2 research outputs found
Iron(III)-Modified Tungstophosphoric Acid Supported on Titania Catalyst: Synthesis, Characterization, and Friedel–Craft Acylation of <i>m</i>‑Xylene
The
Friedel–Craft acylation of <i>m</i>-xylene
with benzoyl chloride over iron-modified tungstophosphoric acid supported
on titania was investigated. It was found that FeTPA/TiO<sub>2</sub> catalyst displayed excellent catalytic performance for this reaction.
Furthermore, a series of catalysts were prepared and characterized
by FT-IR, XRD, BET, NH<sub>3</sub>-TPD, and Py-IR. The results indicated
that both the Lewis acidity and the textural properties presented
significant influences on their catalytic performance. Moreover, the
influence of catalyst calcination temperature to the above reaction
was also studied. The reaction parameters, including reaction temperature,
catalyst dose, and molar ratio of <i>m</i>-xylene to benzoyl
chloride, were optimized, and a 95.1% yield of 2,4-dimethylbenzophenone
was obtained under optimal conditions. Finally, the kinetics of the
benzoylation of <i>m</i>-xylene over 30% FeTPA/TiO<sub>2</sub> was established
Two-Dimensional Imine-Linked Covalent Organic Frameworks as a Platform for Selective Oxidation of Olefins
Two-dimensional imine-linked
covalent organic frameworks with hydroxyl groups, <b>TAPT-DHTA-COF<sub>HX</sub></b> and <b>TAPT-DHTA-COF<sub>DMF</sub></b>, were
respectively constructed by the condensation of 1,3,5-tris-(4-aminophenyl)Âtriazine
and 2,5-dihydroxyl-terephthalaldehyde under solvothermal and reflux
conditions. Both COFs possess excellent thermal stability and a similar
eclipsed stacking structure verified by XRD patterns. However, <b>TAPT-DHTA-COF<sub>HX</sub></b> presented a larger surface area
(2238 m<sup>2</sup>/g) and higher crystallinity than <b>TAPT-DHTA-COF<sub>DMF</sub></b>. Significantly, copper ions are efficiently incorporated
into the pores of these two COFs via the coordination interaction
with hydroxyl groups and imine linkers. The obtained copper-containing
COFs (<b>Cu-COF<sub>HX</sub></b> and <b>Cu-COF<sub>DMF</sub></b>) were employed in the selective oxidation of styrene to benzaldehyde. <b>Cu-COF<sub>HX</sub></b> with superior surface area (1886 m<sup>2</sup>/g) and pore volume (1.11 cm<sup>3</sup>/g) exhibited excellent
catalytic performance and recyclability. This strategy not only provides
a convenient approach to design imine-linked 2D COFs with hydroxyl
groups, but also develops their novel application for catalysis