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Meso-Tetratolylporphyrins Substituted by Pyridinium Groups: Aggregation, Photophysical Properties and Complexation with DNA

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    SYSNO ASEP0101107
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JOstatní články
    TitleMeso-Tetratolylporphyrins Substituted by Pyridinium Groups: Aggregation, Photophysical Properties and Complexation with DNA
    TitleMeso-tetratolyl porfyrinové deriváty substituované pyridiovými skupinami: agregace, fotofyzikální vlastnosti a komplexace s DNA
    Author(s) Procházková, Kristina (UFCH-W)
    Zelinger, Zdeněk (UFCH-W) RID, ORCID
    Lang, Kamil (UACH-T) SAI, RID, ORCID
    Kubát, Pavel (UFCH-W) RID, ORCID, SAI
    Source TitleJournal of Physical Organic Chemistry. - : Wiley - ISSN 0894-3230
    Roč. 17, - (2004), s. 890-897
    Number of pages8 s.
    Languageeng - English
    CountryGB - United Kingdom
    Keywordsporphyrin ; aggregates ; DNA
    Subject RIVCF - Physical ; Theoretical Chemistry
    R&D ProjectsGA203/01/0634 GA ČR - Czech Science Foundation (CSF)
    GA203/02/0420 GA ČR - Czech Science Foundation (CSF)
    GA203/04/0426 GA ČR - Czech Science Foundation (CSF)
    CEZAV0Z4040901 - UFCH-W
    AV0Z4032918 - UACH-T
    AnnotationAggregation of meso-tetratolylporphyrins substituted with two (P2), three (P3) and four (P4) pyridinium groups and their complexation with DNA were studied using UV/Vis and fluorescence spectroscopies, resonance light scattering and circular dichroism. In aqueous solution porphyrins P2-P4 existed in a monomeric form and/or as H- and J-aggregates. The concentration ratio of monomer/aggregates was controlled by the number of cationic substituents, by ionic strength and by temperature. Porphyrin monomers were externally bound to calf thymus DNA with the binding constant of /~106 M-1. Porphyrin aggregates formed chiral assemblies on the DNA template not affecting the duplex melting point. The lifetime of the triplet states of bound monomeric P3 and P4 increased after binding, however it did not prevent the formation of 1O2.
    WorkplaceJ. Heyrovsky Institute of Physical Chemistry
    ContactMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Year of Publishing2005
Number of the records: 1  

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