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Sulfur monoxide thermal release from an anthracene-based precursor, spectroscopic identification, and transfer reactivity.
Joost, Maximilian; Nava, Matthew; Transue, Wesley J; Martin-Drumel, Marie-Aline; McCarthy, Michael C; Patterson, David; Cummins, Christopher C.
Afiliação
  • Joost M; Department of Chemistry, Massachusetts Institute of Technology, Cambridge, MA 02139.
  • Nava M; Department of Chemistry, Massachusetts Institute of Technology, Cambridge, MA 02139.
  • Transue WJ; Department of Chemistry, Massachusetts Institute of Technology, Cambridge, MA 02139.
  • Martin-Drumel MA; Institut des Sciences Moléculaires d'Orsay, CNRS, Université Paris-Sud, Université Paris-Saclay, 91405 Orsay, France.
  • McCarthy MC; Harvard-Smithsonian Center for Astrophysics, Atomic and Molecular Physics Division, Cambridge, MA 02138.
  • Patterson D; Department of Physics, Harvard University, Cambridge, MA 02138.
  • Cummins CC; Department of Chemistry, Massachusetts Institute of Technology, Cambridge, MA 02139; ccummins@mit.edu.
Proc Natl Acad Sci U S A ; 115(23): 5866-5871, 2018 06 05.
Article em En | MEDLINE | ID: mdl-29773708
Sulfur monoxide (SO) is a highly reactive molecule and thus, eludes bulk isolation. We report here on synthesis and reactivity of a molecular precursor for SO generation, namely 7-sulfinylamino-7-azadibenzonorbornadiene (1). This compound has been shown to fragment readily driven by dinitrogen expulsion and anthracene formation on heating in the solid state and in solution, releasing SO at mild temperatures (<100 °C). The generated SO was detected in the gas phase by MS and rotational spectroscopy. In solution, 1 allows for SO transfer to organic molecules as well as transition metal complexes.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Revista: Proc Natl Acad Sci U S A Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Revista: Proc Natl Acad Sci U S A Ano de publicação: 2018 Tipo de documento: Article