Počet záznamů: 1  

Determination of binding constants of cyclodextrin complexes with metal polypyridyl species by affinity CE using their ionic strength corrected and uncorrected actual mobilities

  1. 1.
    SYSNO ASEP0538653
    Druh ASEPA - Abstrakt
    Zařazení RIVZáznam nebyl označen do RIV
    Zařazení RIVNení vybrán druh dokumentu
    NázevDetermination of binding constants of cyclodextrin complexes with metal polypyridyl species by affinity CE using their ionic strength corrected and uncorrected actual mobilities
    Tvůrce(i) Sázelová, Petra (UOCHB-X) RID, ORCID
    Koval, Dušan (UOCHB-X) RID, ORCID
    Severa, Lukáš (UOCHB-X) RID, ORCID
    Teplý, Filip (UOCHB-X) RID, ORCID
    Vigh, G. (US)
    Kašička, Václav (UOCHB-X) RID, ORCID
    Zdroj.dok.Czech Chemical Society Symposium Series - ISSN 2336-7202
    Roč. 18, č. 3 (2020), s. 82
    Poč.str.1 s.
    Forma vydáníTištěná - P
    AkceSjezd českých a slovenských chemických společností /72./
    Datum konání06.09.2020 - 09.09.2020
    Místo konáníPraha
    ZeměCZ - Česká republika
    Typ akceEUR
    Jazyk dok.eng - angličtina
    Země vyd.CZ - Česká republika
    Klíč. slovabinding constants ; affinity capillary electrophoresis ; ionic strength
    Vědní obor RIVCB - Analytická chemie, separace
    Obor OECDAnalytical chemistry
    CEPGA18-02597S GA ČR - Grantová agentura ČR
    Institucionální podporaUOCHB-X - RVO:61388963
    AnotaceThe apparent binding constants and limiting mobilities of the multiply charged complexes of the Δ- and Λenantiomers of [Ru(bpy)3] 2+, [Ru(phen)3] 2+ and [Fe(phen)3] 2+ associates1 with 2,3-diacetylated-6-sulfated-(α,β,γ)- cyclodextrins (CDs) were determined by affinity capillary electrophoresis (ACE)2 . Two limiting models were tested for the ionic strength correction of the actual mobilities based on an empirical relation for the ionic strength correction of multivalent ionic species3 . In model 1, the nominal values of the charge numbers (zS,nom) and analytical concentrations (cS,nom) of the above CD selectors in the background electrolytes (BGEs) were applied for calculation of the BGE ionic strength, as usually. In model 2, the CD selectors were considered as singly charged species (zS = –1) with |zS,nom|-times higher concentrations in the BGE than their analytical concentrations (cS = |zS,nom| × cS,nom) in the calculation of the BGE ionic strength. In all three cases – with uncorrected actual mobilities as well as with actual mobilities corrected according to the two limiting models – the measured effective mobilities of the above enantiomers fit well the theoretical curves of their mobility dependences on the CD selectors concentrations in the BGE, with high average coefficients of determination (R2 = 0.9890–0.9995). The best physico-chemically meaningful values of the apparent binding constants and the limiting mobilities of the enantiomer-CDs complexes with low RSDs were obtained using the actual mobilities of the species involved corrected according to model 2.
    PracovištěÚstav organické chemie a biochemie
    Kontaktasep@uochb.cas.cz ; Kateřina Šperková, Tel.: 232 002 584 ; Jana Procházková, Tel.: 220 183 418
    Rok sběru2021
Počet záznamů: 1  

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