|
density functional calculations |
9 |
|
raman spectroscopy |
9 |
|
photochemistry |
8 |
|
oleds |
7 |
|
gold |
6 |
|
microwave synthesis |
6 |
|
tetradentate ligands |
6 |
|
thermally activated delayed fluorescence (tadf) |
6 |
|
time-resolved spectroscopy |
6 |
|
antibacterial activity |
5 |
|
chemical bonds |
5 |
|
chlorine compounds |
5 |
|
decarboxylation |
5 |
|
electrochemistry |
5 |
|
fluorescence |
5 |
|
igneous zircons |
5 |
|
ligand effects |
5 |
|
light |
5 |
|
metamorphic zircons |
5 |
|
mgo nanoparticles |
5 |
|
phosphorescence |
5 |
|
photochemical reactions |
5 |
|
photophysics |
5 |
|
physics engineering |
5 |
|
platinum |
5 |
|
proteomics |
5 |
|
raman microspectrometry |
5 |
|
rare-earth element |
5 |
|
redox reactions |
5 |
|
schiff base complexes |
5 |
|
spectrum analysis, raman |
5 |
|
tadf |
5 |
|
toxicity |
5 |
|
transient absorption spectroscopy |
5 |
|
tungsten |
5 |
|
ultrafast spectroscopy |
5 |
|
uv/vis spectroscopy |
5 |
|
zircon genesis |
5 |
|
carbanions |
4 |
|
carbene-metal-amide (cma) |
4 |
|
catalysis |
4 |
|
chromophores |
4 |
|
computer simulation |
4 |
|
copper(i) emitter |
4 |
|
c−h activation |
4 |
|
device lifetime |
4 |
|
g-c3n4 |
4 |
|
iron |
4 |
|
laser spectroscopy |
4 |
|
luminescence |
4 |
|
molecular structure |
4 |
|
nanoparticles |
4 |
|
nitrides |
4 |
|
organic light-emitting diode (oled) |
4 |
|
porphyrinoids |
4 |
|
quantum theory |
4 |
|
radical ions |
4 |
|
spectrometry, fluorescence |
4 |
|
thermally-activated delayed fluorescence (tadf) |
4 |
|
time‐resolved spectroscopy |
4 |
|
acetates - chemistry |
3 |
|
acetylation |
3 |
|
acidity |
3 |
|
acids - chemistry |
3 |
|
aldehydes - chemical synthesis - chemistry |
3 |
|
amidation |
3 |
|
amines - chemical synthesis - chemistry |
3 |
|
anti-inflammatory agents, non-steroidal - chemistry |
3 |
|
azo compounds - chemistry |
3 |
|
boron-nitrogen atoms |
3 |
|
bromides - chemistry |
3 |
|
cage compounds |
3 |
|
chemistry, physical |
3 |
|
crystallography, x-ray |
3 |
|
cyanides - chemical synthesis - chemistry |
3 |
|
cyclization |
3 |
|
defects |
3 |
|
delayed fluorescence |
3 |
|
dimethoxybenzoin |
3 |
|
dssc |
3 |
|
energy transfer |
3 |
|
esters - chemical synthesis - chemistry |
3 |
|
h2o2 photosynthesis |
3 |
|
hydrogen-ion concentration |
3 |
|
hydroxyquinolines - chemistry |
3 |
|
ketoprofen |
3 |
|
ketoprofen - chemistry |
3 |
|
kinetics |
3 |
|
lanthanides |
3 |
|
ligands |
3 |
|
macrocyclic compounds - chemical synthesis - chemistry |
3 |
|
models, chemical |
3 |
|
nanographenes |
3 |
|
nonlinear optics |
3 |
|
nucleic acid conformation |
3 |
|
organometallic compounds - chemical synthesis - chemistry |
3 |
|
p-hydroxyphenacyl cage |
3 |
|
pentagon–heptagon rings |
3 |
|
photochemical processes |
3 |
|
photodeprotection |
3 |
|
photoelectron spectroscopy |
3 |
|
photoluminescence |
3 |
|
phototriggers |
3 |
|
photovoltaics |
3 |
|
physics chemistry |
3 |
|
poly a - chemistry |
3 |
|
polycyclic aromatic hydrocarbons |
3 |
|
proton transfer |
3 |
|
proton transport |
3 |
|
protons |
3 |
|
quinoline |
3 |
|
reaction mechanisms |
3 |
|
ruthenium - chemistry |
3 |
|
solutions |
3 |
|
solvent effects |
3 |
|
solvents - chemistry |
3 |
|
spectrophotometry |
3 |
|
spectrophotometry, ultraviolet |
3 |
|
sub-bands |
3 |
|
succinylation |
3 |
|
thermodynamics |
3 |
|
time-resolved resonance |
3 |
|
titanium - chemistry |
3 |
|
transient absorption |
3 |
|
triplet state |
3 |
|
tripodal ligands |
3 |
|
vibration |
3 |
|
water - chemistry |
3 |
|
z-scheme |
3 |
|
zno |
3 |
|
4-benzoylpyridine |
2 |
|
absorption |
2 |
|
acetonitriles - chemistry |
2 |
|
acetophenones - chemistry |
2 |
|
amides - chemistry |
2 |
|
amylose content |
2 |
|
anion |
2 |
|
anions - chemistry |
2 |
|
anthraquinones - chemical synthesis - chemistry |
2 |
|
antiaromaticity. |
2 |
|
aqueous solutions |
2 |
|
atomic force microscopy |
2 |
|
atomic force microscopy (afm) |
2 |
|
aurophilicity |
2 |
|
azupyrene |
2 |
|
benzoin - analogs and derivatives - chemistry |
2 |
|
carbamates - chemistry |
2 |
|
carboxymethylation |
2 |
|
cas-scf |
2 |
|
cationic modification |
2 |
|
cellulose |
2 |
|
charge separation |
2 |
|
circulene |
2 |
|
computational investigation |
2 |
|
copper |
2 |
|
cuprophilicity |
2 |
|
deamidation |
2 |
|
density functional theory |
2 |
|
density functional theory (dft) |
2 |
|
deoxyblebbistatin |
2 |
|
dft calculations |
2 |
|
dlvo theory |
2 |
|
egg white |
2 |
|
electrochemical deposition |
2 |
|
electrodeposition |
2 |
|
electron transfer |
2 |
|
electronic configuration |
2 |
|
electronic structure |
2 |
|
electronic transition |
2 |
|
esters - chemistry |
2 |
|
femtosecond transient absorption |
2 |
|
fluorogen activating protein |
2 |
|
fourier transform infrared spectroscopy |
2 |
|
ft raman spectroscopy |
2 |
|
ft-ir spectra |
2 |
|
functionalized metal oxide surface |
2 |
|
g-c3n4 long-lived charge separation |
2 |
|
geometrical distortion |
2 |
|
gluten |
2 |
|
graphite |
2 |
|
guar gum |
2 |
|
halogenation |
2 |
|
highly oriented pyrolytic graphite (hopg) |
2 |
|
homogeneous catalysis |
2 |
|
hydrocarbons |
2 |
|
hydrogen - chemistry |
2 |
|
hydrogen abstraction |
2 |
|
hydrogen bonding |
2 |
|
intersystem crossing |
2 |
|
intramolecular hydrogen atom transfer |
2 |
|
iodoform |
2 |
|
isomerization |
2 |
|
ketyl radical |
2 |
|
lasing |
2 |
|
light harvesting |
2 |
|
locust bean gum |
2 |
|
luminescence n ligands |
2 |
|
malachite green |
2 |
|
maleinated starch |
2 |
|
metal-metal interactions |
2 |
|
modified starch |
2 |
|
molecular conformation |
2 |
|
n-doping |
2 |
|
nanoparticle |
2 |
|
nitrene insertion |
2 |
|
nmr spectroscopy |
2 |
|
non-alternant topologies |
2 |
|
non-precious metal complex |
2 |
|
oat globulin |
2 |
|
octenyl succinate |
2 |
|
organometallic compounds - chemistry |
2 |
|
oxidation-reduction |
2 |
|
oxidations |
2 |
|
oxygen reduction reaction |
2 |
|
oxygenations |
2 |
|
p ligands |
2 |
|
para-hydroxybenzophenone (p-hbp) |
2 |
|
pasting |
2 |
|
phosphoric acid esters - chemistry |
2 |
|
photochromism |
2 |
|
photoinduced reaction |
2 |
|
photosensitizer |
2 |
|
phototoxicity |
2 |
|
physical properties |
2 |
|
physics |
2 |
|
platinum (pt) |
2 |
|
platinum nanoparticles |
2 |
|
polyoxometalates |
2 |
|
porphyrins - chemistry |
2 |
|
protein conformation |
2 |
|
proteins |
2 |
|
proximal carboxylate cocatalyst |
2 |
|
raman spectra |
2 |
|
raman spectrometry |
2 |
|
red bean globulin |
2 |
|
resonance raman |
2 |
|
resonance raman spectroscopy |
2 |
|
rhenium |
2 |
|
rhodium |
2 |
|
rice globulin |
2 |
|
ruthenium complex |
2 |
|
ruthenium complexes |
2 |
|
silver |
2 |
|
soy protein isolates |
2 |
|
soy proteins isolates |
2 |
|
spray-dried egg white |
2 |
|
starch |
2 |
|
starch esters david |
2 |
|
stereoisomerism |
2 |
|
substitution degree |
2 |
|
succinylated starches |
2 |
|
sulfonic acids - chemistry |
2 |
|
surface modification |
2 |
|
swcnt |
2 |
|
tapping mode atomic force microscopy (tmafm) |
2 |
|
tetrapod |
2 |
|
theoretical calculation |
2 |
|
thermal analysis |
2 |
|
time factors |
2 |
|
time-resolved |
2 |
|
upconversion |
2 |
|
uv-vis spectra |
2 |
|
visible-nir photocatalysis |
2 |
|
water |
2 |
|
whey protein isolates |
2 |
|
xanthan gum |
2 |
|
zinc oxide |
2 |
|
1-bromo-2-iodoethane |
1 |
|
1-chloro-2-iodoethane |
1 |
|
3-hydroxyflavone |
1 |
|
4-chloroaniline |
1 |
|
4-cyanobenzaldehyde |
1 |
|
7-bromo-2-fluorenylnitrenium |
1 |
|
ab initio |
1 |
|
ab initio calculation |
1 |
|
ab initio calculations |
1 |
|
absorption band |
1 |
|
acetylene |
1 |
|
aggregation-induced emission |
1 |
|
aggregation‐induced emission |
1 |
|
aie |
1 |
|
alanine - analogs and derivatives - chemistry - metabolism |
1 |
|
algorithms |
1 |
|
alnnt |
1 |
|
alternative solvents |
1 |
|
amination |
1 |
|
aminobiphenyl compounds - chemistry |
1 |
|
anion–π+ interactions |
1 |
|
anti conformer |
1 |
|
antibacterial cancer cells |
1 |
|
antisymmetries |
1 |
|
aromatic carbonyl compound |
1 |
|
aromatic compounds |
1 |
|
aromaticity |
1 |
|
arylnitrenes |
1 |
|
arylnitrenium ions |
1 |
|
atoms |
1 |
|
azepines - chemical synthesis - chemistry - radiation effects |
1 |
|
azides - chemistry |
1 |
|
azides - chemistry - radiation effects |
1 |
|
azirines |
1 |
|
azobenzene |
1 |
|
b2cat2 |
1 |
|
benzoin |
1 |
|
benzophenones - chemistry |
1 |
|
bifunctional quinone methides |
1 |
|
bimetallic particles |
1 |
|
biphenyl compounds - chemistry |
1 |
|
bond selective excitation |
1 |
|
borylation |
1 |
|
butyrophenone |
1 |
|
c-h activation |
1 |
|
c-h bond activation |
1 |
|
carbenoid |
1 |
|
carbenoids |
1 |
|
carbon nitride |
1 |
|
casscf |
1 |
|
casscf computation |
1 |
|
catalytic properties |
1 |
|
cations |
1 |
|
cations, monovalent |
1 |
|
cell image |
1 |
|
charge trapping |
1 |
|
chemical reaction |
1 |
|
chloro-substituted benzophenone |
1 |
|
column chromatography |
1 |
|
complete active space self-consistent fields |
1 |
|
composites |
1 |
|
computational results |
1 |
|
conical intersection |
1 |
|
control |
1 |
|
cryochemistry |
1 |
|
crystal structure |
1 |
|
crystallization |
1 |
|
cu3p |
1 |
|
cyclen |
1 |
|
cyclodextrin |
1 |
|
cyclopropanation |
1 |
|
cyclopropanes - chemical synthesis |
1 |
|
cyclopropanes - chemistry |
1 |
|
dehalogenation |
1 |
|
dehydroazepines |
1 |
|
density functional theory calculations |
1 |
|
deprotonation |
1 |
|
design for testability |
1 |
|
detention |
1 |
|
dft |
1 |
|
dft calculation |
1 |
|
dichlorocarbene |
1 |
|
dimerization |
1 |
|
disinfection byproducts |
1 |
|
dissociation |
1 |
|
disulfides - chemistry |
1 |
|
dumbbell-shaped platinum complex |
1 |
|
e1bc elimination reaction |
1 |
|
eda complex |
1 |
|
electrocatalysis |
1 |
|
elimination |
1 |
|
embedded |
1 |
|
enzyme models |
1 |
|
esipt |
1 |
|
espt |
1 |
|
ethane |
1 |
|
ethylenes - chemistry |
1 |
|
even–odd effect |
1 |
|
excited state quinone‐conformation induced planarization |
1 |
|
excited states |
1 |
|
excited-state dynamics |
1 |
|
excited-state structural dynamics |
1 |
|
femtosecond transient absorption spectroscopy |
1 |
|
fluorenes - chemistry |
1 |
|
free energy barrier |
1 |
|
gauche conformer |
1 |
|
graphite carbon nitride |
1 |
|
guanosine |
1 |
|
h2 evolution |
1 |
|
haloacetic acid |
1 |
|
halogens - chemistry |
1 |
|
heterocyclic compounds, 1-ring - chemistry - metabolism |
1 |
|
hydrocarbons - chemistry |
1 |
|
hydrocarbons, iodinated - chemistry |
1 |
|
hydrogen evolution |
1 |
|
hydrolysis |
1 |
|
infrared spectroscopy |
1 |
|
intersection |
1 |
|
iodoethane |
1 |
|
ion migration |
1 |
|
isocyanide ligands |
1 |
|
isodichloromethane |
1 |
|
isodihalomethane |
1 |
|
isomers |
1 |
|
isopolyhalomethanes |
1 |
|
ketones - chemistry |
1 |
|
lithium - chemistry |
1 |
|
lithium compounds - chemistry |
1 |
|
methane - analogs & derivatives - chemistry |
1 |
|
methanol |
1 |
|
methanol - chemistry |
1 |
|
methodology |
1 |
|
models, molecular |
1 |
|
molecular dynamics simulation |
1 |
|
molecular models |
1 |
|
molecules |
1 |
|
molybdenum disulfide |
1 |
|
mp2 |
1 |
|
multiple and ordered targeting |
1 |
|
nanocrystals |
1 |
|
narrowband response |
1 |
|
near-infrared photothermal conversion |
1 |
|
nickel oxide cluster |
1 |
|
nitrenes |
1 |
|
nitrenium ion |
1 |
|
nitric oxide |
1 |
|
nitrogen defects |
1 |
|
nucleophiles |
1 |
|
o-h insertion |
1 |
|
octa acid |
1 |
|
oh insertion reaction |
1 |
|
on-site |
1 |
|
organic light‐emitting diodes |
1 |
|
organophosphorus compounds - chemistry - metabolism |
1 |
|
peptides, cyclic - chemistry |
1 |
|
perovskites |
1 |
|
phosphoester |
1 |
|
phosphorus |
1 |
|
photocage |
1 |
|
photocatalysis |
1 |
|
photodetectors |
1 |
|
photodissociation |
1 |
|
photodissociation dynamics |
1 |
|
photodynamic therapy |
1 |
|
photoelectrocatalytic hydrogen evolution |
1 |
|
photoinitiator |
1 |
|
photoisomerization |
1 |
|
photolysis |
1 |
|
photoswitching molecules |
1 |
|
physical chemistry |
1 |
|
planarized intramolecular charge transfer |
1 |
|
polymerization |
1 |
|
porphyrin |
1 |
|
propylene |
1 |
|
protein denaturation |
1 |
|
protein folding |
1 |
|
pt particles |
1 |
|
pt/co |
1 |
|
quantum efficiency |
1 |
|
quinone methide |
1 |
|
quinone methides |
1 |
|
radical |
1 |
|
radical cyclization |
1 |
|
raman |
1 |
|
reactive intermediate |
1 |
|
red phosphorus |
1 |
|
reference standards |
1 |
|
resonance |
1 |
|
resonance raman intensity analysis |
1 |
|
ring opening |
1 |
|
rna - chemistry - metabolism |
1 |
|
room-temperature phosphorescence |
1 |
|
ros |
1 |
|
sensitivity and specificity |
1 |
|
singlet o2 |
1 |
|
singlet state |
1 |
|
solar-driven water evaporation |
1 |
|
solutions - chemistry |
1 |
|
solvent-assisted dehalogenation |
1 |
|
spectrum analysis, raman - methods - standards |
1 |
|
spin conversion |
1 |
|
spin densities |
1 |
|
stereochemistry |
1 |
|
storage |
1 |
|
stormwater |
1 |
|
substituent effect |
1 |
|
support effect |
1 |
|
supramolecular interactions |
1 |
|
suprofen |
1 |
|
ternary cocrystals |
1 |
|
tetraphenylpyrazine |
1 |
|
time resolved spectroscopy |
1 |
|
time-resolved resonance raman |
1 |
|
time-resolved resonance raman spectroscopy |
1 |
|
time‐resolved fluorescence kinetics |
1 |
|
titanium dioxide |
1 |
|
transient spectroscopy |
1 |
|
trap states |
1 |
|
triplet o2 |
1 |
|
triplet state of tpe |
1 |
|
ultrafast transient absorption spectroscopy |
1 |
|
ultraviolet rays |
1 |
|
urban |
1 |
|
vibrational spectra |
1 |
|
water catalyzed |
1 |
|
water chemistry |
1 |
|
x-ray diffraction |
1 |
|
z-scheme heterojunction |
1 |
|
zinc |
1 |
|
zinc - chemistry |
1 |
|
zinc - chemistry - metabolism |
1 |
|
α-cleavage |
1 |
