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오동영,Oh, Dong-Young 대한화학회 1969 대한화학회지 Vol.13 No.3
The experiment have been carried out for the determination of aggregation state of isopolytantalate anion in aqueous solution by using "Ultracentrifuge Method". The molecular weight of this anion at pH 10.7 could be determined as a heptatantalate anion $Ta_7O_{22}^{9-}$.
고주파유도가열 연소합성에 의한 치밀한 WSi<sub>2</sub>-20vol.%SiC 복합재료 제조 및 기계적 특성
오동영,김환철,이상권,손인진,Oh, Dong-Young,Kim, Hwan-Cheol,Lee, Sang-Kwon,Shon, In-Jin 한국분말야금학회 2005 한국분말재료학회지 (KPMI) Vol.12 No.1
Dense $WSi_2$-20vol.%SiC composite was synthesized by high-frequency induction-heated combustion synthesis(HFIHCS) method within 2 minutes in one step from elemental powder mixture of W, Si and C. Simultaneous combustion synthesis and densification were accomplished under the combined effects of an induced current and mechanical pressure. Highly dense $WSi_2$-20vol.%SiC with relative density of up to 97% was produced under simultaneous application of 60MPa pressure and the induced current. The average grain size of $WSi_2$ was about $5.2{\mu}m$. The hardness and fracture toughness values obtained were 1700kg/$mm^2$ and $4.4MPa{\cdot}m^{1/2}$, respectively.
오동영,김충렬,Dong Young Oh,Chung Ryeol Kim Korean Chemical Society 1983 대한화학회지 Vol.27 No.5
5-아릴-1,3,4-옥시티아졸-2-온을 트리에틸포스파이트와 반응시키면 탈황반응에 의해 벤조니트릴과 에틸포스포로티오에이트가 66~94% 수득율로 얻어졌다. 다른 3가의 인화합물 즉, 트리메틸포스파이트, 트리에틸포스핀, 그리고 트리페닐포스핀들과도 같은 탈황반응이 관찰되었다. 그러나 트리페닐포스파이트와는 전혀 반응하지 않았다. 5-아릴-1,3,4-디티아졸-2-온을 트리페닐포스핀과 반응시키면 티오아실 이소시아네이트가 얻어졌다. 이것은 에테르에서 자체적으로 분해되어 벤조니트릴로 변하게 되나 클로로포름에서는 안정하다. 이 두 반응에서 관찰되는 탈황반응은 인이 고리속으로 들어가 고리를 늘인후 분자내에서의 자리옮김 반응에 의해 일어나는 것이라 생각된다. 클로로포름에서 안정한 티오아실 이소시아네이트는 이민과 1,4-고리화 첨가반응을 일으켜 티아다이아지논을 생성하였다. The reactions of various 5-aryl-1,3,4-oxathiazol-2-ones with triethylphosphite resulted in the formation of the corresponding benzonitriles and ethylphosphorothioate by desulfurization reaction in 66∼94% yields. 5-(4-Nitrophenyl)-1,3,4-oxathiazol-2-one was also reacted with trimethylphosphite, triethylphosphine, and triphenylphosphine to give 4-nitrobenzonitrile. But it did not react with triphenylphosphate. The reactions of 5-(4-bromophenyl)-1,2,4-dithiazol-3-one with triphenylphosphine resulted in the formation of 4-bromothiobenzoyl isocyanate and triphenylphosphine thioxide. The thioacyl isocyanate was fragmented into nitrile in ether but was stable in chloroform. This desulfurization reaction observed in each reaction may proceed by the intramolecular rearrangement after insertion of the phosphorus compound into the ring. The stable thioacyl isocyanate in chloroform reacted with imine to give 1,3,5-thiadiazin-4-one via 1,4-cycloaddition reaction.
The Synthesis of Carbamoylsulfenyl Chloride and its Derivatives
문석식,오동영,Surk Sik Moon,Dong Young Oh Korean Chemical Society 1983 대한화학회지 Vol.27 No.2
N-Methylidene-2,6-diethylaniline (III)은 2,6-diethylaniline (II)과 과량의 paraformaldehyde와의 반응으로 만들었으며, 이 화합물 III에서 N=$CH_2$ 프로톤은 AB 스핀계를 나타냈다. 화합물 III과 chlorocarbonylsulfenyl chloride(IV)를 반응시켜서 N-(chloromethyl)-N-(2,6-diethylphenyl)-carbamoylsulfenyl chloride(V)를 합성하였다. 화합물 V와 여러 종류의 알콜을 반응시켜서 Alkyl N-(chloromethyl)-N-(2,6-diethylphenyl)-carbamoylsulfenate esters(VI ${\sim}$XVI)를 71{\sim}$95%의 수득률로 합성하였다. VI${\sim}$XVI은 서서히 분해되지만 S-O 결합이 S=O결합으로 변하지는 않았다. 과량의 알콜은 V의 2가 황과 N-chloromethyl기의 ${\alpha}$-탄소에 대해 친핵성 공격을 할 수 있었으며, 이렇게 하여 생긴 화합물 (XVII, XVIII)은 상당한 안정성을 가지고 있었다. N-Methylidene-2,6-diethylaniline (III) was prepared by the reaction of 2,6-diethylaniline (II) with an excess paraformaldehyde. The protons of N=$CH_2$in the compound III exhibited a second order NMR spectrum. The compound III reacted with bifunctional chlorocarbonylsulfenyl chloride(IV) to give N-(chloromethyl)-N-(2,6-diethylphenyl)-carbamoylsulfenyl chloride(V). The reaction of the compound V with various alcohols resulted in the formation of Alkyl N-(chloromethyl)-N-(2,6-diethylphenyl)-carbamoylsulfenate esters(VI${\sim}$XVI) in 71${\sim}$95% yields. The compound VI${\sim}$XVI decomposed gradually, but the thermal rearrangement of S-O bonding to S=O bonding was not found. The nucleophilic attack of an excess alcohol to the compound Ⅴ was made on both divalent sulfur and ${\alpha}$-carbon of N-chloromethyl group. The corresponding substituted products(XVII, XVIII) had considerable stability.
Carboxyl-Terminated Polybutadiene 의 중합 및 특성에 관한 연구 (제1보). 개시제농도가 수율 및 특성에 미치는 영향
강정부,유경준,권석기,오동영,Jung-Bu Kang,Kyung-Joon You,Suk-Ky Kwon,Dong-Young Oh 대한화학회 1980 대한화학회지 Vol.24 No.5
4,4'-azobis-[4-cyano valeric acid]를 개시제로 하여 라디칼 중합에 의해 carboxyl-terminated polybutadiene을 제조하고, 개시제의 농도가 중합체의 물성에 미치는 영향을 조사하였다. 부타디엔 농도를 일정하게 유지하고, 개시제 농도를 변화시켜 중합한 결과, 개시제농도가 증가함에 따라 카르복실기 함량이 감소하고 중합수율은 개시제농도의 1/2 제곱에 정비례하였으며, 관능도가 2.0을넘어 일반적인 라디칼 중합의 경향과 일치하였다. Carboxyl-terminated polybutadiene was prepared by free-radical polymerization using 4,4'-azobis-[4-cyano valeric acid] as an initiator and the effect of initiator concentration on polymer properties was investigated. Polymerization of the carboxyl-terminated polybutadiene was carried out varying the initiator concentration reacting with a constant butadiene concentration. The carboxyl weight percent decreased with increasing initiator concentration. The conversion was proportional to the square root of initiator concentration, giving a functionality greater than 2.0 which is consistent with the general tendency of free radical polymerization.