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