Protonated serine octamer cluster: structure elucidation by gas-phase H/D exchange reactions.

The H/D exchange kinetics of the protonated serine octamer was investigated by both flow-tube and FT-ICR experiments. The exchange was observed to be bimodal in agreement with previous observations. Quantitative analysis of the experimental results led to site-specific H/D exchange rate constants on the basis of which the structures of both ion populations were deduced.

Letter: some more aspects of formation and stability of the protonated serine octamer cluster.

The formation of protonated serine octamer clusters from homochiral and heterochiral monomer solutions was investigated. The well-established preference for homochiral cluster formation was found to originate from collision-induced dissociation of the less stable ion population B prior to reaching the mass spectrometer's analyzer cell. In addition, collision-induced dissociation experiments were undertaken to investigate the relative stabilities of populations A and B and infrared multi-photon dissociation experiments addressed the relative stabilities of the protonated serine octamer cluster and its metaclusters.

Isolation of isomers based on hydrogen/deuterium exchange in the gas phase.

A method to isolate isomers in a Fourier transform ion cyclotron resonance mass spectrometer on the basis of their different hydrogen/deuterium exchange rates has been developed and applied to the protonated serine octamer cluster. Isolation allows interrogation of each isomer by infrared multi-photon dissociation to determine any differences in the building blocks that form these clusters. The experimental results strongly support previous assignments of an all-zwitterion structure to the slower-exchanging isomer and an all-neutral structure to its faster- exchanging counterpart.

Carbon-fluorine bond activation--looking at and learning from unsolvated systems.

The selective activation of a particular bond in a molecule has always been a desideratum in chemical synthesis. This Feature Article focuses on studying the mechanisms operative in the activation of carbon-fluorine bonds beyond solvated systems, i.e.

Reactions of Group 8, 9, and 10 monocations (Fe+, Co+, Ni+, Ru+, Rh+, Pd+, Os+, Ir+, Pt+) with phosphane in the gas phase.

The reactions of Group 8, 9 and 10 monocations with phosphane were studied under single-collision conditions in a Fourier transform ion cyclotron resonance (FT-ICR) mass spectrometer. Fe(+) is completely unreactive, Co(+) reacts slowly and shows both adduct formation and P-H bond activation, and Ni(+) reacts slowly as well but shows adduct formation only. In contrast to their first-row congeners, the investigated second- and third-row transition metal monocations show facile P-H bond activations.