Special Feature: Tutorial Gas-phase Metal Ion Chemistry

Author(s):  
Ben S. Freiser
Keyword(s):  
ChemInform ◽  
2001 ◽  
Vol 32 (16) ◽  
pp. no-no
Author(s):  
Detlef Schroder ◽  
Christoph A. Schalley ◽  
Helmut Schwarz

2008 ◽  
Vol 86 (3) ◽  
pp. 177-198 ◽  
Author(s):  
Diethard K Böhme

The intrinsic chemical reactivities of ions can be monitored in the gas phase using mass spectrometers that are coupled to appropriate ion sources and reaction cells. Here the author surveys his own experiences over the past 40 years as an ion chemist. He used flow-tube techniques for room temperature measurements of the intrinsic chemical reactivities of a large variety of positive and negative ions, including bare atomic ions, ions found in solution, biological ions, carbonaceous ions, and interstellar, cometary, and ionospheric ions. Progress in the measurement of chemical reactions of these ions with flow-tube mass spectrometry in the author’s laboratory was been driven largely by developments in techniques of ion injection into the flow tube and of ion production (e.g., by electron impact, plasma ionization, and electrospray ionization). Chemical topics that are covered include: acid-base and nucleophilic displacement reactions that have bridged the gap between the gas phase and solution; interstellar ions and their role in molecular synthesis such as the synthesis of amino acids; the chemistry of fullerene cations as a function of charge state; fundamentals and applications of the chemistry of atomic cations with an emphasis on transition metal and lanthanide cations; atomic metal-ion catalysis; and chemical reactions of singly and multiply charged biological anions and cations in the gas phase.Key words: ions, mass spectrometry, kinetics, ion chemistry.


1990 ◽  
Vol 101 (2-3) ◽  
pp. 325-336 ◽  
Author(s):  
Arthur T. Blades ◽  
Palitha Jayaweera ◽  
Michael G. Ikonomou ◽  
Paul Kebarle

2000 ◽  
pp. 640-664 ◽  
Author(s):  
Detlef Schröder ◽  
Christoph A. Schalley ◽  
Helmut Schwarz

1995 ◽  
Vol 73 (12) ◽  
pp. 2263-2271 ◽  
Author(s):  
Christine C.Y. Chow ◽  
John M. Goodings

A pair of laminar, premixed, CH4–O2 flames above 2000 K at atmospheric pressure, one fuel-rich (FR) and the other fuel-lean (FL), were doped with ~10−6 mol fraction of the second-row transition metals Y, Zr, Nb, and Mo. Since these hydrocarbon flames contain natural ionization, metallic ions were produced in the flames by the chemical ionization (CI) of metallic neutral species, primarily by H3O+ and OH− as CI sources. Both positive and negative ions of the metals were observed as profiles of ion concentration versus distance along the flame axis by sampling the flames through a nozzle into a mass spectrometer. For yttrium, the observed ions include the YO+•nH2O (n = 0–3) series, and Y(OH)4−. With zirconium, they include the ZrO(OH)+•nH2O (n = 0–2) series, and ZrO(OH)3−. Those observed with niobium were the cations Nb(OH)3+ and Nb(OH)4+, and the single anion NbO2(OH)2−. For molybdenum, they include the cations MoO(OH)2+ and MoO(OH)3+, and the anions MoO3− and MoO3(OH)−. Not every ion was observed in each flame; the FL flame tended to favour the ions in higher oxidation states. Also, flame ions in higher oxidation states were emphasized for these second-row transition metals compared with their first-row counterparts. Some ions written as members of hydrate series may have structures different from those of simple hydrates; e.g., YO+•H2O = Y(OH)2+ and ZrO(OH)+•H2O = Zr(OH)3+, etc. The ion chemistry for the production of these ions by CI in flames is discussed in detail. Keywords: transition metals, ions, flame, gas phase, negative ions.


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