First Experimental Evidence for the Elusive Tetrahedral Cations [EP3]+ in the Condensed Phase
Condensed phase access to the unprecedented tetrahedral cations [EP3]+ (E = S, Se, Te) was achieved through the reaction of ECl3[WCA] with white phosphorus ([WCA]− = [Al(ORF)4]− and [F(Al(ORF)3)2]−; -RF = -C(CF3)3). Previously, [EP3]+ was only known from gas phase MS investigations. By contrast, the reaction of ECl3[A] with the known P33− synthon Na[Nb(ODipp)3(P3)] (enabling AsP3 synthesis), led to formation of P4. The cations [EP3]+ were characterized by multinuclear NMR spectroscopy in combination with high-level quantum chemical calculations. Their bonding situation is described with several approaches including Atoms in Molecules and Natural Bond Orbital Analysis. The first series of well-soluble salts ECl3[WCA] was synthesized and fully characterized as starting materials for the studies on this elusive class of [EP3]+ cations. Yet, with high fluoride ion affinity values between 775 (S); 803 (Se) and 844 (Te) kJ mol–1, well exceeding typical phosphenium ions, these well-soluble [ECl3]WCA salts could be relevant in view of the renewed interest in strong (also cationic) Lewis acids.