This search combines search strings from the content search (i.e. "Full Text", "Author", "Title", "Abstract", or "Keywords") with "Article Type" and "Publication Date Range" using the AND operator.
Beilstein J. Nanotechnol. 2017, 8, 1878–1888, doi:10.3762/bjnano.8.188
Scheme 1: Synthesis of BODIPY derivatives 2 and 3. i) 2,4-dimethylpyrrole, TFA, DCM, DIPEA, BF3OEt2; ii) 4-(N,...
Scheme 2: Procedure for the preparation of carboxy-functionalized oxi-CNO and fluorescently labelled fluo-CNO...
Figure 1: Emission spectra of BODIPY 3 (blue line: Excitation at 680 nm; emission at 737 nm) and BODIPY 4 (re...
Figure 2: A) Protonated (fluo-CNOs-1a) and non-protonated (fluo-CNOs-1b) forms of fluo-CNOs. B) Emission spec...
Figure 3: Thermogravimetric analysis (TGA) spectra of the functionalized CNOs. TGA (solid lines) and the corr...
Figure 4: Raman spectra of the functionalized CNOs. The Raman spectra are normalized to the G-band at 1580 cm...
Figure 5: Effective hydrodynamic diameter of oxi-CNOs (black line) and fluo-CNOs (red line) in PBS at a conce...
Figure 6: Cellular viability of HeLa cells treated with different concentrations (1, 2, 5, 10 and 20 µg mL−1)...
Figure 7: Confocal fluorescence images of HeLa cells treated with 20 μg mL−1 of fluo-CNOs. (A) PBS for 1 h, p...
Figure 8: Cellular uptake and localization of fluo-CNOs in HeLa cells in acidic conditions (PBS, pH 4.5) obse...
Figure 9: Three-dimensional reconstruction by confocal microscopy of cells incubated for 12 h with 20 µg mL−1...
Beilstein J. Nanotechnol. 2014, 5, 1980–1998, doi:10.3762/bjnano.5.207
Figure 1: HRTEM images of (a) diamond nanoparticles, (b) spherical carbon onions, and (c) polyhedral carbon o...
Figure 2: Typical Raman spectra of pristine CNOs. Reprinted with permission from [21]. Copyright 2013 Elsevier.
Scheme 1: Covalent functionalization pathways for CNOs.
Scheme 2: Covalent functionalization of CNOs by an azomethine ylide addition [25].
Scheme 3: Methods for the covalent functionalization of CNOs by azomethine ylide addition on CNOs and amidati...
Scheme 4: Comparison of the reactivity of small N-CNOs and larger A-CNOs, prepared by different methods [27].
Figure 3: Structure of a CNO–BODA copolymer. (A) CNO starting material (left) and BODA-functionalized CNOs (r...
Scheme 5: Preparation of pyridyl-CNOs and an illustration of their supramolecular interaction with Zn-tetraph...
Scheme 6: Illustration of polymerization reactions on CNOs following initial [2 + 1] cycloaddition reaction o...
Scheme 7: “Tour” functionalization of CNOs and subsequent “click”-addition of a ZnTPP-derivative [37].
Figure 4: First derivative TGA weight-loss curves of pristine CNO (black), treated once (light gray) and trea...
Scheme 8: Fluorophore–CNO conjugates derived from benzoic acid-functionalized CNOs [39-41].
Scheme 9: Schematic overview over the different polymeric structures utilized to functionalize CNOs [43-48].
Figure 5: a) Autofluorescence images of different developmental stages of Drosophila melanogaster from larva ...
Figure 6: High-resolution TEM images of pristine CNOs (left). AFM topographs of pristine CNOs deposited on mi...
Figure 7: Confocal images of azaBODIPY-CNOs in HeLa Kyoto cells (left) and BODIPY-CNOs in MCF-7 cells (right)...
Figure 8: (a) A schematic showing the chemical activation of CNOs in KOH. TEM images of pristine CNO (b), ACN...
Figure 9: Note: The authors of the original report refer to CNOs as onion-like carbon (OLC) (a) Schematic dia...