Loading…

f‐ block MOFs: A Pathway to Heterometallic Transuranics

Abstract A novel series of heterometallic f ‐block‐frameworks including the first examples of transuranic heterometallic 238 U/ 239 Pu‐metal–organic frameworks (MOFs) and a novel monometallic 239 Pu‐analog are reported. In combination with theoretical calculations, we probed the kinetics and thermod...

Full description

Saved in:
Bibliographic Details
Published in:Angewandte Chemie (International ed.) 2022-12, Vol.62 (5)
Main Authors: Park, Kyoung Chul, Kittikhunnatham, Preecha, Lim, Jaewoong, Thaggard, Grace C., Liu, Yuan, Martin, Corey R., Leith, Gabrielle A., Toler, Donald J., Ta, An T., Birkner, Nancy, Lehman‐Andino, Ingrid, Hernandez‐Jimenez, Alejandra, Morrison, Gregory, Amoroso, Jake W., zur Loye, Hans‐Conrad, DiPrete, Dave P., Smith, Mark D., Brinkman, Kyle S., Phillpot, Simon R., Shustova, Natalia B.
Format: Article
Language:English
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Abstract A novel series of heterometallic f ‐block‐frameworks including the first examples of transuranic heterometallic 238 U/ 239 Pu‐metal–organic frameworks (MOFs) and a novel monometallic 239 Pu‐analog are reported. In combination with theoretical calculations, we probed the kinetics and thermodynamics of heterometallic actinide(An)‐MOF formation and reported the first value of a U‐to‐Th transmetallation rate. We concluded that formation of uranyl species could be a driving force for solid‐state metathesis. Density of states near the Fermi edge, enthalpy of formation, band gap, proton affinity, and thermal/chemical stability were probed as a function of metal ratios. Furthermore, we achieved 97 % of the theoretical maximum capacity for An‐integration. These studies shed light on fundamental aspects of actinide chemistry and also foreshadow avenues for the development of emerging classes of An‐containing materials, including radioisotope thermoelectric generators or metalloradiopharmaceuticals.
ISSN:1433-7851
1521-3773