Catalysis in Hydrogen-Bridged Radical Cations

Author:

Jobst Karl J.1,Trikoupis Moschoula A.2

Affiliation:

1. Laboratory Services Branch, Ministry of the Environment, 125 Resources Road, Toronto, ON, Canada, M9P 3V6

2. Environmental Innovations Branch, Ministry of the Environment, 135 St Clair Ave. West, Toronto, ON, Canada, M4V 1P5

Abstract

Hydrogen-bridged radical cations (HBRCs) are an intriguing subclass of ion–molecule complexes. They may act as key intermediates of remarkable stability in both association and dissociation reactions of heteroatom-containing molecular ions. The H-bridge of such an HBRC can promote isomerization of its ionic component by H-transfer. Proton-transport catalysis (PTC) is a prime example. Here, a neutral molecule promotes the smooth transformation of an ion into its H-shift isomer by consecutive proton-transfer reactions. A celebrated case is the water-catalyzed isomerization of CH3OH•+ into its more stable distonic isomer CH2OH2+. Other early studies of PTC also deal with catalyzing 1,2-H shifts in association reactions. This short review focuses on more recent combined experimental and computational studies of catalysis in HBRCs. Mechanisms involving both proton and H atom transfers have been proposed for a variety of systems of H-shift isomers. It has also become clear that PTC is not confined to bimolecular reactions. It also features in the unimolecular chemistry of heteroatom-containing ions, which have a tendency to isomerize to HBRCs en route to their dissociation.

Publisher

SAGE Publications

Subject

Spectroscopy,Atomic and Molecular Physics, and Optics,General Medicine

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