Abstract

AbstractTo extend organoactinide chemistry beyond uranium, reported here is the first structurally characterized transuranic hydrocarbyl complex, Np[η4‐Me2NC(H)C6H5]3 (1), from reaction of NpCl4(DME)2 with four equivalents of K[Me2NC(H)C6H5]. Unlike the UIII species, the neptunium analogue can be used to access other NpIII complexes. The reaction of 1 with three equivalents of HE2C(2,6‐Mes2‐C6H3) (E=O, S) yields [(2,6‐Mes2‐C6H3)CE2]3Np(THF)2, maintaining the trivalent oxidation state.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call