Abstract
The reaction of phenanthroline diamide bearing a bromoaryl moiety on the amide substituent in the presence of palladium catalyst proceeded efficiently to afford multiply-fused phenanthroline derivatives through intramolecular C–H arylation. The obtained diamide derivatives was found to extract lanthanide remarkably highly efficiently with distribution ratio (D: up to ca. 500) and it was also found show the metal-selective extraction (separation factor SF = up to 4.4).
Supplementary materials
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Supporting Information
Description
Experimental section, copies of NMR spectra, and references
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