0435162 - BFÚ 2015 RIV CH eng J - Článek v odborném periodiku
Fojt, Lukáš - Fojta, Miroslav - Grüner, Bohumír - Vespalec, Radim
Electrochemistry of parent and exo-skeletally substituted icosahedral monocarba and dicarbaboranes and their derivatives at the graphite carbon electrode in aqueous phosphate buffers.
Journal of Electroanalytical Chemistry. Roč. 730, SEP15 (2014), s. 16-19. ISSN 1572-6657. E-ISSN 1873-2569
Grant CEP: GA ČR(CZ) GBP206/12/G151
Institucionální podpora: RVO:68081707 ; RVO:61388980
Klíčová slova: Boranes * Carboranes * Glassy carbon electrode
Kód oboru RIV: BO - Biofyzika; CA - Anorganická chemie (UACH-T)
Impakt faktor: 2.729, rok: 2014 ; AIS: 0.575, rok: 2014
DOI: https://doi.org/10.1016/j.jelechem.2014.07.023

Electrochemistry of eight different boron clusters based on 12-vertex icosahedral framework has been studied in water-based electrolytes. This study revealed dependence of the electrochemical behavior on particular exo-skeletal substitution as well as on differences between previously studied divalent clos-o-dodecaborate anion and monovalent [CB11H12](-) anion. Electrochemical response of the latter ion retains the potential of that of the dodecaborate anion, but its relative intensity is considerably lower. Presence of two carbon atoms in parent neutral closo-1,2- and 1,7-dicarbaborane (ortho- and metacarborane) and their respective hydroxyderivative caused a shift of the electrochemical potential to lower values and higher peak sizes than for [CB11H12](-) anion. Most promising behavior for analytical determination in water-based interfaces was found for clusters substituted by OH group. (C) 2014 Elsevier B.V. All rights reserved.
Trvalý link: http://hdl.handle.net/11104/0239090