Explore the words cloud of the RadMag project. It provides you a very rough idea of what is the project "RadMag" about.
The following table provides information about the project.
Coordinator |
THE UNIVERSITY OF SUSSEX
Organization address contact info |
Coordinator Country | United Kingdom [UK] |
Total cost | 1˙584˙202 € |
EC max contribution | 1˙584˙202 € (100%) |
Programme |
1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC)) |
Code Call | ERC-2014-CoG |
Funding Scheme | ERC-COG |
Starting year | 2015 |
Duration (year-month-day) | from 2015-09-01 to 2020-08-31 |
Take a look of project's partnership.
# | ||||
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1 | THE UNIVERSITY OF SUSSEX | UK (BRIGHTON) | coordinator | 1˙050˙608.00 |
2 | THE UNIVERSITY OF MANCHESTER | UK (MANCHESTER) | participant | 516˙439.00 |
3 | KATHOLIEKE UNIVERSITEIT LEUVEN | BE (LEUVEN) | participant | 17˙153.00 |
Single-molecule magnets (SMMs) display magnetic hysteresis that is molecular in origin, and these materials have huge potential to be developed as nano-scale devices. The big challenge is to create SMMs that function without the need for liquid-helium cooling.
This project will develop new SMMs that combine the strong magnetic anisotropy of lanthanide ions with a series of novel radical ligands. Our innovative SMMs will have controllable molecular and electronic structures, which will ultimately enable hysteresis at unprecedented temperatures.
Highly unusual di- and tri-metallic Ln-SMMs are proposed in which the metals are bridged by radicals with heavy Group 15 (phosphorus-bismuth) and Group 16 (sulphur-tellurium) donor atoms. Trimetallic SMMs will also be based on hexaazatriphenylene (HAT) radicals, and dimetallic SMMs will also be based on nindigo radicals, both of which are nitrogen-donor ligands.
The SMM field is dominated by systems with diamagnetic ligands. Our radical ligands have never been used in SMM studies: their diffuse unpaired spin provides a way of switching off the quantum tunnelling mechanisms that otherwise prevent hysteresis. We will exploit the rich electrochemistry of the target ligands: heavy p-block radicals have huge spin densities on the donor atoms; HAT radicals can have up to three unpaired electrons; reduced or oxidized nindigo radicals allow access to redox-switchable SMMs. In the HAT-bridged SMMs, the use of ligands with more than one unpaired electron is unprecedented. The heavy p-block ligands are themselves are novel.
The PI’s approach to SMMs has already established new directions in lanthanide chemistry and in molecular magnetism. He now proposes a new, radical approach to SMMs with potential to re-define the state of the art, and to extend the frontiers of a vibrant multi-disciplinary field. Achieving the aims will provide a major step towards using SMMs for applications at practical temperatures.
year | authors and title | journal | last update |
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2017 |
Thomas Pugh, Nicholas F. Chilton, Richard A. Layfield Antimony-ligated dysprosium single-molecule magnets as catalysts for stibine dehydrocoupling published pages: 2073-2080, ISSN: 2041-6520, DOI: 10.1039/C6SC04465D |
Chem. Sci. 8/3 | 2019-05-30 |
2017 |
Fu-Sheng Guo, Richard A. Layfield Strong direct exchange coupling and single-molecule magnetism in indigo-bridged lanthanide dimers published pages: 3130-3133, ISSN: 1359-7345, DOI: 10.1039/C7CC01046J |
Chem. Commun. 53/21 | 2019-05-30 |
2016 |
Thomas Pugh, Nicholas F. Chilton, Richard A. Layfield A Low-Symmetry Dysprosium Metallocene Single-Molecule Magnet with a High Anisotropy Barrier published pages: 11082-11085, ISSN: 1433-7851, DOI: 10.1002/anie.201604346 |
Angewandte Chemie International Edition 55/37 | 2019-05-30 |
2016 |
Richard Grindell, Veacheslav Vieru, Thomas Pugh, Liviu F. Chibotaru, Richard A. Layfield Magnetic frustration in a hexaazatrinaphthylene-bridged trimetallic dysprosium single-molecule magnet published pages: 16556-16560, ISSN: 1477-9226, DOI: 10.1039/C6DT01763K |
Dalton Trans. 45/42 | 2019-05-30 |
2016 |
Jani O. Moilanen, Nicholas F. Chilton, Benjamin M. Day, Thomas Pugh, Richard A. Layfield Strong Exchange Coupling in a Trimetallic Radical-Bridged Cobalt(II)-Hexaazatrinaphthylene Complex published pages: 5521-5525, ISSN: 1433-7851, DOI: 10.1002/anie.201600694 |
Angewandte Chemie International Edition 55/18 | 2019-05-30 |
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