4.5 Article

Relative Kinetic Reactivities of Boronic Acids and Boronate Ions toward 1,2-Diols

Journal

EUROPEAN JOURNAL OF INORGANIC CHEMISTRY
Volume 2014, Issue 14, Pages 2389-2395

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejic.201400040

Keywords

Kinetics; Reaction mechanisms; Boronic acids; Boronates; Boron

Funding

  1. Japan Society for the Promotion of Science (JSPS KAKENHI) [25410150]
  2. Waseda University [2009B-123, 2011B-179, 2012B-153]
  3. Grants-in-Aid for Scientific Research [25810052, 25410150, 25288027] Funding Source: KAKEN

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The following reaction systems, with and without proton ambiguity, were set up for direct measurements of the rate constants of borate and boronate ions: boric acid [B(OH)(3)] and 4,5-dihydroxy-1,3-benzenedisulfonic acid disodium salt (Tiron); 3-nitrophenylboronic acid [3-NO2PhB(OH)(2)] and Tiron; phenylboronic acid [PhB(OH)(2)] and 4-nitrocatechol; boric acid and 4-nitrocatechol. Each rate constant for boric or boronic acid is larger than that for the conjugate borate or boronate ion for the reaction systems without proton ambiguity. These results explicitly indicate that the widespread belief that the rate constants of boronate ions are several orders of magnitude larger than those of the conjugate boronic acids is erroneous. The relative kinetic reactivities of RB(OH)(2) and RB(OH)(3)(-) were investigated in relation to the linear free energy relationships between the rate constants and acidities of the boronic acids and diols.

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