• Bulletin of the Korean Chemical Society
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• 제9권3호
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• pp.149-152
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• 1988

A mixture of (Z,Z)-3,13-octadecadien-1-yl acetate(1) and its (E,Z)-isomer(2), the sex pheromone of the cherry tree borer, Synanthedon hector Butler was synthesized. (Z)-11-Octadecen-1-al(3) was prepared from 1,10-decandiol. The Wittig reaction the above aldehyde3 with carboethoxymethylenetriphenylphosphorane, or the Wadsworth-Emmons reaction of the above aldehyde3 with the anion of triethylphosphonoacetate gave ethyl (Z,Z)-2,13-octadecadienoate and its (E,Z)-isomer. Deconjugative protonation of ethyl (Z,Z)-2,13-octadecadienoate and its (E,Z)-isomer with potassium hexamethyldisilazide followed by aqueous ammonium chloride work-up afforded stereoselectiv디y ethyl (E,Z)-3,13-octadecadienoate and its (Z,Z)-isomer, respectively, of which stereoselectivity was adjusted to give the product in the required ratio. Exposure of the above deconjugated ester to excess lithium aluminium hydride resulted in formation of the penultimate (Z,Z)-3,13-octadecadien-1-ol and its (E,Z)-isomer. Acetylation of the desired alcohols afford the final products, (Z,Z)-3,13-octadecadien-1-yl acetate(1) and its (E,Z)-isomer(2).

• Bulletin of the Korean Chemical Society
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• 제33권2호
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• pp.420-425
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• 2012

The new organic semiconductors which are composed of divinylbenzene core unit and alkoxynaphthalene on both sides, 1,4-bis-2-(6-octyloxy)naphthalen-2-ylvinylbenzene (BONVB), 1,4-bis-2-(6-decyloxy)naphthalen-2-ylvinylbenzene (BDNVB) and 1,4-bis-2-(6-dodecyloxy)naphthalen-2-ylvinylbenzene (BDDNVB) were synthesized by Wittig reaction. The structures of obtained BONVB, BDNVB and BDDNVB were confirmed by FT-IR and mass spectroscopy. UV-absorption of thin film showed H-aggregates and J-aggregates due to closely packed structure between adjacent molecules. The characterization of vacuum-evaporated films by Xray diffraction (XRD) and atomic force microscopy (AFM) showed that the chain length of alkoxy group affects the crystallinity and morphology. BONVB with octyloxy group showed the mobility of $0.011cm^2/V{\cdot}s$, on/off ratio of $1.31{\times}10^5$, and a subthreshold slope of 0.93 V.

• Journal of Information Display
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• 제10권3호
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• pp.125-130
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• 2009

The new organic semiconductor, which is composed of a divinylbenzene core unit and alkoxynaphthalene on both sides, 1,4-bis-2-(6-hexyloxy)naphthalen-2-yl-vinylbenzene, was synthesized via Wittig reaction. The obtained oligomer was characterized via FT-IR, mass and elemental analysis, UV-visible spectroscopy, cyclovoltammetry, differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA). The vacuum-evaporated film was characterized via X-ray diffraction and atomicforce microscopy (AFM). It formed a highly ordered polycrystalline vacuum-evaporated film and exhibited a good field-effect performance, with a hole mobility of $0.015cm^2/V{\cdot}s$, an on/off ratio of $1.18{\times}10^5$, and a subthreshold slope of 0.69 V when it was deposited at Ts=$90^{\circ}C$ on HMDS-treated $SiO_2$.

• Advances in materials Research
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• 제3권3호
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• pp.175-183
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• 2014

Natural rubber bound phenolic antioxidant, 2,6-di-tert-butyl-4-vinylphenol (2,6-DBVP), was prepared from natural rubber and 2,6-DBVP in both solution and melt state. The 2,6-DBVP had been synthesized from 3,5-di-tert-butyl-4-hydroxybenzaldehyde and methyltriphenylphosphonium iodide ($MePPh_3I$) by Wittig reaction ($0^{\circ}C$ for 2 hrs, $N_2$ atmosphere). The conditions for preparation of natural rubber bound 2,6-DBVP (NR-DBVP) were optimized for both solution state (1 phr BPO and 8 phr 2,6-DBVP at $70^{\circ}C$ for 2 hrs) and for melt state (1 phr BPO and 8 phr 2,6-DBVP at $70^{\circ}C$ for 10 mins, with rotor speed of 60 rpm). A thermoplastic vulcanizate was obtained using a compatibilizer, polypropylene modified with phenolic resin (PhHRJ-PP), in a closed mixer ($180^{\circ}C$ for 3 mins, rotor speed 60 rpm). The antioxidant properties of vulcanized NR-DBVP, using phenolic as the vulcanization system, were similar to NR with the conventional antioxidant BHT. In addition, the antioxidant, water leaching property of the thermoplastic vulcanizate of NR-DBVP/PP were good in comparison to a NR blend with BHT; the morphologies of these thermoplastic vulcanizates were similar.

• Journal of the Korean Wood Science and Technology
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• 제28권3호
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• pp.70-77
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• 2000

산뽕나무 심재추출물 중 다량으로 분리된 stilbenoid인 oxyresveratrol, resveratrol과 이들의 구조유사체를 합성하여 항균 및 항산화활성을 측정하고 화학구조와의 상관관계를 검토하였다. 항균활성은 진균에 대해서는 배지점적법으로, 세균에 대해서는 탁도측정법으로, 그리고 항산화활성은 지질산화억제율과 프리라디칼 소거능을 이용하여 검정하였다. 그 결과, 진균 및 세균에 대한 항균활성은 resveratrol이 oxyresveratrol보다 우수하였으며, 항산화활성은 oxyresveratrol이 resveratrol보다 우수하였다. 또한, Wittig 반응으로 합성한 6종의 stilbenoid의 항균활성은 B-ring의 수산기가 적을수록 활성이 높은 경향을 나타내어. 3,5-dihydroxystilbene (pinosylvin)과 같이 B-ring에 수산기가 없는 경우에 가장 높은 활성을 보였으며, trans type이 cis type보다 활성이 높았다. 그러나, 항산화활성은 B-ring의 수산기가 많을수록 활성이 높았으며, B-ring의 수산기가 ortho-diphenol 구조를 가지는 stilbenoid가 활성이 가장 높아, 2',3,3',5-와 3,3',4',5-tetrahydroxystilbene(piceatannol) 의 경우, 합성항산화제인 BHT보다는 높고 천연항산화제인 ${\alpha}$-tocopherol과는 동등한 효능을 보였다. 이상의 결과, 산뽕나무 심재로부터 단리된 resveratrol과 oxyresveratrol은 항균 및 높은 항산화활성을 가지는 것으로 판명되었으며, B-ring의 수산기의 수와 치환위치가 활성에 큰 영향을 미치는 것으로 판명되었다.