Long-lived (minutes) photoinduced charge separation in a structured periodic mesoporous titania containing 2,4,6-triphenylpyrylium as guest

2,4.6-Triphenylpyrylium (TP+), an electron acceptor, has been included inside the channels of two ordered mesoporous titania (mpTiO(2)). MpTiO(2) contain anatase nanoparticles (3-5 nm) templated by cetylrimethylammonium and differ by the presence or absence of silica domains as binders of the structure. UV irradiation of TP-mpTiO(2) gives rise to a strong EPR signal. This behaviour was not observed for related materials in which TP+ was included inside the channels of MCM-41 or the cavities of zeolite Y. Also, transient spectroscopy shows remarkable differences between TP+ included in mpTiO(2) (charge separation) and in porous silicates (triplet excited state). Based on EPR and laser flash spectroscopic evidence, the occurrence of photo-induced electron transfer from TiO2 as the donor to TP+ as the acceptor leading to a long-lived (minutes at room temperature) charge separated state is proposed.