|
gold |
42 |
|
platinum |
36 |
|
humans |
31 |
|
organic light-emitting diodes |
26 |
|
luminescence |
24 |
|
hepatocellular carcinoma |
22 |
|
phosphorescence |
22 |
|
n-heterocyclic carbenes |
20 |
|
proteomics |
20 |
|
apoptosis |
19 |
|
gold - chemistry |
18 |
|
palladium |
18 |
|
ruthenium |
18 |
|
photochemistry |
17 |
|
porphyrinoids |
17 |
|
silver |
17 |
|
self-assembly |
16 |
|
animals |
15 |
|
homogeneous catalysis |
15 |
|
nanostructures |
15 |
|
antitumor agents |
14 |
|
apoptosis - drug effects |
14 |
|
n-heterocyclic carbene |
14 |
|
thermally activated delayed fluorescence |
14 |
|
cell line, tumor |
13 |
|
iron |
13 |
|
metal-metal interactions |
13 |
|
ruthenium - chemistry |
13 |
|
catalysis |
12 |
|
density functional calculations |
12 |
|
ligands |
12 |
|
mice |
12 |
|
molecular structure |
12 |
|
nasopharyngeal carcinoma |
12 |
|
organic light-emitting devices |
12 |
|
oxidation |
12 |
|
tetradentate ligands |
12 |
|
tungsten |
12 |
|
water - chemistry |
12 |
|
cancer |
11 |
|
cytotoxicity |
11 |
|
c−h activation |
11 |
|
iridium |
11 |
|
photocatalysis |
11 |
|
photophysics |
11 |
|
supramolecular chemistry |
11 |
|
thermally activated delayed fluorescence (tadf) |
11 |
|
alkenes - chemistry |
10 |
|
autophagy - drug effects |
10 |
|
cyclometalation |
10 |
|
diazo compounds |
10 |
|
dna |
10 |
|
electroluminescence |
10 |
|
female |
10 |
|
ligand effects |
10 |
|
ligand-to-ligand charge transfer |
10 |
|
macrocyclic ligands |
10 |
|
n ligands |
10 |
|
nanoparticles |
10 |
|
oleds |
10 |
|
oxidation-reduction |
10 |
|
adult |
9 |
|
aurophilicity |
9 |
|
carbenes |
9 |
|
cells, cultured |
9 |
|
cisplatin |
9 |
|
copper |
9 |
|
crystallography, x-ray |
9 |
|
gels |
9 |
|
luminescent measurements |
9 |
|
male |
9 |
|
metalloporphyrins - pharmacology |
9 |
|
models, molecular |
9 |
|
noncovalent interactions |
9 |
|
platinum complexes |
9 |
|
platinum(ii) complexes |
9 |
|
porphyrin |
9 |
|
rats |
9 |
|
rhodium |
9 |
|
spectrometry, mass, matrix-assisted laser desorption-ionization |
9 |
|
spectrophotometry, ultraviolet |
9 |
|
antineoplastic activity |
8 |
|
asymmetric catalysis |
8 |
|
carbon - chemistry |
8 |
|
coordination complexes - chemistry - toxicity |
8 |
|
electrophosphorescence |
8 |
|
galectin-1 |
8 |
|
light |
8 |
|
metal–metal interactions |
8 |
|
mir-22 |
8 |
|
otx008 |
8 |
|
platinum complex |
8 |
|
porphyrins - chemistry |
8 |
|
semiconductors |
8 |
|
stereoisomerism |
8 |
|
structure elucidation |
8 |
|
tetradentate pt(ii) complexes |
8 |
|
therapeutics |
8 |
|
thiol reactivity |
8 |
|
white emission |
8 |
|
acetylides |
7 |
|
acrosome - physiology |
7 |
|
amines |
7 |
|
amino acid sequence |
7 |
|
antineoplastic agents - chemistry - pharmacology |
7 |
|
bioinorganic chemistry |
7 |
|
coordination complexes - chemistry |
7 |
|
drug screening assays, antitumor |
7 |
|
enantioselectivity |
7 |
|
endoplasmic reticulum - drug effects - pathology |
7 |
|
energy transfer |
7 |
|
fluorescence |
7 |
|
gold(iii) compound |
7 |
|
high efficiency |
7 |
|
hydroxylation |
7 |
|
in situ hybridization, fluorescence |
7 |
|
intermolecular interactions |
7 |
|
metal nanoparticles - chemistry |
7 |
|
metallacycles |
7 |
|
metalloporphyrins - chemistry |
7 |
|
mitochondria |
7 |
|
models, chemical |
7 |
|
molecular sequence data |
7 |
|
nitrides |
7 |
|
oled |
7 |
|
organogold compounds - chemistry - pharmacology |
7 |
|
phosphines - chemistry |
7 |
|
physics engineering |
7 |
|
porphyrins |
7 |
|
protein structure, tertiary |
7 |
|
proteins - genetics - metabolism |
7 |
|
schiff bases |
7 |
|
sequence alignment |
7 |
|
signal transduction - drug effects |
7 |
|
spermatogenesis - physiology |
7 |
|
spermatozoa - cytology - metabolism |
7 |
|
tadf |
7 |
|
testis - cytology - physiology |
7 |
|
tissue distribution |
7 |
|
wound healing |
7 |
|
zinc fingers |
7 |
|
amidation |
6 |
|
antineoplastic agents - pharmacology |
6 |
|
autolysosome |
6 |
|
autophagosome |
6 |
|
breast cancer |
6 |
|
c(sp2)−c(sp2) bond |
6 |
|
c-h bond |
6 |
|
carbenoids |
6 |
|
caspase 3 - metabolism |
6 |
|
cell line |
6 |
|
chemocytotoxic |
6 |
|
cholestenones - pharmacology |
6 |
|
clathrin light chain a |
6 |
|
color-tunable |
6 |
|
cyclization |
6 |
|
dna - chemistry - metabolism |
6 |
|
electronic structure |
6 |
|
fibroblasts |
6 |
|
fibroblasts - cytology - drug effects |
6 |
|
flux |
6 |
|
g quadruplexes |
6 |
|
gene expression regulation, neoplastic - drug effects |
6 |
|
gold - chemistry - pharmacology |
6 |
|
growth arrest and dna damage (gadd) inducible genes |
6 |
|
keratinocytes |
6 |
|
keratinocytes - cytology - drug effects |
6 |
|
kinetics |
6 |
|
lc3 |
6 |
|
lysosome |
6 |
|
membrane potential, mitochondrial - drug effects |
6 |
|
mice, inbred balb c |
6 |
|
microwave synthesis |
6 |
|
molecular wheels |
6 |
|
nanoparticles - therapeutic use |
6 |
|
organic light emitting diodes |
6 |
|
organometallic compounds - chemistry |
6 |
|
organoplatinum compounds - chemistry |
6 |
|
osmium |
6 |
|
phagophore |
6 |
|
photoluminescence |
6 |
|
platinum - chemistry |
6 |
|
porphyrins - chemistry - metabolism - pharmacology |
6 |
|
reactive oxygen species - metabolism |
6 |
|
sarcoplasmic reticulum calcium-transporting atpases - antagonists and inhibitors |
6 |
|
silver - therapeutic use |
6 |
|
small extracellular vesicles |
6 |
|
solution process |
6 |
|
spectrum analysis |
6 |
|
spin-orbit coupling |
6 |
|
stress |
6 |
|
vacuole |
6 |
|
wound healing - drug effects |
6 |
|
1/f noise |
5 |
|
2-de |
5 |
|
3mmlct excited state |
5 |
|
acetaldehyde - analogs & derivatives - metabolism |
5 |
|
acetone - chemistry |
5 |
|
acetylide |
5 |
|
acyl coenzyme a - metabolism |
5 |
|
adducts |
5 |
|
adiponectin |
5 |
|
adipose tissue |
5 |
|
adolescent |
5 |
|
affinity chromatography |
5 |
|
aged |
5 |
|
aggregation forms |
5 |
|
aging |
5 |
|
aging - metabolism |
5 |
|
alkenes |
5 |
|
amination |
5 |
|
amines - chemistry |
5 |
|
antibacterial agents |
5 |
|
anticancer |
5 |
|
antimutagenic agents - pharmacology |
5 |
|
antineoplastic agents - chemical synthesis - pharmacology |
5 |
|
atp |
5 |
|
autophagy |
5 |
|
aza compounds - chemistry |
5 |
|
aziridination |
5 |
|
bioaccumulation |
5 |
|
biotin |
5 |
|
bipolar organic host |
5 |
|
blotting, western |
5 |
|
carcinoma, hepatocellular - metabolism - pathology |
5 |
|
caspases - metabolism |
5 |
|
catechin - analogs & derivatives - pharmacology |
5 |
|
cell imaging |
5 |
|
charge transfer |
5 |
|
chemical bonds |
5 |
|
chemical model reactions |
5 |
|
child |
5 |
|
china |
5 |
|
chlorine compounds |
5 |
|
cohort studies |
5 |
|
color‐tunable |
5 |
|
cu(i)–cu(i) interaction |
5 |
|
cyclopropanation reaction |
5 |
|
cytokines |
5 |
|
c–x bond activation |
5 |
|
deep-red emission |
5 |
|
device lifetime |
5 |
|
dna damage |
5 |
|
drug delivery |
5 |
|
dual fluorescence–phosphorescence |
5 |
|
e. coli |
5 |
|
electrochemistry |
5 |
|
electrophoresis, gel, two-dimensional |
5 |
|
enox2 |
5 |
|
epigallocatechin gallate peracetate |
5 |
|
escherichia coli - genetics |
5 |
|
excited-state halogen-atom transfer |
5 |
|
fluorenes |
5 |
|
food contamination |
5 |
|
gan epilayers |
5 |
|
genipin |
5 |
|
glycosylation |
5 |
|
gold compounds - pharmacology |
5 |
|
gold porphyrin |
5 |
|
gold(iii) |
5 |
|
gold(iii) porphyrin 1a |
5 |
|
groundwater hydraulics |
5 |
|
heat-shock protein |
5 |
|
heat-shock proteins - metabolism |
5 |
|
hela cells |
5 |
|
hepatitis b virus |
5 |
|
hsp27 heat-shock proteins |
5 |
|
hsp70 heat-shock proteins - metabolism |
5 |
|
hydrogen - metabolism |
5 |
|
hydrogen bondings |
5 |
|
hydrogen production |
5 |
|
idronoxil |
5 |
|
imidazoles - metabolism |
5 |
|
interaction profiling |
5 |
|
intercalating agents - chemical synthesis - pharmacology |
5 |
|
ionization time of flight mass spectrometry |
5 |
|
ire1α |
5 |
|
iron - chemistry |
5 |
|
kidney calculi - etiology - urine |
5 |
|
kinetic control |
5 |
|
liquid chromatography-tan-dem mass spectrometry |
5 |
|
liver - drug effects - injuries - metabolism |
5 |
|
liver - metabolism |
5 |
|
liver glycogen - metabolism |
5 |
|
liver injury |
5 |
|
liver neoplasms - metabolism - pathology |
5 |
|
longevity regulator |
5 |
|
low-permeability layer |
5 |
|
luminescent agents - chemistry |
5 |
|
lung cancer |
5 |
|
lysosomal proteolysis |
5 |
|
macrocyclic compounds - chemical synthesis |
5 |
|
mammary neoplasms, experimental - drug therapy |
5 |
|
materials science |
5 |
|
matrix-assisted laser desorption |
5 |
|
medicinal chemistry |
5 |
|
membrane potential |
5 |
|
memory t-cells |
5 |
|
metal-alkynyl complexes |
5 |
|
metallophilic interactions |
5 |
|
methane - analogs & derivatives - chemistry |
5 |
|
methane - analogs and derivatives - chemistry |
5 |
|
middle aged |
5 |
|
mitochondrial proteins - genetics - metabolism |
5 |
|
molecular chaperones - metabolism |
5 |
|
molecular conformation |
5 |
|
multinodular goiter |
5 |
|
multiphase flow |
5 |
|
mutagens - metabolism |
5 |
|
möbius strip |
5 |
|
near-infrared emission |
5 |
|
neoplasm proteins - metabolism |
5 |
|
nf-κb |
5 |
|
nhc–cu(i) complexes |
5 |
|
olefins |
5 |
|
organic light-emitting devices (oleds) |
5 |
|
organic light‐emitting diodes |
5 |
|
organogold compounds - chemistry |
5 |
|
organometallic compounds - chemical synthesis - chemistry |
5 |
|
osmium - chemistry |
5 |
|
outer membrane proteins |
5 |
|
p ligands |
5 |
|
phenylacetaldehyde |
5 |
|
phip |
5 |
|
photochemical reactions |
5 |
|
photooxidation |
5 |
|
phytoestrogen |
5 |
|
pincer ligands |
5 |
|
porphyrin derivative |
5 |
|
prognosis |
5 |
|
proliferation |
5 |
|
protein binding |
5 |
|
protein interaction mapping - methods |
5 |
|
protein staining |
5 |
|
proteins - metabolism |
5 |
|
proteome - metabolism |
5 |
|
quantum theory |
5 |
|
quinoneimido complexes |
5 |
|
recombinant proteins - genetics - metabolism |
5 |
|
redox reactions |
5 |
|
rosiglitazone |
5 |
|
sand box |
5 |
|
schiff base complexes |
5 |
|
sdg9: industry, innovation, and infrastructure |
5 |
|
sensitivity and specificity |
5 |
|
shotgun proteomics |
5 |
|
signaling pathway analysis |
5 |
|
silver - chemistry |
5 |
|
silver ions |
5 |
|
silver nanoparticles |
5 |
|
single emitters |
5 |
|
sirt1 |
5 |
|
sirtuin 1 |
5 |
|
sirtuin 3 |
5 |
|
sirtuins - genetics - metabolism |
5 |
|
spectrometry, mass, electrospray ionization - methods |
5 |
|
surface plasmon resonance absorption |
5 |
|
surface properties |
5 |
|
terpyridine |
5 |
|
tetradentate |
5 |
|
thiazolidinediones - toxicity |
5 |
|
timosaponin aiii |
5 |
|
tmt labeling |
5 |
|
transcription factor yy1 |
5 |
|
transcriptomics |
5 |
|
transition metal complexes |
5 |
|
trefoil knots |
5 |
|
triazines - analysis - chemistry - urine |
5 |
|
triplet state |
5 |
|
ttf1 |
5 |
|
tumor markers, biological - metabolism |
5 |
|
tumour-associated macrophage |
5 |
|
unconfined aquifer |
5 |
|
uncoupling protein 2 |
5 |
|
up-regulation |
5 |
|
uv/vis spectroscopy |
5 |
|
venous infiltration |
5 |
|
visible-light photocatalysis |
5 |
|
xiap |
5 |
|
aatitumor agents |
4 |
|
acylnitrene transfer |
4 |
|
aldehydes - chemistry |
4 |
|
alkyne ligands |
4 |
|
alkynes - chemistry |
4 |
|
and light-emitting devices |
4 |
|
anemarrhena - chemistry |
4 |
|
angiogenesis inhibitors - chemistry - pharmacology |
4 |
|
animal experiment |
4 |
|
anti-hiv agents - chemistry - pharmacology |
4 |
|
anticancer agents |
4 |
|
anticancer compounds |
4 |
|
antigens, viral - immunology |
4 |
|
antimetastasis |
4 |
|
antineoplastic agents - chemical synthesis - chemistry - pharmacology |
4 |
|
antineoplastic agents - chemistry - therapeutic use - toxicity |
4 |
|
antineoplastic agents - chemistry - toxicity |
4 |
|
antineoplastic agents - therapeutic use |
4 |
|
antineoplastic agents, phytogenic - pharmacology |
4 |
|
antineoplastic combined chemotherapy protocols - therapeutic use |
4 |
|
apoptosis - drug effects - physiology |
4 |
|
apoptosis regulatory proteins - genetics |
4 |
|
asparagine synthetase |
4 |
|
azo compounds - chemistry |
4 |
|
bacterial metal resistance |
4 |
|
biofilm |
4 |
|
bioinformatics |
4 |
|
biological targets |
4 |
|
biomarkers |
4 |
|
biosensing techniques - methods |
4 |
|
blue electroluminescence |
4 |
|
bond theory |
4 |
|
boronic esters |
4 |
|
breast carcinogenesis |
4 |
|
c-c bonds |
4 |
|
c-h activation |
4 |
|
c-h insertion |
4 |
|
capping actin protein gelsolin-like |
4 |
|
carbene-metal-amide (cma) |
4 |
|
carbene–metal–amide |
4 |
|
carcinoma - drug therapy |
4 |
|
carcinoma - drug therapy - mortality |
4 |
|
carcinoma, non-small-cell lung - genetics - metabolism - pathology |
4 |
|
caries |
4 |
|
caries arrest |
4 |
|
cariogenic |
4 |
|
catalase - metabolism |
4 |
|
catalyse |
4 |
|
catalyst activity |
4 |
|
catenanes |
4 |
|
cd137 |
4 |
|
cd8+ t cells |
4 |
|
cd8-positive t-lymphocytes - immunology |
4 |
|
cell cycle - drug effects |
4 |
|
cell cycle arrest |
4 |
|
cell differentiation |
4 |
|
cell fractionation |
4 |
|
cell migration |
4 |
|
cell movement - drug effects |
4 |
|
chalcogenolates |
4 |
|
charge-carrier mobility |
4 |
|
chemical proteomics |
4 |
|
chemical stability |
4 |
|
chemistry |
4 |
|
chemotherapeutics |
4 |
|
chlorinated solvent |
4 |
|
cisplatin - therapeutic use |
4 |
|
colon cancer |
4 |
|
colonic neoplasms - drug therapy |
4 |
|
color purity |
4 |
|
columnar structures |
4 |
|
complexes |
4 |
|
contact ion pairs |
4 |
|
controlled study |
4 |
|
coordination complexes - chemistry - therapeutic use - toxicity |
4 |
|
copper complexes |
4 |
|
copper(i) emitter |
4 |
|
cross coupling reactions |
4 |
|
cross-coupling reactions |
4 |
|
crystalline samples |
4 |
|
cyclic amines |
4 |
|
cyclosporine - pharmacology |
4 |
|
cysteine thiol conjugation |
4 |
|
cytochromes c - metabolism |
4 |
|
cytotoxicity, immunologic |
4 |
|
c−n bond formation |
4 |
|
dentine |
4 |
|
device fabrication |
4 |
|
dft calculation |
4 |
|
dielectric |
4 |
|
diosgenin - analogs & derivatives - pharmacology |
4 |
|
dna binding |
4 |
|
dna fragmentation - drug effects |
4 |
|
dna recognition |
4 |
|
dna, neoplasm - drug effects - metabolism |
4 |
|
efflux pump |
4 |
|
electroluminescence measurements |
4 |
|
emission quantum yield |
4 |
|
endocytosis |
4 |
|
endoplasmic reticulum - metabolism |
4 |
|
energy up-conversion |
4 |
|
enzyme inhibitors - chemical synthesis |
4 |
|
enzyme-linked immunosorbent assay |
4 |
|
escherichia coli |
4 |
|
exciplex emission |
4 |
|
excitation light |
4 |
|
field-effect |
4 |
|
flow cytometry |
4 |
|
fluoride |
4 |
|
g-quadruplex dna |
4 |
|
g-quadruplexes |
4 |
|
g-quadruplexes - drug effects |
4 |
|
gene expression profiling - methods |
4 |
|
girdin |
4 |
|
gold (iii) |
4 |
|
gold - administration & dosage |
4 |
|
gold - pharmacology |
4 |
|
gold porphyrins |
4 |
|
gold(i) |
4 |
|
gold(i) emitters |
4 |
|
heat-shock proteins - genetics - metabolism |
4 |
|
herpesvirus 4, human - immunology |
4 |
|
heterocyclic compounds - chemistry |
4 |
|
hfo2 dielectrics |
4 |
|
high k |
4 |
|
high quality |
4 |
|
highly efficient oleds |
4 |
|
hiv reverse transcriptase - antagonists & inhibitors |
4 |
|
hiv-1 - physiology |
4 |
|
hsp60 |
4 |
|
hybrid |
4 |
|
hydroarylation |
4 |
|
immune checkpoint inhibitors |
4 |
|
immune-related adverse effects |
4 |
|
in situ nick-end labeling |
4 |
|
inflammation |
4 |
|
inhibitors |
4 |
|
intercellular communication |
4 |
|
invasion |
4 |
|
iron compounds |
4 |
|
isoxazoles - chemical synthesis |
4 |
|
laser spectroscopy |
4 |
|
ligand reactivity |
4 |
|
luminescence conversion |
4 |
|
luminescent probes |
4 |
|
lung neoplasms - genetics - metabolism - pathology |
4 |
|
lymphocyte activation - immunology |
4 |
|
macrocycles |
4 |
|
macrocyclic compounds - chemistry |
4 |
|
macrophages |
4 |
|
magnetic resonance spectroscopy |
4 |
|
manganese |
4 |
|
melanoma, experimental - drug therapy - mortality |
4 |
|
membrane proteins - genetics |
4 |
|
metabolism |
4 |
|
metal ions |
4 |
|
metallodrugs |
4 |
|
metalloporphyrins - adverse effects - pharmacology - therapeutic use |
4 |
|
metalloporphyrins - pharmacology - therapeutic use |
4 |
|
metal–metal closed-shell interaction |
4 |
|
metastasis |
4 |
|
mitochondria - drug effects - metabolism - physiology |
4 |
|
mitochondria - metabolism |
4 |
|
molecular chaperones - genetics - metabolism |
4 |
|
molecular electronics |
4 |
|
monochromic emission |
4 |
|
nanowires |
4 |
|
nasopharyngeal carcinoma (npc) |
4 |
|
nasopharyngeal neoplasms - blood supply - drug therapy - enzymology - pathology |
4 |
|
nasopharyngeal neoplasms - drug therapy |
4 |
|
natural products |
4 |
|
neoplasm |
4 |
|
neoplasm transplantation |
4 |
|
neovascularization, pathologic - prevention and control |
4 |
|
neuroblastoma |
4 |
|
nf-kappa b - immunology - metabolism |
4 |
|
nitrene transfer |
4 |
|
nitrogen ligands |
4 |
|
non-linear optical properties |
4 |
|
nucleobases |
4 |
|
ofet (organic field-effect transistor) |
4 |
|
onogenes |
4 |
|
operational lifetime |
4 |
|
organic |
4 |
|
organic light-emitting device |
4 |
|
organic light-emitting devices(oleds) |
4 |
|
organic light-emitting diode (oled) |
4 |
|
organic solar cells |
4 |
|
organic thin-film transistor (otft) |
4 |
|
organic thin-film transistors |
4 |
|
organogold compounds - chemical synthesis - pharmacology |
4 |
|
organometallic compounds - chemistry - pharmacology |
4 |
|
organoplatinum compounds - chemistry - metabolism - pharmacology |
4 |
|
otft |
4 |
|
oxalates - chemistry - pharmacology |
4 |
|
oxidative stress - drug effects |
4 |
|
palladium(ii) |
4 |
|
patient-derived xenografts |
4 |
|
pauli repulsion |
4 |
|
pentacene |
4 |
|
pentacene thin-film transistors |
4 |
|
peptides - chemistry |
4 |
|
phosphorescent materials |
4 |
|
phosphorescent platinum(ii) materials |
4 |
|
pi interactions |
4 |
|
pitstop 2 |
4 |
|
platinum compounds - chemistry - pharmacology |
4 |
|
platinum(ii) porphyrin |
4 |
|
platinum(ii) schiff base complex |
4 |
|
platinum(ii) α-diimine arylacetylide complexes |
4 |
|
polarization dependence |
4 |
|
polymer |
4 |
|
polymer light-emitting devices |
4 |
|
polymers |
4 |
|
porphyrins - administration & dosage |
4 |
|
porphyrins - chemical synthesis - chemistry |
4 |
|
porphyrins - chemistry - pharmacology |
4 |
|
powder diffraction |
4 |
|
premetastatic niche |
4 |
|
protein 14-3-3 |
4 |
|
protein kinase b |
4 |
|
proteomics - methods |
4 |
|
proto-oncogene proteins c-myc - chemistry - genetics - metabolism |
4 |
|
pyrazoles - chemistry |
4 |
|
reactive intermediates |
4 |
|
red |
4 |
|
rna, messenger - biosynthesis - genetics |
4 |
|
rna, small interfering - genetics |
4 |
|
rocking curves |
4 |
|
ruthenium - chemistry - pharmacology |
4 |
|
ruv-imido complex |
4 |
|
saponin |
4 |
|
saponins - pharmacology |
4 |
|
schiff bases - chemistry - metabolism - pharmacology |
4 |
|
sensors |
4 |
|
silver - analysis |
4 |
|
silver diamine fluoride |
4 |
|
solubility |
4 |
|
solvents - chemistry |
4 |
|
spatial |
4 |
|
structure-activity relationship |
4 |
|
substrate specificity |
4 |
|
sulfuric acids - chemistry |
4 |
|
superoxide dismutase - metabolism |
4 |
|
t-lymphocytes - virology |
4 |
|
t-lymphocytes, cytotoxic - immunology |
4 |
|
tetradentate o^n^c^n ligand |
4 |
|
thermal proteome profiling |
4 |
|
thermally-activated delayed fluorescence (tadf) |
4 |
|
thioredoxin reductase (trxr) |
4 |
|
tissue-specific immune microenvironment |
4 |
|
topoisomerase i |
4 |
|
toxicity |
4 |
|
transcription factor chop - genetics - metabolism |
4 |
|
transcription factors |
4 |
|
transition-metal-free reaction |
4 |
|
treatment outcome |
4 |
|
tridentate ligands |
4 |
|
tridentate pt(ii) complexes |
4 |
|
trifluoromethyl |
4 |
|
triplet emitter |
4 |
|
triplet emitters |
4 |
|
trisubstituted alkenes |
4 |
|
tuberculosis reactivation |
4 |
|
tumor necrosis factor-alpha - immunology - metabolism |
4 |
|
tumor suppressor protein p53 - genetics - metabolism |
4 |
|
two-photon absorption |
4 |
|
vascular permeability |
4 |
|
vimentin |
4 |
|
viral matrix proteins - chemistry - immunology |
4 |
|
virus replication - drug effects |
4 |
|
volatilization |
4 |
|
white |
4 |
|
x-ray diffraction |
4 |
|
xenograft model antitumor assays |
4 |
|
yellow |
4 |
|
2d magnet |
3 |
|
2d semiconductor |
3 |
|
3d printing |
3 |
|
[60]fullerene |
3 |
|
a. inorganic compounds |
3 |
|
a. nanostructures |
3 |
|
acacia |
3 |
|
acidic vapor |
3 |
|
aerobic oxidation |
3 |
|
agnps. nanostructures |
3 |
|
akt |
3 |
|
albumins - chemistry |
3 |
|
alkadienes - chemistry |
3 |
|
alkenes - chemical synthesis - chemistry |
3 |
|
alkyne |
3 |
|
alkynes |
3 |
|
allenes |
3 |
|
alzheimer disease - metabolism - prevention & control |
3 |
|
amide |
3 |
|
amides - chemical synthesis |
3 |
|
amides - chemistry |
3 |
|
amines - chemical synthesis - chemistry |
3 |
|
amyloid beta-peptides - metabolism |
3 |
|
angiogenesis inhibitors - chemical synthesis - chemistry - pharmacology |
3 |
|
anthracene crystal |
3 |
|
anti-cancer agents |
3 |
|
anti-cancer mechanisms |
3 |
|
anticancer drug |
3 |
|
antimanic agents - pharmacology |
3 |
|
arabinogalactan-protein |
3 |
|
arenes |
3 |
|
arylamine |
3 |
|
asymmetric |
3 |
|
atom/group transfer |
3 |
|
attractive strategies |
3 |
|
azides |
3 |
|
azides - chemistry |
3 |
|
band edge |
3 |
|
beta-amyloid |
3 |
|
biaryls |
3 |
|
bio-inspired catalysts |
3 |
|
bioactive compounds |
3 |
|
biological activities |
3 |
|
biological products - chemistry - pharmacology |
3 |
|
biological reductions |
3 |
|
bipyridines |
3 |
|
bis(η 6-diphenylphosphinobenzene)chromium |
3 |
|
blotting, western - methods |
3 |
|
brain - drug effects - metabolism |
3 |
|
bridging ligands |
3 |
|
burkholderia cepacia |
3 |
|
c-n bond formations |
3 |
|
c. electron microscopy |
3 |
|
c. x-ray diffraction |
3 |
|
camptothecin |
3 |
|
carbene ligands |
3 |
|
carbenoid transfer reactions |
3 |
|
caspase 3 |
3 |
|
caspase 9 - metabolism |
3 |
|
caspases |
3 |
|
cdse/zns quantum dots |
3 |
|
chelating s-ligands |
3 |
|
chelating units |
3 |
|
chemical parameter |
3 |
|
chemical vapour deposition |
3 |
|
chemoselectivity |
3 |
|
chirality |
3 |
|
chirality transfer |
3 |
|
chlorine - chemistry |
3 |
|
chromophores |
3 |
|
cie coordinates |
3 |
|
cis-dihydroxylation |
3 |
|
cleavage reactions |
3 |
|
cluster compounds |
3 |
|
cobalt |
3 |
|
complex cation |
3 |
|
coordination chemistry |
3 |
|
coordination polymers |
3 |
|
crown compounds |
3 |
|
crystal structures |
3 |
|
crystallinity |
3 |
|
crystallization |
3 |
|
cyanides - chemical synthesis - chemistry |
3 |
|
cyclic voltammetry |
3 |
|
cysteine |
3 |
|
cysteine - chemistry |
3 |
|
decomposition temperature |
3 |
|
delayed fluorescence |
3 |
|
delocalized excited state |
3 |
|
density functional theory calculations |
3 |
|
deprotonated oxygen atom |
3 |
|
dft calculations |
3 |
|
dihydroxylation |
3 |
|
dna - chemistry |
3 |
|
dna structures |
3 |
|
dna-binding proteins - antagonists and inhibitors - metabolism |
3 |
|
doping |
3 |
|
doping concentration |
3 |
|
down-regulation - drug effects |
3 |
|
drug compounding |
3 |
|
drug formulation |
3 |
|
drugs, chinese herbal - pharmacology |
3 |
|
efficiency |
3 |
|
electric conductivity |
3 |
|
electron transfer |
3 |
|
electron transport properties |
3 |
|
electron-donor |
3 |
|
electron-donors |
3 |
|
electrons |
3 |
|
electrophoretic mobility shift assay |
3 |
|
electrostatic interactions |
3 |
|
emission lifetime |
3 |
|
energy regions |
3 |
|
epoxidation |
3 |
|
epoxy compounds - chemistry |
3 |
|
ethylenes - chemical synthesis - chemistry |
3 |
|
exciton dynamics |
3 |
|
external heavy-atom effect |
3 |
|
external quantum efficiency |
3 |
|
extracellular signal-regulated map kinases - metabolism |
3 |
|
femtosecond time-resolved fluorescence |
3 |
|
field-effect transistors |
3 |
|
flavonoid |
3 |
|
fluorescent dyes - chemistry |
3 |
|
fluorination |
3 |
|
fluorine plasma |
3 |
|
formulation |
3 |
|
free excitons |
3 |
|
functionalized |
3 |
|
fused-ring systems |
3 |
|
gel-peg-cys |
3 |
|
gold - chemistry - radiation effects - therapeutic use |
3 |
|
gold-corrole |
3 |
|
gquadruplexes |
3 |
|
green photoluminescence |
3 |
|
haloacid |
3 |
|
halophosphate |
3 |
|
hepes buffer |
3 |
|
heterocycles |
3 |
|
heterocyclic compounds, 3-ring - chemistry - pharmacology |
3 |
|
heterocyclic ring system |
3 |
|
heterogeneous catalysis |
3 |
|
hflao |
3 |
|
hflaon |
3 |
|
hfo 2 |
3 |
|
high κ |
3 |
|
high-valent compounds |
3 |
|
high-κ |
3 |
|
high-κ dielectric |
3 |
|
high-κ gate dielectric |
3 |
|
hiv |
3 |
|
hjtio |
3 |
|
hydrogen |
3 |
|
hydrogen - chemistry |
3 |
|
hydrogen peroxide - chemistry |
3 |
|
hydrogen-ion concentration |
3 |
|
ii-vi semiconductors |
3 |
|
imines - chemical synthesis |
3 |
|
imines - chemistry |
3 |
|
in situ interpenetrating network system (ipn) |
3 |
|
indoles |
3 |
|
indoles - chemistry |
3 |
|
insertion reactions |
3 |
|
intercalating agents - chemistry - toxicity |
3 |
|
interferometric autocorrelation |
3 |
|
interpenetrating network system |
3 |
|
iridium complex |
3 |
|
iron catalysis |
3 |
|
iron complexes |
3 |
|
isocyanides |
3 |
|
isomerism |
3 |
|
karstedt’s catalyst |
3 |
|
ketones - chemical synthesis - chemistry |
3 |
|
la incorporation |
3 |
|
light absorption |
3 |
|
light hole exciton |
3 |
|
light-emitting diodes |
3 |
|
lipid nanoparticles |
3 |
|
lipidic formulation |
3 |
|
lithium chloride - pharmacology |
3 |
|
living supramolecular polymerization |
3 |
|
low dimensional ferromagnetism |
3 |
|
low supply voltages |
3 |
|
low-frequency noise |
3 |
|
low-frequency noise (lfn) |
3 |
|
luminance |
3 |
|
luminescence lifetime |
3 |
|
lycium - chemistry |
3 |
|
lycium barbarum |
3 |
|
macrocyclic compounds - chemical synthesis - chemistry |
3 |
|
macromolecular substances - chemical synthesis - chemistry |
3 |
|
magnesium |
3 |
|
magnetic circular dichroism microscopy |
3 |
|
map kinase signaling system - drug effects |
3 |
|
mapk |
3 |
|
mass spectrometry |
3 |
|
mechanistic studies |
3 |
|
medicine, east asian traditional |
3 |
|
melanoma - drug therapy |
3 |
|
melanoma, experimental - drug therapy |
3 |
|
mercury - analysis |
3 |
|
metal medicines |
3 |
|
metal-carbon multiple bonds |
3 |
|
metalation |
3 |
|
metalloporphyrins |
3 |
|
metalloporphyrins - chemical synthesis - chemistry - pharmacology |
3 |
|
metals - chemistry |
3 |
|
metronidazole |
3 |
|
microarray |
3 |
|
microscopy, electron, transmission |
3 |
|
mmlct |
3 |
|
molecular heterostructure |
3 |
|
molecular probe techniques |
3 |
|
molybdenum |
3 |
|
monochloroacetate |
3 |
|
multi-block supramolecular copolymer |
3 |
|
multiphoton absorption (mpa) |
3 |
|
myoglobin - metabolism |
3 |
|
n-ligands |
3 |
|
nanocomposites |
3 |
|
nanoscale phase separation |
3 |
|
nanotubes |
3 |
|
nanowires - chemistry |
3 |
|
neoplasms - drug therapy - physiopathology |
3 |
|
neuroblastoma - drug therapy - enzymology - pathology |
3 |
|
neurons - drug effects - metabolism |
3 |
|
neuroprotection |
3 |
|
neuroprotective agents - pharmacology |
3 |
|
nitrene |
3 |
|
nitrene transfer reactions |
3 |
|
nitrene/imide |
3 |
|
nitric oxide |
3 |
|
nitric oxide - metabolism |
3 |
|
nitrosothiols |
3 |
|
nonradiative decay |
3 |
|
o ligands |
3 |
|
off-resonance |
3 |
|
oligonucleotides - chemistry |
3 |
|
oncogenes |
3 |
|
optical harmonic generation |
3 |
|
organic chemicals - chemistry |
3 |
|
organic chemistry |
3 |
|
organic light emitting diodes (oled) |
3 |
|
organic light-emitting diode |
3 |
|
organic phosphorescence |
3 |
|
organic semiconductors |
3 |
|
organic solar cell |
3 |
|
organic thin film transistors |
3 |
|
organic thin-film transistor |
3 |
|
organic transistor |
3 |
|
organoplatinum compounds - chemical synthesis - chemistry - pharmacology |
3 |
|
osmium complexes |
3 |
|
oxidations |
3 |
|
oxo ligands |
3 |
|
oxygen |
3 |
|
oxygen - chemistry |
3 |
|
oxygen vacancy |
3 |
|
p ligands porphyrinoids |
3 |
|
p38 mitogen-activated protein kinases - metabolism |
3 |
|
passivation |
3 |
|
pentacenes / plasma treatment |
3 |
|
peptides |
3 |
|
periodontitis |
3 |
|
persisters |
3 |
|
phenol - chemistry |
3 |
|
phosphane |
3 |
|
phosphines - chemical synthesis - chemistry |
3 |
|
phosphoproteins - metabolism |
3 |
|
phosphorylation |
3 |
|
phosphotyrosine - metabolism |
3 |
|
photo-conversion |
3 |
|
photo-cytotoxicity |
3 |
|
photochemotherapy - trends |
3 |
|
photocleavage |
3 |
|
photoconversion |
3 |
|
photons |
3 |
|
photosensitizing agents - therapeutic use |
3 |
|
phototoxicity |
3 |
|
pincer ptii complex |
3 |
|
plant extracts - chemistry |
3 |
|
plasma treatment |
3 |
|
platinum - chemistry - radiation effects - therapeutic use |
3 |
|
platinum and palladium |
3 |
|
polymer solar cell |
3 |
|
porcine coronary artery |
3 |
|
porphyromonas gingivalis |
3 |
|
proteins - chemistry |
3 |
|
proto-oncogene proteins c-akt - antagonists and inhibitors - metabolism |
3 |
|
proto-oncogene proteins c-myc - chemistry - drug effects |
3 |
|
proto-oncogene proteins c-myc - genetics |
3 |
|
protons |
3 |
|
pyridines - chemical synthesis - chemistry |
3 |
|
pyridines - chemistry - pharmacology |
3 |
|
radical reactions |
3 |
|
raman spectra |
3 |
|
rats, sprague-dawley |
3 |
|
redox chemistry |
3 |
|
relaxation activity |
3 |
|
reverse transcriptase |
3 |
|
rods (structures) |
3 |
|
room temperature |
3 |
|
ruthenium complexes |
3 |
|
ruthonium |
3 |
|
s ligands |
3 |
|
second-harmonic generation (shg) |
3 |
|
selfassembly |
3 |
|
semiconductor |
3 |
|
silicon dioxide - chemistry |
3 |
|
singlet oxygen - chemistry |
3 |
|
solar cells |
3 |
|
spectrometry, fluorescence |
3 |
|
spectrophotometry - instrumentation |
3 |
|
spectrophotometry, infrared - methods |
3 |
|
spectroscopy |
3 |
|
spectrum analysis, raman |
3 |
|
stacking interactions |
3 |
|
steroids - pharmacology |
3 |
|
substrate binding |
3 |
|
sulfhydryl compounds - chemistry |
3 |
|
supermolecular chemistry |
3 |
|
supported catalysts |
3 |
|
supramolecular polymer |
3 |
|
supramolecular polymerization |
3 |
|
supramolecular polymers |
3 |
|
talao |
3 |
|
tandem mass spectrometry |
3 |
|
target identification |
3 |
|
thermodynamics |
3 |
|
thin-film transistors |
3 |
|
thiol probes |
3 |
|
thiolates |
3 |
|
three-photon absorption |
3 |
|
topoisomerase ii inhibitors - chemistry - toxicity |
3 |
|
transient absorption |
3 |
|
transition-metal (tm) oxides |
3 |
|
triplet exciton |
3 |
|
two-dimensional gel electrophoresis |
3 |
|
tyrosine phosphorylation |
3 |
|
ubiquitinated proteins - metabolism |
3 |
|
ultrasonic irradiation |
3 |
|
vanadium diselenide |
3 |
|
viologen |
3 |
|
water chemistry |
3 |
|
wearable biomedical device |
3 |
|
xenograft |
3 |
|
zinc oxide (zno) |
3 |
|
zrlao |
3 |
|
催化 |
3 |
|
1,2,4-triazolidines |
2 |
|
1,3-dipolar cycloaddition |
2 |
|
1,3-dipolar cycloadditions |
2 |
|
1,4,7-trimethyl-1,4,7-triazacyclononane (me 3tacn) |
2 |
|
8-aminoquinoline |
2 |
|
ab initio powder structure determination |
2 |
|
acetylene - chemistry |
2 |
|
aggregation |
2 |
|
alcohol derivative |
2 |
|
algorithms |
2 |
|
alkaloids - chemical synthesis - chemistry |
2 |
|
alkanes |
2 |
|
alkene |
2 |
|
alkenylation |
2 |
|
alkyl azides |
2 |
|
alkyl carbenes |
2 |
|
alkyl diazomethanes |
2 |
|
alkylation |
2 |
|
allylic alcohol derivative |
2 |
|
allylic carbamate |
2 |
|
allylic compounds |
2 |
|
alzheimer's disease |
2 |
|
amidetriazoles |
2 |
|
ammonia - chemistry |
2 |
|
ammonia annealing |
2 |
|
angiogenesis |
2 |
|
angiogenesis inhibitors - pharmacology - toxicity |
2 |
|
aniline |
2 |
|
anions |
2 |
|
anti-bacterial agents - chemistry - pharmacology |
2 |
|
anti-cancer |
2 |
|
anti-counterfeiting |
2 |
|
anticancer treatment |
2 |
|
antimicrobial materials |
2 |
|
antineoplastic agents - chemistry - pharmacology - therapeutic use |
2 |
|
arene cyclopropanation |
2 |
|
artemisinins - chemical synthesis - chemistry - pharmacology |
2 |
|
aryl halides |
2 |
|
arylation |
2 |
|
asymmetric oxidation |
2 |
|
axial coordination |
2 |
|
benzene derivatives - chemistry |
2 |
|
beta amyloid |
2 |
|
binaphthyl schiff-base ligands |
2 |
|
bioinorganic medicine (無機藥物) |
2 |
|
biological applications |
2 |
|
biomolecular target |
2 |
|
bis(diphenylphorothioyl)amide |
2 |
|
bis-n-heterocyclic carbene |
2 |
|
bisintercalation |
2 |
|
bismuth - chemistry |
2 |
|
buchner reaction |
2 |
|
bulk single crystals |
2 |
|
calixarenes - chemistry - pharmacology |
2 |
|
cancer cell lines |
2 |
|
carbamates - chemistry |
2 |
|
carbazoles - chemistry |
2 |
|
carbene |
2 |
|
carbene complexes |
2 |
|
carbene c–h insertion |
2 |
|
carbenoid |
2 |
|
carbonyl ylide formation |
2 |
|
carboxylic acids - chemistry |
2 |
|
cascade reaction |
2 |
|
caspase-3 |
2 |
|
catalyst |
2 |
|
catenin signaling |
2 |
|
cations - chemistry |
2 |
|
cattle |
2 |
|
cell survival - drug effects |
2 |
|
cellular immunity |
2 |
|
chain structures |
2 |
|
chemical reaction |
2 |
|
chemical structure |
2 |
|
chemistry, physical |
2 |
|
chiral metal complexes |
2 |
|
chiral n-heterocyclic carbenes |
2 |
|
cinnamyl alcohol |
2 |
|
circuits |
2 |
|
circularly polarized luminescence |
2 |
|
cisplatin - pharmacology |
2 |
|
click chemistry |
2 |
|
closed shell |
2 |
|
cobalt catalysis |
2 |
|
color tunable |
2 |
|
coloring agents - chemistry |
2 |
|
combined method |
2 |
|
comparative studies |
2 |
|
complex 1 |
2 |
|
complex compounds. |
2 |
|
computer simulation |
2 |
|
computers |
2 |
|
conducting polymers |
2 |
|
coordination complexes - pharmacology - therapeutic use |
2 |
|
coordination polymer |
2 |
|
copper - chemistry |
2 |
|
copper 4 hydroxythiophenolate |
2 |
|
copper complex |
2 |
|
covid-19 |
2 |
|
cross-conjugation |
2 |
|
cross-linking reagents - chemistry |
2 |
|
cuprophilicity |
2 |
|
cyanides |
2 |
|
cyclometalated gold(iii) compound |
2 |
|
cyclopropanation |
2 |
|
cyclopropanes - chemistry |
2 |
|
cytochrome p-450 enzyme system |
2 |
|
c–h functionalization |
2 |
|
c−c bond formation |
2 |
|
c−h amination |
2 |
|
c−n bond activation |
2 |
|
dehalogenation |
2 |
|
dendrimers |
2 |
|
deubiquitinase |
2 |
|
dft |
2 |
|
diacetylide |
2 |
|
diazo quinone |
2 |
|
diimine |
2 |
|
diseases (疾病) |
2 |
|
dna - drug effects - metabolism |
2 |
|
dna - metabolism |
2 |
|
dna micro-array |
2 |
|
dna topoisomerases, type i - drug effects - metabolism |
2 |
|
dose-response relationship, drug |
2 |
|
drug discovery |
2 |
|
drug stability |
2 |
|
durapatite - chemistry |
2 |
|
dysprosium(iii) |
2 |
|
electro-crystallization |
2 |
|
electrophoresis, polyacrylamide gel |
2 |
|
endoplasmic reticulum stress - drug effects |
2 |
|
enzyme inhibitors - pharmacology - therapeutic use |
2 |
|
enzymes |
2 |
|
epoxy compounds - chemical synthesis - chemistry |
2 |
|
escherichia coli - drug effects |
2 |
|
esters - chemistry |
2 |
|
ethers - chemistry |
2 |
|
evaporation |
2 |
|
exciplex |
2 |
|
excitation sources |
2 |
|
excitation-dependent photoluminescence |
2 |
|
excited state lifetimes |
2 |
|
excited-state decay |
2 |
|
excited-state dynamics |
2 |
|
fast synthesis |
2 |
|
femtoseconds |
2 |
|
fluorescent sensor |
2 |
|
folded structures |
2 |
|
forensic sciences - methods |
2 |
|
glutathione - metabolism |
2 |
|
gold compound |
2 |
|
gold compounds - pharmacology - therapeutic use |
2 |
|
gold nanoparticle |
2 |
|
gold(iii) complexes |
2 |
|
gold/platinum/silver |
2 |
|
green iridium(iii) complex |
2 |
|
heavy metal removal |
2 |
|
hepes - chemistry |
2 |
|
heterocyclic compounds, 2-ring - chemical synthesis |
2 |
|
high-valency |
2 |
|
homogenous catalysis |
2 |
|
host-guest systems |
2 |
|
human carcinoma |
2 |
|
human dna topoisomerase ib |
2 |
|
hydrazones |
2 |
|
hydrocarbons |
2 |
|
hydrocarbons - chemistry |
2 |
|
hydrophobic and hydrophilic interactions |
2 |
|
hydrophobic effect |
2 |
|
hydrothermal synthesis |
2 |
|
hydroxylamines |
2 |
|
hypervalent iodine |
2 |
|
imides |
2 |
|
imines |
2 |
|
iminoiodinanes |
2 |
|
inclusion compounds |
2 |
|
indicators and reagents |
2 |
|
indolocarbazoles |
2 |
|
inhibition |
2 |
|
inorganic chemistry |
2 |
|
intercalation |
2 |
|
intermolecular amino oxyarylation |
2 |
|
intramolecular cyclization |
2 |
|
inverted |
2 |
|
ir(iii) complexes |
2 |
|
iridium - chemistry |
2 |
|
iridium compounds |
2 |
|
iron compounds - chemistry |
2 |
|
isocyanide |
2 |
|
jahn-teller distortion |
2 |
|
lactams |
2 |
|
lactones - chemical synthesis - chemistry - pharmacology |
2 |
|
lasers |
2 |
|
layered compounds |
2 |
|
lewis acids |
2 |
|
ligand–receptor pairs |
2 |
|
lipophilicity |
2 |
|
liquid crystals |
2 |
|
long-lived excited state |
2 |
|
luminesence |
2 |
|
machine learning |
2 |
|
macromolecular substances - chemistry |
2 |
|
mesophases |
2 |
|
mesylates - chemistry |
2 |
|
metal carbenes |
2 |
|
metal nanoparticles - chemistry - ultrastructure |
2 |
|
metal-amide complexes |
2 |
|
metal-carbene complexes |
2 |
|
metal-catalyzed cyclopropanations |
2 |
|
metal-imide complexes |
2 |
|
metal-imido intermediates |
2 |
|
metal-organic frameworks |
2 |
|
metallamacrocycles |
2 |
|
metallocarbenoids |
2 |
|
metallomacrocycle |
2 |
|
metallomacrocycles |
2 |
|
metallophilicity |
2 |
|
metallophthalocyanines |
2 |
|
metalloporphyrins - chemistry - pharmacology |
2 |
|
metalmetal interactions |
2 |
|
metals (金屬) |
2 |
|
metals, heavy - chemical synthesis - chemistry |
2 |
|
methyleneamides |
2 |
|
microspheres |
2 |
|
microwave chemistry |
2 |
|
midkine |
2 |
|
mobility |
2 |
|
monocarborane |
2 |
|
multiblock |
2 |
|
n,o ligands |
2 |
|
nanoparticles and nanostructures |
2 |
|
nanostructures - chemistry |
2 |
|
nanotetrapods |
2 |
|
nanowire |
2 |
|
near-infrared lasers |
2 |
|
nitrene insertion |
2 |
|
nitrogen - chemistry |
2 |
|
nitrogen heterocycles |
2 |
|
nitrosoarenes |
2 |
|
nonheme iron complexes |
2 |
|
nucleic acid conformation |
2 |
|
nucleic acid conformation - drug effects |
2 |
|
oligo(phenylene-ethynylene) |
2 |
|
one-dimensional |
2 |
|
optical band gaps |
2 |
|
organic azides |
2 |
|
organic compounds -- synthesis. |
2 |
|
organic conductor |
2 |
|
organoborane |
2 |
|
organogold compounds - pharmacology - toxicity |
2 |
|
organometallic compounds - chemistry - pharmacology - therapeutic use |
2 |
|
organoplatinum compounds - chemical synthesis - pharmacology |
2 |
|
organoplatinum compounds - chemistry - pharmacology |
2 |
|
osmium compounds - chemistry - pharmacology |
2 |
|
osmium. |
2 |
|
oxido ligands |
2 |
|
oxoiron complexes |
2 |
|
oxycarbamates |
2 |
|
oxygenations |
2 |
|
p, n, s, se, o, te, si-containing ligands |
2 |
|
pargyline - analogs and derivatives - chemical synthesis - chemistry |
2 |
|
phase transitions |
2 |
|
phenyleneethynylene |
2 |
|
phosphanes |
2 |
|
phosphorescent emitters |
2 |
|
photo-redox catalysis |
2 |
|
photophysical properties |
2 |
|
photosensitizing agents - chemistry - pharmacology |
2 |
|
physicochemical phenomena |
2 |
|
physics chemistry - physical chemistry |
2 |
|
platinum compounds - pharmacology - therapeutic use |
2 |
|
platinum-group metals |
2 |
|
polarizing-light optical microscopies |
2 |
|
polycyclic aromatic hydrocarbon derivative |
2 |
|
polymers - chemistry |
2 |
|
polynuclear complexes |
2 |
|
polyoxometalates |
2 |
|
polystyrenes - chemistry |
2 |
|
powder x-ray diffraction |
2 |
|
propylamines - chemical synthesis - chemistry |
2 |
|
proteasome |
2 |
|
protein-labeling |
2 |
|
protonation |
2 |
|
pyridines - chemical synthesis |
2 |
|
pyridines - chemical synthesis - pharmacology |
2 |
|
pyridines - chemistry |
2 |
|
quaternary ammonium compounds - chemical synthesis |
2 |
|
quinoid carbene |
2 |
|
quinoid carbenes |
2 |
|
quinones |
2 |
|
raman spectroscopy |
2 |
|
reaction mechanism |
2 |
|
reaction mechanisms |
2 |
|
receptors |
2 |
|
receptors, ccr5 |
2 |
|
recombinant proteins - antagonists & inhibitors - metabolism |
2 |
|
restriction mapping |
2 |
|
reverse transcriptase polymerase chain reaction |
2 |
|
rhenium |
2 |
|
rhodium - chemistry |
2 |
|
rhodium porphyrin |
2 |
|
rhodium(ii,ii) dimers |
2 |
|
ring opening |
2 |
|
rotaxanes - chemistry |
2 |
|
ruthenium and osmium porphyrins |
2 |
|
ruthenium catalyst |
2 |
|
ruthenium compounds |
2 |
|
ruthenium compounds - pharmacology - therapeutic use |
2 |
|
ruthenium porphyrin |
2 |
|
ruthenium porphyrins |
2 |
|
ruthenium(ii) porphyrins |
2 |
|
ruthenium-oxo and -imido complexes |
2 |
|
ruthenium. |
2 |
|
schiff base ligands |
2 |
|
self-assembly formation |
2 |
|
sensitizers |
2 |
|
silver derivative |
2 |
|
solid-phase synthesis |
2 |
|
soluble polymers |
2 |
|
solvatochromism |
2 |
|
solvent |
2 |
|
solvothermal synthesis |
2 |
|
spectrophotometry |
2 |
|
spectroscopy, fourier transform infrared |
2 |
|
stereoselectivity |
2 |
|
structure |
2 |
|
structure property relationships |
2 |
|
structure-properties relationship |
2 |
|
sublimation yield |
2 |
|
sulfamidates |
2 |
|
sulfides - chemistry |
2 |
|
sulfonic acids - chemistry |
2 |
|
sulfonium compounds - chemical synthesis |
2 |
|
sulfur |
2 |
|
sulfurated frameworks |
2 |
|
surfactant |
2 |
|
temperature |
2 |
|
tert-butyl hydroperoxide |
2 |
|
tetranuclear cu(i) cluster |
2 |
|
tetrathiometalates |
2 |
|
tetrazolium salts |
2 |
|
thermal-annealing free |
2 |
|
thiazoles |
2 |
|
thioether donors |
2 |
|
three-component |
2 |
|
tmtsf |
2 |
|
topoisomerase i inhibitors - chemistry - pharmacology |
2 |
|
transistors, electronic |
2 |
|
tumor cells, cultured |
2 |
|
tumor necrosis factor |
2 |
|
unclassified drug |
2 |
|
vanadium compounds - chemistry - pharmacology |
2 |
|
vapoluminescence |
2 |
|
variable temperature |
2 |
|
vegfrs |
2 |
|
vicinal diamine |
2 |
|
virtual screening |
2 |
|
viscosity |
2 |
|
zigzag chain |
2 |
|
zno nanoparticle |
2 |
|
π-conjugation |
2 |
|
光化学 |
2 |
|
原子或基团转移反应 |
2 |
|
反应机理 |
2 |
|
金属-配体多重键 |
2 |
|
(±)-epi-conocarpan |
1 |
|
1,3-diketones |
1 |
|
2,3-naphtho-10-aza-15-crown-5 |
1 |
|
2,6-dichloropyridine n-oxide |
1 |
|
2-hydroxy-1-naphthoates |
1 |
|
[6,6] phenyl c61 butyric acid methyl ester |
1 |
|
ab initio (从头算) |
1 |
|
ab initio calculations |
1 |
|
acetates - chemistry |
1 |
|
adsorption |
1 |
|
alcohols |
1 |
|
alcohols - chemistry |
1 |
|
aliphatic amine |
1 |
|
alkaloids |
1 |
|
alkene epoxidation |
1 |
|
alkylimido |
1 |
|
allenylidene |
1 |
|
amines - chemical synthesis |
1 |
|
aminoalkynes |
1 |
|
ammonia borane |
1 |
|
aniline compounds - chemistry |
1 |
|
anthracene |
1 |
|
anti-cancer activity |
1 |
|
anti-hiv agents - chemistry |
1 |
|
anti-tumor agents |
1 |
|
anticancer activities |
1 |
|
antiproliferative activities |
1 |
|
asymmetric bromination |
1 |
|
asymmetric chlorination |
1 |
|
asymmetric epoxidation |
1 |
|
aurophilic interaction |
1 |
|
axial ligand |
1 |
|
azamacrocycle complexes |
1 |
|
azurin |
1 |
|
bacterial proteins |
1 |
|
benzyl alcohol |
1 |
|
benzyl chloride |
1 |
|
binuclear complexes |
1 |
|
bioimaging |
1 |
|
bis(diphenylphorothioyl) amide |
1 |
|
black phosphorus |
1 |
|
bpsalan ligand |
1 |
|
butyric acid derivative |
1 |
|
b−h activation |
1 |
|
c - c coupling |
1 |
|
cadmium |
1 |
|
caffeine |
1 |
|
carbamates |
1 |
|
carbene transfer |
1 |
|
carbene transfer reactions |
1 |
|
carbon |
1 |
|
carbonyl ligands |
1 |
|
carboranes |
1 |
|
carbyne complexes |
1 |
|
cascade |
1 |
|
catalytic oxidation |
1 |
|
catalytic property |
1 |
|
cavitands |
1 |
|
cellular uptake |
1 |
|
characterizeation |
1 |
|
chemical formulae |
1 |
|
chemical reactioninter |
1 |
|
chiral |
1 |
|
chiral amine complexes |
1 |
|
chiral diaminodiphosphine |
1 |
|
chiral diiminodiphosphine |
1 |
|
chlorination |
1 |
|
chlorine |
1 |
|
cholesterol - chemistry |
1 |
|
cis-2,3-dihydrobenzofuran |
1 |
|
cocatalyzed |
1 |
|
condensation |
1 |
|
conformation (构象) |
1 |
|
conjugate |
1 |
|
controlled synthesis |
1 |
|
coordination complexes |
1 |
|
copper catalyst |
1 |
|
copper(i) |
1 |
|
copper(i) clusters |
1 |
|
copper(i) iodide |
1 |
|
coupling reaction |
1 |
|
cr-ooxo bond |
1 |
|
critical temperatures |
1 |
|
cross-coupling |
1 |
|
crystal engineering |
1 |
|
crystal structure |
1 |
|
crystal structure determination |
1 |
|
cu(oh)2 |
1 |
|
cubanes |
1 |
|
cuprophilic interactions |
1 |
|
cyano-bridged |
1 |
|
cyclic alkene |
1 |
|
cyclic and rate capability |
1 |
|
cyclic compounds |
1 |
|
cyclic β-keto ester |
1 |
|
cyclometallation |
1 |
|
cytochrome c |
1 |
|
cytochrome c group |
1 |
|
c–h bond functionalization |
1 |
|
dearomative |
1 |
|
dehydrogenation |
1 |
|
diamond-like |
1 |
|
diastereoselectivity |
1 |
|
diazoacetic acid ethyl ester |
1 |
|
diazonium compounds - chemistry |
1 |
|
dinuclear subunit |
1 |
|
dioscin |
1 |
|
dioxygen |
1 |
|
disinfectants - chemistry - pharmacology |
1 |
|
double salts |
1 |
|
drug mechanism |
1 |
|
election transfer |
1 |
|
electrical equipment |
1 |
|
electrochemisiry |
1 |
|
electron density |
1 |
|
electron transport |
1 |
|
electrooxidation |
1 |
|
enantioseparation |
1 |
|
encapsulation |
1 |
|
epoxy compounds - chemical synthesis |
1 |
|
epoxy compounds - chemistry - pharmacology |
1 |
|
europium |
1 |
|
exciplexes |
1 |
|
excited states |
1 |
|
fe(oh)3 |
1 |
|
ferricyanides |
1 |
|
fluorescence resonance energy transfer |
1 |
|
fluorescent |
1 |
|
fret |
1 |
|
förster resonance energy transfer |
1 |
|
gold catalysis |
1 |
|
gold complex |
1 |
|
gold(i) complex (au(i)配合物) |
1 |
|
gold(i)-catalyzed |
1 |
|
gold(iii) catalyst |
1 |
|
gold(iii)-catalyst |
1 |
|
group 6 metals |
1 |
|
halogenation |
1 |
|
hela cell |
1 |
|
hematite |
1 |
|
hepes |
1 |
|
hl-60 cells |
1 |
|
homocysteine |
1 |
|
horses |
1 |
|
host-guest complex (主客體配合物) |
1 |
|
host–guest chemistry |
1 |
|
hydroalkylation |
1 |
|
hydrochloric acid |
1 |
|
hydrogen peroxide - chemistry - pharmacology |
1 |
|
hydrogenation |
1 |
|
imido complexes |
1 |
|
imido/nitrene |
1 |
|
imido/nitrene transfer |
1 |
|
interaction (相互作用) |
1 |
|
intermolecular hydroarylation |
1 |
|
intermolecular n-michael addition |
1 |
|
intramolecular c-h insertion |
1 |
|
intramolecular hydroalkylation |
1 |
|
iodobenzene diacetate |
1 |
|
iron hexacyanide |
1 |
|
isocyanide complexes |
1 |
|
isoxazoles |
1 |
|
ketone |
1 |
|
l-b film |
1 |
|
lactams - chemical synthesis |
1 |
|
lattice stability |
1 |
|
li-ion batteries |
1 |
|
ligand |
1 |
|
ln-fe |
1 |
|
luminescent property |
1 |
|
luminescent ratiometric thermometry |
1 |
|
macrocyclic amine ligands |
1 |
|
magnetic properties |
1 |
|
magnetism |
1 |
|
manganese - chemistry |
1 |
|
manganese complex |
1 |
|
manganese complexes |
1 |
|
mcm- 41 介孔分子筛 |
1 |
|
mercury |
1 |
|
mesoporous materials |
1 |
|
mesoporous molecular sieve mcm-41 |
1 |
|
metal hexacyamide complex |
1 |
|
metal-ligand charge transfer |
1 |
|
metal-organic framework |
1 |
|
metalloporphyrin-catalyzed reactions |
1 |
|
metal–organic framework |
1 |
|
micelles |
1 |
|
mixed ligands |
1 |
|
modification |
1 |
|
molecular amino oxyarylation |
1 |
|
n -boc oxindole |
1 |
|
n-heterocyclic carbene (nhc) |
1 |
|
n-oxide |
1 |
|
nanocomposite |
1 |
|
naphthalene |
1 |
|
new materials |
1 |
|
nobin schiff base |
1 |
|
oligosaccharides - chemistry |
1 |
|
one-pot asymmetric aziridination |
1 |
|
organic anode |
1 |
|
organic synthesis |
1 |
|
organometallic compounds |
1 |
|
oxidants - chemistry |
1 |
|
oxidative carbonylation |
1 |
|
oxo complexes |
1 |
|
p-doped cds |
1 |
|
pd/fe3o4 |
1 |
|
phase junction |
1 |
|
phosphorescent probes |
1 |
|
photochemical studies |
1 |
|
photoexcitation |
1 |
|
photoinduced intramolecular electron transfer |
1 |
|
photoluminescence (光致發光) |
1 |
|
photon |
1 |
|
physics chemistry |
1 |
|
platinum(ii) carbene complexes |
1 |
|
platinum(ii) oligomer |
1 |
|
polymeric complexes |
1 |
|
postsynthetic modification |
1 |
|
potassium terephthalate |
1 |
|
prolinol derivatives |
1 |
|
propargylamines |
1 |
|
propargylic amines |
1 |
|
protein profiling |
1 |
|
proteomic quantitative pathway analysis |
1 |
|
pyrrolidine |
1 |
|
pyrrolo[1,2-a]quinolines |
1 |
|
pyruvates - chemistry |
1 |
|
quenchers |
1 |
|
quenching |
1 |
|
reactive intermediate |
1 |
|
reactive oxygen species |
1 |
|
recyclable |
1 |
|
redox |
1 |
|
rhenium complex |
1 |
|
rhenium complexes |
1 |
|
ruthenium - pharmacology |
1 |
|
ruthenium compounds - chemistry |
1 |
|
ruthenium(ii) porphyrin |
1 |
|
sacrificial-agents-free catalysts |
1 |
|
schiff bases - chemistry |
1 |
|
sensor |
1 |
|
silica nanoparticles |
1 |
|
silver(i) |
1 |
|
silver(i)-catalyzed |
1 |
|
solution dynamic |
1 |
|
solvent effects |
1 |
|
spin coupling |
1 |
|
styrene |
1 |
|
sulfonamides |
1 |
|
supramolecule (超分子) |
1 |
|
suzuki reaction |
1 |
|
synergistic catalysis |
1 |
|
synthesis |
1 |
|
synthetic methods |
1 |
|
tandem reactions |
1 |
|
tertiary amine |
1 |
|
tertiary amines |
1 |
|
thermal stability |
1 |
|
thiols |
1 |
|
thione complexes |
1 |
|
three-component coupling reaction |
1 |
|
trans effect |
1 |
|
trans-stilbene |
1 |
|
transition-metal complex |
1 |
|
triplet excited state |
1 |
|
tripodal ligands |
1 |
|
unactivated alkenes |
1 |
|
urea |
1 |
|
water splitting |
1 |
|
white-light emitting |
1 |
|
x-ray structure |
1 |
|
z-scheme |
1 |
|
zeolite analogues |
1 |
|
zinc |
1 |
|
改性 |
1 |
|
氧化 |
1 |
|
烯烃 |
1 |
|
裹载 |
1 |
|
钌卟啉 |
1 |
