Abstract
Cryogenic ion vibrational predissociation (CIVP) spectroscopy is used to structurally characterize electrochemically (EC)-generated oxidation products of the benchmark compound reserpine. Ionic products were isolated using EC-electrospray ionization (ESI) coupled to a 25 K ion trap prior to injection into a double-focusing, tandem time-of-flight photofragmentation mass spectrometer. Vibrational predissociation spectroscopy was carried out by photoevaporation of weakly bound N2 adducts over the range 800-3800 cm(-1) in a linear (i.e., single photon) action regime, thus enabling direct comparison of the experimental vibrational pattern with harmonic calculations. The locations of the NH and OH stretching fundamentals are most consistent with formation of 9-hydroxyreserpine, which is a different isomer than considered previously. This approach thus provides a powerful structural dimension for the analysis of electrochemical processes detected with the sensitivity of mass spectrometry.
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