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Metallacyclic actinide catalysts for dinitrogen conversion to ammonia and secondary amines.

Polly L ArnoldTatsumi OchiaiFrancis Y T LamRory P KellyMegan L SeymourLaurent Maron
Published in: Nature chemistry (2020)
Chemists have spent over a hundred years trying to make ambient temperature/pressure catalytic systems that can convert atmospheric dinitrogen into ammonia or directly into amines. A handful of successful d-block metal catalysts have been developed in recent years, but even binding of dinitrogen to an f-block metal cation is extremely rare. Here we report f-block complexes that can catalyse the reduction and functionalization of molecular dinitrogen, including the catalytic conversion of molecular dinitrogen to a secondary silylamine. Simple bridging ligands assemble two actinide metal cations into narrow dinuclear metallacycles that can trap the diatom while electrons from an externally bound group 1 metal, and protons or silanes, are added, enabling dinitrogen to be functionalized with modest but catalytic yields of six equivalents of secondary silylamine per molecule at ambient temperature and pressure.
Keyphrases
  • particulate matter
  • air pollution
  • ionic liquid
  • highly efficient
  • room temperature
  • crystal structure
  • single molecule
  • mass spectrometry
  • quantum dots
  • metal organic framework
  • carbon dioxide
  • simultaneous determination