CrossRef enabled

PAC Archives

Archive →

Pure Appl. Chem., 1997, Vol. 69, No. 12, pp. 2497-2510

http://dx.doi.org/10.1351/pac199769122497

ORGANIC AND BIOMOLECULAR CHEMISTRY DIVISION
COMMISSION ON PHYSICAL ORGANIC CHEMISTRY

Compilation and critical evaluation of structure-reactivity parameters and equations: Part 2. Extension of the Hammett σ scale through data for the ionization of substituted benzoic acids in aqueous solvents at 25 C (Technical Report)

J. Shorter

CrossRef Cited-by theme picture

CrossRef Cited-by Linking

  • Audran Gérard, Brémond Paul, Marque Sylvain R.A., Siri Didier, Santelli Maurice: Calculated linear free energy relationships in the course of the Suzuki–Miyaura coupling reaction. Tetrahedron 2014. <http://dx.doi.org/10.1016/j.tet.2014.02.011>
  • Yu Jian-Xin, Hallac Rami R., Chiguru Srinivas, Mason Ralph P.: New frontiers and developing applications in 19F NMR. Progress in Nuclear Magnetic Resonance Spectroscopy 2013, 70, 25. <http://dx.doi.org/10.1016/j.pnmrs.2012.10.001>
  • Pecyna Jacek G., Ringstrand Bryan, Kaszyński Piotr: Transmission of Electronic Effects through the {closo-1-CB9} and {closo-1-CB11} Cages: Apparent Dissociation Constants for Series of [closo-1-CB9H8-1-COOH-10-X] and [closo-1-CB11H10-1-COOH-12-X] Acids. Inrog Chem 2012, 51, 5353. <http://dx.doi.org/10.1021/ic300298e>
  • Sluch Ilya M., Miranda Anthea J., Elbjeirami Oussama, Omary Mohammad A., Slaughter LeGrande M.: Interplay of Metallophilic Interactions, π–π Stacking, and Ligand Substituent Effects in the Structures and Luminescence Properties of Neutral PtII and PdII Aryl Isocyanide Complexes. Inorg. Chem. 2012, 51, 10728. <http://dx.doi.org/10.1021/ic301104a>
  • Lennox Alastair J. J., Lloyd-Jones Guy C.: Organotrifluoroborate Hydrolysis: Boronic Acid Release Mechanism and an Acid–Base Paradox in Cross-Coupling. S J Am Chem Soc 2012, 134, 7431. <http://dx.doi.org/10.1021/ja300236k>
  • Prezhdo Victor V., Prezhdo Marina V., Loginova Lidia P., Zubkova Valentina B.: Influence of Substituents on Phenols Extraction and Dissociation. Separation Science and Technology 2012, 48, 303. <http://dx.doi.org/10.1080/01496395.2012.686551>
  • Szatyłowicz Halina, Krygowski Tadeusz Marek, Jezierska-Mazzarello Aneta: Hydroxyl group as a substituent with varying electronic properties: Effect of strength of H-bonding on charge density changes in Ph–OH…F− complexes. J Mol Model 2011, 17, 125. <http://dx.doi.org/10.1007/s00894-010-0703-y>
  • De Paula Rodrigo, Simões Mário M.Q., Neves M. Graça P.M.S., Cavaleiro José A.S.: Oxidation of styrene and of some derivatives with H2O2 catalyzed by novel imidazolium-containing manganese porphyrins: A mechanistic and thermodynamic interpretation. J Mol Cata A Chem 2011, 345, 1. <http://dx.doi.org/10.1016/j.molcata.2011.05.013>
  • Kopylovich Maximilian N., Mahmudov Kamran T., Guedes da Silva M. Fátima C., Martins Luísa M.D.R.S., Kuznetsov Maxim L., Silva Telma F.S., Fraústo da Silva João J.R., Pombeiro Armando J.L.: Trends in properties of para-substituted 3-(phenylhydrazo)pentane-2,4-diones. J Phys Org Chem 2010, n/a. <http://dx.doi.org/10.1002/poc.1824>
  • Alonso Mercedes, Herradón Bernardo: Substituent effects on the aromaticity of carbocyclic five-membered rings. Phys Chem Chem Phys 2010, 12, 1305. <http://dx.doi.org/10.1039/b917343a>
  • Sadlej-Sosnowska N., Krygowski T.M.: Substituent effect on geometry of the NO and N(CH3)2 groups in para substituted derivatives of nitrosobenzene and N,N-dimethylaniline. chem phys letts 2009, 476, 191. <http://dx.doi.org/10.1016/j.cplett.2009.06.045>
  • Krygowski Tadeusz M., Zachara-Horeglad Joanna E.: Resonance-assisted hydrogen bonding in terms of substituent effect. Tetrahedron 2009, 65, 2010. <http://dx.doi.org/10.1016/j.tet.2009.01.006>
  • Palusiak Marcin, Krygowski Tadeusz M.: Substituent effects in mono- and disubstituted 1,3,5,7-cyclooctatetraene derivatives in natural and planar conformations. New J Chem 2009, 33, 1753. <http://dx.doi.org/10.1039/b905909a>
  • Sayyed Fareed Bhasha, Suresh Cherumuttathu H.: Quantification of substituent effects using molecular electrostatic potentials: additive nature and proximity effects. New J Chem 2009, 33, 2465. <http://dx.doi.org/10.1039/b9nj00333a>
  • Mello Rossella, Royo Jorge, Andreu Cecilia, Báguena-Añó Minerva, Asensio Gregorio, González-Núñez María Elena: On the Reactivity of C(sp3)–H σ-Bonds: Oxygenation with Methyl(trifluoromethyl)­dioxirane. Eur J Org Chem 2008, 2008, 455. <http://dx.doi.org/10.1002/ejoc.200700773>
  • Segala Maximiliano, Takahata Yuji, Chong Delano P., Shamsipur Mojtaba, Alizadeh Kamal, Arshadi Sattar, Yan Shihai, Bu Yuxiang: Geometry, solvent, and polar effects on the relationship between calculated core-electron binding energy shifts (��CEBE) and Hammett substituent (��) constants. Journal of Molecular Structure: THEOCHEM 2006, 758, 61. <http://dx.doi.org/10.1016/j.theochem.2005.10.004>
  • Morley John O., Whittaker Stuart D., McDowell Sean A.C., Moraleda Delphine, El Abed Douniazad, Pellissier H��l��ne, Santelli Maurice: Non-linear optical properties of thienylmethylene anilines and benzylidene aminothiophenes. Journal of Molecular Structure: THEOCHEM 2006, 760, 1. <http://dx.doi.org/10.1016/j.theochem.2005.12.001>
  • Böhm Stanislav, Paŕík Patrik, Exner Otto: Range of validity of the Hammett equation: acidity of substituted ethynylbenzenes. New J Chem 2006, 30, 384. <http://dx.doi.org/10.1039/b512698c>
  • Fu Yao, Liu Lei, Liu Rui, Guo Qing-Xiang: Homolytic bond dissociation energies of 4-substituted bicyclo[2.2.2]octanyl compounds: inductive/field effects on the stabilities of organic radicals. J Phys Org Chem 2005, 18, 529. <http://dx.doi.org/10.1002/poc.891>
  • Shorter John: A history of the international group for correlation analysis in chemistry. J Phys Org Chem 2003, 16, 645. <http://dx.doi.org/10.1002/poc.671>
  • Šima Jozef, Brezová Vlasta: Photochemistry of iodo iron(III) complexes. Coord Chem Rev - 2002, 229, 27. <http://dx.doi.org/10.1016/S0010-8545(02)00018-8>
  • Palát Karel, Waisser Karel, Exner Otto: Infrared intensities of benzene derivatives as a measure of the substituent resonance effect. J Phys Org Chem 2001, 14, 677. <http://dx.doi.org/10.1002/poc.416>
  • Jenkins Aubrey D., Hatada Koichi, Kitayama Tatsuki, Nishiura Takafumi: Revised patterns of reactivity scheme. VII. Revised patterns scheme and its relationship to carbon-13 NMR spectra. J Polym Sci A Polym Chem 2000, 38, 4336. <http://dx.doi.org/10.1002/1099-0518(20001215)38:24<4336::AID-POLA20>3.0.CO;2-4>
  • Jenkins Aubrey D.: THE REVISED PATTERNS OF REACTIVITY SCHEME. PART 6. A GENERAL FORMULATION OF THE SCHEME AND THE “ALTERNATING TENDENCY”. Journal of Macromolecular Science, Part A 2000, 37, 1547. <http://dx.doi.org/10.1081/MA-100102325>
  • Jenkins A.D.: The reactivity of initiator radicals. Poly 1999, 40, 7045. <http://dx.doi.org/10.1016/S0032-3861(99)00078-6>