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Diarylformamides as a safe reservoir and room temperature source of ultra-pure CO for a 'green' rWGS reaction.
Hurtado, Royel; Lou, Lisha; Klerner, Lukas; Inaloo, Iman Dindarloo; Heineman, Frank W; Harder, Sjoerd; Schmid, Günter; Dorta, Romano.
Affiliation
  • Hurtado R; FAU Erlangen Nuremberg, chemistry&pharmacy, GERMANY.
  • Lou L; FAU Erlangen Nuremberg, dip, GERMANY.
  • Klerner L; FAU Erlangen Nuremberg, dip, GERMANY.
  • Inaloo ID; FAU Erlangen Nuremberg, dip, GERMANY.
  • Heineman FW; FAU Erlangen Nuremberg, dip, GERMANY.
  • Harder S; FAU Erlangen Nuremberg, dip, GERMANY.
  • Schmid G; Siemens Energy Global GmbH & Co KG, New Energy Business - Technology & Products, GERMANY.
  • Dorta R; Friedrich-Alexander-Universität Erlangen-Nürnberg: Friedrich-Alexander-Universitat Erlangen-Nurnberg, Chemie und Pharmazie, Egerlandstr. 1, Anorg. Chemie, 91058, Erlangen, GERMANY.
ChemSusChem ; : e202400308, 2024 Jun 14.
Article in En | MEDLINE | ID: mdl-38875288
ABSTRACT
Diarylformamides are shown to be a safe reservoir and source of CO. Perfectly selective decarbonylation is achieved in solution at room temperature with potassium and cesium diarylamide catalysts. Moreover, solvent-free decarbonylations may be run either in a diphenylformamide melt at 70 ºC or, when the bisformamide 9 is used, in the solid state at 88 ºC in virtue of its improved atom economy. These These simple and practical transition-metal-free reactions afford ultra-pure (i.e. dry and solvent-free) CO at moderate temperatures and the byproduct diarylamines are recycled as pure compounds. In the absence of catalysts, diarylformamides 1 and 9 are long-term stable at > 200 ºC.  DFT-calculations indicate a reaction pathway with a rate-determining deprotonation of Ph2NC(O)H and a barrier-free CO elimination from Ph2NC(O)-.
Key words

Full text: 1 Database: MEDLINE Language: En Year: 2024 Type: Article

Full text: 1 Database: MEDLINE Language: En Year: 2024 Type: Article