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Collect. Czech. Chem. Commun. 2004, 69, 2183-2192
https://doi.org/10.1135/cccc20042183

Substituent Effects on the Acidity of Weak Acids. 4. Anilinium Ions

Kenneth B. Wiberg

Department of Chemistry, Yale University, New Haven, CT 06520-8107, U.S.A.

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  • Maksić Zvonimir B., Kovačević Borislav, Vianello Robert: Advances in Determining the Absolute Proton Affinities of Neutral Organic Molecules in the Gas Phase and Their Interpretation: A Theoretical Account. Chem. Rev. 2012, 112, 5240. <https://doi.org/10.1021/cr100458v>
  • Jaramillo Cinthia, Guerra Doris, Moreno Luis Fernando, Restrepo Albeiro: Competitive Substituent Effects on the Reactivity of Aromatic Rings. J. Phys. Chem. A 2010, 114, 6033. <https://doi.org/10.1021/jp9118919>
  • Dumont Elise, Chaquin Patrick: Inductive Effects on Proton Affinity of Benzene Derivatives: Analysis Using Fictitious Hydrogen Atoms. J. Phys. Chem. A 2009, 113, 2990. <https://doi.org/10.1021/jp806871r>
  • Böhm Stanislav, Exner Otto: Revision of the Dual-Substituent-Parameter Treatment; Reaction Series with a Donor Reaction Centre. Collect. Czech. Chem. Commun. 2007, 72, 1158. <https://doi.org/10.1135/cccc20071158>
  • Pasker Felix M., Solcà Nicola, Dopfer Otto: Spectroscopic Identification of Carbenium and Ammonium Isomers of Protonated Aniline (AnH+):  IR Spectra of Weakly Bound AnH+−Ln Clusters (L = Ar, N2). J. Phys. Chem. A 2006, 110, 12793. <https://doi.org/10.1021/jp064571a>
  • Böhm Stanislav, Paŕík Patrik, Exner Otto: Range of validity of the Hammett equation: acidity of substituted ethynylbenzenes. New J. Chem. 2006, 30, 384. <https://doi.org/10.1039/b512698c>