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Influence of Silver Colloid Presence on Stilbazolium Merocyanine Emission

机译:银胶体的存在对提拉唑鎓花青素排放的影响

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摘要

Absorption, fluorescence emission, and fluorescence excitation spectra of stilbazolium merocyanine (1-(n-butyl)-4[(3,5-dimethoxy-4-oxocyclohexa-2,5-dienylidene)ethylidene]-1,4-dihydropyridyne) dye in water solution without and with colloidal silver addition were measured. In the presence of the colloid, besides the absorption band assigned to the protonated species of the dye (at 391 nm), an absorption band related to the free-base species appears at 490 nm. From the absorption and emission spectra, measured at various dye concentrations, follows that the aggregates are not effectively formed. Therefore, the long-wavelength absorption and fluorescence bands have to be related to some dye forms created by the solvatochromic effects. The fluorescence bands of the protonated and the free-base species are located at 559 nm and at about 630 nm, respectively. The shape of the long-wavelength band suggests the occurrence of more than one free-base form of the dye. At some dye and colloid concentrations, the global emission of the sample is enhanced as a result of silver addition. The increase in the emission yield of the dye could be partially due to not only the change in the concentrations of dye forms exhibiting various emission yields but is also due to the resonance surface plasmon effect. Because of the superposition of several effects, before the practical application of merocyanine as an indicator of metal presence in biological samples, its spectral properties in the system investigated should be established.
机译:stilbazolium merocyanine(1-(n-butyl)-4 [(3,5-dimethoxy-4-oxocyclohexa-2,5-dienylidene)ethidene] -1,4-dihydropyridyne)染料的吸收,荧光发射和荧光激发光谱测量在没有和有胶体银的水溶液中的溶解度。在胶体的存在下,除了赋予染料的质子化物质的吸收带(在391 nm处)外,与游离碱物质有关的吸收带在490 nm处出现。从在各种染料浓度下测得的吸收和发射光谱得出,聚集体没有有效形成。因此,长波吸收和荧光带必须与溶剂致变色效应产生的某些染料形式相关。质子化和游离碱物质的荧光带分别位于559 nm和约630 nm。长波带的形状表明存在一种以上的游离碱形式的染料。在某些染料和胶体浓度下,由于添加了银,样品的整体排放得以增强。染料的发射产率的增加不仅可以部分归因于表现出各种发射产率的染料形式的浓度的变化,而且还可以归因于共振表面等离子体激元效应。由于多种效应的叠加,在实际应用花菁作为生物样品中金属存在的指示剂之前,应确定其在被研究系统中的光谱特性。

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