• 제목/요약/키워드: Trifluoromethyl

검색결과 110건 처리시간 0.025초

Washing Effects on Generation of Pretilt Angle in NLC, 5CB, on a Polyimide Surface with Trifluoromethyl Moieties

  • Lee, Sang-Keuk;Hwang, Jeoung-Yeon;Seo, Dae-Shik
    • 한국전기전자재료학회:학술대회논문집
    • /
    • 한국전기전자재료학회 2003년도 춘계학술대회 논문집 디스플레이 광소자분야
    • /
    • pp.133-135
    • /
    • 2003
  • The washing effects on pretilt angle generation in a nematic liquid crystal (NLC), 4-n-pentyl-4’-cyanobiphenyl (5CB) on a rubbed polyimide (PI) surface with trifluoromethyl moiety have been successfully studied. The pretilt angle of 5CB is increased by the washing process on the rubbed PI surface. The surface tension on the rubbed PI surface increases with the rubbing strength RS and then saturated above RS=150 mm. The pretilt angle of 5CB for all washing processes on the rubbed PI surface decreases with the surface tension. We have found that the pretilt angle of 5CB on the rubbed PI surface may be attributed van der walls (VDW) dispersion interaction between the LC molecules and the polymer surfaces having trifluoromethyl moieties.

  • PDF

Synthesis and Characterization of Fluorinated Polyimides for Optical Waveguide Application

  • Han, Kwansoo
    • Macromolecular Research
    • /
    • 제8권4호
    • /
    • pp.165-171
    • /
    • 2000
  • Fluorinated polyimides with high thermal stability, low optical absorption loss in the optical communication wavelengths of 1.3 and 1.55㎛, and low birefringence and water absorption have been investigated for optical waveguide applications. These polyimides were prepared from 2,2-bis(3,4-dicar-boxyphenyl) hexafluoropropane dianhydride (6FDA) with 1,4-bis-(4-amino-2-trifluoromethyl-phenoxy) tetrafluorobenzene (ATPT) , 1,4-bis-(4-amino-2-trifluoromethyl-phenoxy) benzene (ATPB) , and 1,3-bis-(4-amino-2-trifluoromethyl-phenoxy ) 4,6-dichlorobenzene (ATPD ), respectively. The polyimides obtained had glass transition temperatures that ranged from 260 to 280$\^{C}$, and low water absorption less than 0.4% and low optical loss (> 0.2 dB/cm) at 1.3 and 1.55㎛. Birefringency values of polymer films ranged from 0.0041 to 0.0066.

  • PDF

Synthesis and Liquid Crystalline Properties of Dimesogenic Compounds Containing Trifluoromethyl Substituents at Terminal Phenylene Rings and Central Decamethylene Spacer

  • Jo, Byung-Wook;Choi, Jae-Kon;Jin, Jung-Il;Chung, Bong-Yong
    • Bulletin of the Korean Chemical Society
    • /
    • 제11권4호
    • /
    • pp.333-339
    • /
    • 1990
  • A series of new dimesogenic compounds whose mesogens are of aromatic ester or amide type having a trifluoromethyl $(CF_3)$ substituent at the para-position of each terminal phenolic rings were prepared and their liquid crystalline properties were studied by differential scanning calorimetry (DSC) and on a cross-polarizing microscope. The compounds have two identical mesogenic units bracketing a central decamethylene spacer. Trifluoromethyl group appears to favor the formation of smectic phases when it is attached to a phenoxy or anilide terminal. Its group efficiency for mesophase formation seems to be inferior to other common substituents. A thermodynamic analysis of the phase transitions was made and the results were explained in relation to the structures of the compounds.

신규(新規) 살충제(殺蟲劑)인 KH-502 [O,O-Diethyl O-(1-phenyl-3-trifluoromethyl-5-pyrazoyl) thiophosphoric acid ester]의 광(光)에 의한 분해성(分解性) (Photolysis of a New Insecticide KH-502 [O,O-diethyl O-(1-phenyl-3- trifluoromethyl-5-pyrazolyn) thiophosphoric acid ester])

  • 조부연;한대성;양재의
    • 한국환경농학회지
    • /
    • 제12권2호
    • /
    • pp.176-183
    • /
    • 1993
  • 신규 살충제인 KH-502의 안전성을 조사하기 위하여 다양한 조건하에서 광(光) 분해(分解) 실험을 수행하였다. 이 실험에서 KH-502를 acetone 또는 acetonitrile 용액에 첨가한 뒤 태양광선 또는 자외선 $(300{\sim}350nm)$을 조사(照射)하였고, acetone 또는 acetonitrile 용액에는 수분함량, 산소함량이 달랐으며, 부식산,rosebengal 또는 tryptophan이 첨가 되었다. KH-502의 안전성 및 분해경향에 대한 결과를 요약하면 다음과 같다. 1. KH-502의 광분해(光分解)는 자외선을 조사(照射)한 경우와 그렇치 않은 경우에 매우 유의성있는 차이를 보여 주었다. KH-502는 acetone 용매에서 광관여효과에 의해 광분해(光分解)되었으나, acetonitrile 용매 하(下)에서는 광분해되지 않았다. 2. KH-502의 광분해 경향은 열 분해 경향과 판이하게 달랐으며, 광분해산물은 KH-502 oxo형, S-ethyl KH-502, PTMHP 및 몇가지 미지물질 등이었다. 3. acetone 또는 acetonitrile에 첨가된 부식산, rosebengal, tryptophan은 KH-502의 광분해에 광관여효과를 나타내지 않았다. acetone 용매의 용존산소는 acetone과 함께 경쟁적으로 광관여효과를 나타내어 KH-502의 분해를 촉진시켰다. 4. acetone 용매를 부식산 또는 논물로 처리했을때, KH-502의 광분해는 감소하였다.

  • PDF

신규(新規) 살충제(殺蟲劑)인 O, O, O-Diethyl-O-(1-phenyl-3-trifluoromethyl-5-pyrazoyl) thiophosphoric acid ester의 열(熱)에 의한 분해성(分解性) (Thermal Decomposition of A New Insecticide KH-502 [O, O-Diethyl O-(1-phenyl -3-trifluoromethy-5-pyrazoyl) thiophosphoric acid ester])

  • 조부연;한대성
    • 한국환경농학회지
    • /
    • 제11권3호
    • /
    • pp.225-234
    • /
    • 1992
  • Thermal decomposition was conducted to investigate the influence of the various factors on stability of a new insecticide, [O, O-Diethyl O-(1-phenyl-3-trifluoromethyl-5-pyrazoyl) thiophosphoric acid ester : KH-502], in view of those informations applicable for industrial exploitation. In the thermal decomposition experiment, KH-502 was, after mixing with Fe, Cu and adjustment of moisture and pH conditions, subjected to three temperatures, 25, 50, and $100^{\circ}C$. Results for stability, and degradation pattern of KH-502 from the above experiment can be summarized as follows: 1. Main products of the thermal decomposition when this was conducted in the closed system were identified as following five compounds:O, O, O-Triethylthiophosphoric acid(TEPA), 1-Phenyl-3-trifluoromethyl-5-ethoxypyrazole(PTMEP), 1-Phenyl-2-ethyl-3-trifluoromethyl-5-hydroxypyrazole(PETMHP), O, O-Diethyl O-(1-phenyl-3-trifluoromethyl-5-pyrazoyl)phosphoric acid ester(KH-502 oxo form), O, S-Diethyl O-(1-phenyl-3-trifluoromethyl-5-pyrazoyl)phospho rothiolate(S-ethyl KH-502). However, compounds such as oxo form and S-ethyl KH-502 were not identified when the thermal decomposition was proceeded in the open system. 2. KH-502 was stable at 25 and 50$^{\circ}C$, but it was decomposed at 100$^{\circ}C$ following the first-order kinetics at the early stages of decomposition. 3. Rate constants for the thermal decomposition of KH-502 at 100$^{\circ}C$ were in the orders of Cu powder addition 0.344>Cu plate addition 0.21>moisture addition 0.05>closed system=open system=iron addition=pH 5.5 adjustment 0.04>pH 8.5 adjustment 0.027 day$^{-1}$, representing KH-502 was decomposed fast at Cu powder treatment and slow at pH 8.5 adjustment. 4. Half-life for the thermal decomposition of KH-502 at 100$^{\circ}C$ was in the orders of Cu powder addition 2.02

  • PDF

Rotational Photoisomerization of Thioamide, N-5-Trifluoromethyl-6-methoxy-1-thionaphthoyl-N-methylglycine

  • Shim, Sang-Chul;Lee, Sang-Jin
    • Bulletin of the Korean Chemical Society
    • /
    • 제9권4호
    • /
    • pp.236-240
    • /
    • 1988
  • A thioamide, N-5-trifluoromethyl-6-methoxy-1-thionaphthoyl-N-m ethylglycine, undergoes trans${\rightleftharpoons}$cis photoisomerization around C-N bound in solution. Azulene quenching studies showed the photoisomerization to proceed via both singlet and triplet excited states.The total quantum yield of the trans${\rightarrow}$cis photoisomerization is about 0.26, 0.14 from the singlet excited state and 0.12 from the triplet excited state. Intersystem crossing and internal conversion quantum yields were calculated from sensitized photostationary state and a plausible mechanism is proposed.

제초성 Flazasulfuron의 Smile 자리옮김 반응 (Smile Rearrangement of Herbicidal Flazasulfuron)

  • 이광재;김용집;김대황;성낙도
    • Applied Biological Chemistry
    • /
    • 제39권1호
    • /
    • pp.70-76
    • /
    • 1996
  • 일련의 pyridylsulfonyl urea들을 합성하고 25%(v/v) 디옥산 수용액의 넓은 pH범위에서 가수분해 반응속도 상수를 측정하였다. pH-효과, 용매 효과($m{\ll}1,\;n{\ll}3$${\mid}m{\mid}{\ll}{\mid}{\ell}{\mid}$), 일반 염기-효과, 산-해리상수(pKa, 3: 4.9 및 5: lit.4.6), 열역학적 활성화 파라미터(${\Delta}H^{\neq}=0.025\;Kcal.mol.^{-1}$${\Delta}S^{\neq}=0.54{\sim}\;-2.19\;e.u.$) 및 생성물 분석 결과로부터 반응속도식을 유도하고 가수분해 반응 메카니즘을 제안하였다. 즉, 비(H)치환체, 1-(4,6-dimethoxypyrimidine-2-yl)-3-(2-pyridylsulfonyl) urea, 3은 산성용액에서 A-2형(또는 $A_{AC}2$)반응 그리고 염기성 용액 에서는 $(E_1)_{anion}$ 메카니즘으로 가수분해 반응이 일어난다. 반면에 trifluoromethyl-치환체, 1-(4,6-dimethoxypyrimidine-2-yl)-3-(3-trifluorornethyl-2-pyridylsulfonyl) urea, 5(Flazasulfuron)는 산성 용액중에서 $A-S_N2Ar$형의 반응으로 생성된 conjugate acid($5H^+$), 그리고 pH 9.0 이상에서는 $(E_1)_{anion}$$(E_1CB)_R$ 반응으로 생성된 conjugate base(CB)를 거쳐 산성 및 염기성 용액중에서 모두 5원자 고리 중간체를 경유하는 Smile 자리옮김 반응으로 산성에서는 3-trifluoromethyl-2-pyridylpyrimidinyl urea(PPU) 그리고 염기성에서는 3-trifluoromethyl-2-pyridyl-4,6-dimethoxy-pyrimidinyl amine(PPA)을 생성하는 가수분해 반응이 일어남을 알았으며 5는 3보다 약 3.5배 빠른 반응속도를 나타내었다.

  • PDF

새로운 살충제, 1-(2,6-Difluorobenzoy)-3-(3,5-bistrifluoro-methyl-2-chlorophenyl) urea (DBI-3204)의 합성법 (Practical synthesis of a new insecticide, 1-(2,6-difluorobenzoy)-3-(3,5-bistrifluoro-methyl-2-chlorophenyl) urea (DBI-3204))

  • 황일선;김선옥;김중호;정근회
    • 농약과학회지
    • /
    • 제6권2호
    • /
    • pp.105-109
    • /
    • 2002
  • Bezoylphenyl urea계 신규 살충제인 1-(2,6-difluorobenzoyl)-3-(3,5-bistrifluoromethyl-2-chlorophenyl) urea (DBI-3204, HW-3204)를 생산하기 위하여 경제적인 합성법을 확립하였다. 특히 3단계 합성공정에 사용하는 용매를 사염화탄소로 단순화 시켰다. 필수적인 중간체인 3,5-bis(trifluorornethyl)-2-chloroaniline을 92%로 선택적으로 합성하였으며, 2,6-difluorobenzoylisocyanate는 95%, DBI-3204는 약 90%의 좋은 수율로 합성하였다.

Washing Effects on Generation of Pretilt Angle in NLC, 5CB, on a Polyimide Surface with Trifluoromethyl Moieties

  • Lee, Sang-Keuk;Han, Jeong-Min;Hwang, Jeoung-Yeon;Seo, Dae-Shik
    • Transactions on Electrical and Electronic Materials
    • /
    • 제4권1호
    • /
    • pp.21-23
    • /
    • 2003
  • The washing effects on pretilt angle generation in a nematic liquid crystal (NLC), 4-n-pentyl-4'-cyanobiphenyl (5CB) on a rubbed polyimide (PI) surface with trifluoromethyl moiety have been successfully studied. The pretilt angle of 5CB is increased by the washing process on the rubbed PI surface. The surface tension on the rubbed PI surface increases with the rubbing strength RS and then saturated above RS: 150 mm. The pretilt angle of 5CB for all washing processes on the rubbed PI surface decreases with the surface tension. We have found that the pretilt angle of 5CB on the rubbed PI surface may be attributed van der walls (VDW) dispersion interaction between the LC molecules and the polymer surfaces having trifluoromethyl moieties.

Protective Effects of Cinnamic Acid Derivatives on Gastric Lesion

  • Lee, Sun Yi;Hwang, In Young;Jeong, Choon Sik
    • Natural Product Sciences
    • /
    • 제23권4호
    • /
    • pp.299-305
    • /
    • 2017
  • P-methoxycinnamic acid and 3,4,5-trimethoxycinnamic acid are the compounds found in Polygalae Radix, the root of Polygala tenuifolia Willdenow, and have been reported to have hepatoprotective and anti-neurodegenerative effects. On the other hand, there are no reports of their effects on gastric lesions. This study examined the inhibitory effects of cinnamic acids, including p-methoxycinnamic acid, 3,4,5-trimethoxycinnamic acid, and 8 compounds (cinnamic acid, 2-(trifluoromethyl) cinnamic acid, 3-(trifluoromethyl) cinnamic acid, trans-4-(trifluoromethyl) cinnamic acid, 4-(dimethylamino) cinnamic acid, 3,4-(methylenedioxy) cinnamic acid and 3,4-dihydroxycinnamic acid), which were selected based on their presence in medicinal herbs and molecular weight, against gastric lesions. Animal models were used to confirm the protective effects on acute gastritis caused by the administration of HCl/EtOH. Gastric acid inhibition was examined by an acid-neutralizing test and the proton pump ($H^+/K^+$-ATPase) inhibiting activity. In addition, antioxidant tests were performed and the gastric emptying rate was determined. The results showed that cinnamic acid, p-methoxycinnamic acid, and 3,4,5-trimethoxycinnamic acid had an inhibitory effect on gastric lesions.