EPSRC Reference: |
EP/E041337/1 |
Title: |
Synthesis beyond the redox-active tetrathiafulvalene (TTF) molecule: From a topological control in TTF-based macrocycles, towards functional s |
Principal Investigator: |
Skabara, Professor PJ |
Other Investigators: |
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Researcher Co-Investigators: |
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Project Partners: |
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Department: |
Pure and Applied Chemistry |
Organisation: |
University of Strathclyde |
Scheme: |
Standard Research |
Starts: |
31 October 2007 |
Ends: |
29 April 2009 |
Value (£): |
29,761
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EPSRC Research Topic Classifications: |
Chemical Synthetic Methodology |
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EPSRC Industrial Sector Classifications: |
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Related Grants: |
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Panel History: |
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Summary on Grant Application Form |
Functionalised TTFs are pi-electron rich redox-active building blocks which, quite importantly, are stable to many synthetic transformations. In fact, a great variety of applications can be associated with the TTF systems, ranging from solid state electroconducting and magnetic properties of molecular organic metals to molecular/supramolecular systems involving reversible redox, intermolecular charge-transfer and hydrogen-bonding properties of TTF derivatives. This application supports the activities of a COST D31 network by providing funding for travel, consumables and subsistence for visits from four of the COST partners. The aims of the research projects presented here entertain a general theme for incorporating TTF species into thiophene based molecules and macromolecules. The target materials are potential components in electronic devices, such as field effect transistors, magnets and photovoltaics.
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Key Findings |
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Potential use in non-academic contexts |
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Impacts |
Description |
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Summary |
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Date Materialised |
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Sectors submitted by the Researcher |
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Project URL: |
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Further Information: |
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Organisation Website: |
http://www.strath.ac.uk |