• Bulletin of the Korean Chemical Society
• /
• v.29 no.12
• /
• pp.2459-2464
• /
• 2008

• Journal of Pharmaceutical Investigation
• /
• v.21 no.4
• /
• pp.223-230
• /
• 1991

The structural specificity and the chemical dynamics between ${\beta}-cyclodextrin$ and aspirin were studied by FT-IR UN, $^1H$ NMR. $^{13}C NMR$. and FAB-MS spectroscopy in solution and solid state, A stable solid inclusion complex was prepared by the recrystallization method, From the spectral changes of the host and guest molecules, orientational preference for binding in the cyclodextrin cavity was determined.

• Archives of Pharmacal Research
• /
• v.3 no.1
• /
• pp.57-64
• /
• 1980

Carbon-13 NMR spectroscopy(abbreviated CMR) is an extremely powerful strategy for the study of natural organic molecules. The information derivable from CMR is often complementary to that obtianed form proton NMR spectroscopy (PMR). Because of low natural abundance of $^{13}C$ nucleus (1.1%) coupled with low inherent sensitivity relative to $^{1}H$ (about 1/64), CMR experiment is approximately 6000 times less sensitive than PMR. Despite of this, now it is possible to measure CMR of small amount of compound by the development of three significant ingenious techniques, i. e. a) computer time-averaging, b) wide-band (or noise modulated) proton decoupling, and c) pulsed Fourier transform (FT) NMR : For general recognition of CMR, its fundamental aspects of CMR are briefly reviewed.

• Applied Chemistry for Engineering
• /
• v.19 no.1
• /
• pp.133-136
• /
• 2008

In order to decrease carbon dioxide, one of the green house gas, poly(styrene carbonate) has been synthesized from carbon dioxide and styrene oxide with zinc glutarate as a catalyst. The polymer has been identified as an alternating copolymer by spectroscopic analysis, FT-IR, $^1H$-NMR, and $^{13}C$-NMR. The number average molecular weight ($M_n$) of the polymer is $5.0{\times}10^4g/mol$ and the glass transition temperature ($T_g$) is $88^{\circ}C$ and its melting point ($T_m$) is $240^{\circ}C$. The cyclic carbonate, styrene carbonate, has been obtained by thermal degradation of the polymer via the unzipping mechanism.

• Polymer(Korea)
• /
• v.27 no.3
• /
• pp.176-182
• /
• 2003

The fluorine-containing epoxy resin, 2-trifluorotoluene diglycidylether (FER) was prepared by reaction of 2-chloro-${\alpha}$,${\alpha}$,${\alpha}$-trifluorotoluene with glycerol diglycidylether in the presence of pyridine catalyst. Curing behavior of FER/DDM system was investigated using dynamic and isothermal DSC. Cure activation energy (Ea) was determined by Flynn-Wall-Ozawa's equation. The rheological properties of FER/DDM system were studied under isothermal condition using a rheometer. Cross-linking activation energy (Ec) was determined from the Arrhenius equation based on gel time and curing temperature. As a result, the chemical structure of FER was confirmed by FT-IR, $\^$13/C NMR, and $\^$19/F NMR spectroscopy. The cure activation energy of FER/DDM system was 55.4 kJ/mol and conversion and conversion rate were increased with the curing temperature. The cross-linking activation energy of FER/DDM system was 41.6 kJ/mol and gel time was decreased with the curing temperature.

• Applied Chemistry for Engineering
• /
• v.18 no.2
• /
• pp.116-120
• /
• 2007

The synthesis of 1-[2-(3-{7-oxabicyclo[4.1.0]heptyl} 1,1,3,3-tetramethyl-disiloxane (Mono), which is a key intermediate for the synthesis of monomers applied for photopolymer systems based on the cationic ring opening polymerization, was studied. Mono was successfully synthesized by the hydrosilylation reaction of 4-vinyl-1-cyclohexene 1,2-epoxide (VCHO) with an excess amount of 1,1,3,3-tetramethyldisiloxane (TMDS) in the presence of a Speier catalyst. The structure and the purity of Mono were characterized by FT-IR, $^1H-NMR$, and $^{29}Si-NMR$. The optimum conditions for the hydrosilyation reaction were found to be 1:4 molar ratio of VCHO to TMDS and 5 ppm of the catalyst at the temperature of $55^{\circ}C$.

• Applied Chemistry for Engineering
• /
• v.29 no.5
• /
• pp.524-532
• /
• 2018

In this study, two types of amino acids-based anionic biosurfactants such as potassium cocoyl glutamate (CTK) and sodium cocoyl glutamate (CTN) were synthesized from coconut oils and the structure elucidation of CTK and CTN was carried out by using FT-IR, $^1H-NMR$ and $^{13}C-NMR$ spectrophotometries. Measurements of interfacial properties such as static and dynamic surface tensions and emulsification activity showed that both CTK and CTN were surface-active and effective in lowering the interfacial free energy. In particular, the CTK surfactant was found to be more efficient in reducing the interfacial free energy since the larger number of CTK molecules was preferentially adsorbed at the air-water interface due to the higher hydrophobicity and larger mobility of CTK than those of using CTN, indicating possible uses in cosmetics and household products formulation.

• Applied Chemistry for Engineering
• /
• v.25 no.4
• /
• pp.352-356
• /
• 2014

PDMS modified epoxy resin with epoxy group (EMPDMS) was prepared from the reaction of ${\alpha},{\omega}$-aminopropylpolydimethylsiloxane and diglycidyl ether of bisphenol-A (DGEBA) based epoxy resin, and PDMS modified epoxy hybrid compound (EMPDMSH) was prepared by introducing alkylesteraminopropyl alkoxy silane to EMPDMS. Their structures were characterized using FT-IR, $^1H$-NMR and $^{29}Si$-NMR. Coating materials were prepared by mixing EMPDMSH base and solvent. Physical properties of the coating materials coated on epoxy/glass fiber composite film were measured according to the content of PDMS in EMPDMSH. Contact angle of coating film was increased 30 to 71 degree. Adhesive property of coating film was 5B degree better then epoxy or acrylate coating materials, and surface roughness was decreased as increasing in EMPDMSH.

• Polymer(Korea)
• /
• v.26 no.1
• /
• pp.9-17
• /
• 2002

The free radical bulk copolymerizations of perfluoroalkylethyl acrylate(FA) containing perfluoro group ($CF_3(CF_2)_nCH_2CH_2$-; n=5, 7, 9, 11) with styrene were conducted at $60^{\circ}C$ using AIBN as an initiator. Reactivity ratios($r_1$, $r_2$) were determined from monomer feed compositions and the NMR spectroscopically measured copolymer compositions using Kelen-Tudos method. The structures of copolymers were characterized with FT-IR and $^1H-NMR$ analysis. Their thermal properties investigated with DSC and TGA were decreased with increasing the content of fluorinated acrylate in the copolymer. Their surface free energies were calculated with measuring contact angles of the copolymers and PMMA blends with a small amount of them.

• Membrane Journal
• /
• v.22 no.3
• /
• pp.191-200
• /
• 2012

New composite membranes were manufactured by impregnating post-sulfonated poly(arylene ether sulfone)s containing perfluorocyclobutane (PFCB) groups into porous polytetrafluoroethylene (PTFE) films. Two kinds of post-sulfonated poly(arylene ether sulfone)s with two different monomer ratios (sulfonable biphenylene monomer : non-sulfonable sulfonyl monomer = 6 : 4, 4 : 6) were first prepared through three synthetic steps: synthesis of trifluorovinylether-terminated monomers, thermal cycloaddition polymerization and post-sulfonation using chlorosulfonic acid (CSA). The composite membranes were then prepared by adjusting the concentrations (5~20 wt%) of the resulting copolymers impregnated in the PTFE films. The water uptake, ion exchange capacity (IEC) and ion conductivity of the composite membranes were characterized and compared with their unreinforced dense membranes and Nafion. All the synthesized compounds, monomers and polymers were characterized by $^1H$-NMR, $^{19}F$-NMR and FT-IR and the composite membranes were observed with scanning electron micrographs (SEM).