From mass to structure: an aromaticity index for high‐resolution mass data of natural organic matter

Rapid Communications in Mass Spectrometry - Tập 20 Số 5 - Trang 926-932 - 2006
Boris Koch1, Thorsten Dittmar2
1Alfred-Wegener-Institut für Polar- und Meeresforschung, Am Handelshafen 12, 27570 Bremerhaven, Germany
2Florida State University, Department of Oceanography, OSB 311, Tallahassee, FL 32306-4320, USA

Tóm tắt

AbstractRecent progress in Fourier transform ion cyclotron resonance mass spectrometry (FTICRMS) has provided extensive molecular mass data for complex natural organic matter (NOM). Structural information can be deduced solely from the molecular masses for ions with extreme molecular element ratios, in particular low H/C ratios, which are abundant in thermally altered NOM (e.g. black carbon). In this communication we propose a general aromaticity index (AI) and two threshold values as unequivocal criteria for the existence of either aromatic (AI > 0.5) or condensed aromatic structures (AI ≥ 0.67) in NOM. AI can be calculated from molecular formulae which are derived from exact molecular masses of naturally occurring compounds containing C, H, O, N, S and P, and is especially useful for substances with aromatic cores and few alkylations. In order to test the validity of our model index, AI is applied to FTICRMS data of a NOM deep‐water sample from the Weddell Sea (Antarctica), a fulvic acid standard, and an artificial dataset of all theoretically possible molecular formulae. For graphical evaluation a ternary plot is suggested for four‐dimensional data representation. The proposed aromaticity index is a step towards structural identification of NOM and the molecular identification of polyaromatic hydrocarbons in the environment. Copyright © 2006 John Wiley & Sons, Ltd.

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Tài liệu tham khảo

Hertkorn N, 2005, Earth and Environmental Sciences, 391

10.1038/330246a0

Benner R, 2002, Biogeochemistry of Marine Dissolved Organic Matter, 71

10.1021/ac020019f

10.1021/ac0108313

10.1016/S0146-6380(01)00149-8

10.1021/ac026106p

10.1016/j.gca.2005.02.027

10.1021/ci960048p

10.1016/0040-4020(76)80049-X

10.1016/0003-2670(95)00291-7

10.1021/ac034415p

10.1016/j.marchem.2004.06.042

10.1021/es030124m

Dittmar T, 2006, Mar. Chem.

10.1016/j.orggeochem.2004.04.004

10.1007/s00114-004-0550-8

HatcherPG HockadayWC GrannasAM KimS.American Chemical Society Abstracts of the 230th National Meeting 2005.