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Reactive MALDI Mass Spectrometry of Saturated Hydrocarbons: A Theoretical Study

Published

Author(s)

William E. Wallace, Lewandowski Hans, Meier J. Robert

Abstract

Recently it has been shown that the cobaltocenium cation, prepared by the laser ablation of a CoCp(CO)2/fullerene matrix, may react with alkanes and polyethylenes in the gas phase via a dehydrogenation reaction to produce [Co(Cp)2(alkadiene)]+ ions without chain scission (W.E. Wallace, Chem. Commun. 2007, 4525-4527). To better understand these experimental observations density functional calculations were used to obtain the gas-phase binding energies and molecular structures of cobaltocenium, Co(Cp)2+, with 1,3-butadiene, 2,4 hexadiene and 2,3-hexadiene. Calculations were conducted for both cis and trans molecular configurations, in both singlet and triplet electronic states, and with a variety of cyclopentadienyl hapticities. For 1,3 butadiene the 18 electron rule would predict a [Co(η3 Cp)2(η4 1,3 butadiene)]+, however, the lowest energy structure, [Co(η5 Cp)2(η4 1,3 butadiene)]+, has a higher than expected cyclopentadienyl hapticity. In this structure a distance of nearly 0.5 nm between the metal core and the butadiene ligand leads to very little electron sharing. In turn, the lack of orbital overlap leads to a low enthalpy giving the cis butadiene complex a -3.1 kcal/mol binding energy and the trans-butadiene binding a -0.9 kcal/mol binding energy. These low binding energies lead to low levels of charged alkanes in the reactive MALDI process compromising the sensitivity of the method in agreement with experimental observations.
Citation
International Journal of Mass Spectrometry
Volume
292
Issue
1-3

Keywords

alkane, cobaltocene, dehydrogenation, density-functional theory, hydrocarbon, polymer

Citation

Wallace, W. , Hans, L. and Robert, M. (2010), Reactive MALDI Mass Spectrometry of Saturated Hydrocarbons: A Theoretical Study, International Journal of Mass Spectrometry, [online], https://tsapps.nist.gov/publication/get_pdf.cfm?pub_id=904785 (Accessed October 11, 2024)

Issues

If you have any questions about this publication or are having problems accessing it, please contact reflib@nist.gov.

Created May 1, 2010, Updated February 19, 2017