• 충청수학회지
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• 제20권3호
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• pp.245-259
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• 2007

We define and study a concept of $T^f$-space for a map, which is a generalized one of a T-space, in terms of the Gottlieb set for a map. We show that X is a $T_f$-space if and only if $G({\Sigma}B;A,f,X)=[{\Sigma}B,X]$ for any space B. For a principal fibration $E_k{\rightarrow}X$ induced by $k:X{\rightarrow}X^{\prime}$ from ${\epsilon}:PX^{\prime}{\rightarrow}X^{\prime}$, we obtain a sufficient condition to having a lifting $T^{\bar{f}}$-structure on $E_k$ of a $T^f$-structure on X. Also, we define and study a concept of co-$T^g$-space for a map, which is a dual one of $T^f$-space for a map. We obtain a dual result for a principal cofibration $i_r:X{\rightarrow}C_r$ induced by $r:X^{\prime}{\rightarrow}X$ from ${\iota}:X^{\prime}{\rightarrow}cX^{\prime}$.

• Bulletin of the Korean Chemical Society
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• 제20권7호
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• pp.791-795
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• 1999

The crystal structure of a cyclopropane sorption complex of dehydrated fully Ca (2+) -exchanged zeolite X, Ca46Si100Al92O384· 30C3H6 (a = 24.988(4) Å), has been determined by single-crystal X-ray diffraction techniques in the cubic space group Fd3 at 21(1)℃. The crystal was prepared by ion exchange in a flowing stream of 0.05M aqueous Ca(NO3)2 for four days, followed by dehydration at 460℃ and 2×10 (-6) Torr for two days, and exposure to 100 Torr of cyclopropane gas at 21(1)℃. The structure was determined in this atmosphere and refined to the final error indices R1 = 0.068 and R2 = 0.082, with 373 reflections for which I > 3σ (I). In this structure, Ca 2+ ions are located at two crystallographic sites. Sixteen Ca 2+ ions fill the octahedral sites I at the centers of the hexagonal prisms (Ca-O = 2.412(9)Å). The remaining 30 Ca 2+ ions are at sites Ⅱ; each extends 0.46Å into the supercage (an increase of 0.16Å upon C3H6 sorption) where it coordinates to three trigonally arranged framework oxygens at 2.311(8)Å. Each of the 30 cyclopropane molecules was found to complex to Ca 2+ ions at site II by the induced dipole interaction (Ca-C = 2.99(4)Å). All carbon atoms in each cyclopropane molecule are equivalent and equidistant from Ca 2+ ions at site II with which they are associated.

• 한국결정학회지
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• 제5권1호
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• pp.14-19
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• 1994

트리풀르오로메칠트리페닐 1,2,4-트리오키소란(C21H15F3O3)은 삼사정계인 공간군 P1으로 a=10.477(1), b=11.056(1), c=9.917(3)A, a=104.7(1), B=122.7(1), r=63.9(1)°, Z=2, V=867.9(3) A3, Dc=1.43 g/cm3, λ(Mo BCn)=0.71069 A, μ=0.0116 cm-1, F(000)=384, 그리고 I ) 1.0 o(I) 인 1713 개의 관측 된 회절점에 대한 R 값은 0.067 였다. 직접법에 의하여 구조를 풀었으며 전행열-최소자숭법에 의하여 정밀화하였고 C-H결합길이는 0.96 A 에 고정하였다. 106.6°의 두 사이각을 갖는 페닐고리(2)와 고리(3)는 트리오키소란분자평면의 위쪽에 있으나 CF3기와 페닐고리(1)은 아래쪽으로 있다. 트리오키소란 꼬리는 봉투모양의 구조를 갖고 있으며 그의 두 탄소 원자(C(2)와 C(3))는 탄소원자의 내각에 거의 비슷한 각으로 치환기들과 연결되어 있다. 분자들은 van der Waals 힘에 의하여 결합되었고 가장 가까운 거리는 0(2) 와 F(2)(-x, 1+y,1-z) 사이의 3.256 A 이다.

• 분석과학
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• 제18권5호
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• pp.391-395
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• 2005

$[Cd(N_3)_2(2-ethylimidazole)_2]$ 착물을 합성하고 단결정 X-선 회절법으로 구조를 규명하였다. 이 착물은 단사정계, 공간군 Cc, a=16.200(3), b=12.926(3), $c=7.007(1){\AA}$, ${\beta}=102.29(3)^{\circ}$, $V=1433.7(5){\AA}^3$, Z=4로 결정화되었으며, 1874 개의 독립적인 회절반점에 대한 최종 신뢰도 인자 $R_1$ 및 ${\omega}R_2$ 값은 각각 0.0239 및 0.0604 이었다. Cd(II) 금속 원자는 4개의 azido 리간드와 2개의 2-ethylimidazole 리간드의 질소 원자가 배위되어 약간 찌그러진 팔면체 구조를 나타낸다. c 축 방향으로 배열되어 있는 Cd(II) 금속 원자 사이를 azido 리간드가 end-on (${\mu}-1$,1) 형태로 bridge 하고 2-ethylimidazole 리간드가 시스 형태로 결합하여 이 착물은 1차원의 zigzag 사슬 구조를 형성한다.

• 한국ITS학회 논문지
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• 제7권5호
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• pp.1-12
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• 2008

본 논문에서는 고속으로 이동하는 차량에 실시간 교통정보서비스를 연속적으로 제공하기 위하여 C&R 서비스에 대한 개념 및 서비스 시나리오를 제시하고, seamless 서비스 구현에 필요한 정보통신 요소기술들과 C&R 통신시스템의 구조와 제공방법에 대해서 기술하였다 향후, 스마트 하이웨이 서비스는 160km/h 이강 고속으로 이동하는 차량에 실시간 C&R 서비스가 이루어지는 정보통신 환경을 구축하는 개념이라 할 수 있다. 지금까지 DSRC 시스템을 기반하의 환경에서는 저속 차량과 통신이 가능하였으나, 고속 이동 환경에는 한계가 있다. 따라서 본 논문에서는 이러한 문제점을 해결하기 위해서 DSRC 기지국과 다수의 중계기의 핸드오버 기술을 이용함으로써, 고속이동 환경에도 적용 가능하며 스마트 하이웨이 환경에 대응할 수 있는 구조를 제안하였다.

• 한국콘크리트학회:학술대회논문집
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• 한국콘크리트학회 1990년도 봄 학술발표회 논문집
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• pp.66-71
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• 1990

The prediction and estimation of R/C structure behavior subjected to earthquake type loading is partly based on the experimental results of the monotonically increased cyclic loading, rather than that of the irregularly increased cyclic loading. However, actual earthquake is typical random vibration. In this respect, comparing and analysing experimental test results of R/C specimens subjected to monotonically increased cyclic loading and irregularly increased cyclic loading, this study proposes the research direction of irregularly increased cyclic loading during earthquake.

• 한국결정학회지
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• 제12권1호
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• pp.10-13
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• 2001

Compound PdCl₂(PhCN)₂(1) reacted with tert-butylamine(t-BuNH₂) to give trans-[PdCl₂(t-BuNH₂)₂] (2) Compound 2 was characterized by spectroscopy (¹H-NMR, /sup 13/C{¹H}-NMR, and IR) and X-ray diffraction. Crystallographic data for f2: monoclinic space group p2₁/c, a=6.298(1)Å, b=20.740(2)Å, c=10.731(1)Å, β=92.58(1)°, Z=4, R(wR₂)=0.0207(0.0543).

• 한국분말야금학회:학술대회논문집
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• 한국분말야금학회 2002년도 추계학술강연 및 발표대회
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• pp.8-8
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• 2002

TiC core/(Ti,Mo)C rim structure in TiC-$Mo_2C$-Ni base cermet which is generally prepared by sintering below 145$0^{\circ}C$ had been believed to be generated by the solid diffusion of Mo atoms 1 into TiC grains (D. Moskowitz and M.Humenik, 1r.:1966). Afterward, it was clarified that the c core/rim structure is generated by solution/re-precipitation mechanism : (1) $Mo_2C$ grains and s small TiC grains dissolve into the Ni liquid, (2) the dissolved Mo, Ti and C atoms migrate to the s surface of TiC coarse grains, (3) the Mo, Ti and C precipitate on the surface of TiC coarse g grains and form (Ti,Mo)C solid solution rim, and (4) the Ostwald ripening (grain growth by s solution/re-precipitation mechanism) of TiC-core/(Ti,Mo)-rim grains continues, and thus the w width of (Ti,Mo)C rim (at the same time, the grain size) increases with sintering time, etc. ( (H.Suzuki, K.Hayashi and O.Terada: 1973). The TiC-core was found not to disappear even by s sintering at 190$0^{\circ}C$ (ibid.: 1974) Recently, FeSi core/$Fe_2Si_5$-rim structure in Fe-66.7at%Si thermoelectric aIloy was found to also h hardly shrink and disappear by long heating at an appropriate temperature (1999: M.Tajima and K K.hayashD. Then, the authors considered its cause, and clarified experimentaIly that the disappearance of FeSi-core/$Fe_2Ski_5$-rim structure could be attributed to the exhaustion of diffusion-contributable vacancies in core/rim structure (N.Taniguchi and K.Hayashi:2001). At p present, the authors and my coworker are investigating whether the non-disappearance of TiC c core can be explained also from the new hypothesis "Exhaustion of diffusion-contributable v vacancies in corelrim structure".ure".uot;.

• Bulletin of the Korean Chemical Society
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• 제18권3호
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• pp.305-310
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• 1997

The synthesis and characterization of the platinum heterocyclic carboxaldehyde thiosemicarbazone complexes [NC5H4CRNNC(S)NHR'PtCl] (R=H, R'=CH3(1); R=CH3, R'=CH3(2); R=CH3, R=H(3)) and diphenylphosphinophenyl carboxaldehyde thiosemicarbazone complexes [Ph2PC6H4CHNNC(S)NHRPtCl] (R=CH3(5); R=iC3H7(6); R=Ph(7)) are described. Compounds 1-3 were prepared by reaction of Pt(SEt2)2Cl2 with 2-acetylpyridine-4-alkylthiosemicarbazone in the presence of NEt3. Compounds 5-7 were prepared using Pt(SEt2)2Cl2 in toluene with diphenylphosphinophenyl carboxaldehyde alkylthiosemicarbazone. The compounds have been characterized by microanalysis, NMR (1H, 13C, 31P) spectroscopy, and single-crystal X-ray diffraction. X-ray single crystal diffraction analysis reveals that compound 5 is a mononuclear platinum compound with P,N,S-coordination mode.

• 한국결정학회지
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• 제12권3호
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• pp.141-144
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• 2001

Na[Ga(N₃)₄]와 PPh₃의 반응으로부터 이온성 화합물 [Ph₃P(OH)]/sup +/[N₃]/sup -/ (1)이 분리되었다. 화합물1의 구조가 분광학적 방법(¹H-NMR, /sup 13/C{¹H-NMR, IR) 및 X-ray 회절법으로 규명되었다. 화합물1의 결정학 자료 : 사방정계 공간군 P2₁2₁2₁, a = 10.491(4)Å, b=11.603(5)Å, c=13.149(5)Å, Z=4, R(wR₂)=0.0547(0.0978).