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Fischer carbene complexes (6)
Single-crystal X-ray study (6)
Mean (C–C) = 0.003 A° (4)
T = 293 K (4)
Carbenes (Methylene compounds) (3)
Crystals (3)
Chromium compounds (2)
Crystallography (2)
Group 6 transition metals (2)
Mean (C–C) = 0.002 A (2)
Multicarbene complexes (2)
R factor = 0.040 (2)
Spectroscopy (2)
T = 180 K (2)
(Spectro)electrochemistry (1)
1,2,3-triazol-5-ylidenes (1)
2,3′-Bithiophene (1)
3,3′-Bithiophene (1)
Absorption (1)
Al-free SFC (1)
Amines (1)
Anions (1)
Annulated thiophene (1)
Anticancer agents (1)
Aurophilic interactions (1)
Bisphosphonate (1)
C4-position (1)
Cancer (1)
Carbene (1)
Carbene complex (1)
Carbene substituents (1)
Carbenes (Methylene compounds) -- Synthesis (1)
Chemical oxidation (1)
Coinage metals (1)
Complexes stabilized (1)
Crystal structure (1)
Crystallization (1)
Cytotoxicity (1)
Data-to-parameter ratio = 11.0 (1)
Data-to-parameter ratio = 14.9. (1)
Data-to-parameter ratio = 15.0. (1)
Data-to-parameter ratio = 15.1 (1)
Data-to-parameter ratio = 17.9 (1)
Data-to-parameter ratio = 39.3 (1)
Density functional theory (DFT) (1)
Dihydrodesulphurization (1)
Electrochemical analysis (1)
Emissions (1)
Ferrocenyl (1)
Ferrocenyl-substituted 1,2,3-triazol-5-ylidene complexes (1)
Ferrochrome (1)
Fischer (1)
Fischer carbene ligands (1)
Fischer-type carbene complexes (1)
Fischer-type gold(I) (1)
Geigeria aspera (1)
Geigerin (1)
Gold(I) (1)
Group VI transition metals (1)
Heterobi- and -trimetallic complexes (1)
Heterobimetallic gold(I) (1)
Influence of chemical oxidation (1)
Isogeigerin acetate (1)
Isolation of a potassium (1)
Ivalin (1)
Ligand field theory (1)
Ligand transfer reactions (1)
Ligands (Biochemistry) (1)
Manganese (1)
Mesoionic carbene (MIC) (1)
Metal carbonyls -- Reactivity (1)
Modeling (1)
Molecular recognition (1)
Molecules (1)
Mono- and biscarbene complexes (1)
Monocarbene complexes (1)
Multimetal complexes (1)
Multimetal Fischer carbene complexes (1)
NMR spectroscopic analysis method (1)
Nucleophilic attack (1)
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