Prototypical Lewis acids, such as boranes, derive their reactivity from electronic unsaturation. Here, we report the Lewis acidity and catalytic application of electronically saturated phosphorus-centered electrophilic acceptors. Organofluorophosphonium salts of the formula [(C6F5)(3-x)Ph(x)PF][B(C6F5)4] (x = 0 or 1; Ph, phenyl) are shown to form adducts with neutral Lewis bases and to react rapidly with fluoroalkanes to produce difluorophosphoranes. In the presence of hydrosilane, the cation [(C6F5)3PF](+) is shown to catalyze the hydrodefluorination of fluoroalkanes, affording alkanes and fluorosilane. The mechanism demonstrates the impressive fluoride ion affinity of this highly electron-deficient phosphonium center.

A major advance in main-group chemistry in recent years has been the emergence of the reactivity of main-group species that mimics that of transition metal complexes. In this report, the Lewis acidic phosphonium salt [(C 6 F 5 ) 3 PF][B(C 6 F 5 ) 4 ] 1 is shown to catalyze the dehydrocoupling of silanes with amines, thiols, phenols, and carboxylic acids to form the Si-E bond (E = N, S, O) with the liberation of H 2 (21 examples). This catalysis, when performed in the presence of a series of olefins, yields the concurrent formation of the products of dehydrocoupling and transfer hydrogenation of the olefin (30 examples). This reactivity provides a strategy for metalfree catalysis of olefin hydrogenations. The mechanisms for both catalytic reactions are proposed and supported by experiment and density functional theory calculations. fluorophosphonium A wide range of commodity chemicals, petrochemicals, pharmaceuticals, materials, and foods depend on industrial-scale hydrogenation reactions. Catalysts for this process are based on both heterogeneous transition metals materials and homogeneous transition metal complexes. Indeed, it was the discovery of Sabatier (1) in the early 20th century that revealed the utility of amorphous Ni and other metals in hydrogenation processes. Following the dawn of organometallic chemistry in the 1960s, homogeneous catalysts were developed principally based on precious metals (2-4). Although subsequent modifications and optimizations have led to numerous highly selective and efficient catalyst technologies, concerns over cost, natural abundance, and toxicity have prompted efforts to uncover catalysts based on "earth-abundant" elements. The principal targets in these efforts have been the first-row transition metals. Indeed, the groups of Chirik (5, 6), Morris (7), Beller (8), and others (9) have developed remarkably active and selective catalysts based on Fe.Strategies to develop reduction methods using organic or main-group-based reagents have also been explored. For example, use of Hantzsch esters (10), Birch reduction of arenes (11), or the use of B or Al hydrides are effective, albeit stoichiometric reductions. More recently, the advent of "frustrated Lewis pairs" (FLPs) have led to the discovery that combinations of sterically encumbered donors and acceptors act as catalysts for the reductions of imines, enamines, silylenol ethers, olefins, and alkynes (12).To uncover hydrogenation strategies using earth-abundant elements, we have focused our efforts on Lewis acidic phosphorus species. Although Gudat (13), Burford and coworker (14), Yoshifuji (15), and Bertrand and coworker (16), among others, have reported phosphenium cations that demonstrate Lewis acidity, Radosevich and coworkers (17) have exploited the reaction of the unique planar P(III) species with ammoniaborane to give a P(V)H 2 derivative that effects the subsequent reduction of diazobenzene. Although the acidity of P(V) has been exploited previously in ylide reagents (18), Diels-Alder reactions catalysis (19), and add...

No abstract

Organofluorophosphonium salts of the formula [(C6F5)(3-x)Ph(x)PF][B(C6F5)4] (x = 0, 1) exhibit Lewis acidity derived from a low-lying σ* orbital at P opposite F. This acidity is evidenced by the reactions of these salts with olefins, which catalyze the rapid isomerization of 1-hexene to 2-hexene, the cationic polymerization of isobutylene, and the Friedel-Crafts-type dimerization of 1,1-diphenylethylene. In the presence of hydrosilanes, olefins and alkynes undergo efficient hydrosilylation catalysis to the alkylsilanes. Experimental and computational considerations of the mechanism are consistent with the sequential activation and 1,2-addition of hydrosilane across the unsaturated C-C bonds.

Reaction of a 2:1 mixture of B(C6F5)3 and tBu3P with syn-gas results in the stoichiometric reduction of CO to give a formyl derivative which reacts further via an epoxy-borate intermediate to capture CO, affording a heterocylic alkoxyborate. Heating the reaction prompts reaction with H2 to give a borane-oxy-borate derivative, the product of C-O bond cleavage.