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. Org. Chem. 2026, 22, 1196–1204, doi:10.3762/bjoc.22.95
Graphical Abstract
Figure 1: CP-PAH radicals synthesized in our group.
Scheme 1: Synthesis of the nucleophilic outmost ring systems.
Scheme 2: Suzuki coupling and establishment of the undecacyclic ring system.
Scheme 3: Finalization of the radical synthesis.
Figure 2: CW (continuous wave) X-band (9.4214 GHz) EPR spectrum of 7 in toluene (1 mM) at ambient temperature...
Figure 3: Calculated spin densities of 7; blue: α spin, green: β spin (isovalue: 0.004 electrons per bohr; ca...
Scheme 4: Resonance formulas of radical 7. Fully intact benzene rings are highlighted in blue; the indacene u...
Figure 4: Calculated SOMOs of α (left) and β electrons (right) for radical 7 (also termed SOMO and SUMO in th...
Figure 5: Cyclic voltammogram of 7 recorded in THF at room temperature (vs Fc/Fc+, v (THF) = 100 mV s−1; Pt/[...
Figure 6: UV–vis spectrum of radical 7 in CH2Cl2: measured (top), calculated (bottom).
Figure 7: NICS(1)πzz-XY-scan of radical 7 (calculated without mesityl and methyl groups).
Figure 8: ACID isosurface plot of 7 (calculated without mesityl and methyl groups; isosurface value 0.02).