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Self-Aggregates of Cationic meso-Tetratolylporphyrins in Aqueous Solutions

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    SYSNO ASEP0181586
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JOstatní články
    TitleSelf-Aggregates of Cationic meso-Tetratolylporphyrins in Aqueous Solutions
    Author(s) Kubát, Pavel (UFCH-W) RID, ORCID, SAI
    Lang, Kamil (UACH-T) SAI, RID, ORCID
    Procházková, Kristýna (UFCH-W)
    Anzenbacher Jr., P. (US)
    Source TitleLangmuir. - : American Chemical Society - ISSN 0743-7463
    Roč. 19, č. 2 (2003), s. 422-428
    Number of pages7 s.
    Languageeng - English
    CountryUS - United States
    Keywordsporphyrins ; DNA ; point-dipole
    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)
    CEZAV0Z4032918 - UACH-T
    AV0Z4040901 - UFCH-W
    AnnotationAggregation properties of meso-tetratolylporphyrins bearing cationic substituents of a lipophilic nature such as ammonium, pyridinium, phosphonium, sulfonium, and isothiouronium were studied by UV/vis and resonance light scattering spectroscopy. The exciton point-dipole approximation was used to predict the structural alignment of the porphyrin units within the aggregate. The contribution of various types of aggregates depends on the porphyrin substitution, ionic strength, and temperature of aqueous solution of the porphyrin. In general, the preferred structure of an aggregate formed by temperature-induced aggregation is the J-aggregate exhibiting the characteristically narrow, red-shifted Soret band indicating a parallel "side-by-side" arrangement of the porphyrin units. The formation of aggregates of cationic tetratolylporphyrins is controlled by both electrostatic and hydrophobic interactions, Observed aggregation properties of porphyrin derivatives bearing trimethylammonium.
    WorkplaceJ. Heyrovsky Institute of Physical Chemistry
    ContactMichaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196
    Year of Publishing2004

Number of the records: 1  

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