|
helicenes |
6 |
|
nanographenes |
6 |
|
polycyclic aromatic hydrocarbons |
5 |
|
boron-nitrogen atoms |
3 |
|
borylation |
3 |
|
chiroptical properties |
3 |
|
delayed fluorescence |
3 |
|
narrow-band emission |
3 |
|
nitrogen-boron |
3 |
|
pentagon–heptagon rings |
3 |
|
scholl reaction |
3 |
|
1,4-boron migration |
2 |
|
antiaromaticity. |
2 |
|
azupyrene |
2 |
|
boron doping |
2 |
|
boron-nitrogen |
2 |
|
circularly polarized luminescence |
2 |
|
cpl brightness |
2 |
|
density functional theory |
2 |
|
donor-acceptor systems |
2 |
|
graphene nanoribbons |
2 |
|
helical nanographene |
2 |
|
heteroatoms |
2 |
|
macrocycles |
2 |
|
molecular carbons |
2 |
|
n-doping |
2 |
|
negative curvature |
2 |
|
non-alternant topologies |
2 |
|
organic electronics |
2 |
|
oxidation |
2 |
|
polycyclic aromatic hydrocarbons (pahs) |
2 |
|
post-functionalization |
2 |
|
radical cations |
2 |
|
radicals |
2 |
|
scanning tunneling microscopy |
2 |
|
spontaneous resolution |
2 |
|
stacking interactions |
2 |
|
zigzag edges |
2 |
|
1d covalent organic frameworks |
1 |
|
acene |
1 |
|
acenes |
1 |
|
adaptable hosts |
1 |
|
aerobic oxidation |
1 |
|
aie effect |
1 |
|
alkyne annulation |
1 |
|
alkyne aromatization |
1 |
|
amplified spontaneous emission |
1 |
|
annulation |
1 |
|
anthracene |
1 |
|
antiaromaticity |
1 |
|
aromaticity |
1 |
|
atom manipulation |
1 |
|
azepines. |
1 |
|
azomethine ylides |
1 |
|
azulene |
1 |
|
biradical |
1 |
|
biradicals |
1 |
|
bistetracene |
1 |
|
bn-coordinated compounds |
1 |
|
bodipy |
1 |
|
bottom-up synthesis |
1 |
|
charge trapping memory |
1 |
|
circumacenes |
1 |
|
curved nanographenes |
1 |
|
cycloaddition |
1 |
|
cyclopenta-fused polycyclic aromatic hydrocarbons |
1 |
|
diels–alder reaction |
1 |
|
donor–acceptor |
1 |
|
doping |
1 |
|
electrocatalyst |
1 |
|
electron paramagnetic resonance |
1 |
|
electron spin resonance spectroscopy |
1 |
|
electronic structure |
1 |
|
field effect transistors |
1 |
|
figure-eight |
1 |
|
fluorescence |
1 |
|
four contiguous heptagons |
1 |
|
geometrically |
1 |
|
graphene |
1 |
|
graphene molecules |
1 |
|
graphenoids |
1 |
|
heterocycles |
1 |
|
hetroartoms |
1 |
|
hydrogen bonding |
1 |
|
isomers |
1 |
|
large stokes shift |
1 |
|
liquid phase |
1 |
|
magnetism |
1 |
|
metalloporphyrin |
1 |
|
molecular geometry |
1 |
|
molecular magnetism |
1 |
|
molecular packing |
1 |
|
multiple resonance |
1 |
|
nanographene |
1 |
|
nanoribbons |
1 |
|
nanostructures |
1 |
|
nbn doping |
1 |
|
nitrogen doping |
1 |
|
nitrogen heterocycles |
1 |
|
non-alternant topology |
1 |
|
non-contact atomic force microscopy |
1 |
|
non-hexagonal pairs |
1 |
|
nonalternant extension |
1 |
|
nonalternant polycyclic aromatic hydrocarbons |
1 |
|
nonhexagonal rings |
1 |
|
nonplanarity |
1 |
|
oled device |
1 |
|
on-surface chemistry |
1 |
|
on-surface synthesis |
1 |
|
open-shell polycyclic aromatic hydrocarbons |
1 |
|
optical properties |
1 |
|
optoelectronic properties |
1 |
|
organic synthesis |
1 |
|
oxygen reduction |
1 |
|
peri -acenes |
1 |
|
peropyrene |
1 |
|
perylenes |
1 |
|
photocatalysis |
1 |
|
photophysical properties |
1 |
|
polycyclic arenes |
1 |
|
polycyclic aromatic hydrocarbon |
1 |
|
polycyclic conjugated hydrocarbons (pchs) |
1 |
|
polycyclic hydrocarbons |
1 |
|
polyimides |
1 |
|
polymer frameworks |
1 |
|
polymer functionalization |
1 |
|
porous nanoparticles |
1 |
|
processability |
1 |
|
pyrene |
1 |
|
pyrolysis |
1 |
|
quantum information processing |
1 |
|
quantum properties |
1 |
|
radicaloids |
1 |
|
regioselectivity |
1 |
|
ring expansion |
1 |
|
saddle conformation |
1 |
|
scanning tunneling spectroscopy |
1 |
|
self assembly |
1 |
|
singlet biradicals |
1 |
|
spectroelectrochemistry |
1 |
|
stimulated emission |
1 |
|
sulfur-doped cove-edged graphene nanoribbons |
1 |
|
supramolecular assembly |
1 |
|
supramolecular structure |
1 |
|
supramolecular-doped polymer |
1 |
|
topological quantum computing |
1 |
|
transient absorption |
1 |
|
transistor memories |
1 |
|
zigzag |
1 |
|
zigzag-edge |
1 |
