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Using Voltammetry to Measure the Relative Hydrogen-Bonding Strengths of Pyridine and Its Derivatives in Acetonitrile.

Chemphyschem : a European journal of chemical physics and physical chemistry (2017-06-14)
Malcolm E Tessensohn, Yu Rong Koh, Sihao Lim, Hajime Hirao, Richard D Webster
RESUMEN

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

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Sigma-Aldrich
2-Methylpyridine, 98%
Sigma-Aldrich
2,6-Lutidina, ReagentPlus®, 98%
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2,6-Di-tert-butylpyridine, ≥97%
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Pyrimidine, ≥98.0%
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4-(Trifluoromethyl)pyridine, 97%
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Pyridazine, 98%