On the rate of boronate ester formation inortho-aminomethyl-functionalised phenyl boronic acids
- 1 February 2013
- journal article
- research article
- Published by Taylor & Francis in Supramolecular Chemistry
- Vol. 25 (2), 79-86
- https://doi.org/10.1080/10610278.2012.740044
Abstract
The role of the ortho-aminomethyl functional group in phenyl boronic acids for sugar complexation is a topic of debate. To decipher its effect on the kinetics of boronate ester formation, we first performed pseudo-first-order kinetics analyses at five pH values up to 4 mM in fructose, revealing a first-order kinetic dependence upon fructose. Under these conditions, the reaction is in equilibrium and does not reach completion, but at 50 mM fructose saturation is achieved, revealing zero-order dependence upon fructose. This indicates rate-determining creation of an intermediate prior to reaction with fructose, which we propose involves leaving group departure of inserted solvent. Furthermore, the region of kinetics displaying zero-order dependence has a kinetic isotope effect of 1.42, showing involvement of a proton transfer in the leaving group departure. The ratio of forward and reverse rate constants branching from the intermediate shows that fructose is several thousand times more nucleophilic than the solvent. Overall, the data support a mechanism where the ortho-aminomethyl group lowers the pK a of the proximal boronic acid and acts as a general acid (as an ammonium) to facilitate leaving group departure. Consequently, by microscopic reversibility the resulting amine must perform general base catalysis to deliver fructose.Keywords
This publication has 18 references indexed in Scilit:
- Boronic acid building blocks: tools for sensing and separationChemical Communications, 2011
- Supramolecular ChemistryPublished by Wiley ,2009
- Peptide Borono Lectins (PBLs): A New Tool for Glycomics and Cancer DiagnosticsChemBioChem, 2007
- Boronic Acids in Saccharide RecognitionPublished by Royal Society of Chemistry (RSC) ,2006
- Boronic AcidsPublished by Wiley ,2005
- Regulating the fluorescence intensity of an anthracene boronic acid system: a B–N bond or a hydrolysis mechanism?Bioorganic Chemistry, 2004
- Study of the Mechanism of Electron-Transfer Quenching by Boron−Nitrogen Adducts in Fluorescent SensorsThe Journal of Physical Chemistry B, 2003
- Boronic Acid-Based SensorsCurrent Organic Chemistry, 2002
- Novel photoinduced electron-transfer sensor for saccharides based on the interaction of boronic acid and amineJournal of the Chemical Society, Chemical Communications, 1994
- Preparation of chromatographic sorbents with chiral cavities for racemic resolutionJournal of Chromatography A, 1978