Publication | Closed Access
Bis(phosphoryl)‐Bridged Biphenyls by Radical Phosphanylation: Synthesis and Photophysical and Electrochemical Properties
89
Citations
35
References
2011
Year
Diversity Oriented SynthesisEngineeringRadical PhosphanylationPhotochemistryπ-Conjugated CompoundsNatural SciencesDiversity-oriented SynthesisOrganometallic ElectrochemistrySynthetic PhotochemistryOrganic ChemistryElectrochemical PropertiesChemistryUnique Electron-accepting ScaffoldElectronic StructureSynthetic ChemistryBiomolecular Engineering
The efficient fourfold radical phosphanylation of 2,2,2′,2′-tetrabromobiphenyl with a bis(stannyl)phosphane followed by oxidation produces a highly strained biphenyl with two phosphoryl bridges (see picture). Extended π-conjugated compounds consisting of this core unit can be also synthesized by using the same approach. The two phosphoryl bridges significantly alter the electronic structure, making this biphenyl a unique electron-accepting scaffold.
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