@article {571, title = {[Co(Co)(5)][(CF3)(3)BF]: A stable salt of a homoleptic trigonal-bipyramidal metal-carbonyl cation}, journal = {Angewandte Chemie-International Edition}, volume = {42}, number = {18}, year = {2003}, note = {ISI Document Delivery No.: 681QPTimes Cited: 11Cited Reference Count: 34}, pages = {2077-2079}, type = {Article}, keywords = {ACIDS, ANIONS, borates, carbonyl ligands, CO, cobalt complexes, MOLECULAR-STRUCTURE, RH, structure elucidation, superacids, UNDECAFLUORODIANTIMONATE(V), VIBRATIONAL-SPECTRA, X-RAY-DIFFRACTION}, isbn = {1433-7851}, url = {://000183047100021}, author = {Bernhardt, E. and Finze, M. and Willner, H. and Lehmann, C. W. and Aubke, F.} } @article {425, title = {A F-19 nuclear magnetic resonance study of the conjugate Bronsted-Lewis superacid HSO3F-SbF5. Part II}, journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie}, volume = {80}, number = {9}, year = {2002}, note = {ISI Document Delivery No.: 607YFTimes Cited: 4Cited Reference Count: 31}, month = {Sep}, pages = {1265-1277}, type = {Article}, abstract = {Solutions of SbF5 in HSO3F with x(SbF5) = 0.012 to 0.405 are studied by 500 MHz H-1 NMR (299 K) and 471 MHz F-19 NMR (213-250 K), using NMR tubes fitted with fluoropolymer lining. The initial process during dissolution is the fast solvolysis of monomeric SbF5 in HSO3F according to SbF5 + nHSO(3)F left arrow SbF5 - n(SO3F)(n) + nHF (n = 1, 2). All HF formed during solvolysis will no longer be removed by reaction with glass, but will remain in the superacid system. Besides participation in the fast formation of various fluoro-fluorosulfato anions [SbF6 - n(SO3F)(n)](-) (n = 0, 1, 2) and acidium ions [H2X](+)((solv.)) (X= F, SO3F), HF is involved in slow-exchange reactions of the type [SbF6 - n(SO3F)(n)](-)((solv.)) + HF left arrow [SbF7 - n(SO3F)(n- 1)](-)((solv.)) + HSO3F (n = 1, 2) detected because of a delay of 3 months between sample preparation and measurements and confirmed by repeating theses measurements after a further 3 months. There are three notable differences to our earlier study, affecting concentrations of the fluoro-fluorosulfato antimonate anions observed: (i) in dilute solutions [SbF6](-) is formed in high concentrations (34.7-76.1\%), with [Sb2F11](-) now clearly detected at intermediate to high SbF5 concentrations (up to 5.8\%); (ii) bis-fluorosulfato anions (cis-, trans-[SbF4(SO3F)(2)](-)) are found in much lower concentrations only, which decrease further with time, while tris-fluorosulfato anions ([SbF3(SO3F)(3)](-)) are now no longer observed; (iii) these reduced concentrations of poly-fluorosulfato anions in dilute solutions are responsible for the formation of fewer mu-SO3F-oligomers at lower concentrations, when more SbF5 is added. As a consequence, the HSO3F-SbF5 magic acid system is now less complex than found previously and only seven anionic species are clearly observed.}, keywords = {ANTIMONY PENTAFLUORIDE, antimony(V) fluoroanions, F-19 NMR, H-1 NMR, HF-SBF5, MEDIA, RELATIVE ACIDITY, SBF5, solvolysis, superacids, SYSTEMS}, isbn = {0008-4042}, url = {://000178817800011}, author = {Kuhn-Velten, J. and Bodenbinder, M. and Brochler, R. and Hagele, G. and Aubke, F.} }