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Spectroelectrochemistry (2)
Synthesis (2)
T = 293 K (2)
1,2,3-Triazol-5-ylidene (TRZ) (1)
1,2,3-triazol-5-ylidenes (1)
2,3′-Bithiophene (1)
2,5-Diferrocenylthiophene (1)
3,3′-Bithiophene (1)
Absorption (1)
Alkyne hydrothiolation reactions (1)
Alkynes (1)
Annulated thiophene (1)
Annulated thiophenes (1)
Anticancer agents (1)
Aurophilic interactions (1)
Base-free rhodium(I) (1)
Biferrocene Fischer carbene complexes (1)
Bis(triazolium)carbazole (1)
C4-position (1)
Carbazolide Gold(III) (1)
Carbene (1)
Carbenes (Methylene compounds) -- Synthesis (1)
Carbon−amine−carbon (CHNC) (1)
Carbon−ether−carbon (COC) (1)
Catalyzes (1)
Chemical oxidation (1)
Chromium(0) (1)
Coinage metals (1)
Complexes stabilized (1)
Computational study (1)
Cytotoxic Bis(1,2,3-triazol-5-ylidene) (1)
Data-to-parameter ratio = 11.0 (1)
Data-to-parameter ratio = 15.1 (1)
Deoxyribonucleic acid (DNA) (1)
DFT calculations (1)
Dihydrodesulphurization (1)
Electrochemical (1)
Electrochemical analysis (1)
Emissions (1)
ESR spectroscopy (1)
Facile transmetalation (1)
Ferrocene (1)
Ferrocenyl aminocarbene (1)
Ferrocenyl-substituted 1,2,3-triazol-5-ylidene complexes (1)
Ferrochrome (1)
Fischer (1)
Fischer carbene complex (1)
Fischer carbene complex (FCC) (1)
Fischer carbenes (1)
Fischer-type gold(I) (1)
Gold(I) (1)
Group VI transition metals (1)
Heterobimetallic gold(I) (1)
Hydrogenation (1)
Hydrothiolation (1)
Influence of chemical oxidation (1)
Interactions (1)
Intramolecular electronic (1)
Iridium (1)
Iridium(I) (1)
Isolation of a potassium (1)
Ligand field theory (1)
Ligands (Biochemistry) (1)
Manganese (1)
Meridional coordination (1)
Metal (Au, Ag) (1)
Metal carbonyls -- Reactivity (1)
Metal precursors (1)
Metal-metal interaction (1)
Metalemetal interaction (1)
Mono- and biscarbene complexes (1)
Monocarbene complexes (1)
Multimetal complexes (1)
Multimetal Fischer carbene complexes (1)
N-donor functionalized (1)
NMR spectroscopic analysis method (1)
Nucleophilic attack (1)
Observation (1)
Organic light emitting device (OLED) (1)
Pincer complexes (1)