2017
DOI: 10.1021/acs.jpca.7b04395
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X-ray Absorption Spectroscopy of Aliphatic Organic Sulfides

Abstract: Organic sulfides, sometimes called thioethers, are important in a variety of materials with diverse roles in biology and the environment. They also contribute a significant proportion of the sulfur in fossil fuels. We have studied a range of aliphatic sulfides using a combination of sulfur K-edge X-ray absorption spectroscopy and density functional theory calculations. We show that the sulfur K-edge near-edge X-ray absorption spectra of aliphatic organic sulfides comprise two intense transitions in the near-ed… Show more

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Cited by 11 publications
(25 citation statements)
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References 40 publications
(64 reference statements)
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“…The higher energy intense transition shows substantial S–C σ* character (LUMO+3), also involving the aromatic ring. The two intense groups of transitions are related to those of the alkyl sulfides, but with the order reversed . A similar phenomenon has been noted by Mijovilovich et al for benzyl sulfide and benzyl phenyl sulfide …”
Section: Resultssupporting
confidence: 81%
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“…The higher energy intense transition shows substantial S–C σ* character (LUMO+3), also involving the aromatic ring. The two intense groups of transitions are related to those of the alkyl sulfides, but with the order reversed . A similar phenomenon has been noted by Mijovilovich et al for benzyl sulfide and benzyl phenyl sulfide …”
Section: Resultssupporting
confidence: 81%
“…Sulfur K-edge X-ray absorption spectroscopy (XAS) has been used previously to probe the sulfur speciation in complex specimens, including fossil fuels. Our previous work has demonstrated the technique’s sensitivity to a series of thiophenes including solution tautomers, , to organic disulfides, and to a range of different cyclic and acyclic alkyl sulfides . Here we report upon the sulfur K-edge XAS of both aryl and aryl–alkyl sulfides and show how these differ from those of the alkyl sulfides …”
Section: Introductionmentioning
confidence: 84%
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“…Functional group Oxidation state (Waldo et al 1991;Xia et al 1998;Vairavamurthy 1998) (George et al 2014;Pickering et al 2016;Cotelesage et al 2017).…”
Section: Compoundmentioning
confidence: 99%