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Beilstein J. Org. Chem. 2025, 21, 798–799, doi:10.3762/bjoc.21.62
Beilstein J. Org. Chem. 2024, 20, 2732–2738, doi:10.3762/bjoc.20.231
Graphical Abstract
Figure 1: (a) Chemical structure and schematic illustration of the charge-separated state of a triad molecule...
Figure 2: Differential scanning calorimetry analysis for the phase transition of liposomes (1 mM phospholipid...
Figure 3: UV–vis absorption spectra of liposomes (1 mM phospholipid) with C60 (a) or a cationic derivative of...
Figure 4: Fluorescence spectra of 1-pyrenebutyric acid (PyBA) in cationic derivative of C60 (catC60)-loaded l...
Figure 5: Photoinduced generation of reactive oxygen species (ROS) by cationic derivative of C60 (catC60)-loa...
Beilstein J. Org. Chem. 2024, 20, 777–786, doi:10.3762/bjoc.20.71
Figure 1: a) Synthesis of C60–oligopeptide conjugates 5a–c and b) synthesis of compound 3. Fulleropyrrolidine...
Figure 2: Structure of C60–oligo-Lys (5a), C60–oligo-Glu (5b), and C60–oligo-Arg (5c) and images of dissolved...
Figure 3: DLS diagrams of C60–peptide conjugates 5a (1 mM, in Milli-Q® water), 5b (1 mM, in Milli-Q® water or...
Figure 4: UV–vis spectra of C60–peptide conjugates 5a and 5b (20 μM in Milli-Q® water for 5a and in pH 9.0 TR...
Figure 5: 1H NMR spectrum of C60–peptide conjugate 5a in D2O (above) and of the precursor monoadduct in CDCl3...
Figure 6: 13C NMR spectrum of C60–peptide conjugate 5a in D2O and of the precursor monoadduct in CDCl3 at 150...
Figure 7: a) X-band ESR spectra of the 4-oxo-TEMP adduct with 1O2 generated by C60–oligo-Lys (5a) and rose be...