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Photoinduced electron transfer reactions of pyranine with benzoquinone and titanium dioxide
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The fluorescence quenching of pyranine by benzoquinone in acetonitrile medium was studied using steady‐state and time‐resolved fluorescence techniques. The quenching process was characterized by a Stern–Volmer plot, which displayed a linear aspect. From the linear plot, the bimolecular quenching rate constant was obtained. The obtained rate constants are within diffused controlled limits. The results show that benzoquinone can efficiently quench the fluorescence of pyranine with dynamic quenching rate constants in the order of 1010 M–1 s–1, suggesting that the pyranine can act as a good electron donor for photoinduced electron transfer in artificial photosynthesis and organic solar cells. In addition, the electron injection dynamics of a pyranine/titanium dioxide semiconductor film was also investigated and electron injection from the excited state pyranine into the conduction band of titanium dioxide is suggested. These preliminary results hold promise for the possibility of using pyranine in dye‐sensitized solar cells. Copyright © 2016 John Wiley & Sons, Ltd. 相似文献
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川芎嗪,丹参对豚鼠输尿管电位的影响 总被引:2,自引:0,他引:2
本工作研究了川芎嗪、丹参对豚鼠输尿管电位的影响。用0.5mg/ml、1.0mg/ml、2.0mg/ml、4.0mg/ml的川芎嗪分别注射豚鼠静脉,结果显示对豚鼠输尿管电位有不同的抑制作用。用1:80、1:40、1:20、1:10的丹参分别注射豚鼠静脉,也对豚鼠输尿管电位有不同的抑制作用。结果表明,丹参具扩张小动脉的作用,川芎嗪、丹参对输尿管平滑肌起了Ca^2+的拮抗剂的作用。 相似文献
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Van Dongen JT Ammerlaan AM Wouterlood M Van Aelst AC Borstlap AC 《Annals of botany》2003,91(6):729-737
An important function of the seed coat is to deliver nutrients to the embryo. To relate this function to anatomical characteristics, the developing seed coat of pea (Pisum sativum L.) was examined by light- and cryo-scanning electron microscopy (cryo-SEM) from the late pre-storage phase until the end of seed filling. During this time the apparently undifferentiated seed coat tissues evolve into the epidermal macrosclereids, the hypodermal hourglass cells, chlorenchyma, ground parenchyma and branched parenchyma. Using the fluorescent symplast tracer 8-hydroxypyrene-1,3,6-trisulfonic acid, it could be demonstrated that solutes imported by the phloem move into the chlorenchyma and ground parenchyma, but not into the branched parenchyma. From a comparison with literature data of common bean (Phaseolus vulgaris L.) and broad bean (Vicia faba L.), it is concluded that in the three species different parenchyma layers, but not the branched parenchyma, may be involved in the post-phloem symplasmic transport of nutrients in the seed coat. In pea, the branched parenchyma dies during the storage phase, and its cell wall remnants then form the boundary layer between the living seed coat parenchyma cells and the cotyledons. Using cryo-SEM, clear images were obtained of this boundary layer which showed that many intracellular spaces in the seed coat parenchyma are filled with an aqueous solution. This is suggested to facilitate the diffusion of nutrients from the site of unloading towards the cotyledons. 相似文献
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Marcel De Cuyper Marcel Joniau Hugo Dangreau 《Biochemical and biophysical research communications》1980,95(3):1224-1230
The application of continuous free-flow electrophoresis in the liposome field is described. The technique is able to distinguish between artificial phospholipid vesicles as a function of their surface charge. This made possible to follow intervesicular interactions between differently charged bilayer structures. As an example, we present evidence for a relatively fast, spontaneous phospholipid transfer between dimyristoylphosphatidylcholine and mixed dimyristoylphosphatidylcholine/dimyristoylphosphatidylglycerol vescles. 相似文献
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Neutral methylanthracene (MA), anionic trisodium 8-hydroxy-1,3,6-pyrenetrisulfonate, (pyranine), and cationic 3,6-diamino-10-methylacridinium chloride (acriflavine), have been used as fluorescence probes to investigate effects of osmotic shrinkage on neutral, cationic and anionic dipalmitoyl-D,L-α-phosphatidylcholine liposomes. The determined fluorescence polarizations in the liposomes and in solvents of known viscosities afforded the estimation of the microviscosities of the environments of these probes. The viscosity reported by pyranine for anionic and that by acriflavine for cationic single compartment liposomes, ~1.0 cP, indicate the aqueous environments of these probes. Increased viscosities following osmotic shrinkages have been rationalized in terms of changing the nature of the liposome entrapped water. Following the release of free water, some bound water is also released as the result of osmotic shrinkage. The determined shrinkage rates support this postulate. The viscosity of the environment of pyranine in cationic, 9.6 ± 0.3 cP, and that of acriflavine in anionic single compartment liposomes, 74 ± 5 cP, indicate electrostatic attractions of the probes to the charged liposome surface. Osmotic shrinkage results in lowering the viscosity of the environments of the probes presumably because the more concentrated sodium chloride replaces them from their sites. The high viscosities reported by MA, ~ 1000 cP, suggest the intercalation of this probe in the phospholipid bilayers. Osmotic shrinkage does not alter the environment of MA. However, in the presence of cholesterol, the viscosities reported by MA are greater than in its absence. These data contradict previous NMR, ESR and X-ray results as well as those obtained in the present work from osmotic shrinkage rates. The need for care in interpreting data obtained by the use of fluorescence probes is emphasized. 相似文献
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