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Beilstein J. Nanotechnol. 2025, 16, 1504–1521, doi:10.3762/bjnano.16.106
Figure 1: Structural formulae of ligands, amine linkers, disulfide reducing agents, and clickable dyes used i...
Figure 2: Legend of labeling schemes used within the figures throughout the text. Left column: the black circ...
Figure 3: FTIR and UV–vis characterization of IONP-PPA and controls. (A) FTIR spectra of i) IONP-PPA, (ii) ED...
Figure 4: High-resolution C 1s XPS spectra of i) IONP-3,4-DHBA, ii) IONP-PPA, and iii) EDC-free PPA control. ...
Figure 5: Amine concentration study of EDC/NHS-activated (left column), and EDC-free controls (right column),...
Figure 6: Structural formulae of the primary amine dyes used in this study.
Figure 7: FTIR spectra of CySH products and controls. (A) the fingerprint region showing i) IONP-CySH, ii) ED...
Figure 8: High-resolution S 2p XPS spectra of i) IONP-CySH and ii) the EDC-free CySH control.
Figure 9: Characterization of the thiol–maleimide coupling products and controls with CySH. (A) UV–vis spectr...
Figure 10: UV–vis spectra of MeOH- and MeOH/benzene-washed Cy3-maleimide treated IONP-3,4-DHBA controls. i) Me...
Figure 11: UV–Vis and XPS characterization of DTT-treated IONPs. (A) UV–vis spectra of the thiol–maleimide cou...
Figure 12: UV–vis and XPS characterization of TCEP- and THPP-treated IONPs. (A) UV–vis spectrum of thiol–malei...
Figure 13: UV–vis characterization of IONP-3,5-DHBA CuAAC and thiol–maleimide coupling controls. (A) UV–vis of...