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Sökning: onr:"swepub:oai:research.chalmers.se:8acf1c89-b996-4db5-a357-ca087a838804" > Mixed valence radic...

Mixed valence radical cations and intermolecular complexes derived from indenofluorene-extended tetrathiafulvalenes

Christensen, M. A. (författare)
Köpenhamns universitet,University of Copenhagen
Parker, C. R. (författare)
Köpenhamns universitet,University of Copenhagen
Sorensen, T. J. (författare)
Köpenhamns universitet,University of Copenhagen
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de Graaf, Sebastian Erik, 1986 (författare)
Chalmers tekniska högskola,Chalmers University of Technology
Morsing, T. J. (författare)
Köpenhamns universitet,University of Copenhagen
Brock-Nannestad, T. (författare)
Köpenhamns universitet,University of Copenhagen
Bendix, J. (författare)
Köpenhamns universitet,University of Copenhagen
Haley, M. M. (författare)
University of Oregon
Rapta, P. (författare)
Slovak University of Technology Bratislava
Danilov, Andrey, 1961 (författare)
Chalmers tekniska högskola,Chalmers University of Technology
Kubatkin, Sergey, 1959 (författare)
Chalmers tekniska högskola,Chalmers University of Technology
Hammerich, O. (författare)
Köpenhamns universitet,University of Copenhagen
Nielsen, M. B. (författare)
Köpenhamns universitet,University of Copenhagen
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 (creator_code:org_t)
2014-10-20
2014
Engelska.
Ingår i: Journal of Materials Chemistry C. - : Royal Society of Chemistry (RSC). - 2050-7526 .- 2050-7534. ; 2:48, s. 10428-10438
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Engineering of mixed-valence (MV) radical cations and intermolecular complexes based on pi-extended tetrathiafulvalenes (TTFs) is central for the development of organic conductors. On another front, redox-controlled dimerization of radical cations has recently been recognized as an important tool in supramolecular chemistry. Here we show that pi-extended TTFs based on the indenofluorene core, prepared by Horner-Wadsworth-Emmons reactions, undergo reversible and stepwise one-electron oxidations and that the detectable, intermediate radical cation forms remarkably strong intermolecular MV ([neutral.cation]) and pi-dimer ([cation.cation]) complexes with near-infrared radical cation absorptions. The radical cation itself seems to be a so-called Class III MV species in the Robin-Day classification. The formation of MV dimers was corroborated by ESR spectroelectrochemical studies, revealing two slightly different ESR signals upon oxidation, one assigned to the MV dimer and the other to the cation monomer. Crystals of the radical cation with different anions (PF6- , BF4-, and TaF6-) were grown by electrocrystallization. Conductance studies revealed that the salts behave as semiconductors with the hexafluorotantalate salt exhibiting the highest conductance. Using a custom-built ESR spectrometer with sub-femtomole sensitivity, the magnetic properties of one crystal were investigated. While the spin-to-spin interaction between radical cations was negligible, a high cooperativity coupling to the microwave field was observed - as a result of an exceptionally narrow spin line width and high spin density. This could have great potential for applications in quantum computation where crystalline spin ensembles are exploited for their long coherence times.

Ämnesord

TEKNIK OCH TEKNOLOGIER  -- Materialteknik (hsv//swe)
ENGINEERING AND TECHNOLOGY  -- Materials Engineering (hsv//eng)
TEKNIK OCH TEKNOLOGIER  -- Annan teknik (hsv//swe)
ENGINEERING AND TECHNOLOGY  -- Other Engineering and Technologies (hsv//eng)

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