Counterion influence on chemical shifts in strychnine salts. (11th March 2013)

• Record Type: Journal Article
• Authors: Metaxas, Athena E.; Cort, John R.
• Is Part Of: Magnetic resonance in chemistry. Volume 51:Number 5(2013:May)
• Page Start: 292
• Page End: 298
• Publication Date: 2013-03-11
• Subjects: Nuclear magnetic resonance spectroscopy -- Periodicals; Chemistry, Organic -- Periodicals; Magnetic resonance -- Periodicals; 538.36
• DOI: 10.1002/mrc.3945
• Languages: English
• ISSNs: 0749-1581

Abstract

<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>The highly toxic plant alkaloid strychnine is often isolated in the form of the anion salt of its protonated tertiary amine. Here, we characterize the relative influence of different counterions on ¹H and ¹³C chemical shifts in several strychnine salts in D₂O, methanol‐<italic>d</italic>₄ (CD₃OD), and chloroform‐<italic>d</italic> (CDCl₃) solvents. In organic solvents but not in water, substantial variation in chemical shifts of protons near the tertiary amine was observed among different salts. These secondary shifts reveal differences in the way each anion influences electronic structure within the protonated amine. The distributions of secondary shifts allow salts to be easily distinguished from each other as well as from the free base form. Slight concentration dependence in chemical shifts of some protons near the amine was observed for two salts in CDCl₃, but this effect is small compared with the influence of the counterion. Distinct chemical shifts in different salt forms of the same compound may be useful as chemical forensic signatures for source attribution and sample matching of alkaloids such as strychnine and possibly other organic acid and base salts. Copyright © 2013 John Wiley &amp; Sons, Ltd.</p> </abstract>