Juan Diwu University of Notre Dame, Notre Dame, in 46556 Wednesday, Nov

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Juan Diwu University of Notre Dame, Notre Dame, in 46556 Wednesday, Nov

Glenn T. Seaborg Center Special Seminar Using Phosphonates to Probe Structural Differences Between the Transuranium Elements and Their Proposed Surrogates Juan Diwu University of Notre Dame, Notre Dame, IN 46556 Wednesday, Nov. 16, 5:10 p.m., Bldg. 70A, Rm. 3377 Transuranium elements, especially plutonium, play a special role in advanced technological societies, being responsible for both significant electrical energy production and nuclear weapon arsenals. However, owing to their radioactivity and toxicity, the related research is severely restricted. One of the outcomes of this is the use of less toxic and less or non-radioactive surrogates for transuranium elements. These include early transition metals, especially Zr4+, lanthanides (e.g. Ce4+ and Eu3+), and the early actinides, thorium and uranium. The most central question is: do these surrogates actually mimic the chemistry of transuranics? In this work, we focused on the actinide diphosphonate system, for their importance in nuclear remediation and actinide separation processes, to answer the aforementioned question. Recently, we have successfully crystallized trivalent, tetravalent and hexavalent transuranic diphosphonate compounds as well as their surrogates. In the trivalent series, plutonium and americium compounds were synthesized. Most of the lanthanide compounds were also crystallized for the purpose of comparison. In the tetravalent series, Ce4+ and Pu4+ were mainly explored, along with Th4+, U4+ and Np4+. The structural types vary from zero-dimensional clusters, one-demensional chains, to three-dimensional frameworks. PuO22+ phenylenediphosphonate is the only transuranic hexavalent compound that we were able to synthesize. There are a number of uranyl phases that can be compared to. Additionally, in order to study the interaction between different elements, experiments of mixing Np4+ and Pu4+ with both each other and with Ce4+ or UO22+ were conducted, which yielded both ordered and disordered heterobimetallic 4f/5f and 5f/5f phosphonates. In most of the series, significant differences are found between transuranium elements and their surrogates. There are examples where isostructural series exist, but transuranium elements still have their unique properties, which are not mimicked by the surrogates. Host: Ken Raymond (510) 642-7219 [email protected] | Admin. Assistant: Susan Meux (510) 486-6145 Ernest Orlando Lawrence Berkeley National Laboratory | One Cyclotron Road, Berkeley, California 94720 .

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Rational Ligand Design for U(VI) and Pu(IV)* by Géza Szigethy BA
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NJC Accepted Manuscript This is an Accepted Manuscript, which has been through the Royal Society of Chemistry peer review process and has been accepted for publication. Accepted Manuscripts are published online shortly after acceptance, before technical editing, formatting and proof reading. Using this free service, authors can make their results available to the community, in citable form, before we publish the edited article. We will replace this Accepted Manuscript with the edited and formatted Advance Article as soon as it is available. You can find more information about Accepted Manuscripts in the Information for Authors. Please note that technical editing may introduce minor changes to the text and/or graphics, which may alter content. The journal’s standard Terms & Conditions and the Ethical guidelines still apply. In no event shall the Royal Society of Chemistry be held responsible for any errors or omissions in this Accepted Manuscript or any consequences arising from the use of any information it contains. www.rsc.org/njc Page 1 of 3 New Journal of Chemistry New Journal of Chemistry RSCPublishing The structure determination of uranocene and the first COT lanthanide complexes Cite this: DOI: 10.1039/x0xx00000x a Kenneth N. Raymond Received 00th January 2012, Accepted 00th January 2012 DOI: 10.1039/x0xx00000x www.rsc.org/ Manuscript This paper results from my introductory talk at the attention in the general organometallic community, since it was the symposium “Frontiers of Organo-f-Element Chemistry.” first representative of an entirely new class of π-bonded sandwich Although my active research in organoactinide and - complexes.” lanthanide chemistry ended early in my career, it led to an interest in actinide coordination chemistry that continues to My involvement in this chemistry began in the first year or so of my this day; I am a member of the actinide research group of the appointment as an assistant professor.
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