• 대한방사선기술학회지:방사선기술과학
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• 제29권3호
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• pp.147-155
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• 2006

기체 저장제로서 제올라이트의 구조와 기체분자의 유출입 기전을 이해하기 위해 완전히 탈수된 $K_3-A$들을 제조하고 $K_3Na_8H-A(R_1=0.0478,\;R_2=0.0458$ 및 $a=12.257(1){\AA}$)의 결정구조들을 Pm3m 입방 공간군에서 단결정 X-ray 회절 방법으로 연구하였다. 진공 탈수된 $K_3Na_8H-A$의 결정구조에 있어서, 단위세포 당 3개의 $K^+$ 이온들이 8-ring(0.0, 0.4531, 0.4531) 상에 존재하였고, 단위세포 당 8개의 $Na^+$ 이온들이 6-oxygen ring들의 중앙에 위치하였다. 8-ring상에 존재하는 각 $K^+$ 이온들은 두 가지 종류의 골격산소 원자들로 부터 각각 $2.87(2){\AA}$과 $2.79(1){\AA}$의 거리를 가지고 있었다. 이러한 값들은 이미 기존에 알려진 $K_{12}Na-A$의 값들보다 더 짧은 값으로 이들의 이온 반경들을 고려할 때 더 타당한 값들이였다. $K^+$ 이온들의 정확한 위치들은 8-ring들의 중앙으로부터 약 $0.8{\AA}$ 떨어져 있었다. 이러한 결과는 제올라이트 골격을 안전화시켜 기체분자들의 효과적인 유출입 통제와 저장을 가능하게 하며, 유효 부피 극대화를 이루어 더 많은 기체 저장을 할 수 있으므로 병원에서 사용하는 산소 저장 용기를 더욱더 소형임은 물론 산소가 필요한 응급환자 들을 위한 휴대하기 간편한 용기를 만들어 줄 것으로 예상된다.

• Journal of Pharmaceutical Investigation
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• 제13권1호
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• pp.1-9
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• 1983

The effect of humidity on crystallization and polymorphic transformation of hydrous aluminum oxide under various humidity at $37^{\circ}$ was examined by means of X-ray diffraction, scanning electron micrograph, IR spectra and DTA. The humidity was an important factor influencing crystallization of hydrous aluminum oxide. The growth or crystal was strongly accelerated by humidity. The aging process is assumed that it is composed of two seperate steps, an increase of the diffraction around $36{\sim}42^{\circ}$, and an appearance and its development of the peak at $18{\sim}20^{\circ}$ of $2{\theta}$ value. The former is considered to be nucleation and the latter correspond to the growth period on crystallization. The crystalline form of aging products was various depending on the degree of humidity, directly it leads to the eventual formation of bayerite in more than 72%, $b{\"{o}}hmite$ in 50% and resembled to Nordstandite in 0% relative humidity, respectively but once formed, it was mostly stable in each surroundings and does not transform to the other more stable form in solid state even after aging for five years. The mechanism responsible for aging is further polymerization process of six-membered rings by deprotonation-dehydration reaction in which positively charged polynuclear hydroxy aluminum complexes formed in the presence of moisture are joined at their edges by double hydroxide bridges.

• Journal of Pharmaceutical Investigation
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• 제26권1호
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• pp.55-59
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• 1996

The crystal structure of diflunisal, 2',4'-difluoro-4-hydroxy-3-biphenyl-carboxylic acid, was determined by single crystal X-ray diffraction technique. The compound was recrystallized from a mixture of acetone and water in monoclinic, space group C2/c, with $a\;=\;34.666(6),\;b\;=\;3.743(1),\;c\;=\;20.737(4)\;{\AA},\;{\beta}=\;110.57(2)^{\circ}$, and Z = 8. The calculated density is $1.324\;g/cm^3$. The structure was solved by the direct method and refined by full matrix least-squares procedure to the final R value of 0.045 for 1299 observed reflections. It was found that the molecules in the crystal are partially disordered, that is, the two equivalent conformers $(180^{\circ}$ rotated ones through C(1)-C(7)) are packed alternatively without regular symmetry or sequence. The two phenyl rings of the biphenyl group is tilted to each other by the dihedral angle of $43.3^{\circ}$. The carboxyl group at the salicylic moiety is just coplanar to the phenyl ring, and the planarity of this salicylic moiety is stabilized by an intramolecular hydrogen bond of O(3)-H(O3) O(2). The molecules are dimerized through the intermolecular hydrogen bonds at the carboxyl group in the crystal.

• 통합자연과학논문집
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• 제6권4호
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• pp.197-204
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• 2013

The crystal structure of the potential active 4,6-dimethyl-9-phenyl-8,12-dioxa-4,6-diazatetracyclo [8.8.0.02,7.013,18] octadeca-2(7),13,15,17-tetraene-3,5,11-trione 2-ethoxyphenyl (2E)-but-2-enoate ($C_{22}H_{18}N_2O_5$) has been determined from single crystal X-ray diffraction data. In the title compound crystallizes in the monoclinic space group $P_12_1/c_1$ with unit cell dimension a=15.2039(8), b=12.3888(6) and c= 9.8162(5) [alpha & $gamma=90^{\circ}$ beta=98.113(2)]. In the structure fused pyrone and pyran rings each adopt a sofa/envelop conformation. The crystal structure is stabilized by intramolecular C-H... O hydrogen bond interaction.

• 한국윤활학회:학술대회논문집
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• 한국윤활학회 2002년도 proceedings of the second asia international conference on tribology
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• pp.135-136
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• 2002

Molybdenum Nitrided (MoNx) films were deposited by DC planar magnetron sputtering. Silicon wafers and real nitrided stainless steel piston rings are employed as substrates. 12 different combinations of nitrogen and argon partial pressure, from 1:7 to 7:1, were applied to deposit MoNx films. X-ray diffraction (XRD) was used to determine the phase structures of films. When nitrogen vs. argon partial pressure is 1:7, the film is mainly $Mo_2N$ phase. With increase of nitrogen partial pressure, MoN phase emerges, but $Mo_2N$ phase still exists. Composition analysis with atomic emission spectrometry (AES) also agreed with this. The films have very high nanohardness (max 2400Hv) and good adhesion to the substrates.

• 한국결정학회지
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• 제11권1호
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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.

• Journal of information and communication convergence engineering
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• 제12권2호
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• pp.83-88
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• 2014

The simultaneous suppression of sidelobes and the sharpening of the central peak in the process of diffraction pattern detection based on asymmetric apodization have been investigated. Asymmetric apodization is applied to a semicircular array of two-dimensional (2D) aperture functions, which is a series of 'coded-phase arrays of semicircular rings randomly distributed over the central circular region of a pupil function' and is similar to that used in the field of diffractive optics. The point spread function (PSF) of an imaging system with asymmetric apodization of the discrete type has been found to possess a good side with suppressed sidelobes, whereas its bad side contains enhanced sidelobes. Further, the diffracted field characteristics are obtained in the presence of these aperture functions. Asymmetric apodization is helpful in improving the performance of the optical gratings or 2D arrays used in real-time imaging techniques.

• Archives of Pharmacal Research
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• 제19권2호
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• pp.160-162
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• 1996

The structural analysis of tolfenamic acid, 2-[(3-chloro-2-methylphenyl)-amino]benzoic acid, was performed by single crystal X-ray diffraction technique. The compound was recrystallized from a mixture of ether and toluene in triclinic, space group $P2_1/c, \;with\; \partial=3.914(1), \; b=22.\; 020(2), \; c=14.271(1)\;{\AA}, \beta.=94.68(1)^{\circ}, $ and Z=4. The calculated density is $1.418 g/cm^3$. The structure was solved by the direct method and refined by full matrix least-squares procedure to the final R value of 0.039 for 1773 independent reflections. In the molecule, carboxyl group at the anthranilic acid is coplanar to the phenyl ring. The dihedral angle between the two aromatic rings of the molecule is $44.2^{\circ}$ The molecules are dirnerized through the intermolecular hydrogen bonds at the carboxyl group in the crystal.

• Bulletin of the Korean Chemical Society
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• 제20권8호
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• pp.905-909
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• 1999

Reaction of tetrahomodioxa p-phenylcalix[4]arene with ethyl bromoacetate and potassium carbonate in ace-tone leads to the title tetra ester derivative, 7,13,21,27-tetra-phenyl-29,30,31,32 -tetrakis(ethoxycarbonyl)meth-oxy-2,3,16,17-tetrahomo-3,17-dioxacalix[4]arene, its structure was determined by NMR spectra as 1,4-alternate conformation. The molecular structure has been solved by X-ray diffraction methods. The molecule has a conformation with pseudo center of symmetry. The benzene ring A is up, ring C is down, B and D rings are flat with respect to the plane of the macrocyclic ring.

• Bulletin of the Korean Chemical Society
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• 제12권5호
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• pp.525-529
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• 1991

A simple route is described for the selective functionalization of calixarene at the para positions of phenyl rings. Calix[4]arene tetraacetate 2, obtained from the treatment of calix[4]arene with acetic anhydride, undergoes Fries rearrangement to yield the diametrically para substituted p-diacetylcalix[4]arene 3 in 80% yield. The crystal and molecular strucutre has been determined by X-ray diffraction method. The crystals are orthorhombic, space group Pna21, with a = 11.121 (3), b = 10.374 (3), c = 21.690 (6) $\AA$ and Z = 4. The structure was solved by direct method and refined by full-matrix least-squares methods to final R of 0.036 for 1795 observed reflections. Each hydroxyl hydrogen atom is disordered over two positions. The macrocycle exists in the cone conformation which is determined by the strong circular intramolecular flip-flop type hydrogen bonds of phenolic OH, while crystal packing effects of the diametrically para-acetyl substituents seem to be responsible for the distortion of the cone conformation.