|
ruthenium |
12 |
|
gold |
11 |
|
supramolecular chemistry |
10 |
|
homogeneous catalysis |
9 |
|
structure elucidation |
8 |
|
alkenes - chemistry |
7 |
|
asymmetric catalysis |
7 |
|
molecular structure |
7 |
|
iron |
6 |
|
models, molecular |
6 |
|
molecular wheels |
6 |
|
porphyrinoids |
6 |
|
porphyrins |
6 |
|
ruthenium - chemistry |
6 |
|
aurophilicity |
5 |
|
catalysis |
5 |
|
cyclopropanation reaction |
5 |
|
density functional calculations |
5 |
|
enantioselectivity |
5 |
|
gold - chemistry |
5 |
|
macrocyclic compounds - chemical synthesis |
5 |
|
metal-alkynyl complexes |
5 |
|
metallacycles |
5 |
|
metalloporphyrins - chemistry |
5 |
|
metal–metal interactions |
5 |
|
möbius strip |
5 |
|
n ligands |
5 |
|
olefins |
5 |
|
osmium |
5 |
|
phosphines - chemistry |
5 |
|
quinoneimido complexes |
5 |
|
stereoisomerism |
5 |
|
trefoil knots |
5 |
|
acylnitrene transfer |
4 |
|
amination |
4 |
|
aza compounds - chemistry |
4 |
|
carbenes |
4 |
|
carbenoids |
4 |
|
catalyst activity |
4 |
|
chalcogenolates |
4 |
|
chemical stability |
4 |
|
crystallography, x-ray |
4 |
|
c−h activation |
4 |
|
c−n bond formation |
4 |
|
diazo compounds |
4 |
|
electronic structure |
4 |
|
glycosylation |
4 |
|
hydroxylation |
4 |
|
iron compounds |
4 |
|
macrocyclic compounds - chemistry |
4 |
|
macrocyclic ligands |
4 |
|
metal ions |
4 |
|
methane - analogs & derivatives - chemistry |
4 |
|
molecular conformation |
4 |
|
nitrogen ligands |
4 |
|
porphyrins - chemical synthesis - chemistry |
4 |
|
reactive intermediates |
4 |
|
ruv-imido complex |
4 |
|
self-assembly |
4 |
|
spectrometry, mass, electrospray ionization - methods |
4 |
|
sulfuric acids - chemistry |
4 |
|
trifluoromethyl |
4 |
|
trisubstituted alkenes |
4 |
|
water - chemistry |
4 |
|
[60]fullerene |
3 |
|
aldehydes - chemistry |
3 |
|
alkenes |
3 |
|
amidation |
3 |
|
arylamine |
3 |
|
asymmetric |
3 |
|
aziridination |
3 |
|
bio-inspired catalysts |
3 |
|
bis(η 6-diphenylphosphinobenzene)chromium |
3 |
|
c-h activation |
3 |
|
c-h bond |
3 |
|
carbene ligands |
3 |
|
carbenoid transfer reactions |
3 |
|
carbon - chemistry |
3 |
|
catenanes |
3 |
|
chelating s-ligands |
3 |
|
chlorine - chemistry |
3 |
|
cis-dihydroxylation |
3 |
|
crystal structures |
3 |
|
crystallization |
3 |
|
dft calculations |
3 |
|
electrochemistry |
3 |
|
epoxy compounds - chemistry |
3 |
|
ethylenes - chemical synthesis - chemistry |
3 |
|
hydrogen - chemistry |
3 |
|
iron catalysis |
3 |
|
isomerism |
3 |
|
ketones - chemical synthesis - chemistry |
3 |
|
ligands |
3 |
|
magnetic resonance spectroscopy |
3 |
|
manganese |
3 |
|
mass spectrometry |
3 |
|
metal-carbon multiple bonds |
3 |
|
metallophilic interactions |
3 |
|
metalloporphyrins |
3 |
|
metals - chemistry |
3 |
|
models, chemical |
3 |
|
molybdenum |
3 |
|
n-ligands |
3 |
|
natural products |
3 |
|
nitrene transfer |
3 |
|
nitrene/imide |
3 |
|
nitrides |
3 |
|
o ligands |
3 |
|
osmium - chemistry |
3 |
|
osmium complexes |
3 |
|
oxidation |
3 |
|
oxidation-reduction |
3 |
|
oxygen - chemistry |
3 |
|
p ligands porphyrinoids |
3 |
|
palladium |
3 |
|
peptides - chemistry |
3 |
|
phenol - chemistry |
3 |
|
phosphines - chemical synthesis - chemistry |
3 |
|
platinum |
3 |
|
porphyrin |
3 |
|
porphyrins - chemistry |
3 |
|
proteins - chemistry |
3 |
|
protons |
3 |
|
rhodium |
3 |
|
ruthenium complexes |
3 |
|
ruthonium |
3 |
|
spectrophotometry, infrared - methods |
3 |
|
spectrophotometry, ultraviolet |
3 |
|
thiolates |
3 |
|
1,4,7-trimethyl-1,4,7-triazacyclononane (me 3tacn) |
2 |
|
alkanes |
2 |
|
alkyne ligands |
2 |
|
amines |
2 |
|
amines - chemistry |
2 |
|
axial coordination |
2 |
|
binaphthyl schiff-base ligands |
2 |
|
catalyst |
2 |
|
chiral metal complexes |
2 |
|
chirality |
2 |
|
cis-β complexes |
2 |
|
cluster compounds |
2 |
|
coordination polymer |
2 |
|
copper |
2 |
|
copper complexes |
2 |
|
cyclization |
2 |
|
cyclopropanation |
2 |
|
c−n bond activation |
2 |
|
dendrimers |
2 |
|
epoxidation |
2 |
|
homogenous catalysis |
2 |
|
hydroxylamines |
2 |
|
imides |
2 |
|
imines |
2 |
|
imines - chemistry |
2 |
|
iridium |
2 |
|
kinetics |
2 |
|
luminescence |
2 |
|
metal-amide complexes |
2 |
|
metal-carbene |
2 |
|
metal-carbene complexes |
2 |
|
metal-catalyzed cyclopropanations |
2 |
|
metal-imide complexes |
2 |
|
metallamacrocycles |
2 |
|
metallophthalocyanines |
2 |
|
methyleneamides |
2 |
|
n-heterocyclic carbenes |
2 |
|
nitrene transfer reactions |
2 |
|
nitrosoarenes |
2 |
|
nonheme iron complexes |
2 |
|
oxidations |
2 |
|
oxoiron complexes |
2 |
|
photochemistry |
2 |
|
ru(ii)-salen |
2 |
|
ruthenium and osmium porphyrins |
2 |
|
ruthenium-oxo and -imido complexes |
2 |
|
schiff base ligands |
2 |
|
singlet oxygen - chemistry |
2 |
|
structure |
2 |
|
sulfamidates |
2 |
|
supported catalysts |
2 |
|
synthesis |
2 |
|
tetrathiometalates |
2 |
|
催化 |
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 |
|
allosteric effect |
1 |
|
amine (胺) |
1 |
|
amino acid ester (氨基酸酯) |
1 |
|
application |
1 |
|
bis(amine)iron(ii) porphyrin (鐵（ⅱ）卟啉二胺) |
1 |
|
electrochemisry |
1 |
|
equilibrium dialysis |
1 |
|
hypochromic effect (减色效应) |
1 |
|
iron porphyrin (鐵卟啉) |
1 |
|
iron(ii) |
1 |
|
lmct band (lmct谱带) |
1 |
|
manganese porphyrin |
1 |
|
manganese porphyrin (錳卟啉) |
1 |
|
manganese porphyrin thiolate |
1 |
|
mechanism of dipole-dipole (偶极-偶极机理) |
1 |
|
n-butylamine |
1 |
|
ni(i)-serum albumin (ni(ⅱ)-血清白蛋白) |
1 |
|
ni(ii)-serum albumin |
1 |
|
nmr |
1 |
|
reduction |
1 |
|
ruthenium porphyrin complexes |
1 |
|
structural characterization |
1 |
|
successive stability constants |
1 |
|
synthesis (合成) |
1 |
|
synthesis method |
1 |
|
systhesis characterization (合成;表征) |
1 |
|
uv-vis |
1 |
