M
Marisa J. Monreal
Researcher at Los Alamos National Laboratory
Publications - 31
Citations - 884
Marisa J. Monreal is an academic researcher from Los Alamos National Laboratory. The author has contributed to research in topics: Uranium & Molten salt. The author has an hindex of 14, co-authored 27 publications receiving 811 citations. Previous affiliations of Marisa J. Monreal include California State University & University of California, Los Angeles.
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Journal ArticleDOI
A Weak Interaction between Iron and Uranium in Uranium Alkyl Complexes Supported by Ferrocene Diamide Ligands
TL;DR: In this paper, the existence of a donor-acceptor, weak interaction between iron and uranium has been shown, supported by ferrocene diamide ligands, along with corresponding cationic species.
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Synthesis and characterization of three-coordinate Ni(III)-imide complexes.
Vlad M. Iluc,Alexander J. M. Miller,John S. Anderson,Marisa J. Monreal,Mark P. Mehn,Gregory L. Hillhouse +5 more
TL;DR: A new family of low-coordinate nickel imides supported by 1,2-bis(di-tert-butylphosphino)ethane was synthesized and it was indicated that the unpaired electron is mostly localized on the imide nitrogen for the Ni(III) complexes.
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UI4(1,4-dioxane)2, [UCl4(1,4-dioxane)]2, and UI3(1,4-dioxane)1.5: Stable and Versatile Starting Materials for Low- and High-Valent Uranium Chemistry
Marisa J. Monreal,Robert K. Thomson,Thibault Cantat,Nicholas E. Travia,Brian L. Scott,Jaqueline L. Kiplinger +5 more
TL;DR: In this paper, the uranium(III) and uranium(IV) iodide complexes UI3(1,4-dioxane)1.5 and UI4(1.4-dimethyl iodide)2 have been easily prepared in high yield by reacting uranium turnings with a 1,4dioxANE solution of iodine under mild conditions.
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Redox processes in a uranium bis(1,1'-diamidoferrocene) complex.
TL;DR: Oxidation of a uranium(IV) bis(1,1'-diamidoferrocene) gives a compound which is best described as a mixed-valence bisferrocene complex in which uranium mediates the electronic communication.
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Scandium Alkyl Complexes Supported by a Ferrocene Diamide Ligand
TL;DR: In this paper, the scandium dimethylbenzyl complex Sc(fc[NSi(t-Bu)Me2]2] 2 ) was used as a starting material for the synthesis of the corresponding chloride-bridged dimer, (2-Cl)2, which, in turn, led to a Scandium bis(neo-pentyl) ate salt, Li[2-Np2].