• 한국광물학회지
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• 제22권4호
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• pp.407-415
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• 2009

전자빔 조사를 조사량에 따라 단계별로 수행하면서 전자빔을 조사하는 동안 다이아몬드 내에서 일어나는 질소관련 결함의 변화와 색상의 변화를 분광학적 방법으로 측정 분석하였다. 일반적으로 질소의 양이 적을수록 공공이 쉽게 생성되며 A집합체보다 B집합체가 많은 시료에서 공공이 빠르게 생성된다는 결과를 보였다. 그 이유로 공공의 생성 정도가 전자빔에 의해 파괴될 수 있는 크기를 가진 결함의 양 즉, platelets에 비례한다는 결론을 추론할 수 있었다. 그리고 조사량이 증가할수록 옅은 녹색을 지닌 청색에서 짙은 청색으로 변화한다. 이러한 청색의 발현은 GR1센터의 점진적인 증가로 GR1센터 흡수포논에 의한 흡수띠의 영역은 더욱 확장되어 가시광선이 투과하는 최고 파장대가 530 nm에서 500 nm로 이동하면서 나타나는 현상이다.

• Bulletin of the Korean Chemical Society
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• 제14권5호
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• pp.561-567
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• 1993

The twelve macrocycle (L) complexes of cadmium(II) nitrate have been synthesized: $CdL(NO_3)_2$. All the complexes have been indentified by elemental analysis, electric conductivity measurements, IR and NMR spectroscopic techniques. The molar electric conductivities of the complexes in water and acetonitrile solvent were in the range of 236.8-296.1 $cm^2{\cdot}mol^{-1}{\cdot}ohm^{-1}$ at 25$^{\circ}$C. The characteristic peaks of macrocycles affected from Cd(II) were shifted to lower frequencies as compared with uncomplexed macrocycles. A complex with 1,4,8,11-tetrakis(methylacetato)-1,4,8,11-tetraaza cyclodecane (L4) exhibited two characteristic bands such as strong stretching (1646 $cm^{-1})$, and weaker symmetric stretching band (1384 $cm^{-1})$. NMR studies indicated that all nitrogen donor atoms of macrocycles have greater affinity to cadmium(II) metal ion than do the oxygen atoms. The $^{13}$C-resonance lines of methylene groups neighboring the donor atom such as N and S were shifted to a direction of high magnetic field and the order of chemical shifts were $L_1 < L_2 < L_3 < L_6 < L_4$. Also the chemical shifts values were larger than those of methylene groups bridgeheaded in side-armed groups. This result seems due to not only the strong interaction of Cd(Ⅱ) with nitrogen donors according to the HSAB theory, but weak interaction of Cd(Ⅱ) and COO- ions or sulfur which is enhanced by the flexible methylene spacing group in side-armed groups. Thus, each additional gem-methyl pairs of L_3, L_4\;and\; L_6$ macrocycles relative to $L_1, L_2,\;and\;L_5$ leads to an large enhancement in Cd(II) affinity. ^{13}C$-NMR spectrum of the complex with $L_{12}$ (1,5,9,13-tetracyclothiacyclohexadecane-3,11-diol) reveals the presence of two sets of three resonance lines, and intensities of the each resonance line have the ratio of 1 : 2 : 2. This molecular conformation is predicted as structure of tetragonal complex to be formed by coordinating two sulfur atoms and the other two sulfur atoms which is affected by OH-groups.

• 헤리티지:역사와 과학
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• 제48권4호
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• pp.4-23
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• 2015

출토 청동유물은 매장 상태에서 구성 성분, 제작기법, 매장 환경 등에 의해 형태 및 화학적으로 특성을 가지는 부식층이 형성된다. 안정한 상태의 부식층은 유물을 보호할 뿐만 아니라 유물의 정보를 담고 있으며, 이를 통한 부식층의 특성과 메커니즘 이해는 보존처리 시 중요한 자료가 된다. 화합물의 화학적 정보를 구별하고 분석이 가능한 분석 방법 중에 라만분광분석법은 원소분석이 주로 이루어졌던 미세영역에 대해서 화합물의 화학적 정보 및 구조에 대한 정확한 정보를 얻을 수 있는 분석방법이다. 이에 본 연구에서는 출토 청동용기에 대해서 라만분광분석을 실시하여 출토 청동유물의 부식층의 특성을 확인하고 SEM-EDS 분석을 병행하여 종합적인 고찰을 하고자 하였다. 분석 결과 출토 청동유물의 외부 부식층에서는 구리 화합물인 malachite와 부식 환경에 기인한 albite, quartz, microcline 등과 같은 토양 및 점토 광물이 혼재되어 층을 형성하고 있다. 이는 매장 상태에서 부식이 진행되었음을 보여 줄 수 있다. 내부 부식층에서는 cuprite가 확인되며 일부 라만스펙트럼에서 나타나는 차이는 산화주석과 같은 혼재되어 있는 화합물에 의한 간섭으로 추정된다. 또한 내부 부식층에 존재하는 납 편석은 PbO, $PbSO_4$, $PbCO_3$ 형태로 존재하거나 cuprite로 대체되는 것을 확인하였다. 조사 샘플의 수가 적고 매장 토양에 대한 정보의 부족으로 일반적인 결론을 내릴 수는 없지만, 이러한 결과들을 통해서 청동유물에서 나타나는 부식과정과 오랜 시간 부식된 청동에서만 나타날 수 있는 특성들을 명확히 규명할 수 있다면 진위판별에 적용 가능성이 있다. 따라서 다양한 출토 유물에 대한 분석과 부식 환경까지 종합적으로 검토하는 추가적 연구가 필요할 것으로 사료된다.

• Bulletin of the Korean Chemical Society
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• 제24권4호
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• pp.484-488
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• 2003

Polycarbosilanes containing diacetylene and organosilacyclic groups, such as poly(1,1-diethynyl-1-silacyclopent-3-ene), poly(1,1-diethynyl-3-triethylsilyl-1-silacyclopent-3-ene), and poly(1,1-diethynyl-1- silacyclobutane), were synthesized by the Glaser oxidative coupling polymerization reactions of 1,1-diethynyl-1-silacyclopent-3-ene, 1,1-diethynyl-3-triethylsilyl-1-silacyclopent-3-ene, and 1,1-diethynyl-1-silacyclobutane, respectively. These materials are almost insoluble in usual organic solvents such as $CHCl_3$ and THF. The polymers were characterized by using several spectroscopic methods in solid state. FTIR spectra of all the polymeric materials show that the characteristic C≡C stretching frequencies appear at 2146-2170 $cm^{-1}$, in particular. The polymers in the solid state show that the strong maximum excitation peaks appear at 255-257 nm and the strong maximum fluorescence emission bands at 401-402 nm. About 71-87% of the initial polymer weights remain at 400 ℃ in nitrogen according to thermogravimetric analysis.

• Bulletin of the Korean Chemical Society
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• 제34권6호
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• pp.1637-1642
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• 2013

We carried out the melt copolymerization reactions of 1,2-bis(diethylamino)tetramethyldisilane with several aryldiols such as, 4,4'-biphenol, 4,4'-isopropylidenediphenol, 9H-fluoren-9,9-dimethanol, and 4,4'-(9-fluorenylidene) bis(2-phenoxyethanol) to afford poly[oxy(arylene)oxy(tetramethyldisilylene)]s containing fluorescent aromatic chromophore groups in the polymer main chain: poly[oxy(4,4'-biphenylene)oxy(tetramethyldisilylene)], poly[oxy{(4,4'-isopropylidene) diphenylene}oxy(tetramethyldisilylene)], poly[oxy(9H-fluorene-9,9-dimethylene) oxy(tetramethyldisilylene)], and poly[oxy{4,4'-(9-fluorenylidene)bis(2-phenoxyethylene)}oxy(tetramethyldisilnylene)]. These prepared materials are soluble in common organic solvents such as $CHCl_3$ and THF. The obtained polymers were characterized by several spectroscopic methods such as $^1H$, $^{13}C$, and $^{29}Si$ NMR. Further, FTIR spectra of all the polymers exhibited characteristic Si-O stretching frequencies at 1014-1087 $cm^{-1}$. These polymeric materials in THF showed strong maximum absorption peaks at 268-281 nm, strong maximum excitation peaks at 263-291 nm, and strong maximum fluorescence emission bands at 314-362 nm due to the presence of tetramethyldisilylene and several arylene chromophores in the polymer main chain. TGA thermograms indicated that most of the polymers were stable up to $200^{\circ}C$ with a weight loss of 3-16% in nitrogen.

• Fibers and Polymers
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• 제5권3호
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• pp.239-244
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• 2004

Solution-cast films of polymethylmethacrylate (PMMA) and polyurethane (PU) containing polymeric styryl dye up to 5 % by weight were prepared to investigate their acid-sensitivity and mechanical and thermal properties. Original red samples due to styryl dye turned out yellow very rapidly as they were exposed to acid vapor of hydrochloric acid or p-toluenesulfonic acid. According to UV/VIS spectroscopic measurements, characteristic peak intensities near 430 nm and 520 nm increased or decreased relatively with exposed amounts of acid, respectively. Both PMMA and PU samples showed uniform color distribution due to a good miscibility between polymer and dye which can be evidenced by measurements of glass transition temperature. No significant difference in acid-sensitivity was found between PU and PMMA except relative absorbance. However, dependence of their mechanical properties on dye content was somewhat different with PU or PMMA. In case of PMMA, modulus and breaking stress increased up to about 50 % with increasing dye content, whereas those of PU samples showed only slight increase. It was ascribed to whether the matrix polymer was in the glassy or rubbery state.

• BMB Reports
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• 제43권11호
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• pp.766-771
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• 2010

The biological evaluation of a new synthesized Pt(II)-complex, 2,2'-bipyridin Butylglycinato Pt(II) nitrate, an anti-tumor component, was studied at different temperatures by fluorescence and far UV circular dichroism (CD) spectroscopic methods. Human serum albumin (HSA) and human tumor cell line K562 were as targets. The Pt(II)-complex has a strong ability to quench the intrinsic fluorescence of HSA. Binding and thermodynamic parameters of the interaction were calculated by fluorescence quenching method. Far-UV-CD results showed that Pt(II)-complex induced increasing in content of $\alpha$ helical structure of the protein and stabilized it. The 50% cytotoxic concentration ($Cc_{50}$) of complex was determined using MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide) assay at different incubation times. Also, fluorescence staining with DAPI (4,6-diamidino-2-phenylindole) revealed some typical nuclear changes, which are characteristic of apoptosis. Above results suggest that Pt (II) complex is a promising anti-proliferative agent and should execute its biological effects by inducing apoptosis.

• 폴리머
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• 제27권6호
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• pp.603-608
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• 2003

신디오탁틱 폴리스티렌 (5-PS)는 시료의 처리 조건에 따라 여러 구조를 가지며 열처리에 따른 고체상의 구조 전이현상을 보여준다 서로 다른 s-PS 사슬 및 결정 구조를 가지는 시료들을 상온에서 220 $^{\circ}C$까지 온도를 올려가며 열처리하여 준비한 후 FTIR과 FT-Raman 분광계를 이용하여 구조의 변화를 조사하였다. 빠른 결정화 속도 때문에 DSC 실험으로 측정하기 힘든 x-PS 시료의 열처리 시간에 따른 결정화도 변화를 결정 부분과 비결정 부분 infrared특성피크 세기에 따라 측정한 후 Beer-Lambert 법칙에 적용하여 조사할 수 있었다.

• Food Science and Biotechnology
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• 제15권1호
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• pp.107-111
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• 2006

Kernel oils of Lindera erythrocarpa seeds had high level of unusual fatty acid. Picolinyl ester of this unknown fatty acid showed molecular ion at m/z = 317 with other diagnostic ions such as m/z = 151, 191 (40 amu between two peaks), 204, and 218 on GC-MS. Characteristic peak at $720\;cm^{-1}$ appeared in IR spectrum. In $^1H-NMR$ spectrum both methylene protons at C-3 and C-6 resonated at ${\delta}2.309$ and ${\delta}2.012$, and methine protons of double bond resonated in lower magnetic field centered at ${\delta}5.296$ (C-4) and ${\delta}5.387$ (C-5) as multiplet (J = 9.7Hz). In $^{13}C-NMR$, signals at ${\delta}22.669$ and ${\delta}27.048$ were due to C-3 and C-6 of ${\delta}^4$-monoenoic acid. Results obtained from spectroscopic measurements confirmed unknown fatty acid as cis-4-tetradecenoic acid (cis-4-$C_{14:1}$). Main fatty acid components of oils were cis-4-$C_{14:1}$ (44.5-45.1%), oleic acid ($C_{18:1}$), 20.4-21.3%), and lauric acid ($C_{12:0}$, 11.6-12.4%), along with trace amounts of cis-4-$C_{12:1}$ and cis-4-$C_{16:1}$.

• KSBB Journal
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• 제15권6호
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• pp.673-676
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• 2000

호염성 세균이 갖는 특성 즉, 다른 균에 의한 오염 감소, 세포벽 파괴의 수월성, 용매를 이용하지 않는 색소추출 등을 응용하기 위한 기초 자료를 얻기 위하여 호염성 세균인 Haloarcular sp. EH-1 으로부터 추출한 천연색소를 bioreactor 에서 배양한 후 색소의 함량을 조사한 결과 3 L 용량에서는 8 83.1 mg%, 5 L 용량에서는 82.7 mg%의 카로테노이드를 함 유하는 것으로 나타났다 이들의 주된 성분은 $\beta$-c따otene (8.1 %), $\beta$-hydroxyechinenone (42.0%) 및 astaxanthin(25.0% )으로 동정 되었으며, 이들 성분을 동정하기 위하여 표품과의 co- TLC, co-HPLC, 가시부 홉수스펙트럼, 화학적 변화 등을 조사하였다.