|
absolute configuration |
2 |
|
chirality |
2 |
|
corannulene |
2 |
|
fullerenes |
2 |
|
nanostructures |
2 |
|
1,2-disubstituted-3,4,5,6- tetraethylbenzenes |
1 |
|
1,3,5,7,9-pentasubstituted corannulene |
1 |
|
1,3,5-trisubstituted-2,4,6-triethylbenzene |
1 |
|
1,4-di-x-2,3,5,6-tetraethylbenzenes |
1 |
|
13 c nmr |
1 |
|
2d self-assembly |
1 |
|
ab initio calculations |
1 |
|
ab initio structure |
1 |
|
afterglow organic light-emitting diode |
1 |
|
aids |
1 |
|
alkynes |
1 |
|
allow extension of the |
1 |
|
ally1 cations |
1 |
|
annulenes |
1 |
|
anthracene |
1 |
|
api production |
1 |
|
arenes |
1 |
|
aromatic chemistry |
1 |
|
aromatic diimides |
1 |
|
aromaticity |
1 |
|
aromaticity scale |
1 |
|
aryl hydrocarbon receptor |
1 |
|
arylbromides |
1 |
|
atropisomerism |
1 |
|
basicity |
1 |
|
benzene |
1 |
|
benzo[a]pyrene |
1 |
|
bipyridine ligands |
1 |
|
bond length alternation |
1 |
|
bond-length alternations |
1 |
|
bowl-shaped arenes |
1 |
|
buckybowl |
1 |
|
buckybowl-graphene hybrids |
1 |
|
buckybowls |
1 |
|
c 60 |
1 |
|
c-f activation |
1 |
|
c-glycosides |
1 |
|
c-nucleosides |
1 |
|
cahn–ingold–prelog system |
1 |
|
carbon nanotube |
1 |
|
carbon nanotubes |
1 |
|
carbonylation |
1 |
|
carboranes |
1 |
|
cations |
1 |
|
chemistry institutes uzh |
1 |
|
chiral auxiliaries |
1 |
|
chlorine |
1 |
|
circular dichroism |
1 |
|
circular dichroism spectroscopy |
1 |
|
clafqo |
1 |
|
close contacts |
1 |
|
cobalt |
1 |
|
computation |
1 |
|
computational chemistry |
1 |
|
coordination chemistry |
1 |
|
copper |
1 |
|
copper surface |
1 |
|
corannulenes |
1 |
|
correlated rotation |
1 |
|
cross-coupling |
1 |
|
crystal engineering |
1 |
|
curved aromatic compounds |
1 |
|
cyclic voltammetry |
1 |
|
cyclohexatriene |
1 |
|
cycloisomerism |
1 |
|
cyclophanes |
1 |
|
defective graphene |
1 |
|
demetallation |
1 |
|
density functional calculations |
1 |
|
density functional theory |
1 |
|
diels-alder cycloaddition |
1 |
|
diene |
1 |
|
differential scanning calorimetry |
1 |
|
dna recognition |
1 |
|
domino synthesis |
1 |
|
dynamic gearing |
1 |
|
dynamic nmr spectroscopy |
1 |
|
dynamical disorder |
1 |
|
dynamics |
1 |
|
electrochemistry |
1 |
|
electrophilic aromatic bromination |
1 |
|
enantioselectivity |
1 |
|
encapsulation |
1 |
|
equivalents |
1 |
|
fivefold-symmetry |
1 |
|
fluorescence |
1 |
|
fluorides |
1 |
|
fluorination |
1 |
|
fluorine |
1 |
|
fluorine compounds |
1 |
|
fluorobenzene |
1 |
|
fullerene |
1 |
|
fullerene fragments |
1 |
|
fullerene mimic |
1 |
|
fused-ring systems |
1 |
|
generated from otherwise unreactive aryl fluorides |
1 |
|
geodesic polyarenes |
1 |
|
graphene |
1 |
|
helical structures |
1 |
|
history of chemistry |
1 |
|
hiv |
1 |
|
homochirality |
1 |
|
host-guest systems |
1 |
|
hydrido |
1 |
|
hydrocarbon |
1 |
|
hydrogen-storage |
1 |
|
hyperconjugation |
1 |
|
indenocorannulenes |
1 |
|
institute of organic chemistry uzh |
1 |
|
integrase |
1 |
|
ionization energies |
1 |
|
iridacyclopentadiene |
1 |
|
kilogram scale |
1 |
|
laboratory for process chemistry |
1 |
|
lewis acids |
1 |
|
ligand design |
1 |
|
lipid synthesis |
1 |
|
lipidic cubic phase |
1 |
|
lipids |
1 |
|
macrocycles |
1 |
|
materials science |
1 |
|
membrane proteins |
1 |
|
mesophases |
1 |
|
metal surfaces |
1 |
|
metal-arene complexes |
1 |
|
metallacyclopentadiene |
1 |
|
mills–nixon effect |
1 |
|
molecular compression |
1 |
|
molecular design |
1 |
|
molecular electronics |
1 |
|
molecular evolution |
1 |
|
molecular gears |
1 |
|
molecular machines |
1 |
|
molecular presses |
1 |
|
molecular receptors |
1 |
|
molecular recognition |
1 |
|
multiple phosphorescence |
1 |
|
n ligands |
1 |
|
n-bromosuccinimide |
1 |
|
nitrogen heterocycles |
1 |
|
nomenclature |
1 |
|
noncovalent interactions |
1 |
|
nonlinear optics |
1 |
|
oligoacetylenes |
1 |
|
organic semiconductors |
1 |
|
organocatalysis |
1 |
|
origins of chirality |
1 |
|
oxidation |
1 |
|
pah |
1 |
|
palladium catalysis |
1 |
|
pentaindenocorannulene |
1 |
|
phase behavior |
1 |
|
phase transition |
1 |
|
phase transitions |
1 |
|
photochemistry |
1 |
|
photoelectron spectroscopy |
1 |
|
photoluminescence |
1 |
|
photophysical properties |
1 |
|
photophysics |
1 |
|
photorefractive polymers |
1 |
|
photovoltaic |
1 |
|
physical organic |
1 |
|
pi interactions |
1 |
|
pinwheel |
1 |
|
polar-π effects |
1 |
|
polyaromatic hydrocarbons |
1 |
|
polycycles |
1 |
|
polycyclic aromatic hydrocarbons |
1 |
|
polymers |
1 |
|
polymorphism |
1 |
|
process chemistry |
1 |
|
quantitative pcr |
1 |
|
quasielastic neutron scattering |
1 |
|
racemic state |
1 |
|
raman spectroscopy |
1 |
|
reductive coupling |
1 |
|
retroviral vector |
1 |
|
room-temperature phosphorescence |
1 |
|
ruthenium |
1 |
|
scanning probe microscopy |
1 |
|
scanning tunneling microscopy |
1 |
|
self-assembled monolayers |
1 |
|
self-assembly |
1 |
|
silicon cations |
1 |
|
silyl cations |
1 |
|
small-angle x-ray scattering |
1 |
|
solar cells |
1 |
|
solvent effects |
1 |
|
spiro-bicarbazolium salts |
1 |
|
spontaneous resolution |
1 |
|
stacking interactions |
1 |
|
staudinger reduction |
1 |
|
stereochemistry |
1 |
|
stereoselective synthesis |
1 |
|
stm |
1 |
|
structure-activity relationships |
1 |
|
substituted aromatic alkyl halides |
1 |
|
sumanene |
1 |
|
supported catalysts |
1 |
|
supramolecular chemistry |
1 |
|
synchrotron x-ray diffraction |
1 |
|
synthetic biology |
1 |
|
synthetic methods |
1 |
|
taqman |
1 |
|
temperature sensing |
1 |
|
template synthesis |
1 |
|
tetraarylammonium salts |
1 |
|
triethylbenzene scaffold |
1 |
|
triptycene |
1 |
|
two-dimensional glass |
1 |
|
vancomycin |
1 |
|
x-ray photoelectron spectroscopy |
1 |
|
π interactions |
1 |
