Beilstein J. Org. Chem.2024,20, 32–40, doi:10.3762/bjoc.20.5
., graphitic carbon nitride) in the form of 10–30 nm-sized stacks is also demonstrated using the present amphiphiles.
Keywords: aromaticmicelle; nanocarbon; nonionic surface modification; pyridinium; water-solubilization; Introduction
Nanocarbons, such as fullerenes, graphenes, and carbon nanotubes, are
present amphiphile is originated from bent aromatic amphiphile AA [12][13], composed of two anthracene panels linked by a m-phenylene spacer with two cationic side-chains, which assembles into an aqueous ≈2 nm-sized aromaticmicelle with broad host functions [14][15][16][17][18][19][20][21]. Replacement
and structure of aromatic micelles
Aromaticmicelle (PA-CH3)n was facilely generated via dissolution of PA-CH3 (2.1 mg, 4.3 μmol) in water (8.6 mL). The 1H NMR spectrum of PA-CH3 in D2O showed significantly upfield-shifted signals (Δδ = −2.73 ppm for Hb) compared to the spectrum in CD3OD, in a manner
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Graphical Abstract
Figure 1:
a) Previous methods for the water-solubilization and modification of nanocarbons (NCs). b) Bent aro...