• Bulletin of the Korean Chemical Society
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• 제21권8호
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• pp.761-762
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• 2000

• Bulletin of the Korean Chemical Society
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• 제14권4호
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• pp.524-526
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• 1993

• 한국자기학회지
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• 제21권5호
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• pp.151-156
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• 2011

전기도금법으로 제작한 CoPt 자성막의 두께가 자기상호작용과 자기적 성질에 미치는 영향을 잔류자기화 곡선과 자기이력 곡선을 측정 분석하여 규명하였다. CoPt 자성막의 두께가 증가함에 따라 수직 보자력과 포화자화가 증가하였으나 각형비는 급격히 감소하였다. 잔류자화 곡선의 분석결과로부터 모든 시료의 주된 자기상호작용 기구는 쌍극자 상호작용이며, 시료의 두께가 증가함에 따라 상호작용의 세기가 증가함을 알 수 있었다.

• Bulletin of the Korean Chemical Society
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• 제7권3호
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• pp.170-178
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• 1986

The NMR chemical shift arising from 4d electron angular momentum and 4d electron angular momentum and 4d electron spin dipolar-nuclear spin angular momentum interactions for a $4d^1$ system in a strong crystal field environment of trigonal symmetry, when the threefold axis is chosen to be the axis of quantization axis, has been examined. A general expression using the nonmultipole expansion method (exact method) is derived for the NMR chemical shift. From this expression all the multipolar terms are determined. We observe that along the (100), (010), (110), and (111) axes the NMR chemical shifts are positive while along the (001) axis, it is negative. We observe that the dipolar term (1/R3) is the dominant contribution to the NMR chemical shift except for along the (111) axis. A comparison of the multipolar terms with the exact values shows also that the multipolar results are exactly in agreement with the exact values around $R{\geqslant}0.2$ nm. The temperature dependence analysis on the NMR chemical shifts may imply that along the (111) axis the contribution to the NMR chemical shift is dominantly pseudo contact interaction. Separation of the contributions of the Fermi and the pseudo contact interactions would correctly imply that the dipolar interaction is the dominant contribution to the NMR chemical shifts along the (100), (010), (001), and (110) axes, but along the (111) axis the Fermi contact interaction is incorrectly the dominant contribution to the NMR chemical shift.

• Bulletin of the Korean Chemical Society
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• 제23권3호
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• pp.437-440
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• 2002

A variety of 1,2,3-triazole derivatives bearing acyclic sugar moieties of DHPG and iso-NDG were synthesised by Diels-Alder reaction. None of the new compounds display any interesting biological activity.

• Bulletin of the Korean Chemical Society
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• 제14권3호
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• pp.384-388
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• 1993

• Bulletin of the Korean Chemical Society
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• 제14권5호
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• pp.539-540
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• 1993

• Bulletin of the Korean Chemical Society
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• 제17권7호
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• pp.595-599
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• 1996

1,3-Dipolar cyclization of various nitrile oxides with 3(2H)- and 2(5H)-furanones regioselectively furnished the corresponding syn-addition products of 3-oxotetrahydro-furano[4,5-d]isoxazolines and 2-oxotetrahydrofurano[3,4-d]isoxazolines.

• 한국염색가공학회지
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• 제23권4호
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• pp.284-289
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• 2011

Poly(phenylene sulfide)(PPS) films were photooxidized under UV/ozone irradiation. The effect of UV energy on the surface properties of the UV-irradiation PPS films were investigated by the measurement of reflectance, surface roughness, and contact angle. Reflectance decreased at the wavelength of 400nm and the surface roughness increased with increased UV energy. The improvement in hydrophilicity with increased $O_{1s}/C_{1s}$ was caused by the introduction of hydrophilic $SO_2$ bond. Surface energy increased from 46.6 to $78.3mJ/m^2$ with increased UV energy up to $21.2J/cm^2$. Also zeta potential decreased with increased UV energy. The increased dyeability to cationic dyes may be due to the photochemically introduced anionic and dipolar dyeing sites on the PPS films surfaces.he photochemically introduced anionic and dipolar dyeing sites on the PPS films surfaces.

• Macromolecular Research
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• 제15권6호
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• pp.533-540
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• 2007

We designed and successfully synthesized UV curable, functional acrylate monomers having a polarizing group, i.e., an electron-withdrawing and/or electron-donating group for the optical materials of high refractive index. Optical polymer films made from the functional methacrylate monomers were achieved with photo crosslinking under UV illumination. A monomer having amino and cyano groups (Dimer-CN) exhibited the highest refractive index ($n_{TE}$=1.595 at 850nm) among the studied methacrylate derivatives, due to the large polarizability of the dipolar monomer structures with electron-donating and withdrawing groups. By controlling the compositions of the functional acrylate monomer of copolymers, the refractive indices of the polymers were readily adjusted within a wide range of 1.498-1.595. The copolymers showed a high glass transition temperature $(T_g)$ and good thermal stability, which are desirable for optical applications. $T_g$ and $T_{10%}$ (10%-weight loss occurred) of the copolymers ranged from $120-140^{\circ}C$ and from $329-387^{\circ}C$, respectively.