• 공업화학
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• 제10권6호
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• pp.828-831
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• 1999

Meso-(mesityl)dipyrromethane(MS-DPM)과 4-nitrobenaldehyde로부터 5,15-bis(mesityl)-10,20-bis(4-amino)porphyrin[mesityl-$TPP(NH_2)$]을 합성하였다. Mesityl-$TPP(NH_2)$는 UV spectrophotometer[Soret-band(438 nm), Q-band(526, 572, 611 nm)]와 $^1H$-NMR spectroscopy에 의해 그 구조를 확인하였다. 3,3',4,4'-Benzophenone tetracarboxylic dianhydride(BTDA)와 2,2-bis(4-(4-aminophenoxy)-phenyl)hexafluoropropane(BAPHF)를 mesityl-$TPP(NH_2)$와 축합시켜 porphyrin 구조를 포함하는 copolyimide를 합성하였다. 제조된 copolyimide 역시 UV spectrophotometer [Soret-band (428 nm), Q-band (558 nm, 599 nm)]와 FT-IR spectrophotometer를 이용하여 그 구조를 확인하였고, 열분석 결과 $T_g$와 $T_m$은 각각 220.7와 $369.2^{\circ}C$였다.

• 대한화학회지
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• 제26권4호
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• pp.218-223
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• 1982

chl-a는 $5.12{\times}10-6M$ 이상의 농도와 건조된 ethyl ether, benzene, iso-octane중에 소중합체로 존재하고 이 용매에 n-prOH를 소량씩 가할때 단위체로 변함을 확인하였다. 형광은 중합체인 경우에 세게 나타나지만 중합정도에 따라 변하며 단위체인 경우는 약하게 나타났다. 그리고 n-prOH를 용매에 가할 때 흡광과 형광의 ${\lambda}_{max}$은 모두 장파장쪽으로 이동하였다. soret/red band의 비는 흡광도가 감소할수록 작아졌으며 chl-a의 농도에 따른 흡광도는 $1.0{\times}10^{-6}$M 정도의 용액에서 최대값을 나타냈다.

• Bulletin of the Korean Chemical Society
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• 제19권8호
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• pp.825-830
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• 1998

The electrocatalytic reduction of dioxygen by Co(TTFP)(Y)2 {Y=H2O or HO-} is investigated by cyclic voltammetry, spectroelectrochemistry, hydrodynamic voltammetry at a glassy carbon electrode in dioxygen-saturated aqueous solutions. Electrocatalytic reduction of dioxygen by CoⅡ(TTFP)(Y)2 establishes a pathway of 2e- reduction to form hydrogen peroxide, and then the generated hydrogen peroxide is reduced to water by CoⅠ(TTFP)(Y)2 at more negative potential. CoⅡ(TTFP)(Y)2 may bind dioxygen to produce the adduct complex [CoⅡ-O2 or CoⅢ-O2] which exhibits a Soret band at 411 nm and Q band at 531 nm.

• 한국축산식품학회지
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• 제44권2호
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• pp.408-429
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• 2024

The color, lipid oxidation, heme iron (HI) and non-heme iron (NHI) contents, metmyoglobin content and Soret band of myoglobin of ground pork subjected to supercritical CO₂ treatment under different conditions, or to heat treatment (40℃, 2 h) and subsequent storage at 4℃ were evaluated during 9-day period. Supercritical CO₂ treatment significantly increased CIE L^* and CIE b^* values of ground pork during subsequent storage, while the HI content was slightly affected. In general, CIE a^* value and metmyoglobin content were decreased. Supercritical CO₂ treatment for 2 h could increase the thiobarbituric acid-reactive substances (TBARS) value, while treatment for 1 h or less had no effect. The NHI content could be increased only after treatment at above 40℃ or 17.2 MPa for 2 h. The Soret band of myoglobin was shifted to longer wavelength. Increasing treatment temperature from 35℃ to 45℃ could increase CIE L^*, CIE a^*, CIE b^* and TBARS values, HI and NHI contents of the ground pork, while decreasing metmyoglobin content. As the treatment pressure increased from 13.8 MPa to 20.7 MPa, CIE b^* and TBARS values were decreased, while the NHI and metmyoglobin contents were increased. However, the other parameters were unchanged. Extending exposure time from 0.5 h to 2 h could increase CIE L^*, CIE b^* and TBARS values, HI contents, while decreasing CIE a^* value and metmyoglobin content. Correlation analysis showed that the TBARS value was significantly and negatively correlated with the HI content or metmyoglobin content in samples treated at 40℃ or above for 2 h.

• Bulletin of the Korean Chemical Society
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• 제29권8호
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• pp.1533-1538
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• 2008

Porphyrins generally bind DNA in two different ways with respect to the mixing ratio; monomeric binding at a low mixing ratio and outside stacking at a high mixing ratio. In the present study, CTDNA binding property of a planar structured porphyrin, 5,10,15,20-tetrakis(N-methyl-4-pyridin-4-yl-phenyl)porphyrin (referred to as B-TMPyP) was investigated using absorption, CD, LD, and $LD^r$ spectroscopies. B-TMPyP produced a bisignate CD band, even at the lowest mixing ratio, indicating that B-TMPyP may not have a monomeric binding mode. From the observations of the spectral changes to the absorption, CD, and LD spectra in mixing ratio dependent titrations, B-TMPyP seems to have a quite different stacking type compared to that for the binding of $H_2$TMPyP. Moreover, B-TMPyP produced a CD band of opposite shape in the Soret band region. A qualitative explanation for the observed optical differences is also given.

• 한국미생물·생명공학회지
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• 제19권5호
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• pp.470-476
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• 1991

Peroxidase를 다량 함유하는 식물체를 검색할 목적으로 십자화과 식물 9종에 대하여 효소활성 분포를 조사하였다. 검색한 식물체 중 배추 뿌리에서 본 효소의 활성이 강하게 나타나 배추 뿌리로 부터 본 효소의 정제를 행하였다. 정제된 효소는 분자량 50,000의 단량체로서 pH 7.0, $50^{\circ}C$에서 최적 활성을 나타내었다. phenol 및 phenol이 유도체가 좋은 기질로 작용하였으며 pyrogallol에 대한 $H_2O_2$의 Km 값은 1.6mM이었다. 본 효소는 406nm 에서 soret 흡수대를 나타내어 다른 peroxidase와 마찬가지로 분자내 보결분자단으로 heme을 가지고 있음을 알았다. 정제된 배추뿌리 기원의 효소는 면역화학적, 전기영동적 성질이 horseradish 기원의 peroxidase와 유사하였다.

• Journal of Photoscience
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• 제9권2호
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• pp.364-366
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• 2002

Photoadaptation of Chlorobium (Cb.) phaeobacteroides was investigated under dim and strong light intensity. Absorption spectra of these whole cellIs were different each other. The Soret band intensity and the Qy bandwidth of BChl e in c디l grown under dim light intensity were smaller and more broadened than those under strong light intensity. From HPLC analysis of the pigments, total carotenoid (Car) / bacterochorolphyll (BChl) e ratio of cell increased wi1h increase of light intensities. But camposition of BChl e hamologs almost unchanged. Cb. phaeobacteroides contains 11 kinds of Car including isorenieratene and beta-isorenieratene as major Car. The campositions of Car were different for cells grown under dim and strong light intensities. In conclusion, Cb. phaeobacteroides changes total amount and canposition of Car to adapt various light intensities, while homolog canposition of BChle unchange.

• Bulletin of the Korean Chemical Society
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• 제19권4호
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• pp.439-444
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• 1998

The protonation of tetraphenylporphyrin (TPP) in acidic organic solutions was analyzed by acid titrimetric and temperature-dependent absorption measurements. Competition between the protonation of free base TPP $(TPPH_2)$ and the solvation of proton by near solvent molecules determines the equilibrium of the diprotonated TPP $(TPPH_4^{2+})$ formation. The diprotonated TPP exists as an ion pair complex with the acid counterions, which are found to affect the degree of red shift of the Soret band. The rotation of the phenyl rings also plays an important role in the diprotonation, as suggested by the decrease in the degree of diprotonation for the fluorophenyl TPP derivatives whose phenyl ring rotation is significantly hindered relative to normal TPP. The difference of fluorescence lifetime between $TPPH_2 \;({\pi}_{FL}=19.6\;ns)\; and\; TPPH_4^{2+} \;({\pi}_{FL}=2.1 \;ns)$ was used advantageously to measure the rate of protonation in the excited state. The protonation of TPPH2 are found to occur much slower than the diffusion of protons from bulk solution to the porphyrin ring. The monoprotonated TPP is suggested to be the transient species for the diprotonation process.

• BMB Reports
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• 제42권4호
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• pp.223-226
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• 2009

We measured the pH-induced spectral changes of yeast iso-1-cytochrome c on silver nanoparticle surfaces using surface-enhanced resonance Raman scattering (SERRS) at 457.9 nm. At a pH of ~3, the Met80 ligand in yeast iso-1-cytochrome c is assumed to dissociate, leading to a marked conformational change as evidenced by the vibrational spectral shifts. The Soret band at ~410 nm in the UV-Vis spectrum shifted to ~396 nm at pH~3, indicating a transition from a low spin state to a high spin state from a weak interaction with a water molecule. Thus, SERRS spectroscopy can measure the pH-induced denaturalization of cyt c adsorbed on metal nanoparticle surfaces at a lower concentration with a better sensitivity than ordinary resonance Raman spectroscopy.

• Bulletin of the Korean Chemical Society
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• 제26권11호
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• pp.1728-1734
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• 2005

The interactions of Cu(II)-meso-Tetrakis(n-N-methylpyridiniumyl)porphyrin (n = 2,3,4), respectively referred to as o-, m- and p-CuTMPyP, and DNA, poly$[d(A-T)_2]$ and poly$[d(G-C)_2]$ were investigated by circular and linear dichroism (CD and LD). In the o-CuTMPyP case, in which the rotation of the pyridinium ring is prevented, the shape of the CD spectrum when associated to DNA and poly$[d(A-T)_2]$ resembles and is characterized by a positive band at a low drug to DNA concentration ratio (R ratio) and is bisignate at a high R ratio. The former CD spectrum shape has been attributed to porphyrin that is bound monomerically outside of DNA while the latter can be attributed to those that are stacked. When o-CuTMPyP is bound to poly$[d(G-C)_2]$, the excitonic CD appeared at a relatively high R ratio. In contrast, a characteristic negative CD band in the Soret region was apparent for both m- and p-CuTMPyP when bound to DNA and poly$[d(G-C)_2]$ at the low R ratios, indicating that the porphyrin molecule intercalates. However, the DNA is bent near the intercalation site and the plane of the porphyrin molecule tilts relative to the DNA helix axis, as judged by the magnitude of the reduced LD. Various stacking patterns were identified by the shape of the CD spectrum for m- and p-CuTMPyP when bound to poly$[d(A-T)_2]$. Three species for the former complex and two for the latter complex were found which may reflect the extent of the stacking.