In this paper, we report the synthesis and physico-chemical investigation of two uranylsalophen receptors, bearing either one or two anthracenyl moieties appended to the salophen skeleton. Despite the presence of the anthracenyl fluorophores, no fluorescence emission was detected. Photophysical data and cyclic voltammetric experiments show that photoinduced electron transfer from the anthracene-localised first singlet excited state to the metal centre is strongly exergonic, thus suggesting that this is the main fluorescence quenching mechanism in these complexes. The investigated compounds are photoreactive upon UV irradiation, yielding either anthracene photooxidation or photodimerisation products depending on the specific complex and the experimental conditions.
F. Yafteh Mihan, S. Bartocci, A. Credi, S. Silvi, A. Dalla Cort (2013). Synthesis and photochemical behavior of novel Uranyl salophen complexes bearing anthracenyl side arms. SUPRAMOLECULAR CHEMISTRY, 25, 109-115 [10.1080/10610278.2012.752089].
Synthesis and photochemical behavior of novel Uranyl salophen complexes bearing anthracenyl side arms
CREDI, ALBERTO;SILVI, SERENA;
2013
Abstract
In this paper, we report the synthesis and physico-chemical investigation of two uranylsalophen receptors, bearing either one or two anthracenyl moieties appended to the salophen skeleton. Despite the presence of the anthracenyl fluorophores, no fluorescence emission was detected. Photophysical data and cyclic voltammetric experiments show that photoinduced electron transfer from the anthracene-localised first singlet excited state to the metal centre is strongly exergonic, thus suggesting that this is the main fluorescence quenching mechanism in these complexes. The investigated compounds are photoreactive upon UV irradiation, yielding either anthracene photooxidation or photodimerisation products depending on the specific complex and the experimental conditions.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.