Vanadium oxide anion cluster reactions with methyl isobutyrate and methyl methacrylate monomer and dimer: a study by FT/ICR mass spectrometry

Citation
A. Dinca et al., Vanadium oxide anion cluster reactions with methyl isobutyrate and methyl methacrylate monomer and dimer: a study by FT/ICR mass spectrometry, INT J MASS, 183, 1999, pp. 73-84
Citations number
52
Categorie Soggetti
Spectroscopy /Instrumentation/Analytical Sciences
Journal title
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY
ISSN journal
13873806 → ACNP
Volume
183
Year of publication
1999
Pages
73 - 84
Database
ISI
SICI code
1387-3806(19990301)183:<73:VOACRW>2.0.ZU;2-E
Abstract
Laser ablation of vanadium pentoxide (V2O5) powder produces VO3-, V2O5-, V3 O7-, V3O8-, and V4O10- cluster ions which have subsequently been reacted wi th methyl isobutyrate, methyl methacrylate monomer and its dimer in the ion cell region of a Fourier transform ion cyclotron resonance mass spectromet er. Gas phase ion/molecule chemistry has revealed that reactivity decreases with increased mass of the vanadium oxide cluster anions. VO3-, V2O5-, and V3O7- ions react with the three reagents, methyl isobutyrate, methyl metha crylate and its dimer, respectively, either by addition of a whole reagent molecule or an associated fragment. All products formed are a result of par allel processes. V4O10- undergoes no reaction for reaction times of up to 5 00 s, while V3O8- adds a water molecule. Although the ions possess a net ne gative charge, the reactive site toward electron rich reagents such as meth yl isobutyrate, methyl methacrylate and its dimer is the under-coordinated vanadium atom. This observation is supported by the lack of reactivity towa rd the studied reagents by those anions (V3O8- and V4O10-) whose most likel y stable structures contain fully coordinated vanadium atoms. (C) 1999 Else vier Science B.V.