• 제목/요약/키워드: cyclohexene

검색결과 94건 처리시간 0.022초

Antimicrobial Activity of Essential Oil of Pinus koraiensis Seed Against Pathogens Related to Acne

  • Choi, Jae-Wan;Kim, Ran
    • KSBB Journal
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    • 제29권3호
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    • pp.179-182
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    • 2014
  • The purpose of the present research was to evaluate the antimicrobial activity of the essential oil extracted from Pinus koraiensis seed against pathogens related to acne. The essential oil was extracted by steam distillation method. The chemical compositions of essential oil were analyzed by GC-MS. Alpha-pinene (29.87%), D-limonene (19.26%), betapinene (11.19%), beta-myrcene (3.84%), n-hexadecanoi acid (3.2%), beta-caryphyllene (2.72%), and cyclohexene (2.17%) were main components. This essential oil had antimicrobial activities against Malasseizia furfur, Propionibacterium acnes, and Staphylococcus epidermidis.

Coupling Reaction of CO2 with Epoxides by Binary Catalytic System of Lewis Acids and Onium Salts

  • Bok, Taekki;Noh, Eun Kyung;Lee, Bun Yeoul
    • Bulletin of the Korean Chemical Society
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    • 제27권8호
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    • pp.1171-1174
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    • 2006
  • Various off-the-shelf Lewis acids in conjunction with various onium salts are screened for coupling reaction of $CO_2$ with epoxides. Among the tested ones, $VCl_3/n-Bu_4NOAc$, $VCl_3/(n-Bu_4NCl$ or PPNCl), $FeCl_3/ n-Bu_4NOAc$, and $FeCl_3/ n-Bu_4NOAc$are proved to be highly active. Propylene oxide, epichlorohydrin, styrene oxide, and cyclohexene oxide can be converted over 90% yields to the corresponding cyclic carbonates without the use of organic solvents under mild conditions by 0.1-1.0 mol% catalyst charge.

Alignment of smectic liquid crystals on newly synthesized photo-reactive polyimide with chalcone moiety

  • Song, Dong-Mee;Shin, Dong-Myung;Kim, Jae-Hoon;Kim, Il
    • 한국정보디스플레이학회:학술대회논문집
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    • 한국정보디스플레이학회 2002년도 International Meeting on Information Display
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    • pp.479-482
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    • 2002
  • Benzylideneacetophenones are known as chalcones[1]. The chalcone has been known to be a photo-isomerizable and photo-dimerizable chromophore. The chalcone derivatives were prepared by base-catalyzed condensation of aldehydes and acetophenones, which were substituted with various alkyl chains. The synthesized chalcone was introduced into the t-BOC protected diamine through William synthesis reaction. Photocrosslinkable polyimide was prepared via one-step imidization reaction of DOCDA (5-(2,5-dioxotetrahydro furyl}-3-methyl-3-cyclohexene-1,2-dicarboxylic anhydride) and the chalcone introduced diamine using isoquinoline (5 wt%) in m-cresol. The polyimide solutions were spin-coated onto the quartz, silicone wafer and glass substrates and the obtained thin films were irradiated obliquely with linearly polarized UV light.

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Autoxidation of Cycloalkenes by the System “Molecular Oxygen-bis(acetylacetonato) Cobalt (II) Complex-butyraldehyde”

  • Fang, Zhao;Tang, Rui-Ren;Zhang, Rui-Rong;Huang, Ke-long
    • Bulletin of the Korean Chemical Society
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    • 제30권10호
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    • pp.2208-2212
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    • 2009
  • Oxidation of cycloalkenes with $O_2$ promoted by heterogeneous bis(acetylacetonato) cobalt (II) complex catalyst which can be recycled has been performed under mild conditions. It was found that $\beta$-ionone, cyclohexene, 1-methylcyclohexene, and $\alpha$-ionone were efficiently oxidized with $O_2$ in the presence of Co (II) complex and butyraldehyde at $55\;{^{\circ}C}$. A simple treatment of the resulting products led to epoxides as predominant products and a small amounts of allylic oxides, the chemoselectivity for the former being 82.1 - 90.8% with a 70.6 - 98.6% substrate conversion. On the other hand, oxidation of 1-phenylcyclohexene, 1-cyclohex-1-enylethan-1-one, $\alpha$-pinene, and $\beta$-pinene gave allylic oxides as major products.

The Rapid and Efficient Synthesis of Bromohydrins from Olefins under HBr/H2O2 System by Visible Light Induced

  • Tang, Rui-Ren;Gong, Nian-Hua
    • Bulletin of the Korean Chemical Society
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    • 제30권8호
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    • pp.1832-1834
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    • 2009
  • A simple and safe method has been presented for conversion of olefins into bromohydrins using hydrogen bromide and hydrogen peroxide as bromide source by visible light induced within a very short time to get high yield bromohydrins along with a little mount dibromo-product. In this paper, cyclohexene is firstly carried out as the model substrate and investigated the bromination under HBr/$H_2O_2$ system using 150 W incandescent light irradiated in C$Cl_4$ within short time to get good yield of 2-bromocyclohexanol along with a little mount of 1,2-dibromocyclohexane; then, a series of alkenes are brominated to corresponding bromohydrins using the same protocol.

Low-Temperature Processable Polyimide Gate Insulator and Hybridization Approach for High Performance Pentacene Thin Film Transistor

  • Ahn, Taek;Kim, Jin-Woo;Yi, Mi-Hye
    • 한국정보디스플레이학회:학술대회논문집
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    • 한국정보디스플레이학회 2007년도 7th International Meeting on Information Display 제7권1호
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    • pp.871-874
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    • 2007
  • We have synthesized a novel fully soluble and low-temperature processable polyimide gate insulator (KSPI) through one-step condensation polymerization. For the preparation of KSPI, 5- (2,5-dioxytetrahydrofuryl)-3-methly-3-cyclohexene- 1,2-dicarboxylic anhydride (DOCDA) and 4,4- diaminodiphenylmethane (MDA) were used as monomers and fully imidized KSPI was completely soluble in organic solvents like ${\gamma}-butyrolactone$ and 2-butoxyethanol, etc.

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Syntheses and Reactivites with Olefins of Ruthenium(IV) Oxo/Ruthenium(II)-Aqua Complexes that Contain 2,6-Bis(N-pyrazolylpyridine)

  • Jo, Du-Hwan;Yeo, Hwan-Jin
    • Bulletin of the Korean Chemical Society
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    • 제14권6호
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    • pp.682-686
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    • 1993
  • The syntheses and reactivities with olefins of $[Ru^{II}(L_3)(L_2)OH_2]^{2+}$ $[L_3$= 2,6-bis(N-pyrazolyl)pyridine(bpp), 2,6-bis(3,5-dimethyl-N-pyrazolyl)pyridine $(Me_4bpp);\;L_2$= 2,2'-bipyridine(bpy), 4,4'-dimethyl-2,2'-bipyridine $(Me_2bpy)$] are described. Their spectral and redox properties in aqueous solution were investigated. Evidence for each one electron redox process for the $Ru^{IV}-Ru^{III}$ and $Ru^{III}-Ru^{II}$ couples has been obtained. Oxidation of $[Ru^{II}(bpp)(bpy)OH_2]^{2+}$ with $Ce^{IV}$ gave $[Ru^{IV}(bpp)(bpy)O]^{2+}$. The $[Ru^{IV}$= 0 complex is paramagnetic $({\mu}_{eff}=2.82)$ and the complexes $[Ru(L_3)(L_2)OH_2]^{2+}$ are robust catalysts for the oxidation of styrene, cyclohexene, and cyclooctene with cooxidant such as NaOCl. Product distributions and selectivities are discussed by varying the number of the substituted-methyl group in the ring.

1,4-Dibora-2-cyclohexene 유도체들의 합성과 그 성질 (Synthesis and Properties of 1,4-Diboracyclohexene-2 Derivatives)

  • 엄재국;호동기
    • 대한화학회지
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    • 제34권5호
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    • pp.490-497
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    • 1990
  • 1,4-dibora-2-cyclohexene 고리화합물 8을 합성하기 위한 두 가지 방법이 개발되었다. 방법 i)은 1,2-bis(dichloroaluminyl)ethane을 출발물질로 하는데 이 물질은 AlCl$_2$ 부분을 BCl$_2$로 치환시켜준다. 1,2-bis(dichloroaluminyl)ethane에 결합된 염소를 BI$_3$로 교환시켜 대응되는 요오드 화합물을 얻고 이 화합물을 alkynes와 반응시켜 헤테로고리화합물 8a, b를 많이 얻었다. 방법 ii)는 B$_2$Cl$_4$를 alkynes에 부가시켜 얻어지는 염소화합물에 BI$_3$를 치환시켜 bis(diiodoboryl)ethane유도체를 얻고 이 화합물에 alkynes와 산화환원반응을 하여줌으로 8c, d를 얻는다. 요오드 유도체인 8a는 pyridine 부가물인 9a를 생성하고 또 ether와 반응하여 ethoxy 유도체인 8e를 생성시킨다. 요오드 유도체의 dimethyl amino 치환제가 8f이다. 8a-d와 AlMe$_3$를 반응시켜 대응되는 methyl유도체인 8g-j를 얻고 이들 화합물은 THF속에서 칼륨과 반응시켜 불안정한 라디칼 음이온이 생성되고 여기서 ESR 결과가 측정된다. 8g-j의 전기화학적인 실험이 비가역적인 환원반응으로 나타났다. 8g-j화합물은 (C$_5$H$_5$)CO(C$_2$H$_4$)$_2$와 반응하여 중간체인 16개 VE(valence electron)를 갖는 착물 (C$_5$H$_5$)Co(8)이 얻어지는데 이 화합물은 다시 C-H 활성화에 의해 대응되는 붉은색의 1,4-diboracyclohexene 착물 10을 생성하게 된다. 착물 10h와 10j의 X-ray 구조가 결정되었다.

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전자선 조사에 의한 고리지방족/DGEBA 에폭시 블렌드 시스템의 경화 및 기계적 특성 (Cure and Mechanical Behaviors of Cycloaliphatic/DGEBA Epoxy Blend System using Electron-Beam Technique)

  • 이재락;허건영;박수진
    • 폴리머
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    • 제27권3호
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    • pp.210-216
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    • 2003
  • Benzylquinoxalinium hexafluoroantimonate를 함유한 4-vinyl-1-cyclohexene diepoxide (VCE)/diglycidyl ether of bisphenol-A (DGEBA) 에폭시 블렌드를 전자선을 사용하여 경화하였다. 그리고 VCE에서 DGEBA의 함량이 경화 거동, 열적 그리고 기계적 특성에 미치는 영향을 연구하였다. VCE/DGEBA 블렌드계의 조성은 100 : 0, 80 : 20, 60 : 40, 40 : 60, 20 : 80, 및 0 : 100 wt%로 하였다. 경화 거동과 열안정성은 근적기선 분광기와 열중량 분석기로 각각 측정하였다. 또한 기계적 계면 특성을 연구하기 위하여 경화된 시편의 임계응력 세기인자 ( $K_{IC}$) 실험을 수행하였다. 그 결과 DGEBA 함량 증가와 함께 수산화기와 카보닐기에 기인한 짧은 곁사슬 구조와 사슬 절단의 감소가 근적외선 분광법에 의해서 측정되었다. 그리고 열안정성 인자들로서 초기 열분해 온도 (IDT), 최대 무게 감량시 온도 ( $T_{max}$), 그리고 분해 활성화 에너지 ( $E_{d}$)는 DGEBA 함량 증가와 함께 증가하였다. 이러한 결과들은 DGEBA 함량 증가에 따른 점도의 감소와 안정된 방향족 고리 구조, 그리고 graftedIPN구조로 설명될 수 있었다. 또한 최대 $K_{IC}$ 값은 40 : 60 wt%에서 보였다.보였다..

Ga(Ⅲ), In(Ⅲ) 및 Tl(Ⅲ) 금속이온을 포함한 Metalloporphyrin 착물의 촉매적 특성 (Catalytic Activity of Ga(Ⅲ)-, In(Ⅲ)- and Tl(Ⅲ)-porphyrin Complexes)

  • 박유철;나훈길;김성수
    • 대한화학회지
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    • 제39권5호
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    • pp.364-370
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    • 1995
  • 비산화-환원 금속인 Ga(III), In(III), TI(III)을 포함하는 금속 포르피린을 촉매제로 NaOCl을 산화제로 하여 올레핀의 촉매적 산화반응을 $CH_2Cl_2$에서 연구하였다. 포르피린은 $(p-CH_3O)TPP,\;(p-CH_3)TPP,\;TPP,\;(p-F)TPP,\;(p-Cl)TPP $그리고 $(F_20)TPP$를 사용하였다. 올레핀은 $(p-CH_3O)-,\;(p-CH_3)-,\;(p-H)-,\;(p-F)-,\;(p-Cl)-,\;(p-Br)styrene$ 그리고 cyclopentene, cyclohexene을 사용하였다. 올레핀 산화반응에서 기질의 전환율(%)은 금속 포르피린 및 기질의 치환기 효과와 중심 금속이온 성질에 따라 고찰하였다. TPP 치환기에 따른 전환율의 변화는 $p-CH_3O$ < $p-CH_3$ < H < p-F < p-Cl 순서로 증가하였다. 이러한 증가는 TPP의 $4{\sigma}$값의 증가 순서와 일치하였다. 기질의 치환기에 따른 전환율의 변화는 $p-CH_3O$ > $p-CH_3$ > H > p-Cl > p-Br 순서로 치환기의 ${\sigma}^+$값이 증가할수록 오히려 감소하였다. 올레핀의 산화 반응에서 In(III)-, Tl(III)-포르피린은 Ga(III)-포르피린에 비하여 높은 촉매 활성을 나타내었다.

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