• Korean Journal of Crystallography
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• v.10 no.1
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• pp.20-27
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• 1999

CaF2 단결정을 흑연도가니를 사용하여 He 분위기 하에서 탄만법으로 성장시켰다. 수화방지를 위해 PbF2를 출발물질에 도포하였다. 열구배에 따른 계면의 움직임인 성장속도는 배플판에 의해 성공적으로 조절되었다. 결정성장의 최적조건은 온도구배가 37℃/cm, 냉각속도가 10℃/hr 및 2.5tw% PbF2를 사용한 경우로, 성장속도는 약 3.2 mm/hr이었으며, 위로 볼록한 고액계면을 갖는 단결정이 성장되었다. IR분석 결과, 1500∼4000 cm-1(6.7∼2.5 ㎛)영역에서 약 96%의 투과도를 보였다. 결함밀도를 측정하기 위해, 성장축에 수직 및 수평으로 절단한 면을 농축 H2SO4에서 약 30분간 에칭하여 간섭현미경으로 관찰한 결과, 각각 3.4×104/cm2였다. 이러한 결과는 수화에 따른 성장된 단결정의 투명도의 경향과 일치하였다. 결정에 대한 XRD분석 결과 우선성장 방향은 <311>이었다.

• Korean Journal of Crystallography
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• v.10 no.1
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• pp.28-32
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• 1999

The title compound consisting of a calix[4]arene molecule with four phenyl rings arranged alternately in anti-orientation fashion, two propyloxy groups attached on the upper rim of calix[4]arene, and polyther chain with two phyenyl rings attached on the lower rim of calix[4]arene offers a big cavity inside a molecule with might a potential for forming host-guest complexes.

• Korean Journal of Crystallography
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• v.16 no.1
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• pp.11-20
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• 2005

Six basic symmetries and five Bravais lattices existing in the two-dimensional lattice are derived and then ten two-dimensional point groups are classified by each of five Bravais lattices. Finally seventeen two-dimensional space groups belonging to the ten point groups are studied.

• Korean Journal of Crystallography
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• v.16 no.1
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• pp.1-5
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• 2005

The structure of the title compound has been determined by single-crystal X-ray diffraction work. The crystals are orthorhombic, space group $Pna2_1$ with a=11.095(3), b=21.834(7), c=12.574(4) $\AA$, and R1=0.0667. The average carbon bond length in aromaticity In the molecule is 1.386(1) $\AA$ and the average single bond length linking the central benEene ring and peripheral phenyl rings is 1.491(3) $\AA$. The average dihedral angle between the central benzene ring and each of six peripheral phenyl rings is $67.1(1)^{\circ}$ and the average dihedral angle between neighboring two phenyl rings is $55.0(1)^{\circ}$. Thus the molecule adopts a quasi-propeller configuration with approximate six-fold rotation symmetry.

• Korean Journal of Crystallography
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• v.11 no.1
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• pp.1-5
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• 2000

An another symmetric cone conformational isomer of p-tert-butylcalix[4]arene hexanoate(C/sub 68/H/sub 96/O/sub 8/) was prepared and was determined by X-ray diffraction method. The crystals are orthorhombic, Pbca, a=20.625(3) Å, b=21.291(3)Å, c=30.22(4)Å, V=13271(2)ų and Z=8. The intensity data were collected on an Enraf-Noninus CAD-4 diffractometer with a graphite monochromated Mo-Kα radiation. The structure was solved by direct method and refined by least-squares calculations to a final R value of 0.138 for 2394 observed reflections. The molecular conformation is distorted symmetric cone with the flattening B and D phenyl rings.

• Korean Journal of Crystallography
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• v.11 no.1
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• pp.10-15
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• 2000

Compound trans-[FeH(NCS(i-Pr)-S)(dppe)₂](1) reacted with isopropyl iodide (i-PrI) to give an Fe(II)-organic isothiocyanide complex, trans-[FeH(NCS(i-Pr)-S)(dppe)₂]I (2). Compound 2 was structurally characterized, in which the hydride ligand appears to be involved in the "dihydrogen" bonding, M-H…H-C. Crystallographic data for 2: monoclinic space group P2₁/n, a=13.490(2)Å, b=17.269(3)Å, c=21.384(3)Å, β=90.682(7)°, Z=4, R(wR₂)=0.0348(0.0894).

• Korean Journal of Crystallography
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• v.11 no.1
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• pp.34-41
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• 2000

The group-theoretical approach analyzing the domain structure and the domain wall orientations of the ferroelastic crystal was introduced. These theoretical results were investigated by comparing them with the experimental results of several ferroelastic crystals, CsPbCl₃, Pb₃(PO₄)₂, and LiCsSO₄, which were grown by the Czochralski and solution methods, respectively. both results were agreed well and also consistent with those of previous works such s the strain method and the geometrical consideration. The group-theoretical approach showed that the ferroelastic domain walls must be the crystallographical prominent planes with fixed indices and classified by the symmetry elements characterizing the permissible domain walls. So the group-theoretical approach could be suggested as a new method for analyzing the structure of the ferroelastic domain and domain walls.

• Korean Journal of Crystallography
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• v.11 no.1
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• pp.46-51
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• 2000

The molecular structures of 2-SC₄H₃CH=NN(H)C/sub 6/H/sub 5/(C/sub 11/H/sub 10/N₂S) and (GaMe₂)₂(2-SC₄H₃CH=NNC/sub 6/H/sub 5/)₂(C/sub 26/H/sub 30/Ga₂N₄S₂) have been determined by X-ray diffraction. Crystallographic data for 2-SC₄H₃CH=NN(H)C/sub 6/H/sub 5/:orthorhombic space group P2₁2₁2₁, a=6.108(1)Å, b=7.593(1)Å, c=22.356(2)Å, V=1037.1(3)ų, Z=4, R=0.0613. Crystallographic data for (GaMe₂)₂(2-SC₄H₃CH=NNC/sub 6/H/sub 5/)₂:monoclinic space group P2₁/n, a=15.996(2) Å, c=9.879(3)Å, β=100.07.(2)°, V=2764.599)ų, Z=4, R=0.0503.

• Korean Journal of Crystallography
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• v.11 no.1
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• pp.52-57
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• 2000

Hydrothermal synthesis of find CeO₂ powder has been investigated. Synthesis was performed with Ce(NO₃)₃·6H₂O, in ethanol and water solution. Mineralizer were NH₄OH and KOH and reaction for the powder synthesis has performed at 130℃. The morphology of CeO₂ was nearly spherical in using NH₄OH and cubic form in KOH. Particle size increased with addition of NH₄OH. Ethanol solution was effective to reduced the agglomeration.

• Korean Journal of Crystallography
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• v.11 no.4
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• pp.191-194
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• 2000

Bi/sub 12/SiO/sub 20/, Bi/sub 12/GeO/sub 20/ and Bi/sub 12/O/sub 20/ compounds with the sillenite crystal structure were synthesized and sintered into the dense ceramic bodies. An analyses of the microwave dielectric properties of the Si, Ge and Ti sillenites showed a permittivity (e) of ∼40 and a negative temperature coefficient of the resonant frequency for all analogues (from -20 to -40 ppm/K). The Qxf value of the Si and Ge sillenites was measured to be ∼8.000 GHz. The Ti analogue shows a significantly lower Qxf value(∼2.500 GHz) and is sensitive to the heat-treatment conditions. By increasing the sintering temperature the size of the grains increases, which correlates with an increase in the Qxf value.