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  Light-Induced Radical Formation and Isomerization of an Aromatic Thiol in Solution Followed by Time-Resolved X-ray Absorption Spectroscopy at the Sulfur K-Edge

Ochmann, M., von Ahnen, I., Cordones, A. A., Hussain, A., Lee, J. H., Hong, K., et al. (2017). Light-Induced Radical Formation and Isomerization of an Aromatic Thiol in Solution Followed by Time-Resolved X-ray Absorption Spectroscopy at the Sulfur K-Edge. Journal of the American Chemical Society, 139(13), 4797-4804. doi:10.1021/jacs.6b12992.

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 Creators:
Ochmann, Miguel1, 2, 3, Author           
von Ahnen, Inga2, Author
Cordones, Amy A.4, Author
Hussain, Abid1, 2, 3, Author           
Lee, Jae Hyuk4, Author
Hong, Kiryong4, 5, Author
Adamczyk, Katrin2, 3, Author
Vendrell, Oriol6, Author
Kim, Tae Kyu5, Author
Schoenlein, Robert W.4, Author
Huse, Nils2, 3, Author
Affiliations:
1International Max Planck Research School for Ultrafast Imaging & Structural Dynamics (IMPRS-UFAST), Max Planck Institute for the Structure and Dynamics of Matter, Max Planck Society, ou_2266714              
2Department of Physics, University of Hamburg and Center for Free Electron Laser Science, 22761 Hamburg, Germany, ou_persistent22              
3Max Planck Institute for the Structure and Dynamics of Matter, 22761 Hamburg, Germany, ou_persistent22              
4Ultrafast X-ray Science Lab, Chemical Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States, ou_persistent22              
5Department of Chemistry and Chemistry Institute of Functional Materials, Pusan National University, Busan 46241, South Korea, ou_persistent22              
6Center for Free-Electron Laser Science, DESY and The Hamburg Centre for Ultrafast Imaging, 22607 Hamburg, Germany, ou_persistent22              

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 Abstract: We applied time-resolved sulfur-1s absorption
spectroscopy to a model aromatic thiol system as a promising method for tracking chemical reactions in solution. Sulfur-1s absorption spectroscopy allows tracking multiple sulfur species with a time resolution of ∼70 ps at synchrotron radiation facilities. Experimental transient spectra combined with high-level electronic structure theory allow identification of a radical and two thione isomers, which are generated upon illumination with 267 nm radiation. Moreover, the regioselectivity of the
thione isomerization is explained by the resulting radical frontier orbitals. This work demonstrates the usefulness and potential of time-resolved sulfur-1s absorption spectroscopy for tracking multiple chemical reaction pathways and transient products of sulfur-containing molecules in solution.

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Language(s): eng - English
 Dates: 2016-12-222017-02-202017-02-20
 Publication Status: Issued
 Pages: 8
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1021/jacs.6b12992
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Title: Journal of the American Chemical Society
  Other : J. Am. Chem. Soc.
  Abbreviation : JACS
Source Genre: Journal
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Publ. Info: Washington, DC : American Chemical Society
Pages: - Volume / Issue: 139 (13) Sequence Number: - Start / End Page: 4797 - 4804 Identifier: ISSN: 0002-7863
CoNE: https://pure.mpg.de/cone/journals/resource/954925376870