ABSTRACT
The secondary amine participating asymmetric reductive amination remains an unsolved problem in organic synthesis. Here we show for the first time that secondary amines are capable of effectively serving as N-sources in direct asymmetric reductive amination to afford corresponding tertiary chiral amines with the help of a selected additive set under mild conditions (0-25 °C). The applied chiral phosphoramidite ligands are readily prepared from BINOL and easily modified. Compared with common tertiary chiral amine synthetic methods, this procedure is much more concise and scalable, as exemplified by the facile synthesis of rivastigmine and N-methyl-1-phenylethanamine.
ABSTRACT
Single crystalline, non-toxicity, and long-term stability graphene quantum dots (GQDs) were modified onto the AgVO3 nanoribbons by a facile hydrothermal and sintering technique which constructs a unique heterojunction photocatalyst. Characterization results indicate that GQDs are well dispersed on the surface of AgVO3 nanoribbons and GQD/AgVO3 heterojunctions are formed, which can greatly promote the separation efficiency of photogenerated electron-hole pairs under visible light irradiation. By taking advantage of this feature, the GQD/AgVO3 heterojunctions exhibit considerable improvement on the photocatalytic activities for the degradation of ibuprofen (IBP) under visible light irradiation as compared to pure AgVO3. The photocatalytic activity of GQD/AgVO3 heterojunctions is relevant with GQD ratio and the optimal activity is obtained at 3wt% with the highest separation efficiency of photogenerated electron-hole pairs. Integrating the physicochemical and photocatalytic properties, the factors controlling the photocatalytic activity of GQD/AgVO3 heterojunctions are discussed in detail. Moreover, potential photocatalytic degradation mechanisms of IBP via GQD/AgVO3 heterojunctions under visible light are proposed.
