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Beilstein J. Org. Chem. 2020, 16, 1554–1563, doi:10.3762/bjoc.16.127
Graphical Abstract
Figure 1: FTIR analysis of βNS-CDI 1:4, before and after treatment for 4 h in H2O at 40 °C, synthesized with ...
Figure 2: Thermogravimetric analysis of β-CD-based carbonate nanosponges, obtained through solution (DMF) and...
Figure 3: Thermogravimetric analysis of α, β and γ-CD-based carbonate nanosponges, obtained through ball-mill...
Figure 4: Adsorption of organic dyes by ball-mill synthesized β-CD-based carbonate nanosponges. Conditions: a...
Figure 5: ζ-Potential of bm cyclodextrin nanosponges with relative STDev (mV).
Figure 6: Hydrolysis of the imidazoyl carbonyl group in water at 40 °C.
Figure 7: Nitrogen content in weight % in cyclodextrins NS-CDI from ball mill synthesis. a) comparison betwee...
Figure 8: Simplified schematic reaction and procedure for obtaining the dye-functionalized βNS-CDI. Surface z...
Beilstein J. Org. Chem. 2014, 10, 2586–2593, doi:10.3762/bjoc.10.271
Figure 1: FTIR spectra of branched β-CD polymer (a), cross-linked β-CD nanosponge (b) and pyromellitic dianhy...
Figure 2: SEC curves of the β-CD-based polymer before (solid line) and after ultrafiltration with cut-off siz...
Figure 3: Thermogravimetric curves of the β-CD-based polymer after ultrafiltration with cut-off size of 3000 ...
Figure 4: Raman (a) and FTIR–ATR (b) spectra of the branched β-CD-based polymer in the wavenumber range of 15...
Figure 5: Ratio between the intensity of the bands assigned to ester groups (ICO1) and to the free carboxylic...
Figure 6: NMR spectra of fluorescein in D2O solution (a) and in the presence of the hyper-branched β-CD polym...
Figure 7: UV–vis spectrum of fluorescein with increasing amounts of hyper-branched β-CD polymer. pH range: 8....
Beilstein J. Org. Chem. 2012, 8, 1305–1311, doi:10.3762/bjoc.8.149
Scheme 1: Enantiodifferentiating photoisomerizations of 1Z and 2ZZ sensitized by β- and γ-cyclodextrin nanosp...
Scheme 2: Representative enantiodifferentiating photosensitization of 1Z and 2ZZ with conventional and supram...
Figure 1: (a) Circular dichroism spectra of 3 (67 μg/mL) (black), 4 (67 μg/mL) (red) and 5 (50 μg/mL) (blue) ...
Figure 2: Circular dichroism spectra of 3 (67 μg/mL) (a) in water at pH 1.9 (black), 4.0 (red), 7.5 (green) a...