Related Experiment Video
Updated: Nov 1, 2025

Assessment of Boron Doped Diamond Electrode Quality and Application to In Situ Modification of Local pH by Water Electrolysis
Published on: January 6, 2016
Facile proton-coupled electron transfer enabled by coordination-induced E-H bond weakening to boron
Anthony Wong1, Arunavo Chakraborty1, Deependra Bawari2
1Department of Chemistry and Biochemistry, University of California, Santa Barbara, CA 93106, USA. menard@chem.ucsb.edu.
Abstract:
We report the facile activation of aryl E-H (ArEH; E = N, O, S; Ar = Ph or C6F5) or ammonia N-H bonds via coordination-induced bond weakening to a redox-active boron center in the complex, (1-). Substantial decreases in E-H bond dissociation free energies (BDFEs) are observed upon substrate coordination, enabling subsequent facile proton-coupled electron transfer (PCET). A drop of >50 kcal mol-1 in H2N-H BDFE upon coordination was experimentally determined.
More Related Videos
Related Concept Videos
Hydroboration-Oxidation of Alkenes
Electrophiles
While a positive electrophile, like a proton, reacts due to its vacant, low-energy 1s orbital, the...
Exceptions to the Octet Rule
Regioselectivity and Stereochemistry of Hydroboration
Hydroboration proceeds in a concerted fashion with the attack of borane on the π bond, giving a cyclic four-centered transition state. The –BH2 group is bonded to the less substituted carbon and –H to the more substituted carbon. The concerted nature requires the simultaneous addition of –H and –BH2 across the same face of the alkene giving syn stereochemistry.
Hydrogen Bonds
Hydrogen Bonds
Hydrogen Bonds Control the World!
Because hydrogen has very weak electronegativity when it binds with a strongly electronegative atom, such as oxygen or nitrogen, electrons in the bond are unequally shared....

