کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1234666 | 1495279 | 2012 | 7 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Photoinduced electron-transfer from imidazole derivative to nano-semiconductors Photoinduced electron-transfer from imidazole derivative to nano-semiconductors](/preview/png/1234666.png)
Bioactive imidazole derivative absorbs in the UV region at 305 nm. The interaction of imidazole derivative with nanoparticulate WO3, Fe2O3, Fe3O4, CuO, ZrO2 and Al2O3 has been studied by UV–visible absorption, FT-IR and fluorescence spectroscopies. The imidazole derivative adsorbs strongly on the surfaces of nanosemiconductor, the apparent binding constants for the association between nanomaterials and imidazole derivative have been determined from the fluorescence quenching. In the case of nanocrystalline insulator, fluorescence quenching through electron transfer from the excited state of the imidazole derivative to alumina is not possible. However, a possible mechanism for the quenching of fluorescence by the insulator is energy transfer, that is, energy transferred from the organic molecule to the alumina lattice. Based on Forster's non-radiation energy transfer theory, the distance between the imidazole derivative and nanoparticles (r0 ∼ 2.00 nm) as well as the critical energy transfer distance (R0 ∼ 1.70 nm) has been calculated. The interaction between the imidazole derivative and nanosurfaces occurs through static quenching mechanism. The free energy change (ΔGet) for electron transfer process has been calculated by applying Rehm–Weller equation.
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► Fluorescence quenching from excited state of imidazole to alumina is not possible.
► Energy transfer from the organic molecule to the alumina lattice.
► r0 ∼ 2.00 nm as well as R0 ∼ 1.70 nm has been calculated.
► The interaction occurs through static quenching mechanism.
► ΔGet for electron transfer process has been calculated by Rehm–Weller equation.
Journal: Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy - Volume 89, April 2012, Pages 187–193