Fifty years have passed since the foundation of organometallic neptunium chemistry, and yet only a handful of complexes have been reported, and even fewer have been fully characterized. Yet, increasingly, combined synthetic/spectroscopic/computational studies are demonstrating how covalently bonding, soft, carbocyclic organometallic ligands provide an excellent platform for advancing the fundamental understanding of the differences in orbital contributions and covalency in f-block metal-ligand bonding. Understanding the subtleties is the key to the safe handling and separations of the highly radioactive nuclei. This review describes the complexes that have been synthesized to date and presents a critical assessment of the successes and difficulties in their analysis and the bonding information they have provided. Because of increasing recent efforts to start new Np-capable air-sensitive inorganic chemistry laboratories, the importance of radioactivity, the basics of Np decay and its ramifications (including the radiochemical synthesis of one organometallic compound), and the available anhydrous starting materials are also surveyed. The review also highlights a range of instances in which important differences in the chemical behavior between Np and its closest neighbors, uranium and plutonium, are found.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acs.chemrev.7b00192 | DOI Listing |
Inorg Chem
April 2023
Department of Chemistry, University of California Irvine, Irvine, California 92697, United States.
1,3,5-Trimethyl-1,3,5-triazacyclohexane (Metach) readily complexes uranium triiodide to form (Metach)UI. The complex is soluble in THF and arenes and can function as a source of UI to form organometallic U(III) complexes. When dissolved in pyridine (py), (Metach)UI forms (Metach)UI(py).
View Article and Find Full Text PDFInorg Chem
March 2020
Department of Chemistry, University of Nevada Reno, 1664 North Virginia Street, Reno, Nevada 89557-0216, United States.
Organometallic uranium complexes that can activate small molecules are well-known. In contrast, there are no known organometallic trans-uranium species capable of small-molecule transformations. Using density functional theory, we previously showed that changing actinide-ligand bonds from U-O groups to Np-N- (amide/imido) bonds makes redox small-molecule activation more energetically favorable for Np species.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
October 2019
Department of Chemistry, University of Missouri, Columbia, 601 S. College Avenue, Columbia, MO, 65211, USA.
To extend organoactinide chemistry beyond uranium, reported here is the first structurally characterized transuranic hydrocarbyl complex, Np[η -Me NC(H)C H ] (1), from reaction of NpCl (DME) with four equivalents of K[Me NC(H)C H ]. Unlike the U species, the neptunium analogue can be used to access other Np complexes. The reaction of 1 with three equivalents of HE C(2,6-Mes -C H ) (E=O, S) yields [(2,6-Mes -C H )CE ] Np(THF) , maintaining the trivalent oxidation state.
View Article and Find Full Text PDFInorg Chem
May 2019
Department of Chemistry , University of Nevada Reno, 1664 North Virginia Street , Reno , Nevada 89557-0216 , United States.
There is recent interest in organometallic complexes of the trans-uranium elements. However, preparation and characterization of such complexes are hampered by radioactivity and chemotoxicity issues as well as the air-sensitive and poorly understood behavior of existing compounds. As such, there are no examples of small-molecule activation via redox reactivity of organometallic trans-uranium complexes.
View Article and Find Full Text PDFChemistry
February 2019
European Commission-Joint Research Centre, Directorate for Nuclear Safety and Security-G. I. 5, Postfach 2340, 76125, Karlsruhe, Germany.
Recent developments and results from the organometallic chemistry of the actinides are reviewed. In the last one and a half years the structural data of about 15 organometallic complexes of transuranium actinides (Np or Pu) have been published, all involving π-ligands in the coordination sphere of the metal ion. On the basis of these data, a comparison of these molecules is presented.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!