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Redox potentials and binding enhancement of fullerene and fullerene-cyclodextrin systems in water and dimethylsulfoxide

  1. 1.
    SYSNO ASEP0334005
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleRedox potentials and binding enhancement of fullerene and fullerene-cyclodextrin systems in water and dimethylsulfoxide
    TitleRedox potenciály a zvýšení komplexace fullerenu a systémů fullerene=cyklodextrin ve vodě dimethylsulfoxidu
    Author(s) Pospíšil, Lubomír (UFCH-W) RID, ORCID
    Hromadová, Magdaléna (UFCH-W) RID, ORCID, SAI
    Gál, Miroslav (UFCH-W)
    Kocábová, Jana (UFCH-W) RID
    Sokolová, Romana (UFCH-W) RID, ORCID, SAI
    Filippone, S. (FR)
    Yang, J. (FR)
    Guan, Z. (FR)
    Rassat, A. (FR)
    Zhang, Y. (FR)
    Source TitleCarbon. - : Elsevier - ISSN 0008-6223
    Roč. 48, č. 1 (2010), s. 153-162
    Number of pages10 s.
    Languageeng - English
    CountryUS - United States
    Keywordselectrochemistry ; fullerenes ; fullerene-cyclodextrin systems
    Subject RIVCG - Electrochemistry
    R&D ProjectsGA203/09/0705 GA ČR - Czech Science Foundation (CSF)
    GA203/08/1157 GA ČR - Czech Science Foundation (CSF)
    GP203/09/P502 GA ČR - Czech Science Foundation (CSF)
    LC510 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    ME09114 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    OC 140 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    CEZAV0Z40400503 - UFCH-W (2005-2011)
    UT WOS000272018800019
    DOI10.1016/j.carbon.2009.08.043
    AnnotationThe formal redox potentials of electron transfer reactions of fullerene, methanofullerene, fullerene-cyclodextrin complex and methanofullerene conjugates with cyclodextrins in aqueous and dimethylsulfoxide solutions are reported. These new compounds are surface active and retain the redox activity of C-60 even in aqueous medium. Compounds have been characterized by an electrochemical admittance technique, which offers an advantage of separating faradaic and capacitive properties. Observed difference of formal redox potentials of the free fullerene forms and their cyclodextrin-containing compounds were used to determine the binding enhancement. Results are interpreted in terms of inter-molecular host-guest interactions of C-60-cyclodextrin conjugates.
    WorkplaceJ. Heyrovsky Institute of Physical Chemistry
    ContactMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Year of Publishing2010
Number of the records: 1  

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