95953-45-0Relevant academic research and scientific papers
Synthesis and structure of ionic liquids containing the [Al(OC 6H4CN)4]- anion
Lund, Henrik,Harloff, Joerg,Schulz, Axel,Villinger, Alexander
, p. 754 - 764 (2013/07/04)
The synthesis, structure, and physical properties of ionic liquids (IL) bearing the novel [Al(O-C6H4-CN)4]- ion as counterion to the commonly used [NR4]+, [PR 4]+ and imidazolium ions are reported. Both the influence of the alkyl chain length as well as the functionalization with cyano groups is studied. These ILs are easily obtained by reaction of Ag[Al(O-C 6H4-CN)4] with the corresponding ammonium, phosphonium, and imidazolium halides. The stability towards electrophilic cations was investigated. All prepared salts have a window for the liquid phase of ca. 200 °C and are thermally stable up to 450 °C. The solid-state structures reveal only weak cation-anion and anion-anion interactions in accord with the observed low melting points (glass transition points). Copyright
Flash-Photolysis Generation and Reactivities of Triarylmethyl and Diarylmethyl Cations in Aqueous Solutions
McClelland, Robert A.,Kanagasabapathy, V. M.,Banait, Narinder S.,Steenken, Steen
, p. 3966 - 3972 (2007/10/02)
A series of 18 triarylmethyl cations and 10 diarylmethyl cations have been generated by nanosecond laser flash photolysis of cyanide, 4-cyanophenyl ether, and acetate precursors in acetonitrile/water (AN/W) solutions and first-order rate constants for their reaction with the solvent (ks) have been directly measured following the decay in their optical density.In the standard solvent employed, 1:2 AN/W, the triarylmethyl cations which were studied had ks values at 20 deg C ranging from 1E1 s-1 (for the 4,4',4''-(MeO)3-substituted ion) to 9*1E6 s-1 (4,4'-(CF3)2), while diarylmethyl cations had ks values ranging from 1E5 s-1 (4,4'-(MeO)2) to 3*1E7 s-1 (4,4'-Me2).The parent diphenylmethyl cation and its derivative with one 4-methyl substituent were too short-lived (s of varying the amounts of acetonitrile were investigated for several cations.As water is added to 100percent acetonitrile, ks increases significantly, but at around 15percent by volume water, there is a leveling and from that point to 100percent water, ks is almost unchanged, decreasing by about 20percent.A plot of log ks versus ?+ constructed for the triarylmethyl cations shows significant deviations from linearity for the points for the ? donors, in the direction which indicates that ?+ is underestimating the stabilizing effect of these substituents for a fully formed cation.A plot versus ?C+, a parameter obtained from the analysis of NMR spectra of solutions of carbocations, is reasonably linear.A two-parameter correlation indicates that polar andresonance interactions of substituents do not proceed in parallel along the reaction coordinate, the addition of water to cation resulting at the transition state in the loss of 73percent of the equilibrium resonance effect but only a 33percent loss of the polar effect.A rate-equilibrium plot (log ks versus pKR) was constructed which covers 23 pKR units.A single line of slope 0.64 can be drawn to include the entire set of data for both triarylmethyl and diarylmethyl cations.From a small extrapolation the ks value for the tert-butyl cation in water is obtained as 1E10.5 s-1.
