Izvorni znanstveni članak
Gas Phase Ligation Kinetics of Metal Monocations with Pyrene
Snježana P. Kazazić
APA 6th Edition
Kazazić, S., Kazazić, S.P., Klasinc, L., Rožman, M. i Srzić, D. (2005). Gas Phase Ligation Kinetics of Metal Monocations with Pyrene. Croatica Chemica Acta, 78 (2), 269-274. Preuzeto s https://hrcak.srce.hr/21
MLA 8th Edition
Kazazić, Saša, et al. "Gas Phase Ligation Kinetics of Metal Monocations with Pyrene." Croatica Chemica Acta, vol. 78, br. 2, 2005, str. 269-274. https://hrcak.srce.hr/21. Citirano 05.07.2022.
Chicago 17th Edition
Kazazić, Saša, Snježana P. Kazazić, Leo Klasinc, Marko Rožman i Dunja Srzić. "Gas Phase Ligation Kinetics of Metal Monocations with Pyrene." Croatica Chemica Acta 78, br. 2 (2005): 269-274. https://hrcak.srce.hr/21
Kazazić, S., et al. (2005). 'Gas Phase Ligation Kinetics of Metal Monocations with Pyrene', Croatica Chemica Acta, 78(2), str. 269-274. Preuzeto s: https://hrcak.srce.hr/21 (Datum pristupa: 05.07.2022.)
Kazazić S, Kazazić SP, Klasinc L, Rožman M, Srzić D. Gas Phase Ligation Kinetics of Metal Monocations with Pyrene. Croatica Chemica Acta [Internet]. 2005 [pristupljeno 05.07.2022.];78(2):269-274. Dostupno na: https://hrcak.srce.hr/21
S. Kazazić, S.P. Kazazić, L. Klasinc, M. Rožman i D. Srzić, "Gas Phase Ligation Kinetics of Metal Monocations with Pyrene", Croatica Chemica Acta, vol.78, br. 2, str. 269-274, 2005. [Online]. Dostupno na: https://hrcak.srce.hr/21. [Citirano: 05.07.2022.]
The gas-phase ligation of M+ ions with pyrene is reviewed. The M+ (M = Al, K, V, Cr, Fe, Co, Ni, Cu, Nb, Mo, Ru, Ag, Sn, Ta, W, Re, Pt, Au, Hg, Pb, Bi and U) were produced by a single laser shot. Gaseous pyrene was already present in the Fourier transform mass spectrometer (FTMS). The reaction proceeded by consecutive ligations, sometimes accompanied by expulsion of a part (usually H2) of the ligand. Charge transfer (when the neutral metal has a higher ionization energy than the pyrene), pyrene dimerization, oxidation by residual oxygen, and protonation by ubiquitous water in the instrument may also take place. Reaction progression was followed by varying the delay time between the shot and the mass-spectrometric assay of the ions. If electronically-excited M+, which might have been produced by the laser pulse, was interfering with the reaction, these ions and their products were swept out of the FTMS chamber prior to initiation of the time delay specified above.
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