The effect of hydrosulphurization on stable carbon isotopic compositions of free and sulphur-bound lipids

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Scientific paper

1-Decene was subjected to hydrosulphurization under phase-transfer conditions at room temperature. Compound-specific isotope analysis revealed that 1-decene becomes enriched in 13 C with increasing yields of sulphurization whilst the sulphur compounds formed are initially depleted in 13 C compared to the starting substrate. The average carbon isotopic fractionation effect of the reaction on the two carbon atoms involved is ca. -20 . Sedimentary sulphur compounds, however, do not show this fractionation effect indicating that either a different sulphurization reaction with different isotope effects has occurred or that functionalized lipids may have been fully sulphurized.

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