| نویسندگان | Maasoumeh Jafarpour,Mehri Salimi tabas |
| نشریه | Applied Organometallic Chemistry |
| شماره صفحات | 5093-5101 |
| شماره سریال | 33 |
| شماره مجلد | 10 |
| ضریب تاثیر (IF) | 2.319 |
| نوع مقاله | Full Paper |
| تاریخ انتشار | 2019 |
| رتبه نشریه | ISI |
| نوع نشریه | الکترونیکی |
| کشور محل چاپ | ایران |
| نمایه نشریه | JCR،Scopus |
چکیده مقاله
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.
لینک ثابت مقاله