|
gold |
17 |
|
organic light-emitting diodes |
13 |
|
palladium |
12 |
|
photochemistry |
12 |
|
organic light-emitting devices |
11 |
|
phosphorescence |
11 |
|
luminescence |
10 |
|
photocatalysis |
10 |
|
tetradentate ligands |
10 |
|
n-heterocyclic carbenes |
9 |
|
thermally activated delayed fluorescence (tadf) |
9 |
|
tungsten |
9 |
|
ligand-to-ligand charge transfer |
8 |
|
platinum |
8 |
|
light |
7 |
|
density functional calculations |
6 |
|
intermolecular interactions |
6 |
|
3mmlct excited state |
5 |
|
acetone - chemistry |
5 |
|
aggregation forms |
5 |
|
bipolar organic host |
5 |
|
carbon - chemistry |
5 |
|
chemical bonds |
5 |
|
chlorine compounds |
5 |
|
color‐tunable |
5 |
|
coordination complexes - chemistry |
5 |
|
cu(i)–cu(i) interaction |
5 |
|
c–x bond activation |
5 |
|
deep-red emission |
5 |
|
dual fluorescence–phosphorescence |
5 |
|
excited-state halogen-atom transfer |
5 |
|
gold - chemistry |
5 |
|
high efficiency |
5 |
|
hydrogen - metabolism |
5 |
|
hydrogen production |
5 |
|
luminescent measurements |
5 |
|
metal-alkynyl complexes |
5 |
|
metal–metal interactions |
5 |
|
microwave synthesis |
5 |
|
near-infrared emission |
5 |
|
nhc–cu(i) complexes |
5 |
|
oleds |
5 |
|
organic light‐emitting diodes |
5 |
|
organogold compounds - chemistry |
5 |
|
oxidation |
5 |
|
oxidation-reduction |
5 |
|
photochemical reactions |
5 |
|
photooxidation |
5 |
|
photophysics |
5 |
|
platinum complexes |
5 |
|
platinum(ii) complexes |
5 |
|
porphyrinoids |
5 |
|
quantum theory |
5 |
|
redox reactions |
5 |
|
sdg9: industry, innovation, and infrastructure |
5 |
|
single emitters |
5 |
|
solution process |
5 |
|
supramolecular chemistry |
5 |
|
tetradentate pt(ii) complexes |
5 |
|
trefoil knots |
5 |
|
visible-light photocatalysis |
5 |
|
water - chemistry |
5 |
|
antitumor agents |
4 |
|
bond theory |
4 |
|
c−h activation |
4 |
|
energy up-conversion |
4 |
|
gold(i) |
4 |
|
iron |
4 |
|
laser spectroscopy |
4 |
|
metal–metal closed-shell interaction |
4 |
|
nitrides |
4 |
|
organic light-emitting devices (oleds) |
4 |
|
pauli repulsion |
4 |
|
pincer ligands |
4 |
|
self-assembly |
4 |
|
silver |
4 |
|
tadf |
4 |
|
thermally activated delayed fluorescence |
4 |
|
thiol reactivity |
4 |
|
thioredoxin reductase (trxr) |
4 |
|
transition metal complexes |
4 |
|
triplet emitters |
4 |
|
two-photon absorption |
4 |
|
attractive strategies |
3 |
|
bioactive compounds |
3 |
|
c-h bond |
3 |
|
c-n bond formations |
3 |
|
cancer |
3 |
|
chirality transfer |
3 |
|
chromophores |
3 |
|
cyclometalation |
3 |
|
dna damage |
3 |
|
electron transfer |
3 |
|
external heavy-atom effect |
3 |
|
femtosecond time-resolved fluorescence |
3 |
|
gold - chemistry - radiation effects - therapeutic use |
3 |
|
hydrogen |
3 |
|
insertion reactions |
3 |
|
isocyanides |
3 |
|
kinetic control |
3 |
|
living supramolecular polymerization |
3 |
|
mechanistic studies |
3 |
|
mmlct |
3 |
|
multi-block supramolecular copolymer |
3 |
|
neoplasms - drug therapy - physiopathology |
3 |
|
nonradiative decay |
3 |
|
photo-cytotoxicity |
3 |
|
photochemotherapy - trends |
3 |
|
photocleavage |
3 |
|
photosensitizing agents - therapeutic use |
3 |
|
phototoxicity |
3 |
|
pincer ptii complex |
3 |
|
platinum - chemistry - radiation effects - therapeutic use |
3 |
|
platinum and palladium |
3 |
|
spin-orbit coupling |
3 |
|
substrate binding |
3 |
|
supramolecular polymerization |
3 |
|
transient absorption |
3 |
|
viologen |
3 |
|
water chemistry |
3 |
|
amination |
2 |
|
anti-counterfeiting |
2 |
|
asymmetric catalysis |
2 |
|
aurophilicity |
2 |
|
bis-n-heterocyclic carbene |
2 |
|
catalysis |
2 |
|
chiral n-heterocyclic carbenes |
2 |
|
circularly polarized luminescence |
2 |
|
diacetylide |
2 |
|
diimine |
2 |
|
excitation-dependent photoluminescence |
2 |
|
iridium compounds |
2 |
|
porphyrins |
2 |
|
ruthenium compounds |
2 |
|
sensitizers |
2 |
|
transition metal catalysts |
2 |
