Superácido (Portuguese Wikipedia)

Analysis of information sources in references of the Wikipedia article "Superácido" in Portuguese language version.

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doi.org

dx.doi.org

  • Himmel D, Goll SK, Leito I, Krossing I (2010). «A Unified pH Scale for All Phases». Angew. Chem. Int. Ed. 49 (38): 6885–6888. PMID 20715223. doi:10.1002/anie.201000252 
  • Himmel D, Goll SK, Leito I, Krossing I (2010). «A Unified pH Scale for All Phases». Angew. Chem. Int. Ed. 49 (38): 6885–6888. PMID 20715223. doi:10.1002/anie.201000252 
  • Gillespie, R. J.; Peel, T. E.; Robinson, E. A. (1 de outubro de 1971). «Hammett acidity function for some super acid systems. I. Systems H2SO4-SO3, H2SO4-HSO3F, H2SO4-HSO3Cl, and H2SO4-HB(HSO4)4». Journal of the American Chemical Society. 93 (20): 5083–5087. ISSN 0002-7863. doi:10.1021/ja00749a021. The work of Jorgenson and Hartter formed the basis for the present work, the object of which was to extend the range of acidity function measurements into the super acid region, i.e., into the region of acidities greater than that of 100% H2SO4. 
  • George A. Olah, Schlosberg RH (1968). «Chemistry in Super Acids. I. Hydrogen Exchange and Polycondensation of Methane and Alkanes in FSO3H–SbF5 ("Magic Acid") Solution. Protonation of Alkanes and the Intermediacy of CH5+ and Related Hydrocarbon Ions. The High Chemical Reactivity of "Paraffins" in Ionic Solution Reactions». Journal of the American Chemical Society. 90 (10): 2726–7. doi:10.1021/ja01012a066 
  • Olah, George A. (2005). «Crossing Conventional Boundaries in Half a Century of Research». Journal of Organic Chemistry. 70 (7): 2413–2429. PMID 15787527. doi:10.1021/jo040285o 
  • Herlem, Michel (1977). «Are reactions in superacid media due to protons or to powerful oxidising species such as SO3 or SbF5?». Pure and Applied Chemistry. 49: 107–113. doi:10.1351/pac197749010107Acessível livremente 
  • Michael Röper, Eugen Gehrer, Thomas Narbeshuber, Wolfgang Siegel "Acylation and Alkylation" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2000. doi:10.1002/14356007.a01_185
  • Gillespie, R. J.; Peel, T. E. (1 de agosto de 1973). «Hammett acidity function for some superacid systems. II. Systems sulfuric acid-[fsa], potassium fluorosulfate-[fsa], [fsa]-sulfur trioxide, [fsa]-arsenic pentafluoride, [sfa]-antimony pentafluoride and [fsa]-antimony pentafluoride-sulfur trioxide». Journal of the American Chemical Society. 95 (16): 5173–5178. ISSN 0002-7863. doi:10.1021/ja00797a013 

nih.gov

ncbi.nlm.nih.gov

  • Himmel D, Goll SK, Leito I, Krossing I (2010). «A Unified pH Scale for All Phases». Angew. Chem. Int. Ed. 49 (38): 6885–6888. PMID 20715223. doi:10.1002/anie.201000252 
  • Himmel D, Goll SK, Leito I, Krossing I (2010). «A Unified pH Scale for All Phases». Angew. Chem. Int. Ed. 49 (38): 6885–6888. PMID 20715223. doi:10.1002/anie.201000252 
  • Olah, George A. (2005). «Crossing Conventional Boundaries in Half a Century of Research». Journal of Organic Chemistry. 70 (7): 2413–2429. PMID 15787527. doi:10.1021/jo040285o 

psc.edu

web.archive.org

worldcat.org

  • Gillespie, R. J.; Peel, T. E.; Robinson, E. A. (1 de outubro de 1971). «Hammett acidity function for some super acid systems. I. Systems H2SO4-SO3, H2SO4-HSO3F, H2SO4-HSO3Cl, and H2SO4-HB(HSO4)4». Journal of the American Chemical Society. 93 (20): 5083–5087. ISSN 0002-7863. doi:10.1021/ja00749a021. The work of Jorgenson and Hartter formed the basis for the present work, the object of which was to extend the range of acidity function measurements into the super acid region, i.e., into the region of acidities greater than that of 100% H2SO4. 
  • Ruff, F. (Ferenc) (1994). Organic reactions : equilibria, kinetics, and mechanism. Csizmadia, I. G. Amsterdam: Elsevier. ISBN 0444881743. OCLC 29913262 
  • Gillespie, R. J.; Peel, T. E. (1 de agosto de 1973). «Hammett acidity function for some superacid systems. II. Systems sulfuric acid-[fsa], potassium fluorosulfate-[fsa], [fsa]-sulfur trioxide, [fsa]-arsenic pentafluoride, [sfa]-antimony pentafluoride and [fsa]-antimony pentafluoride-sulfur trioxide». Journal of the American Chemical Society. 95 (16): 5173–5178. ISSN 0002-7863. doi:10.1021/ja00797a013