Beilstein J. Org. Chem.2024,20, 1207–1212, doi:10.3762/bjoc.20.103
achieved with one-pot Suzuki–Miyaura coupling to arrange phenylene rings and pyridinylene rings in an alternating fashion. Analyses with UV–vis spectroscopy showed changes in the photophysical properties with nitrogendoping, and X-ray crystallographic analyses experimentally revealed the presence of
biased charges on the peripheral nitrogen atoms.
Keywords: cross coupling; macrocycles; nitrogendoping; UV–vis spectroscopy; X-ray charge density analysis; Introduction
Graphitic carbonaceous sheets of graphene continue to attract considerable attention, which lead us to explore structural defects
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Graphical Abstract
Figure 1:
Nitrogen-doped nanocarbons. (a) Schematic illustration of pyridinic nitrogen atoms installed at the...