88276-90-8Relevant articles and documents
Silica iminopyridine-functionalized nanomaghemite enhances the oxygenation activity and durability of simple Co(II) salophen complex
Jafarpour, Maasoumeh,Keikha, Narges,Rezaeifard, Abdolreza
, (2020)
A novel magnetically recoverable catalyst was produced by coordinative attachment of Co(II) salophen complex to silica iminopyridine (SIPy)-functionalized-γ-Fe2O3 magnetic nanoparticles (SMNP?SIPy/Co(II) salophen). The vibration spectra and compositional data provided sufficient evidences for the structural integrity of as-prepared organic–inorganic nanohybrid. The magnetic nanocatalyst proved to be an efficient and selective heterogeneous catalyst for oxidation of different benzylic alcohols and featured higher catalytic activity and stability than that of homogenous counterpart. A TOF of 151 h?1 and TON of more than 322 were obtained for oxidation of 4-cholrobenzyl alcohol in this catalytic system. The supported catalyst could easily be recovered from the reaction mixture by an external magnetic field and reused for subsequent experiments with consistent catalytic activity.
Heterogeneous Fenton-like activity of novel metallosalophen magnetic nanocomposites: Significant anchoring group effect
Keikha, Narges,Rezaeifard, Abdolreza,Jafarpour, Maasoumeh
, p. 32966 - 32976 (2019)
Two new pyridine and thiolate anchoring groups were prepared to functionalize γ-Fe2O3 nanoparticles for coordinative attachment of simple Fe(iii)- and Mn(iii)salophen complexes. Four new magnetically recoverable composites were characterized by several analytical techniques such as FT-IR, XRD, TGA, EDS compositional analysis and VSM to confirm superparamagnetic properties. TEM images revealed the nanostructure nature of composites with size ranging between 20 and 40 nm. A heterogeneous advanced oxidation process for degradation of some organic dyes as water pollution compounds using an aqueous solution of H2O2 were successfully exploited. Several key parameters including the metal center in the salophen complex, initial pH, catalyst dosage, H2O2 and dye concentration and temperature were investigated. A significant effect of the anchoring ligand on the degradation efficiency and catalyst stability was documented. The superior catalytic activity and particularly durability of the thiolate-based catalysts were demonstrated in comparison with their Py counterparts. Rate constants of 0.21, 0.17, 0.23 and 0.11 min-1 were obtained for degradation of rhodamine B (RhB), methylene blue (MB), methyl orange (MO), and crystal violet (CV). Finally, a photoluminescence probing technology and radical scavenging measurements were carried out to elucidate the active species involved in the process.
Supramolecular photocatalyst of Palladium (II) Encapsulated within Dendrimer on TiO2 nanoparticles for Photo-induced Suzuki-Miyaura and Sonogashira Cross-Coupling reactions
Eskandari, Ameneh,Jafarpour, Maasoumeh,Rezaeifard, Abdolreza,Salimi, Mehri
, (2019/08/20)
In this study, synthesis, characterization and catalytic performance of a novel supramolecular photocatalytic system including palladium (II) encapsulated within amine-terminated poly (triazine-triamine) dendrimer modified TiO2 nanoparticles (Pd (II) [PTATAD] @ TiO2) is presented. The obtained nanodendritic catalyst was characterized by FT-IR, ICP-AES, XPS, EDS, TEM, TGA and UV-DRS. The as-prepared nanodendritic catalyst was shown to be highly active, selective, and recyclable for the Suzuki–Miyaura and Sonogashira cross-coupling of a wide range of aryl halides including electron-rich and electron-poor and even aryl chlorides, affording the corresponding biaryl compounds in good to excellent yields under visible light irradiation. This study shows that visible light irradiation can drive the cross-coupling reactions on the Pd (II) [PTATAD] @ TiO2 under mild reaction conditions (27–30?°C) and no additional additives such as cocatalysts or phosphine ligands. So, we propose that the improved photoactivity predominantly benefits from the synergistic effects of Pd (II) amine-terminated poly (triazine-triamine) dendrimer on TiO2 nanoparticles that cause efficient separation and photogenerated electron–hole pairs and photoredox capability of nanocatalyst which all of these advantages due to the tuning of band gap of catalyst in the visible light region.