• Bulletin of the Korean Chemical Society
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• 제31권5호
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• pp.1204-1208
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• 2010

Anion recognition via hydrogen-bonding interactions could be monitored with changes in UV-vis absorption spectra and in some cases easily monitored with naked eye. Urea receptors 1 and 2 connected with both an azo group and a nitrophenyl group as a signaling group for color change proved to be an efficient naked eye receptor for the fluoride ion. The anion recognition phenomena of the receptors 1 and 2 via hydrogen-bonding interactions were investigated through UV-vis absorption and $^1H$ NMR spectra.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2006년도 추계학술대회 논문집 Vol.19
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• pp.166-167
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• 2006

Dendrimers represent a new class of synthetic macromolecules characterized by a regularly branched treelike structure. Multiple branching yields a large number of chain ends that distinguish dendrimers from conventional star-like polymers and microgels. The azobenzene dendrimer is one of the dendrimeric macromolecules that include the azo-group exhibiting a photochromic character. Due to the presence of the charge transfer element of the azo-group and its rod-shaped structure, these compounds are expected to have potential interest in electronics and photoelectronics, especially in nonlinear optics. In the present paper, we give pressure stimulation to organic thin films and detect the induced displacement current. Functional photoisometrization organic molecular the photo-stimulus to organic monomolecular L-films and LB films of dendrimer and 8A5H were performed. The 8A5H organic monolayer in case of pressure stimulus occurred that positive course but in case of the photo-stimulus compared positive and negative. It is assumed that generation forms of displacement current were measured when photo-stimulus for Impression.

• 공업화학
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• 제9권1호
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• pp.66-70
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• 1998

정보전자 기기의 디스플레이용 재료로 사용되는 액정/고분자 복합재료의 매트릭스로 사용하기 위한 새로운 선형 및 가교형 측쇄 액정고분자를 제조하기 위하여 필요한 저분자 액정 중간체들을 합성하고 이들의 액정 특성을 살펴보았다. Alkyl spacer의 길이가 다르고 연결기로서 azo기를 그리고 말단기로서 cyano를 공통적으로 가지고 다른 한 말단기로서 bromoalkyl(AZO(n)), azidoalkyl(AZI(n)) 및 amonoalkyl(ALC(n))기를 가지는 저분자 액정 들의 합성을 하였으며 IR, NMR 및 원소분석을 통하여 이를 확인할 수 있었다. 또한 DSC thermogram 및 편광현미경 관찰로부터 이들 저분자 액정들은 모두 일정한 온도 영역에서 네마틱 상의 액정성을 발현하는 것을 알았다. 또한, 저분자 액정 분자들이 spacer 길이, 즉 $-(CH_2)n-$의 n이 짝수 및 홀수로 변화함에 따라 분자 내의 conformation 변화에 따른 $T_{KN}$과 $T_{NI}$의 값이 전형적인 even-odd 변화 현상을 나타내었다.

• 한국염색가공학회:학술대회논문집
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• 한국염색가공학회 2008년도 제39차 학술발표회
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• pp.23-24
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• 2008

본 연구는 고 세탁견뢰도 특성을 가진 Phthalimed계 염료를 합성하고, 일반 PET 섬유 및 해도형 PET에 염색하여 염색거동과 견뢰도 특성에 대해 알아보았다. 대부분의 염료는 5급 이상의 세탁견뢰도를 가지며, 몇가지 염료는 70%이상의 염착률을 가진다.

• 한국섬유공학회:학술대회논문집
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• 한국섬유공학회 1996년도 추계 학술발표회
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• pp.105-110
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• 1996

• 대한화학회지
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• 제16권5호
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• pp.320-327
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• 1972

韓國産 土炭의 흄酸의 性狀(分子量, 分子式 및 示性式)과 基應用(田沓用 土壤改良制 및 溶性燐質 肥料製造)에 關해서 이미 硏究報韓 바가 있으나, 흄酸의 構造를 推定하는데 있어서, 未及한 鮎이 있어서, 이의 補完策으로서 aromatic diazonium salt를 coupling 시켜, phenolic-OH group 의 結合狀態를 살펴보고 各種 aromatic diazonium salt와 흄酸 및 니트로흄酸에 依해서 얻어진 生成物들을 Azo 染料로 利用함으로서 應用策의 一環을 講究했다.

• KIEE International Transactions on Electrophysics and Applications
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• 제11C권4호
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• pp.146-149
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• 2001

The functionalized dendrimer containing 48 azobenzene was synthesized. Many isolated featureless domains were explicitly observed even at the air/water interface. Also, these monolayers were representatively observed, showing the change of surface pressure with irradiation time and wavelength. In AFM images, larger domains irregularly shaped structures on the top, while smaller ones were free from such defects. In the optical absorption spectra of the monolayer films by UV irradiation and heat treatment, only the photoiosmerization of the G4-48 Azo monolayers was observed, revealing a decrease of absorbance peaks without any change of the spectral shape. This suggests that the functional group and the symmetric chain affect optical behavior and morphological change.

• Bulletin of the Korean Chemical Society
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• 제30권5호
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• pp.1143-1146
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• 2009

[$Mn_{12}O_{12}(azo-L)_{16}(H_2O)_4$] (1), a new Mn12 single molecule magnet containing a photochromic azobenzene ligand, has been successfully synthesized by substitution of acetate ligand of Mn12 with 6-[4-{4-hexyloxyphenyl( azo)}-phenoxy]hexanoic-1-acid. The reversible photoisomerization of the azobenzene group was confirmed by UV-visible absorption spectroscopy. The temperature and field dependence of dc susceptibility and the temperature and the frequency dependence of ac susceptibility were measured for the cis and the trans isomer of 1. The magnetization value of the cis isomer in dc measurement is higher than that of the trans isomer. The cis isomer of 1 has a slower relaxation because cis-trans photoisomerization of the azobenzene group in peripheral ligands induces changes in its structure and dipole moment.

• 대한전기학회:학술대회논문집
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• 대한전기학회 2006년도 추계학술대회 논문집 전기물성,응용부문
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• pp.10-11
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• 2006

The azobenzene dendrimer is one of the dendrimeric macromolecules that include the azo-group exhibiting a photochromic character. Due to the presence of the charge transfer element of the azo-group and its rod-shaped structure, these compounds are expected to have potential interest in electronics and photoelectronics, especially in nonlinear optics. In the present paper, we give pressure stimulation to organic thin films and detect the induced displacement current. Functional photoisometrization organic molecular the photo-stimulus to organic monomolecular L films and LB films of dendrimer and SASH were performed. The SASH organic monolayer in case of pressure stimulus occurred that positive course but in case of the photo-stimulus compared positive and negative. It is assumed that generation forms of displacement current were measured when photo-stimulus for impression.

• Advances in materials Research
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• 제1권4호
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• pp.299-310
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• 2012

This article describes the synthesis of a novel N-substituted pyrrole monomer containing an azobenzene group. The 2-[N-ethyl-N-[4-[(4-nitrophenyl) azo]-phenyl] amino] ethyl-3-chloropropionate (RedII) compound was synthesized via reaction of 4-nitro-4'-[N-ethyl-N-(2-hydroxyethyl)-amino] azobenzene (RedI) and 3-chloropropionic acid. RedII was reacted with the potassium salt of pyrrole then 2-[N-ethyl-N-[4-[(nitro phenyl) azo] phenyl] amino] ethyl-N-pyrrolyl propionate (Py-RedII) was prepared. Chemical polymerization of Py-RedII and copolymerization of Py-RedII with pyrrole carried out using $FeCl_3$. Poly (2-[N-ethyl-N-[4-[(nitro phenyl) azo] phenyl] amino] ethyl-N-pyrrolyl propionate) (PPy-RedII) was characterized by UV, IR, $^1HNMR$, $^{13}CNMR$ spectroscopies. Electropolymerization of Py-RedII and electroco-polymerization of Py-RedII and pyrrole were studied using conventional three electrodes system, Ag/AgCl reference electrode, platinum counter electrode and GC disk working electrode. Scanning electron microscopy (SEM), thermogravimetry analysis (TGA) and differential scanning calorimetry (DSC) were used for thermal and rheological studies. The TGA curve of PPy-RedII demonstrated a high thermal stability up to 200°C and its DSC thermogram showed two endothermic peaks at 88 and $122^{\circ}C$. The glass transition temperature of the polymer was found to be above the room temperature. Electrical conductivities of PPy-RedII and it's copolymer with pyrrole (PPy-RedII-co-Py) were studied by the four-probe method and produced conductivities of $7.5{\times}10^{-4}$ and $6.5{\times}10^{-3}Scm^{-1}$, respectively.