VOLURAD

Single-molecule magnets based on the orbitally-degenerate spin centers and stable organic radicals complexes

 Coordinatore UNIVERSITE LYON 1 CLAUDE BERNARD 

 Organization address address: BOULEVARD DU 11 NOVEMBRE 1918 NUM43
city: VILLEURBANNE CEDEX
postcode: 69622

contact info
Titolo: Dr.
Nome: Javier
Cognome: Olaiz
Email: send email
Telefono: 33472697600
Fax: 33472697609

 Nazionalità Coordinatore France [FR]
 Totale costo 269˙096 €
 EC contributo 269˙096 €
 Programma FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call FP7-PEOPLE-2011-IIF
 Funding Scheme MC-IIF
 Anno di inizio 2012
 Periodo (anno-mese-giorno) 2012-07-23   -   2014-07-22

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITE LYON 1 CLAUDE BERNARD

 Organization address address: BOULEVARD DU 11 NOVEMBRE 1918 NUM43
city: VILLEURBANNE CEDEX
postcode: 69622

contact info
Titolo: Dr.
Nome: Javier
Cognome: Olaiz
Email: send email
Telefono: 33472697600
Fax: 33472697609

FR (VILLEURBANNE CEDEX) coordinator 269˙096.40

Mappa


 Word cloud

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

   storage    ground    single    magnetic    molecule    radicals    magnets    molecular    spin    anisotropy    structural    temperatures    magnetization    complexes    blocking    density    interactions    polynuclear    carriers    metal    ions    theoretical   

 Obiettivo del progetto (Objective)

'The finding some polynuclear complexes can behave like magnets on the molecular level attracted much attention, opening perspectives for their applications in processing devices or for high density information storage carriers. To manifest single-molecule magnet (SMM) behaviour a polynuclear complex should have a high-spin ground-state and strong negative anisotropy (D). The energy barrier, U, separating two spin orientations (up-down) is proportional to the product of │D│ and square of spin, S. Therefore the larger the D and S values are the higher the U barriers should be and the longer the magnetization might be blocked. However, such single-molecule magnetization is so far only observed at temperatures too low to allow an application. The project aims to rise the blocking temperature by increasing the U. Our approach is based on heterospin polynuclear complexes assembling involving orbitally-degenerated 4d, 5d metal centres (Os, Ru) and 3d metal ions or/and nitroxide radicals. If the utilisation of the first guaranties the strong anisotropy, the use of the stable radicals as ligands and bridges assures well isolated high spin ground-state owing to the strong exchange interactions between spin carriers. The synthesis work will be complemented with structural analysis and magnetic studies of these systems to elucidate the magnetic interactions as well the magnetic anisotropy in conjunction with theoretical magneto-structural analysis. A major goal of the project is to discover some rules for the rational design of polynuclear cluster systems with elevated blocking temperatures. The project results will document the coordination chemistry of 4d and 5d ions with nitroxides, a field lacking of fundamental results. The complexes will bring experimental opportunity to test and improve theoretical models. The project might be considered as a step toward molecular spintronics. Prototypes of devices could be envisioned if the right property shows up at liquid nitrogen.'

Introduzione (Teaser)

Single-molecule magnets (SMMs) could lead to high-density information storage based on spin flips in single molecules. Scientists developed new magnetic materials rationally designed to overcome current bottlenecks to widespread implementation.

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