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机构地区:[1]北京理工大学化工与材料学院,北京100081 [2]北京大学化学与分于工程学院,北京100871
出 处:《高等学校化学学报》1997年第10期1703-1705,共3页Chemical Journal of Chinese Universities
基 金:国家自然科学基金
摘 要:The deprotonation of an amphiphilic porphyrin, meso-tetra (p-hydroxylphenyl)porphyrin with a hexadecyl chain(THPPH2), has been observed by means of UV-Visspectroscopy in CTAB micellar solutions. With increasing of PH values, the Soret band shiftsfrom 424 nm to 441nm, and the four-Q bands (520 nm, 560 nm, 595nm, 655 nm) aredisappeared while two new Q-bands are appeared at 585 nm and 675 nm, which is similar tometal-porphyrin, means that the deprotonation of porphyrin takes place. Comparing withthe spectra in an other solutions, the spectral characteration of THPPH2 in neutral and inbasic CTAB solutions is similar to that in CHCI3 and basic aqueous solutions respectively,suggesting that the solubilizing location of THPPH2 takes a change from inner to the outer of theCTAB micellars with the PH value of solutions increasing between 6. 20 and 11. 19.The deprotonation of an amphiphilic porphyrin, meso-tetra (p-hydroxylphenyl)porphyrin with a hexadecyl chain(THPPH2), has been observed by means of UV-Visspectroscopy in CTAB micellar solutions. With increasing of PH values, the Soret band shiftsfrom 424 nm to 441nm, and the four-Q bands (520 nm, 560 nm, 595nm, 655 nm) aredisappeared while two new Q-bands are appeared at 585 nm and 675 nm, which is similar tometal-porphyrin, means that the deprotonation of porphyrin takes place. Comparing withthe spectra in an other solutions, the spectral characteration of THPPH2 in neutral and inbasic CTAB solutions is similar to that in CHCI3 and basic aqueous solutions respectively,suggesting that the solubilizing location of THPPH2 takes a change from inner to the outer of theCTAB micellars with the PH value of solutions increasing between 6. 20 and 11. 19.
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