Tris(perfluoroalkyl) compounds can be characterized using techniques such as NMR spectroscopy, IR spectroscopy, and mass spectrometry. The fluorine atoms in the perfluoroalkyl groups can result in characteristic shifts in NMR spectra.
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Articles of Spectroscopic Properties
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Flavonoids synthesis. I. Synthesis and spectroscopic properties of flavones with two hydroxy and five methoxy groups at C-2',3',4',5,6,6',7 and C-2',3,4',5,5',6,7
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4H-1-Benzopyran-4-one,
3-hydroxy-2-(4-hydroxy-2,5-dimethoxyphenyl)-5,6,7-trimethoxy-
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Syntheses, structures, spectroscopic properties, and thermal behavior of nickel(II) mixed-ligand complexes with N,N,N′,N′- tetramethylethylenediamine, benzoylacetonate, and a halide anion
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dibromo(N,N,N',N'-tetramethylethane-1,2-diamine)nickel(II)
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Related entries
Synthesis
Characterization
Reactivity
Structures
Syntheses
Solubility
Crystal structures
Deprotection
CO
applications
Novel
Purification
Stability
Toxicity
Preparation
Coupling Reaction
Start with a suitable starting material
Ligand Exchange
Protecting group strategy
Facile Synthesis
One common method is to react the perfluoroalkyl Grignard reagents (RFMgX) with a suitable arsenic or antimony compound. The reaction proceeds as follows
Cationic
Introduction of Methoxy Groups
Hetarenium Salts
Pentafluoropyridine
Dimethylamino
N,N'-disubstituted
Thioureas
Potential biological interest
Nickel(II)
Mixed-ligand complexes
N,N,N′,N′-tetramethylethylenediamine
Benzoylacetonate
Halide anion
Thermal behavior
Carbyne
Molybdenum and tungsten
Tripodal
Nitrogen, phosphorus, and sulfur donor ligands
Polyfunctionally substituted
MIII
Cl3 N
P3 + n
Rh
Tripodal tridentate phosphine
1,1,1-tris(dimethylphosphinomethyl)ethane
2,6and 2,7-naphthyridines
Arylene-ethynylenes