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Using Voltammetry to Measure the Relative Hydrogen‐Bonding Strengths of Pyridine and Its Derivatives in Acetonitrile
Author(s) -
Tessensohn Malcolm E.,
Koh Yu Rong,
Lim Sihao,
Hirao Hajime,
Webster Richard D.
Publication year - 2017
Publication title -
chemphyschem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.016
H-Index - 140
eISSN - 1439-7641
pISSN - 1439-4235
DOI - 10.1002/cphc.201700560
Subject(s) - chemistry , acetonitrile , dication , pyridine , electrochemistry , steric effects , cyclic voltammetry , aqueous solution , protonation , hydrogen bond , inorganic chemistry , acceptor , hydrogen , stoichiometry , redox , medicinal chemistry , photochemistry , molecule , stereochemistry , organic chemistry , electrode , ion , physics , condensed matter physics
The voltammetric behavior of 2,3,5,6‐tetramethyl‐1,4‐phenylenediamine was found to be able to differentiate the hydrogen acceptor abilities of electroinactive pyridine compounds in acetonitrile. Weak and strong hydrogen acceptors were distinguished through the onset of a third oxidation process that came about at sub‐stoichiometric amounts of strong hydrogen acceptors, but not in the presence of weak hydrogen acceptors. This additional oxidation reaction occurred at a potential between the two 1 e − ‐oxidation reactions that phenylenediamines typically undergo (i.e. E P ox(1) < E P ox(3) < E P ox(2) , with E P ox(1) and E P ox(2) representing the electrochemical conversion of the neutral phenylenediamine into the radical cation and thereafter to the quinonediimine dication) as well as at the expense of the second electrochemical reaction. E P ox(2) and E P ox(3) were observed to shift towards less positive potentials with increasing concentrations of weak or strong hydrogen acceptors, respectively, whereas E P ox(1) remained virtually unaffected. This allows the electrochemical parameters Δ E P ox(1, 2) =| E P ox(1) − E P ox(2) | and Δ E P ox(1, 3) =| E P ox(1) − E P ox(3) | to be employed as measures of the hydrogen‐bonding strengths within each category, to which they were found to be highly reproducible and responsive to steric, electronic, inductive, and mesomeric effects. The electrochemical findings concur with available aqueous p K a data of the protonated pyridine compounds but were, however, in poor agreement with results obtained by density functional theory calculations.