INIS
triplets
100%
molecules
67%
excited states
66%
fluorescence
65%
water
63%
energy
52%
relaxation
52%
solvents
47%
populations
41%
environment
35%
deactivation
35%
resonance
33%
free energy
31%
ground states
31%
dna
29%
luminescence
27%
spin
25%
photochemistry
24%
comparative evaluations
24%
yields
22%
barriers
21%
guanine
19%
potential energy
19%
internal conversion
18%
absorption spectra
18%
dynamics
18%
rna
18%
glycine
18%
levels
17%
liquids
16%
pyrimidines
15%
electrostatics
15%
aqueous solutions
15%
hydrogen
14%
hybrids
14%
energy gap
14%
quantum mechanics
14%
shells
14%
surfaces
14%
l-s coupling
14%
design
13%
alanines
13%
lifetime
13%
nuclear magnetic resonance
12%
mechanics
12%
nucleosides
12%
values
11%
density functional method
11%
coupling constants
11%
nmr
11%
Chemistry
Excited State
49%
Relaxation
47%
Nucleobase
38%
Triplet State
37%
Intersystem Crossing [Singlet->triplet]
31%
Ground State
31%
Deoxyribonucleic Acid
29%
Delayed Fluorescence
28%
Gibbs Free Energy
25%
Internal Conversion
24%
NMR Spectroscopy
23%
Density Functional Theory
21%
Guanine
18%
RNA
18%
Band Gap
15%
Aqueous Solution
15%
Spin-Orbit Coupling
14%
Alanine
13%
CCSD
13%
Hydrogen Bonding
13%
k·p perturbation theory
13%
Photophysics
11%
Photochemistry
11%
Photochemical Reaction
11%
Isothiazole
11%
Spin-Spin Coupling Constant
11%
Solvation
10%
Thymine
10%
Potential Energy Surface
10%
Energy Barrier
10%
Molecular Mechanic
10%
Organic Molecule
10%
Luminiscence Type
9%
L-Alanine
9%
Selenium
9%
2,6-Diaminopurine
9%
Uracil
9%
Cytidine
9%
Tautomer
9%
Potential Energy Hypersurface
9%
Chirality
9%
Organic Radical
9%
Liquid Water
9%
Electron Transport
9%
Electron Transfer
9%
Photoluminescence
9%
Borylation
9%
Rearrangement Reaction
9%
Dielectric Constant
9%
Excited Triplet State
9%
Keyphrases
Water Environment
13%
Free Energy Gradient
10%
Energy Gradient
10%
S2 State
9%
Exciton Relaxation
9%
DNA Duplex
9%
7-Deazaguanine
9%
Photo-initiated
9%
Free Energy Landscape
9%
CH3Br
9%
SN2 Reaction
9%
Pyrimidine Analogues
9%
2,6-diaminopurine
9%
Resonant-type
9%
State Recovery
9%
Organic Radicals
9%
Optical Interface
9%
Chirality
9%
Water Solvent
9%
Stabilization Mechanism
9%
Zwitterionization
9%
Fluorescent nucleosides
9%
Energy Splitting
9%
Prompt Fluorescence
9%
C-H Arylation
9%
Blue-green Emission
9%
Bimolecular
9%
Photolesions
9%
SOS1
9%
8-azapurines
9%
6-Thioguanine (6-TG)
6%
Bright States
6%
Nse5
6%
EOM-CCSD
6%
Biradical
6%
