• 제목/요약/키워드: Phenyl boronic acid

검색결과 7건 처리시간 0.018초

Synthesis and characterization of star-shaped imide compounds

  • Jeon, Eunju;Yoon, Tae-Ho
    • Rapid Communication in Photoscience
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    • 제1권1호
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    • pp.19-20
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    • 2012
  • Novel star-shaped imide compounds containing electron-donating triphenylamine and/or electron-withdrawing bis(trifluoromethyl)phenyl side groups were synthesized via a two-step process. First, 3,6-dibromo-benzene-1,2,4,5-tetracarboxylic acid (2B4BA) was reacted with 4-aminophenyl (diphenylamine) (ATPA) or 3,5-bis(trifluoromethyl)aniline (6FA) by imide reaction. Then, Suzuki coupling reaction was carried out on these compounds with 4-(N,N-diphenylamino)-1-phenyl boronic acid (BTPA) or 3,5-bis(trifluoromethyl)phenyl boronic acid (6FBB), resulting in 3,6-bis[4-(diphenylamino)phenyl]-N,N'-bis[4-(diphenylamino) phenyl]-pyromellitimide (TPTPPI), 3,6-bis[3,5-bis(trifluoro methyl) phenyl]-N,N'-bis[3,5-bis(trifluoromethyl) phenyl]-pyro mellitimide (6F6FPI) or 3,6-bis[4-(diphenylamino)phenyl]-N,N'-bis[3,5-bistrifluoromethyl)phenyl]-pyromellitimide (6FTPPI). The imide compounds obtained were characterized by NMR, FT-IR, DSC, TGA, melting point analyzer, EA, and solubility measurements. In addition, their optical and electrical properties were evaluated by fluorescence spectroscopy, UV-vis spectroscopy, and cyclic voltammetry (CV). 6F6FPI exhibited deep blue emission (443 nm), along with high $T_m$ ($382^{\circ}C$) and relatively high $T_g$ ($148^{\circ}C$).

Development of Analytical Methods for Insect Moulting Hormone $({\beta}-Ecdysone)$ by HPLC/UV Using Boronate Derivatization

  • Shim, Jae-Han;Kim, In-Seon;Lim, Kye-Taek
    • Applied Biological Chemistry
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    • 제41권4호
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    • pp.251-256
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    • 1998
  • The analytical method of ${\beta}-ecdysone$, the insect moulting hormone, by high performance liquid chromatograph (HPLC) with UV detector was developed using boronic ester derivatization and applied to the extracts of Ajuga iva, Silene otites and Schistocerca egg. Derivatization of yield with methyl-, butyl-, and phenyl-boronate was completed under mild conditions with 20-hydroxyecdysone. The conversion ratios of boronate were estimated to be 70% in methylboronic acid, 89% in butylboronic acid and 93% in phenylboronic acid. Phenylboronate showed a high sensitivity and demonstrated an effective separation on HPLC. The optimum temperature and reaction time for derivative formation were $25^{\circ}C$ and 20 min. respectively. ${\beta}-Ecdysone$ was effectively identified in extracts of Ajuga iva, Silene otites and Schistocerca egg by the HPLC method.

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Analysis of 3-MCPD and 1,3-DCP in Various Foodstuffs Using GC-MS

  • Kim, Wooseok;Jeong, Yun A;On, Jiwon;Choi, Ari;Lee, Jee-yeon;Lee, Joon Goo;Lee, Kwang-Geun;Pyo, Heesoo
    • Toxicological Research
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    • 제31권3호
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    • pp.313-319
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    • 2015
  • 3-Monochloro-1,2-propanediol (3-MCPD) and 1,3-dichloro-2-propanol (1,3-DCP) are not only produced in the manufacturing process of foodstuffs such as hydrolyzed vegetable proteins and soy sauce but are also formed by heat processing in the presence of fat and low water activity. 3-MCPD exists both in free and ester forms, and the ester form has been also detected in various foods. Free 3-MCPD and 1,3-DCP are classified as Group 2B by the International Agency for Research on Cancer. Although there is no data confirming the toxicity of either compound in humans, their toxicity was evidenced in animal experimentation or in vitro. Although few studies have been conducted, free 3-MCPD has been shown to have neurotoxicity, reproductive toxicity, and carcinogenicity. In contrast, 1,3-DCP only has mutagenic activity. The purpose of this study was to analyze 3-MCPD and 1,3-DCP in various foods using gas chromatography-mass spectrometry. 3-MCPD and 1,3-DCP were analyzed using phenyl boronic acid derivatization and the liquid-liquid extraction method, respectively. The analytical method for 3-MCPD and 1,3-DCP was validated in terms of linearity, limit of detection (LOD), limit of quantitation, accuracy and precision. Consequently, the LODs of 3-MCPD and 1,3-DCP in various matrices were identified to be in the ranges of 4.18~10.56 ng/g and 1.06~3.15 ng/g, respectively.

붕소/실리콘 졸로 도포된 목재의 열위험성 평가 (Heat Risk Assessment of Wood Coated with Boron/Silicone Sol)

  • 진의;정영진
    • 한국화재소방학회논문지
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    • 제33권3호
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    • pp.9-20
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    • 2019
  • 본 연구는 붕소/실리콘 화합물을 건축 내장재용 목재에 도포한 후 화재위험성을 열 위험성에대하여 화재성능지수와 화재성장지수를 중심으로 조사하였다. 화합물은 Boric acid와 Boronic acid 유도체를 Tetraethoxyorthosilicate와 반응시켜 합성하였다. 열방출 성질은 Cone calorimeter (ISO 5660-1)를 사용하여 측정하였으며 편백나무를 사용하였다. 화재강도는 외부 열 유속(External heat flux)을 50 kW/㎡로 고정시켰다. 연소시킨 후 측정된 화재성능지수는 편백나무와 비교하여 Boric acid/silicone (BA/Si) sol이 1.6배, Isobutylboronic Acid/silicone 졸 (IBBA/Si)과 Phenyl boronic acid/silicone 졸 (PBA/Si)은 각각 1.1배 증가하였다. 화재성능지수에 의한 화재위험성은 BA/Si < IBBA/Si ≈ PBA/Si 순으로 증가하였다. 화재성장지수는 편백나무와 비교하여 BA/Si와 IBBA/Si는 각각 94%, 8% 감소하였고 PBA/Si는 17% 증가하였다. 화재성장지수에 의한 화재위험성은 BA/Si < IBBA/Si < PBA/Si 순으로 증가하였다. 화재위험성을 종합적으로 평가하면 BA/Si < IBBA/Si < PBA/Si 순으로 높았다.

Electroluminescent Properties of Spiro[fluorene-benzofluorene]-Containing Blue Light Emitting Materials

  • Jeon, Soon-Ok;Lee, Hyun-Seok;Jeon, Young-Min;Kim, Joon-Woo;Lee, Chil-Won;Gong, Myoung-Seon
    • Bulletin of the Korean Chemical Society
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    • 제30권4호
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    • pp.863-868
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    • 2009
  • New spiro[fluorene-7,9′-benzofluorene]-based blue host material, 5-phenyl-spiro[fluorene-7,9′-benzofluorene] (BH-1P), was successfully prepared by reacting 5-bromo-spiro[fluorene-7,9′-benzofluorene] (1) with phenyl boronic acid through the Suzuki reaction. 5-(N,N-Diphenyl)amino-spiro[fluorene-7,9′-benzofluorene] (BH-1DPA) and diphenyl-[4-(2-[1,1;4,1]terphenyl-4-yl-vinyl)-phenyl]amine (BD-1) were used as dopant materials. 2,5-Bis-(2',2"- bipyridin-6-yl)-1,1-diphenyl-3,4-diphenylsilacyclopentadiene (ET4) and Alq3 were used as electron transfer materials. Their UV absorption, photoluminescence and thermal properties were examined. The blue OLEDs with the configuration of ITO/DNTPD/$\alpha$-NPD/BH-1P:5% dopant/$Alq_3$ or ET4/LiF-Al prepared from the BH-1P host and BH-1DPA and BD-1 dopants showed a blue EL spectrum at 452 nm at 10 V and a luminance of 923.9 cd/$m^2$ with an efficiency of 1.27 lm/W at a current density of 72.57 mA/$cm^2$.

임상검체에서 분리된 그람음성막대균으로부터 카바페넴 내성 유전자 검출 (Detection of the Carbapenem Resistance Gene in Gram-negative Rod Bacteria Isolated from Clinical Specimens)

  • 양병선
    • 대한임상검사과학회지
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    • 제54권3호
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    • pp.179-191
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    • 2022
  • 본 연구는 공중보건에 위협이 되고 있는 carbapenemase 유전자형 중 blaKPC, blaNDM, blaIMP, blaVIM, blaOXA-48-like 유전자의 표현형적 검사 및 분자진단으로 검출하고 관련 유전자 분포 양상에 대해 알아보았다. 표현형적 검사결과 MHT는 41균주 모두에서 양성을 확인하고, CIT는 meropenem+PBA는 18균주 및 meropenem+EDTA에서 8균주의 양성을 확인하였다. PCR 결과 blaKPC 28균주, blaNDM 25균주, blaIMP 5균주, blaVIM 1균주, blaOXA-48-like 13균주에서 증폭 산물을 확인하였다. 또한 blaKPC+blaNDM 7균주, blaKPC+blaIMP 1균주, blaNDM+blaOXA-48-like 1균주, blaNDM+blaVIM 1균주, blaKPC+blaNDM+blaIMP 4균주, blaKPC+blaNDM+blaOXA-48-like 4균주를 확인하였다. 실시간 중합효소 연쇄반응을 이용한 융해 곡선 분석결과는 PCR 결과와 100% 일치함을 확인하였다. 결론적으로 real-time PCR을 이용한 신속하고 특이성이 높은 CRE 조기진단을 통한 유전자 확인은 제한된 치료 옵션과 높은 사망률로 공중 보건 위협을 고조하는 CRE의 감시, 진단 및 치료를 개선할 수 있으며 전염을 방지하기 위한 효과적인 항균 치료 및 시기적절한 감염 통제가 가능할 것으로 사료된다.