Protective effect of the perchlorophenyl group in organophosphorus chemistry

Abstract

The homoleptic phosphine with the bulky perchlorophenyl group, (C₆Cl₅)₃P (1), exhibits trigonal pyramidal structure (TPY-3), yet considerably flattened: Σ(C–P–C') = 321.0(1)°. Key steric and electronic properties of this simple organophosphorus species have been estimated by calculation. Attending to its characteristic features, 1 can be rated as a deactivated phosphine, where the less-basic P atom is sterically shielded by the bulky C₆Cl₅ groups. This marked inertness notwithstanding, it has been possible to obtain (under harsh conditions) derivatives with phosphorus in high oxidation state, namely the phosphine oxide (C₆Cl₅)₃PO (2) and the difluorophosphorane (C₆Cl₅)₃PF₂ (3). These four- and five-substituted derivatives respectively exhibit trigonal pyramidal (TPY-4) and trigonal bipyramidal (TBPY-5) structures. The Σ(C–P–C') value steadily increases along the series 1–3, according to the referred structural variation. The P–C bond length is, in turn, invariably maintained at about 185 pm regardless of the different oxidation state, the increasing number of substituents around the P atom and the overall geometry. The hypervalent difluorophosphorane (C₆Cl₅)₃PF₂ (3) dissociates one of the axial fluorides in the gas phase giving rise to the fluorophosphonium cation [(C₆Cl₅)₃PF]⁺, as detected by mass spectrometry. This cation is identified as a Lewis superacid.