https://www.selleckchem.com/products/Dasatinib.html Superacids have been the source of much spectacular chemistry but very little interesting physics despite the fact that the states of cations formed by transfer of the superacid proton to molecular bases can approach that of the cations in free space. Indeed, some of the very strongest acids, such as HPF6 and HAlCl4, have no independent existence due to lack of screening of the bare proton self-energy their acidities can only be assessed by study of the conjugate bases. Here we show that, by allowing the protons of transient HAlCl4 and HAlBr4 to relocate on pentafluoropyridine, PFP (a very weak base that is stable to superacids), we can create glass forming protic ionic liquids (PILs) that are themselves superacids but, being free of superacid vapors, are of benign character. At Tg, conductivities exceed "good" ionic liquid values by 9 decades, so must be superprotonic. Anomalous Walden plots confirm superprotonicity.An unprecedented copper-catalyzed multicomponent radical-based reaction involving alkenes, P(O)H compounds, sulfur powder, and Togni reagent II at room temperature has been developed. A variety of highly functionalized CF3-containing S-alkyl phosphorothioates can be directly prepared from a wide range of activated and unactivated alkenes. Moreover, this protocol highlights its potential in the late-stage functionalization of complex molecules and opens up a new avenue for the construction of C(sp3)-S-P bonds.The reaction of the vanadium(III) tris(silylamide) VN(SiMe3)23 with LiAlH4 in diethyl ether gives the highly unstable mixed-metal polyhydride [V(μ2-H)6[AlN(SiMe3)22]3][Li(OEt2)3] (1), which was structurally characterized. Alternatively, performing the same reaction in the presence of 12-crown-4 affords a rare example of a structurally verified vanadium terminal hydride complex, [VHN(SiMe3)23][Li(12-crown-4)2] (2). The corresponding deuteride 2D was also prepared using LiAlD4. In contrast, no hydrid