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Beilstein J. Org. Chem. 2024, 20, 1011–1019, doi:10.3762/bjoc.20.89
Graphical Abstract
Figure 1: XPS spectra for ACFs and FeCp2-ACFs-150. Peaks without labels originate from the indium substrate u...
Figure 2: XPS spectrum for FeCp2-ACFs-150 in the Fe2p region shown with fitting curves.
Figure 3: XPS spectra of (left) FeCp2-ACFs-150 and (right) ACFs in the C1s region with fitting curves.
Figure 4: Raman spectra for ACFs and FeCp2-ACFs-150. Each raw data (black) was fitted to the G-band (blue) an...
Figure 5: The raw infrared spectrum for FeCp2 (black) and differential absorbance spectra for FeCp2-ACFs-55 (...
Figure 6: The temperature (T) dependence of the magnetic susceptibility χ for FeCp2-ACFs-150, ACFs, and FeCp2...
Figure 7: a) ESR spectra of ACFs and FeCp2-ACFs-55 with different excitation microwave power. Each spectrum w...
Figure 8: The square root of the excitation microwave power dependence of the relative ESR intensities for AC...
Beilstein J. Org. Chem. 2013, 9, 1156–1163, doi:10.3762/bjoc.9.129
Figure 1: (a) Graphical presentation of Pd–Ag co-plating and sequential removal of Ag to give a porous Pd sur...
Figure 2: Schematic diagram of experimental setup used for the catalytic hydrogenation of p-nitrophenol.
Scheme 1: Hydrogenation of p-nitrophenol with formic acid.
Figure 3: Influence of temperature on the conversion of 0.01 M p-nitrophenol with 0.1 M formic acid at 30 °C ...
Figure 4: Effect of residence time on the conversion of 0.01 M p-nitrophenol with 0.1 M formic acid at 30 °C ...
Figure 5: Effect of the concentration of formic acid on the conversion of 0.01 M p-nitrophenol. The formic ac...
Figure 6: Effect of pH on the conversion of 0.01 M p-nitrophenol by using 0.05 M formic acid. The porous PdO ...
Figure 7: Long-term testing for continuous hydrogenation of 0.01 M p-nitrophenol with 0.05 M formic acid in t...