UNCLE

UNCLE: Uranium in Non-Conventional Ligand Environments

 Coordinatore THE UNIVERSITY OF NOTTINGHAM 

Spiacenti, non ci sono informazioni su questo coordinatore. Contattare Fabio per maggiori infomrazioni, grazie.

 Nazionalità Coordinatore United Kingdom [UK]
 Totale costo 999˙996 €
 EC contributo 999˙996 €
 Programma FP7-IDEAS-ERC
Specific programme: "Ideas" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call ERC-2009-StG
 Funding Scheme ERC-SG
 Anno di inizio 2010
 Periodo (anno-mese-giorno) 2010-02-01   -   2014-09-30

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    THE UNIVERSITY OF NOTTINGHAM

 Organization address address: University Park
city: NOTTINGHAM
postcode: NG7 2RD

contact info
Titolo: Dr.
Nome: Stephen Taylor
Cognome: Liddle
Email: send email
Telefono: +44(0)115 8467167
Fax: +44(0)115 951 3563

UK (NOTTINGHAM) hostInstitution 999˙996.00
2    THE UNIVERSITY OF NOTTINGHAM

 Organization address address: University Park
city: NOTTINGHAM
postcode: NG7 2RD

contact info
Titolo: Mr.
Nome: Paul
Cognome: Cartledge
Email: send email
Telefono: +44 115 951 5679
Fax: +44 115 951 3633

UK (NOTTINGHAM) hostInstitution 999˙996.00

Mappa


 Word cloud

Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.

clean    unknown    gallium    bonds    actinide    pi    reactivity    table    uranium    chemistry    periodic    ligands    transition    conventional       metal    nuclear    waste   

 Obiettivo del progetto (Objective)

'Metal-metal bonds are fundamental to generating step-changes in our knowledge because the periodic table is composed mainly of metals. The PI has recently made a breakthrough by making the first covalent uranium-gallium bond which exhibits sigma- and pi-donation from gallium to uranium. It is a direct model for the unknown isolobal uranium(IV)-CO " unit, and is very significant to explaining why the widely used N-heterocyclic carbenes are so good at supporting transition metal catalysts and extracting uranium from solutions containing lanthanides such as found in nuclear waste clean up. This result opens the way to non-conventional ligand complexes of uranium and the previous limitation of conventional halide or C-, N-, or O-donor ligands for uranium will be overcome using non-conventional transition metal ligands to establish a new field of uranium-metal bonds. This work will deliver new compounds which will take our understanding of actinide structure, bonding, magnetism and reactivity to a higher platform of understanding, thus bringing an area of the periodic table, which lags behind all others, up to speed and beyond. This project will deliver a whole new field of actinide chemistry, provide unique and hitherto unknown atom efficient reactivity patterns, generate models for the too-hot-to-handle neptunium and plutonium which are present in nuclear waste, and precipitate new ways of thinking about how to solve nuclear waste clean up. This will induce a paradigm shift in uranium chemistry and will be directly included in textbooks of the future. This project will deliver mobile, high calibre, inter-/multi-disciplinary researchers, reversing a strategic skills shortage and retaining them for future employment and benefit to science, industry, and society in Europe.'

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