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Equilibrium ^2H/^1H fractionation in organic molecules: III. Cyclic ketones and hydrocarbons

Wang, Ying and Sessions, Alex L. and Nielsen, Robert J. and Goddard, William A., III (2013) Equilibrium ^2H/^1H fractionation in organic molecules: III. Cyclic ketones and hydrocarbons. Geochimica et Cosmochimica Acta, 107 . pp. 82-95. ISSN 0016-7037. doi:10.1016/j.gca.2013.01.001.

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Quantitative interpretation of stable hydrogen isotope ratios (^2H/^1H) in organic compounds is greatly aided by knowledge of the relevant equilibrium fractionation factors (ε_(eq)). Previous efforts have combined experimental measurements and hybrid Density Functional Theory (DFT) calculations to accurately predict equilibrium fractionations in linear (acyclic) organic molecules ( Wang et al., 2009a and Wang et al., 2009b), but the calibration produced by that study is not applicable to cyclic compounds. Here we report experimental measurements of equilibrium ^2H/^1H fractionation in six cyclic ketones, and use those data to evaluate DFT calculations of fractionation in diverse monocyclic and polycyclic compounds commonly found in sedimentary organic matter and petroleum. At 25, 50, and 75 °C, the experimentally measured ε_(eq) values for secondary and tertiary H_α in isotopic equilibrium with water are in the ranges of −130‰ to −150‰ and +10‰ to −40‰ respectively. Measured data are similar to DFT calculations of εeq for axial H_α but not equatorial H_α. In tertiary C_α positions with methyl substituents, this can be understood as a result of the methyl group forcing H_α atoms into a dominantly axial position. For secondary C_α positions containing both axial and equatorial H_α atoms, we propose that axial H_α exchanges with water significantly faster than the equatorial H_α does, due to the hyperconjugation-stabilized transition state. Interconversion of axial and equatorial positions via ring flipping is much faster than isotopic exchange at either position, and as a result the steady-state isotopic composition of both H’s is strongly weighted toward that of axial H_α. Based on comparison with measured ε_(eq) values, a total uncertainty of 10–30‰ remains for theoretical ε_(eq) values. Using DFT, we systematically estimated the ε_(eq) values for individual H positions in various cyclic structures. By summing over all individual H positions, the molecular equilibrium fractionation was estimated to be −75‰ to −95‰ for steroids, −90‰ to −105‰ for hopanoids, and −65‰ to −100‰ for typical cycloparaffins between 0 and 100 °C relative to water. These are distinct from the typical biosynthetic fractionations of −150‰ to −300‰, but are similar to equilibrium fractionations for linear hydrocarbons (Wang et al., 2009b). Thus post-burial H exchange will generally remove the ∼50–100‰ biosynthetic fractionations between cyclic isoprenoid and n-alkyl lipid molecules, which can be used to evaluate the extent of H exchange in sedimentary organic matter and oils.

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Sessions, Alex L.0000-0001-6120-2763
Nielsen, Robert J.0000-0002-7962-0186
Goddard, William A., III0000-0003-0097-5716
Additional Information:© 2013 Elsevier Ltd. Received 18 February 2012; accepted in revised form 1 January 2013; available online 12 January 2013. We thank Dr. Arndt Schimmelmann for the analysis of 2H-enriched organic standards employed here. We also acknowledge Dr. George Cody and Dr. Thomas Miller for helpful discussions and Lichun Zhang for help in the lab. This work was supported by National Science Foundation (NSF) Grant #EAR-0645502 to ALS. Associate editor: Edwin Schauble.
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Official Citation:Ying Wang, Alex L. Sessions, Robert J. Nielsen, William A. Goddard III, Equilibrium 2H/1H fractionation in organic molecules: III. Cyclic ketones and hydrocarbons, Geochimica et Cosmochimica Acta, Volume 107, 15 April 2013, Pages 82-95, ISSN 0016-7037, 10.1016/j.gca.2013.01.001. (
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:37824
Deposited By: Ruth Sustaita
Deposited On:09 Apr 2013 18:23
Last Modified:09 Nov 2021 23:31

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