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Ionization Constants of Four Dinitrophenols in Water at 25 °C

Thermodynamic ionization constants of 2,3-, 2,5-, 3,4-, and 3,5-dinitrophenols in aqueous solution at 25° C have been determined by a spectrophotometric method. The respective values found, expressed as pK, are 4.95(9), 5.21(0), 5.42(2), and 6.69(2). pK has also been determined potentiometrically fo...

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Autores principales: Robinson, Robert A., Davis, Marion Maclean, Paabo, Maya, Bower, Vincent E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: [Gaithersburg, MD] : U.S. Dept. of Commerce, National Institute of Standards and Technology 1960
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5287089/
https://www.ncbi.nlm.nih.gov/pubmed/32196173
http://dx.doi.org/10.6028/jres.064A.034
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author Robinson, Robert A.
Davis, Marion Maclean
Paabo, Maya
Bower, Vincent E.
author_facet Robinson, Robert A.
Davis, Marion Maclean
Paabo, Maya
Bower, Vincent E.
author_sort Robinson, Robert A.
collection PubMed
description Thermodynamic ionization constants of 2,3-, 2,5-, 3,4-, and 3,5-dinitrophenols in aqueous solution at 25° C have been determined by a spectrophotometric method. The respective values found, expressed as pK, are 4.95(9), 5.21(0), 5.42(2), and 6.69(2). pK has also been determined potentiometrically for 2,3- and 3,5-dinitrophenols; the respective values obtained are 4.98 and 6.66. The experimental pK values for all six dinitrophenols are lower than the calculated values based on pK data for phenol and the mononitrophenols. Spectral absorption curves are presented for the ionized and unionized forms of the four dinitrophenols.
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spelling pubmed-52870892020-03-18 Ionization Constants of Four Dinitrophenols in Water at 25 °C Robinson, Robert A. Davis, Marion Maclean Paabo, Maya Bower, Vincent E. J Res Natl Bur Stand A Phys Chem Article Thermodynamic ionization constants of 2,3-, 2,5-, 3,4-, and 3,5-dinitrophenols in aqueous solution at 25° C have been determined by a spectrophotometric method. The respective values found, expressed as pK, are 4.95(9), 5.21(0), 5.42(2), and 6.69(2). pK has also been determined potentiometrically for 2,3- and 3,5-dinitrophenols; the respective values obtained are 4.98 and 6.66. The experimental pK values for all six dinitrophenols are lower than the calculated values based on pK data for phenol and the mononitrophenols. Spectral absorption curves are presented for the ionized and unionized forms of the four dinitrophenols. [Gaithersburg, MD] : U.S. Dept. of Commerce, National Institute of Standards and Technology 1960 1960-08-01 /pmc/articles/PMC5287089/ /pubmed/32196173 http://dx.doi.org/10.6028/jres.064A.034 Text en https://creativecommons.org/publicdomain/zero/1.0/ The Journal of Research of the National Bureau of Standards Section A is a publication of the U.S. Government. The papers are in the public domain and are not subject to copyright in the United States. Articles from J Res may contain photographs or illustrations copyrighted by other commercial organizations or individuals that may not be used without obtaining prior approval from the holder of the copyright.
spellingShingle Article
Robinson, Robert A.
Davis, Marion Maclean
Paabo, Maya
Bower, Vincent E.
Ionization Constants of Four Dinitrophenols in Water at 25 °C
title Ionization Constants of Four Dinitrophenols in Water at 25 °C
title_full Ionization Constants of Four Dinitrophenols in Water at 25 °C
title_fullStr Ionization Constants of Four Dinitrophenols in Water at 25 °C
title_full_unstemmed Ionization Constants of Four Dinitrophenols in Water at 25 °C
title_short Ionization Constants of Four Dinitrophenols in Water at 25 °C
title_sort ionization constants of four dinitrophenols in water at 25 °c
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5287089/
https://www.ncbi.nlm.nih.gov/pubmed/32196173
http://dx.doi.org/10.6028/jres.064A.034
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