The Selectivity of Charged Phenyl Radicals in Hydrogen Atom Abstraction Reactions with Isopropanol

• Published in: The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory Vol. 112; no. 40; pp. 9708 - 9715
• Main Authors: Jing, Linhong, Guler, Leonard P, Pates, George, Kenttämaa, Hilkka I
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 09.10.2008
• Subjects: 2-Propanol - chemistry; A: Kinetics, Spectroscopy; Benzene - chemistry; Deuterium - chemistry; Ethanol - chemistry; Hydrogen - chemistry; Kinetics; Substrate Specificity
• ISSN: 1089-5639; 1520-5215
• DOI: 10.1021/jp802257m

The vertical electron affinity is demonstrated to be a key factor in controlling the selectivity of charged phenyl radicals in hydrogen atom abstraction from isopropanol in the gas phase. The measurement of the total reaction efficiencies (hydrogen and/or deuterium atom abstraction) for unlabeled and partially deuterium-labeled isopropanol, and the branching ratios of hydrogen and deuterium atom abstraction, by using a Fourier transform ion cyclotron resonance (FT-ICR) mass spectrometer, allowed the determination of the selectivity for each site in the unlabeled isopropanol. Examination of hydrogen atom abstraction from isopropanol by eight structurally different radicals revealed that the preferred site is the CH group. The selectivity of the charged phenyl radicals correlates with the radical’s vertical electron affinity and the reaction efficiency. The smaller the vertical electron affinity of a radical, the lower its reactivity, and the greater the preference for the thermodynamically favored CH group over the CH3 group or the OH group. As the vertical electron affinity increases from 4.87 to 6.28 eV, the primary kinetic isotope effects decrease from 2.9 to 1.3 for the CD group, and the mixture of primary and α-secondary kinetic isotopes decreases from 6.0 to 2.4 for the CD3 group.