• 한국의학물리학회지:의학물리
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• 제12권1호
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• pp.79-94
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• 2001

생물학적 조직(Biological Tissue)에서 얻어내는 형광(Fluorescence)은 산란(Scattrering), 흡수(Absorption), 그리고 형광체(Fluorophores)가 원인이 되는, 인트린식 형광(Intrinsic Fluorescence)들에 관한 정보를 갖고 있다. 생물학적 조직의 형광스펙트럼은 조직 내에 존재하는 흡수체(Absorber)와 산란물질(Scatters)들의 영향을 받기 때문에 다른 조직의 생화학적인 인트린식 형광을 선형적인 조합으로 해석할 수 없었다. 생물학적 조직 같은 터비드 매질(Turbid Media)로부터 실험적으로 형광을 얻어서 산란과 흡수의 영향을 조사하기 위하여 본 연구소에서 제작한 장치를 소개하고, 넓은 범위의 흡수체와 산란물질의 농도를 갖고 제작한 조직 팬텀(Tissue Phantom)에 대한 형광과 반사(Reflectance) 스펙트럼을 측정하였다. 형광스펙트럼에 존재하는 산란과 흡수의 왜곡(Distortion)을 제거하기 위하여, 반사스펙트럼에 포함된 산란과 흡수 정보를 이용하는 ‘광자 이동 모델(Photon Migration Model)’을 적용하였고, 이러한 조직모델에 대한 인트린식 형광을 얻었다 연구 결과, 모델 값과 실제 인트린식 형광 스펙트럼이 훌륭하게 일치함을 확인하였다. 이런 연구를 하게된 동기는, 인간의 조직이 병들어서 진화하면 조직의 생화학적 구성의 변화가 발생하고 이때 인트린식 형광의 변화가 생기기 때문이다 결론적으로, 조직에 대한 실시간 광학적 생검에서 병든 조직과 정상조직을 단지 형광스펙트럼만으로 구분하는 것은 어렵지만, 인트린식 형광을 이용하면 가능하다.

• 한국염색가공학회지
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• 제6권1호
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• pp.28-32
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• 1994

The synthesis and absorption spectra of squarvlium(SQ) dyes and croconium(CR) dyes were .studied. Absorption spectra of SQ dye in various solvents exhibited a negative solvatochrornism. Thus, it was suggested that the structure of SQ dye may be a highly polar structure. The λ$_{max}$ of CR dyes undergoes a bathochromic shift of about 100nm compared with the corresponding SQ dyes. This shift can be calculated by the Pariser-Parr-Pople molecular orbital method. From the PPP MO calculation results, we found that SQ dye and CR dye have a almost same Highest Occupied Molecular Orbital(HOMO) level(SQ : -8.0eV, CR : -8.09eV). On the other hand, energy levels of Lowest Unoccupied Molecular Orbital(LUMO) of SQ and CR dyes are -4.09eV and -4.13eV respectively. Thus, replacement of five membered ring by four membered ring in SQ dye causes a large bathochromic shift.t.

• Macromolecular Research
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• 제12권5호
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• pp.501-506
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• 2004

We have investigated the spectral properties of DNA, including its electric absorption, circular and linear dichroism (CD and LD), and fluorescence emission, in the DNA-linear polyethyleneimine (LPEI) and DNA-branched polyethyleneimine (BPEI) complexes at various polymer concentrations. The spectral properties of both complexes are similar. We observed a relatively moderate change in the absorption and CD spectra at low amine/DNA phosphate (NIP) ratios (< 0.5), followed by a drastic collapse within the N/P range from 0.8 and 1.0. The absorption and CD spectra recovered as the N/P ratio increased to ca. 1.2. In contrast, the LD and emission of ethidium intercalated between the DNA bases decreased almost linearly at N/P ratios between 0.0 and 1.0. These spectra never recovered at higher N/P ratios. We believe that the moderate changes in the spectrum at low N/P ratios occurred because of electrostatic interactions between DNA and BPEI, while the collapsed spectra at N/P ratios between 0.5 and 1.5 occurred because of condensation/aggregation of the DNA. Considering the structure of the polymers, we suggest that the secondary amino group of LPEI and all three amino groups of BPEI are equally involved in DNA condensation.

• 천문학회보
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• 제38권1호
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• pp.62.1-62.1
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• 2013

The Cassini/Visual Infrared Mapping Spectrometer (VIMS) observed the sun through the atmosphere of Titan, and provided vertically-resolved 63 spectra from 49 km to 987 km for the 1 - 5 micron range (Bellucci, 2008). Bellucci et al. (2009) analyzed selected spectral ranges where the band absorptions of $CH_4$ and CO are strong by constructing synthetic spectra including $CH_4$ and CO lines, but without including haze absorptions in their synthetic spectra. Kim et al. (2011) and Sim et al. (2013) were able to extract detailed spectral features of fundamental (Dv = 1) and overtone (Dv = 2) bands of the haze from the VIMS spectra by excluding the adjacent influences of strong $CH_4$ absorptions using a radiative transfer program, which includes effects of absorption and emission of lines of these molecules, and absorption and scattering of haze particles. In this presentation, we extend our detailed analyses to other remaining wavelengths in order to provide the spectral characteristics of the Titanian haze for the entire 1 - 5 micron range and to identify any additional haze spectral features and an unidentified feature near 4.3 microns reported by Bellucci et al. (2009).

• 대한화학회지
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• 제43권1호
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• pp.1-7
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• 1999

이 논문에서는 광화학적 방법을 이용하여 금속 콜로이드 입자를 반도체 나노입자를 함유한 수용액내에서 제조하여 그 광학적 특성을 관찰하였다. 형성된 금속입자는 사용된 반도체 입자에 따라 다른 경향을 나타낸다. Au 금속 입자를 CdS 입자를 함유한 수용액내에서 제조한 경우 일반적인 금속 입자의 Plasmon Resonance의 특성을 보이는 반면 Ag금속 입자를 AgBr 입자를 함유한 용액내에서 제조한 경우 Red-Shift 현상을 보였고, 그 정도는 UV 조사량에 따라 달라졌다. 이러한 금속 Plasmon Resonance의 Red-Shift 현상을 Effective Medium 이론을 이용하여 이론적으로 설명하였다.

• Bulletin of the Korean Chemical Society
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• 제32권12호
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• pp.4171-4175
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• 2011

Bio-functionalized gold nanoparticles (AuNPs), which bio-specifically interact with biotin-(strept)avidin, were investigated in this study. AuNPs were functionalized with a synthetically-provided biotin-linked thiol (BLT), which was synthesized by amidation of the active ester of biotin with 2-mercaptoethylamine. The BLT-attached AuNP was bio-specific for streptavidin, making it potentially useful for biosensor applications. To test the bio-specific interactions, the colors, absorption spectra and TEM images were investigated for proteins such as streptavidin, cytochrome C, myoglobin and hemoglobin. The colors and absorption spectra changed when streptavidin was added to the BLT-attached AuNP solution. However, the color and spectra did not change when the other proteins were added to the same solution. These results show that the AuNPs provided a colloidal solution with excellent stability and highly selective absorption characteristics for streptavidin as a target molecule. Proteins were also screened in order to identify a general strategy for the use of optical biosensing proteins based on AuNPs. In addition, TEM images confirmed that streptavidin led the BLT-attached AuNPs to aggregate or precipitate.

• Bulletin of the Korean Chemical Society
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• 제34권11호
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• pp.3211-3217
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• 2013

Density functional theory (DFT) and time-dependent DFT (TD-DFT) calculations have been employed to investigate the molecular structures and absorption spectra of three D-${\pi}$-A-type organic dyes (C1-1, D5 and TH208) containing identical ${\pi}$-spacers and electron acceptors, but different aromatic amine electron-donating groups (tetrahydroquinoline, triphenylamine and phenothiazine). The coplanar geometries indicate that the strong conjugation is formed in the dyes. The electronic structures suggest that the intramolecular charge transfer from the donor to the acceptor occurs, and the electron-donating ability of tetrahydroquinoline is stronger than those of triphenylamine and phenothiazine. The computed orbital energy levels of these dyes confirm that the electrons could be injected from the excited dyes to the semiconductor conduction band and the oxidized dyes could be reduced effectively by electrolyte. The TD-DFT results show that the CAM-B3LYP/6-31+G(d, p) is suitable for calculating the absorption spectra. The first absorption band for these dyes is assigned to the HOMO${\rightarrow}$LUMO and HOMO-1${\rightarrow}$LUMO transitions.

• Bulletin of the Korean Chemical Society
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• 제22권8호
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• pp.837-841
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• 2001

The electronic absorption and Raman spectra of $\alpha\omega-diphenylpolyenyl$, anions Ph(CH)nPh- (DPn- , n = 3, 5, 7, 9, and 13), with odd number of carbons at the polyene part, have been studied in the tetrahydrofuran (THF) solutions and in their solid film states, respectively. In the case of Raman spectra for DPn- , the frequencies and relative intensities of some Raman peaks regularly change with the increase of polyene chain length. The spectral patterns of anions (DPn- ) are very similar with those of radical anion (DPn${\cdot}$- ). However, the C=C stretching peaks of DPn- anions are observed in the 25-35 cm-1 higher frequency region than those of DPn${\cdot}$- radical anions. In the case of long chain models such as DP9- and DP13- , the C=C stretching peaks are observed in even higher frequency region than those of the corresponding neutral polyenes such as DP8, DP10, and DP12. The Raman patterns of DPn- anions in the THF solutions are similar with those in their solid film states. On the other hand, their electronic absorption spectra show a considerable difference each other. The n- ${\pi}*$ electronic absorption bands of DPn- anions in the THF solutions have been observed in the 0.27-0.39 eV lower energy region than those in their solid film states due to the solvent effects on polyene anions.

• 한국결정성장학회지
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• 제33권6호
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• pp.294-302
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• 2023

Ni-Mn-Zn ferrite, Ni_0.5-xMn_xZn_0.5Fe₂O₄(0 ≤ x ≤ 0.5)를 sol-gel 법으로 합성하여 Mn 치환량 x에 따른 결정 구조와 미세구조, 자기적 특성, 고주파 특성, 그리고 전자기파 흡수 특성을 연구하였다. Mn의 함량이 증가함에 따라 보자력 (H_C)에 큰 변화 없이 포화자화값(M_S)이 연속적으로 감소하는 것을 확인하였다. Ni-Mn-Zn ferrite-epoxy(10 wt%) 복합체에 대하여 0.1~18 GHz 주파수 범위에서 고주파 복소 유전율(ε', ε'') 및 복소 투자율(µ', µ'') spectra를 측정하고 전송선 이론을 통하여 전자기파 흡수 특성을 평가하였다. 각 시료는 1.5~2.5 GHz 및 6~11 GHz 범위에서 최소 반사손실 RL_min < -40 dB를 만족하는 1, 2차 강한 전자기파 흡수 영역이 존재하였고, Mn이 치환됨에 따라 RL_min 주파수는 저주파 방향으로 이동하였다. 또한 Ni-Zn ferrite(x = 0) 시료에 대하여 자기장(H)을 100 Oe에서 최대 400 Oe까지 단계적으로 인가한 상태로 ε', ε'', µ', µ'' spectra를 얻고 전자기파 흡수 특성을 평가하였다. 인가자장의 증가에 따라 시료의 강자성 공명 주파수가 증가하기 때문에 µ', µ'' spectra도 고주파 방향으로 단계적으로 이동해갔으며 최대 전자기파 흡수 주파수도 이에 대응하여 이동하였다. 이는 Ni-Mn-Zn ferrite에서 전자기파의 흡수는 자기적 손실에 의존하기 때문이며 Mn의 치환이나 인가자장에 의해 µ', µ'' spectra를 조절하면 전자기파 흡수 주파수도 조절할 수 있음을 보여준다. Ni-Zn ferrite-epoxy는 2.8~11.6 GHz에서 RL < -10 dB를 만족하는 광대역 전자기파 흡수 특성을 보였다.

• Bulletin of the Korean Chemical Society
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• 제33권2호
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• pp.597-600
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• 2012

Polyynes were formed by laser ablation of a graphite target in deionized water ($H_2O$ and $D_2O$) and various organic solvents such as acetonitrile, n-hexane, and c-hexane and were identified by analyzing ultraviolet (UV) absorption and Raman spectra. We assigned the major UV absorption peaks that coincided with the electronic transitions corresponding to linear polyyne chains. The UV absorption peak intensities of a polyyne solution decreased as the holding temperature of the solution increased. Also, the absorption spectra of polyynes obtained by laser ablation of a graphite target at different volume fractions of $H_2O$ and $D_2O$ were examined.