کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1305486 | 1498938 | 2015 | 4 صفحه PDF | دانلود رایگان |
• Lanthanide(III) mono- and bisporphyrins possess similar photoinduced properties.
• Irradiation accelerates their slow transformation to each other.
• During the photolysis at the Soret-band, a radical type intermediate can be observed.
• However, during the irradiation at the Q-bands, a stable photoproduct appears.
• This species is undetectable in the case of post-transition metal ions.
Water-soluble, early lanthanide(III) mono- and bisporphyrin complexes possess very similar UV–Vis absorption as well as photophysical and photochemical properties, as a consequence of a special type of aggregation, through the peripheral substituents. In the absence of the bidentate, O-donor acetate ligand, bisporphyrin can form too, which has slightly redshifted and broadened absorption bands, compared to those of the monoporphyrin. Also the bisporphyrin displays a blueshifted and less intense fluorescence, related to the free-base porphyrin. The formation of complexes and the transformation between the mono- and bisporphyrins are very slow reactions in dark at room temperature. These reactions are accelerated by the photolysis of the system, which are considerable by-processes of the photoredox degradation. Depending on the wavelength of irradiation, two types of photoproducts can appear: during the photolysis at the Soret-band, a radical type intermediate can be observed, which disappears in dark. However, during the irradiation at the Q-bands, a new photoproduct appears, which is stable in dark and undetectable in the case of post-transition metal ions' out-of-plane porphyrin complexes.
During the photolysis of lanthanide(III) porphyrins at the Soret-band, a radical type intermediate can be observed, which disappears in dark. However, during the irradiation at the Q-bands, a new photoproduct appears, which is stable in dark and undetectable in the case of post-transition metal ions' out-of-plane porphyrin complexes.Figure optionsDownload as PowerPoint slide
Journal: Inorganic Chemistry Communications - Volume 52, February 2015, Pages 60–63