Skip to main navigation Skip to search Skip to main content

Gas-Phase Coordination of Phosphine-Chalcogenides to the Uranyl Cation

  • Christopher A Zarzana
  • , JungSoo Kim
  • , Brittany Dawn Marie Hodges
  • , Jonathan Martens
  • , W. C. M. Berden
  • , Cristian Celis-Barros
  • , Thomas Albrecht-Schoenzart
  • , Madeline Martelles

Research output: Contribution to conferencePoster

Abstract

It is generally believed that actinides exhibit an increased covalency in bonding to soft-donor atoms such as nitrogen and sulfur compared to the lanthanides. The explanation is that the greater spatial extent of the 5f orbitals in the actinides compared to the 4f orbitals in the lanthanides accounts for this behavior. However, recent computational studies on lanthanide and actinide complexes with sulfur-donor atom ligands suggest that while calculated metrics of bond covalency could increase for actinide complexes with sulfur ligands, the overall stability of the complexes decreased. While many studies of actinide covalency were conducted in the condensed phases, this work investigates the intrinsic interaction between actinides and soft-donor ligands compared with oxygen in the gas phase.
Original languageEnglish
StatePublished - 2024
Event72nd ASMS Conference on Mass Spectrometry and Allied Topics - Anaheim, United States
Duration: Jun 2 2024Jun 6 2024

Conference

Conference72nd ASMS Conference on Mass Spectrometry and Allied Topics
Country/TerritoryUnited States
CityAnaheim
Period06/2/2406/6/24

Keywords

  • 37 - INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY
  • 38 - RADIATION CHEMISTRY, RADIOCHEMISTRY, AND NUCLEAR CHEMISTRY
  • uranyl
  • gas-phase
  • triphenylphosphine chalcogenides
  • IRMPD
  • mass spectrometry
  • CID

INL Publication Number

  • INL/CON-24-76430
  • 188611

Fingerprint

Dive into the research topics of 'Gas-Phase Coordination of Phosphine-Chalcogenides to the Uranyl Cation'. Together they form a unique fingerprint.

Cite this