences of the character of amides and also the acidity of alcohols. In this work we have studied at first the influences of amides with electron withdrowing and donating character upon the formation of carbamates. From our results we have found that there is no remarkable influence of amides on account of the yield or the reactivity. We have also found that this reaction does not initiate without base. Therefore we have concluded that the formation of isocyanate intermediate in the process of carbamate preparation occurs by a spontaneous intramolecular synchronous rearrangement and not by the free nitrene formation, and that the catalytic effect of a base, which acts to displace a nitrogen bonded proton of the amide and initiates the reaction, must be accounted as an important factor.
6개원소로 이루어진 짝이중결합화합물과 AsCl_3와의 반응
주완철,육명화,김용주 成均館大學校 科學技術硏究所 1983 論文集 Vol.34 No.2
6개의 원소로 이루어진 오르토히드록시짝이중결합화합물, 즉 시남알데히드-오르토-히드록시아닐(cinnam-aldehyde-ortho-hydroxyanil), 벤질모노히드록시아닐(benzil-mono-hydroxyanil), 오르토-히드록시벤잘아세톤페논(ortho-hydroxy benzalacetophenone)과 알진트리클로라이드(AsCI_3)와의 반응으로부터 고체반응생성물을 분리해 냈다. 이들 반응생성물의 적외선 및 자외선분광학으로부터, 이들 모든 반응생성물은 비소의 전하이동착물임을 획인했다. 이 반응으로부터 3원자가 비소화합물의 화학적거동이 인의 3원자가 화합물과 유사하지 않다는 것을 알 수 있었다. Solid products were isolated by the reaction of orthohydroxy-6-membered conjugated system such as cinnamaldehyde-ortho-hydroxyanil, benzil-mono-orthohydroxyanil and ortho-hydroxybenzalacetophenon with AsCl_3. All of these products were confirmed to be Charge-transfer complexes of As from the examination of IR and UV spectra. It could be found that the chemical behavior of trivalent As is not analogous with that of triv alent P.
1-Silacyclopentadiene으로부터 Silylene을 합성하는데 대한 연구
공영건,주완철 成均館大學校 科學技術硏究所 1983 論文集 Vol.34 No.1
1-Spiro(tetraphenyl-1-silacyclopentadiene) was obtained from the reaction of 1, 2, 3, 4-tetraphenylbutadiene anion with tetrachlorosilane in ether. This spiro compound is treated with phenylacetylene at 350℃ in sealed tube. From this reaction, pentaphenylbenzene and polymer like silicon compound which are byproducts of silylene formation, are isolated. The reaction product which must be formed from the reaction of silylene and phenylacetylene, is now under investigation.
1,1-Dimethyl-2,5-bis(trimethylsilyl)-3,4-diphenyl-1-silacyclopenta-2,4-diene의 합성
공영건,주완철,Young Kun Kong,Wan-Chul Joo 대한화학회 1986 대한화학회지 Vol.30 No.6
Phenyltrimethylsilylacetylene과 리듐의 반응으로 부터 1,4-bis(trimethylsilyl)-2,3-diphenyl-1,4-butadene dianion이 형성되었다. 이 반응생성물과 dichlorodimethylsilane을 반응시키면 1,1-dimethyl-2,5-bis(trimethylsilyl)-3,4-diphenyl-1-silacyclopenta-2,4-diene이 얻어졌다. 이와 함께 분리된 1,4-bis(trimethylsilyl)-2,3-diphenyl-1,3-butadiene은 알칼리 매질에서 가수분해되어 생성된 화합물로 보인다. From the reaction of phenyltrimethylsilylacetylene with lithium, 1,4-bis(trimethylsilyl)-2,3-diphenyl-1,4-butadene dianion was formed. The reaction of dianion with dichlorodimethylsilane affords 1,1-dimethyl-2,5-bis(trimethylsilyl)-3,4-diphenyl-1-silacyclopenta-2,4-diene. In addition 1,4-bis(trimethylsilyl)-2,3-diphenyl-1,3-butadiene was isolated. It seems to be hydrolized product in alkali medium.