Probing gas phase catalysis by atomic metal cations with flow tube mass spectrometry.

The evolution and applications of flow tube mass spectrometry in the study of catalysis promoted by atomic metal ions are tracked from the pioneering days in Boulder, Colorado, to the construction and application of the ICP/SIFT/QqQ and ESI/qQ/SIFT/QqQ instruments at York University and the VISTA-SIFT instrument at the Air Force Research Laboratory. The physical separation of various sources of atomic metal ions from the flow tube in the latter instruments facilitates the spatial resolution of redox reactions and allows the separate measurement of the kinetics of both legs of a two-step catalytic cycle, while also allowing a view of the catalytic cycle in progress downstream in the reaction region of the flow tube. We focus on measurements on O-atom transfer and bond activation catalysis as first identified in Boulder and emphasize fundamental aspects such as the thermodynamic window of opportunity for catalysis, catalytic efficiency, and computed energy landscapes for atomic metal cation catalysis.

Relativistic Effects in the Ligation of Atomic Coinage Metal Cations with O and CH: Anomalous Formation of Relativistic Mono- and Bis-adducts with Au.

The interaction of the atomic coinage metal cations Cu, Ag, and Au with O, a weak ligand, and CH, a strong ligand, was investigated with measurements of rate coefficients of ligation and quantum-chemical computations of ligation energies with an eye on relativistic effects going down the periodic table. Strong "third row enhancements" were observed for both the rate coefficients of ligation and ligation energies with the O ligand and for the formation of both the mono- and bis-adducts of M and the monoadduct of M(CH). The computations revealed that the third-row enhancement in the ligation energy is attributable to a relativistic increase in the ligation energy.

Ligation Kinetics as a Probe for Non-Covalent Electrostatic Bonding and Electron Solvation of Alkali and Alkaline Earth Cations with Ammonia.

Mono-ligation kinetics were measured for ammonia reacting with atomic cations in the first two groups of the periodic table (K, Rb, Cs and Ca, Sr, Ba). Also, mono-ligation energies were computed using density functional theory (DFT) in an attempt to assess the role of non-covalent electrostatic interactions in these chemical reactions. The measurements were performed at room temperature in helium bath gas at 0.

Ligation kinetics as a probe for gas-phase ligand field effects: Ligation of atomic transition metal cations with ammonia at room temperature.

The kinetics of ammonia ligation to atomic first and second row transition metal cations were measured in an attempt to assess the role of ligand field effects in gas-phase ion-molecule reaction kinetics. Measurements were performed at 295 ± 2 K in helium bath gas at 0.35 Torr using an inductively coupled plasma/selected-ion flow tube tandem mass spectrometer.

Multi-component ion modifiers and arcing suppressants to enhance differential mobility spectrometry for separation of peptides and drug molecules.

The optimization of ion/molecule chemistry in a differential mobility spectrometer (DMS) is shown to result in improved peak capacity, separation, and sensitivity. We have experimented with a modifier composed of multiple components, where each component accomplishes a specific task on mixtures of peptides and small drug molecules. Use of a higher proton affinity modifier (hexanol) provides increased peak capacity and separation.