Isolating fluorinated carbocations

Using carboranes as counterions, fluorinated benzyl-type carbocations such as (p-FC(6)H(4))(2)CF(+), (p-FC(6)H(4))(CH(3))CF(+) and fluorinated trityl ions are readily isolated for X-ray and IR structural characterization

Phosphazene cations.

Cations derived from (NPCl2)3, hexachloro-cyclo-triphosphazene, the weakly basic precursor of phosphazene polymers, have been prepared using strongly electrophilic reagents based on carborane anions. N-protonated, N-methylated, and N-silylated adducts of (NPCl2)3 have been isolated and characterized by X-ray crystallographic and spectroscopic methods. The normally potent chloride-abstracting silyl reagents of the type R3Si(carborane) are unable to abstract chloride from (NPCl2)3, even though the coordinatively unsaturated N2P2Cl5+ cation is widely accepted as a reactive intermediate in the ring-opening polymerization of (NPCl2)3

Hydrogen bonding versus hyperconjugation in condensed-phase carbocations.

Hyperconjugative stabilization of positive charge in tertiary carbocations is the textbook explanation for their stability and low frequency νCH bands in their IR spectra have long been taken as confirming evidence. While this is substantiated in the gas phase by the very close match of the IR spectrum of argon-tagged t-butyl cation with that calculated under C(s) symmetry, the situation in condensed phases is much less clear. The congruence of νCH(max) of t-Bu(+) in superacid media (2830 cm(-1)) with that in the gas phase (2834 cm(-1)) has recently been shown to be accidental. Rather, νCH(max) varies considerably as a function of counterion in a manner that reveals the presence of significant C-H···anion hydrogen bonding. This paper addresses the question of the relative importance of hyperconjugation versus H-bonding. We show by assigning IR spectra in the νCH region to specific C-H bonds in t-butyl cation that the low frequency νCH(max) band in the IR spectrum of t-butyl cation, long taken as direct evidence for hyperconjugation, appears to be due mostly to H-bonding. The appearance of similar low frequency νCH bands in the IR spectra of secondary alkyl carboranes such as i-Pr(CHB11Cl11), which have predominant sp(3) centres rather than sp(2) centres (and are therefore less supportive of hyperconjugation), also suggests the dominance of H-bonding over hyperconjugation

Superacidity of boron acids H2(B12X12) (X = Cl, Br).

Acid remarks: The anhydrous diprotic boron acids H(2)(B(12)X(12)) (X = Cl, Br; see picture, B orange, X green) are the first examples of diprotic superacids and may be the strongest acids yet isolated. Both protons protonate benzene to give benzenium ion salts that are stable at room temperature. These acids owe their existence to the stability of the icosahedral B(12) cluster with its dinegative charge buried beneath a layer of halide substituents

Superacidity of boron acids H2(B12X12) (X = Cl, Br).

Acid remarks: The anhydrous diprotic boron acids H(2)(B(12)X(12)) (X = Cl, Br; see picture, B orange, X green) are the first examples of diprotic superacids and may be the strongest acids yet isolated. Both protons protonate benzene to give benzenium ion salts that are stable at room temperature. These acids owe their existence to the stability of the icosahedral B(12) cluster with its dinegative charge buried beneath a layer of halide substituents

Phosphazene cations.

Cations derived from (NPCl2)3, hexachloro-cyclo-triphosphazene, the weakly basic precursor of phosphazene polymers, have been prepared using strongly electrophilic reagents based on carborane anions. N-protonated, N-methylated, and N-silylated adducts of (NPCl2)3 have been isolated and characterized by X-ray crystallographic and spectroscopic methods. The normally potent chloride-abstracting silyl reagents of the type R3Si(carborane) are unable to abstract chloride from (NPCl2)3, even though the coordinatively unsaturated N2P2Cl5+ cation is widely accepted as a reactive intermediate in the ring-opening polymerization of (NPCl2)3

Hydrogen bonding versus hyperconjugation in condensed-phase carbocations.

Hyperconjugative stabilization of positive charge in tertiary carbocations is the textbook explanation for their stability and low frequency νCH bands in their IR spectra have long been taken as confirming evidence. While this is substantiated in the gas phase by the very close match of the IR spectrum of argon-tagged t-butyl cation with that calculated under C(s) symmetry, the situation in condensed phases is much less clear. The congruence of νCH(max) of t-Bu(+) in superacid media (2830 cm(-1)) with that in the gas phase (2834 cm(-1)) has recently been shown to be accidental. Rather, νCH(max) varies considerably as a function of counterion in a manner that reveals the presence of significant C-H···anion hydrogen bonding. This paper addresses the question of the relative importance of hyperconjugation versus H-bonding. We show by assigning IR spectra in the νCH region to specific C-H bonds in t-butyl cation that the low frequency νCH(max) band in the IR spectrum of t-butyl cation, long taken as direct evidence for hyperconjugation, appears to be due mostly to H-bonding. The appearance of similar low frequency νCH bands in the IR spectra of secondary alkyl carboranes such as i-Pr(CHB11Cl11), which have predominant sp(3) centres rather than sp(2) centres (and are therefore less supportive of hyperconjugation), also suggests the dominance of H-bonding over hyperconjugation

Readily Available Onio-Substituted Methyleneiminium Salts: Single Precursors for a Variety of Aminocarbenes

5 páginas, 1 figura, 3 esquemas.From amides to carbenes: Phosphonio-substituted iminium salts are readily available from the corresponding amides in a one-pot reaction. Deprotonation followed by substitution reactions affords a variety of transient and stable amino carbenes.We are grateful to the ACS/PRF (38192-AC4) and RHODIA for financial support of this work, and to the Spanish Ministerio de Educacion, Cultura y Deporte for a postdoctoral fellowship (S C).Peer reviewe