Journal
CHEMPHYSCHEM
Volume 14, Issue 8, Pages 1670-1675Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/cphc.201300107
Keywords
donoracceptor systems; EPR spectroscopy; fullerenes; perchlorotriphenylmethide; UV; Vis spectroscopy
Funding
- Spanish Direccion General de Investigacion (DGI) [CTQ2010-19501/BQU]
- Generalitat de Catalunya [2009SGR00516]
- bilateral CSIC-NFBR project [2008RU0073]
- RFBR [09-03-91291-INIS-a, 13-03-01291-a]
- Presidium of the RAS [8]
- European project ERC StG [2012-306826]
- CIBER-BBN
- VI National RDi Plan
- Iniciativa Ingenio
- Consolider Program
- CIBER Actions
- Instituto de Salud Carlos III
- European Regional Development Fund
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We show that electron transfer from the perchlorotriphenylmethide anion (PTM) to Y@C82(C2v) is an instantaneous process, suggesting potential applications for using PTM to perform redox titrations of numerous endohedral metallofullerenes. The first representative of a Y@C82-based salt containing the complex cation was prepared by treating Y@C82(C2v) with the [K+([18]crown-6)]PTM salt. The synthesis developed involves the use of the [K+([18]crown-6)]PTM salt as a provider of both a complex cation and an electron-donating anion that is able to reduce Y@C82(C2v). For the first time, the molar absorption coefficients for neutral and anionic forms of the pure isomer of Y@C82(C2v) were determined in organic solvents with significantly different polarities.
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