Utilizing the Perfluoronaphthalene Radical Cation as a Selective Deelectronator to Access a Variety of Strongly Oxidizing Reactive Cations.

Abstract

A selective deelectronation reagent with very high potential of +2.00 (solution) / +2.41 V (solid-state) vs. Fc+/0 and based on a room temperature stable perfluoronaphthalene (naphthaleneF) radical cation salt was developed and applied. The solid-state deelectronation of commercial naph-tha-leneF with [NO]+[F{Al(ORF)3}2]- generates [naphthaleneF]+∙[F{Al(ORF)3}2]- (ORF = OC(CF3)3) in gram scale. Thermo-chemical analysis unravels the solid-state de-electronation potential of the starting [NO]+-reagent to be +2.34 V vs. Fc+/0 with [F{Al(ORF)3}2]- counterion, but only +1.14 V vs. Fc+/0 with the small [SbF6]- ion. Selective reactions demonstrate the selectivity of [naphthaleneF]+∙ for deelectronation of a multitude of organ(ometall)ic molecules and elements in solution: providing the molecular struc-tures of the acene dications [tetracene]2+, [pentacene]2+ or spectroscopic evi-dence for the carbo-nyl complex of the ferrocene dication [Fc(CO)]2+, the [P9]+ cation from white phosphor-us, the solvent-free copper(I) salt starting from copper metal and the dicationic Fe(IV)-scorpionate complex [Fe(sc)2]2+.